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Nutrients, Volume 12, Issue 4 (April 2020) – 323 articles

Cover Story (view full-size image): Treating sarcopenia in older individuals remains a challenge, and nutritional interventions present promising approaches in individuals that perform limited physical exercise. We assessed the efficacy of leucine administration to evaluate whether the regular intake of this essential amino acid can improve muscle mass, muscle strength and functional performance and respiratory muscle function in institutionalized older individuals.View this paper.
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22 pages, 517 KiB  
Article
Social-Psychological Factors in Food Consumption of Rural Residents: The Role of Perceived Need and Habit within the Theory of Planned Behavior
by Jiaqi Huang, Gerrit Antonides and Fengying Nie
Nutrients 2020, 12(4), 1203; https://doi.org/10.3390/nu12041203 - 24 Apr 2020
Cited by 20 | Viewed by 6074
Abstract
To address the problem of malnutrition in poor rural areas of China, this study aims to examine the effects of social-psychological factors in food consumption of rural residents in poor counties of Southwest China. In addition, it investigates the role of perceived need [...] Read more.
To address the problem of malnutrition in poor rural areas of China, this study aims to examine the effects of social-psychological factors in food consumption of rural residents in poor counties of Southwest China. In addition, it investigates the role of perceived need and habit within the theory of planned behavior (TPB) in predicting food consumption. A survey with random sampling was conducted on rural residents (n = 424), and the theoretical frameworks of both the standard and extended TPB were applied for comparison purposes. Structural equation modeling was applied to test the relationships among constructs. Consumption of five food items was studied, respectively: meat, eggs, dairy, fish, and fruits. Results showed that incorporation of perceived need and habit substantially increased the explanatory power of the TPB, but these factors only had significant direct effects on intention rather than behavior. Perceived need and habit are stronger predictors of intention than any other TPB construct for consumption of all food items except for meat. We found indirect effects of the constructs in the extended TPB model on consumption to be different across food items. Practical implications to improve consumption of different food items were proposed accordingly. Full article
(This article belongs to the Section Nutrition and Public Health)
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<p>Specification of the extended theory of planned behavior (TPB) model and tested hypotheses.</p>
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18 pages, 1966 KiB  
Article
Monobutyrin and Monovalerin Affect Brain Short-Chain Fatty Acid Profiles and Tight-Junction Protein Expression in ApoE-Knockout Rats Fed High-Fat Diets
by Thao Duy Nguyen, Frida Fåk Hållenius, Xue Lin, Margareta Nyman and Olena Prykhodko
Nutrients 2020, 12(4), 1202; https://doi.org/10.3390/nu12041202 - 24 Apr 2020
Cited by 18 | Viewed by 4936
Abstract
Monobutyrin (MB) and monovalerin (MV), esters of short-chain fatty acids (SCFAs), have previously been shown to reduce liver cholesterol and inflammation in conventional rats fed high-fat diets. This study explored the potential effects of MB and MV in hypercholesterolemic apolipoprotein E-knockout (ApoE-/-) rats. [...] Read more.
Monobutyrin (MB) and monovalerin (MV), esters of short-chain fatty acids (SCFAs), have previously been shown to reduce liver cholesterol and inflammation in conventional rats fed high-fat diets. This study explored the potential effects of MB and MV in hypercholesterolemic apolipoprotein E-knockout (ApoE-/-) rats. ApoE-/- rats were fed three high-fat (HF) diets, pure or supplemented with MB or MV (1%), for 5 weeks. One group of conventional rats (C) was also fed the pure high-fat diet and another group of ApoE-/- rats a low-fat (LF) diet. Blood and liver lipids, urinary lactulose/mannitol, SCFAs (blood and brain), tight junction proteins (small intestine and brain), and inflammation-related markers (blood, brain, and liver) were analyzed. MV supplementation elevated serum high-density lipoprotein (HDL) cholesterol and valeric acid concentration (p < 0.05), while the amounts of isovaleric acid in the brain were reduced (p < 0.05). MB increased butyric acid amounts in the brain, while the plasma concentration of interleukin 10 (IL-10) was lowered (p < 0.05). Both MV and MB upregulated the expression of occludin and zonula occludens-1 (ZO-1) in the brain (p < 0.05). Supplementation of MB or MV affected HDL cholesterol, the expression of tight junction proteins, and SCFA profiles. MB and MV may therefore be promising supplements to attenuate lipid metabolic disorders caused by high-fat intake and genetic deficiency. Full article
(This article belongs to the Special Issue Diet, Gut Microbiota and Metabolic Disorders)
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<p>Changes in (<b>a</b>) lactulose (µM), (<b>b</b>) mannitol (mM), and (<b>c</b>) lactulose/mannitol in urine, and mucosal thickness (µm) in the (<b>d</b>) duodenum and (<b>e</b>) jejunum of conventional rats fed a pure high-fat diet (C), or Apolipoprotein E-knockout (ApoE-/-) rats fed a low-fat diet (LF) or high-fat diet (HF), pure or supplemented with 1% monobutyrin (MB) or monovalerin (MV) for 5 weeks (<span class="html-italic">n</span> = 10/group). Rats from the C, HF, MB, MV and LF groups are shown as ●, ■, ▼, ♦ and ▲, respectively. Values are means ± SEM. * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01.</p>
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<p>Gene expression of tight junction proteins (zonula occludens (ZO)-1 and occludin) and short-chain fatty acid receptors (G-protein-coupled receptor 43/GPR43 and GPR109A) in the jejunal (<b>a</b>–<b>d</b>) and brain (<b>e</b>–<b>h</b>) tissues of conventional rats fed a pure high-fat diet (C), or Apolipoprotein E-knockout (ApoE-/-) rats fed a low-fat diet (LF) or high-fat diet (HF), pure or supplemented with 1% monobutyrin (MB) or monovalerin (MV) for 5 weeks (<span class="html-italic">n</span> = 8–10/group). Rats from the C, HF, MB, MV and LF groups are shown as ●, ■, ▼, ♦ and ▲, respectively. Box and whisker plots with error bars indicate minimum and maximum values, while central lines represent median and means shown as “+”. * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01.</p>
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<p>Changes in cytokines and liver enzymes in conventional rats fed a pure high-fat diet (C), or Apolipoprotein E-knockout (ApoE-/-) rats fed a low-fat diet (LF) or high-fat diet (HF), pure or supplemented with 1% monobutyrin (MB) or monovalerin (MV) for 5 weeks (<span class="html-italic">n</span> = 8/group). Interleukin-1beta (IL-1β, pg/mL) in (<b>a</b>) aortic plasma and (<b>b</b>) brain homogenates, (<b>c</b>) aortic plasma IL-10 (pg/mL), and (<b>d</b>) portal vein serum alanine transaminase activity (ALT) activity (mU/mL). Rats from the C, HF, MB, MV and LF groups are shown as ●, ■, ▼, ♦ and ▲, respectively. Data are presented as means ± SEM. * <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>Total weight gain (<b>a</b>), final body weight (<b>b</b>), and food efficiency ratio (<b>c</b>) in conventional rats fed a pure high-fat diet (C), or Apolipoprotein E-knockout (ApoE-/-) rats fed a low-fat diet (LF) or high-fat diet (HF), pure or supplemented with 1% monobutyrin (MB) or monovalerin (MV) for 5 weeks (<span class="html-italic">n</span> = 10/group). Rats from the C, HF, MB, MV and LF groups are shown as ●, ■, ▼, ♦ and ▲, respectively. Data are presented as means ± SEM. * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01, *** <span class="html-italic">p</span> &lt; 0.001.</p>
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<p>Projection to Latent Structures-Discriminant Analysis (PLS-DA) plot summaries of the effects of monobutyrin (MB) and monovalerin (MV) on short-chain fatty acids (SCFAs) and biomarkers in conventional rats fed a pure high-fat diet (C), or Apolipoprotein E-knockout (ApoE-/-) rats fed a low-fat diet (LF) or high-fat diet, pure (HF) or supplemented with 1% MB or MV for 5 weeks. (<b>a</b>) The score scatter plot shows separation patterns among the groups, with each circle denoting one rat having all values of the variables included in the loading plot; (<b>b</b>) alterations of the measured variables (shown as 4-angle stars) as an effect of the experimental diets (shown as circles). ACE, acetic acid; BUT, butyric acid; PRO, propionic acid; ISV, isovaleric acid; VAL, valeric acid; ALT, alanine transaminase, IL, interleukin; HDL-c, high-density lipoprotein cholesterol; br, brain; si; small intestine; ZO-1, zonula occludens-1; GPR, G-protein-coupled receptor.</p>
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15 pages, 1077 KiB  
Article
Plasma Adipokines Profile in Prepubertal Children with a History of Prematurity or Extrauterine Growth Restriction
by María Dolores Ordóñez-Díaz, Mercedes Gil-Campos, Katherine Flores-Rojas, María Carmen Muñoz-Villanueva, Concepción María Aguilera-García, María Jose de la Torre-Aguilar and Juan Luis Pérez-Navero
Nutrients 2020, 12(4), 1201; https://doi.org/10.3390/nu12041201 - 24 Apr 2020
Cited by 6 | Viewed by 3365
Abstract
Adipose tissue programming could be developed in very preterm infants with extrauterine growth restriction (EUGR), with an adverse impact on long-term metabolic status, as was studied in intrauterine growth restriction patterns. The aim of this cohort study was to evaluate the difference in [...] Read more.
Adipose tissue programming could be developed in very preterm infants with extrauterine growth restriction (EUGR), with an adverse impact on long-term metabolic status, as was studied in intrauterine growth restriction patterns. The aim of this cohort study was to evaluate the difference in levels of plasma adipokines in children with a history of EUGR. A total of 211 school age prepubertal children were examined: 38 with a history of prematurity and EUGR (EUGR), 50 with a history of prematurity with adequate growth (PREM), and 123 healthy children born at term. Anthropometric parameters, blood pressure, metabolic markers and adipokines (adiponectin, resistin, leptin) were measured. Children with a history of EUGR showed lower values of adiponectin (μg/mL) compared with the other two groups: (EUGR: 10.6 vs. PREM: 17.7, p < 0.001; vs. CONTROL: 25.7, p = 0.004) and higher levels of resistin (ng/mL) (EUGR: 19.2 vs. PREM: 16.3, p =0.007; vs. CONTROL: 7.1, p < 0.001. The PREM group showed the highest values of leptin (ng/mL), compared with the others: PREM: 4.9 vs. EUGR: 2.1, p = 0.048; vs. CONTROL: 3.2, p = 0.029). In conclusion, EUGR in premature children could lead to a distinctive adipokines profile, likely associated with an early programming of the adipose tissue, and likely to increase the risk of adverse health outcomes later in life. Full article
(This article belongs to the Section Nutrition and Metabolism)
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<p>Concentration of adiponectin (<b>A</b>), leptin (<b>B</b>) and resistin (<b>C</b>) in prepubertal children with a history of prematurity and extrauterine growth restriction (EUGR) (<span class="html-italic">n</span> = 38), premature without EUGR (PREM) (<span class="html-italic">n =</span> 50) and control children (<span class="html-italic">n =</span> 123). Values are expressed as medians and interquartile ranges. * Median value was significantly different from that of the PREM group with <span class="html-italic">p</span> &lt; 0.05. ** Median value was significantly different from that of the CONTROL group with <span class="html-italic">p</span> &lt; 0.05 (Mann–Whitney <span class="html-italic">U</span> test). <span class="html-italic">p</span>, probability adjusted for gestational age, birth weight and length. Adiponectin: EUGR vs. PREM <span class="html-italic">p</span> &lt; 0.001, EUGR vs. CONTROL <span class="html-italic">p</span> &lt; 0.001; PREM vs. CONTROL <span class="html-italic">p</span> = 0.004. Leptin: EUGR vs. PREM <span class="html-italic">p</span> = 0.048, EUGR vs. CONTROL <span class="html-italic">p</span> = 0.214, PREM vs. CONTROL <span class="html-italic">p</span> = 0.029. Resistin: EUGR vs. PREM <span class="html-italic">p</span>= 0.007, EUGR vs. CONTROL <span class="html-italic">p</span> &lt; 0.001, PREM vs. CONTROL <span class="html-italic">p</span> &lt; 0.001.</p>
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<p>Concentration of adiponectin (<b>A</b>), leptin (<b>B</b>) and resistin (<b>C</b>) in prepubertal children with a history of prematurity and extrauterine growth restriction (EUGR) (<span class="html-italic">n</span> = 38), premature without EUGR (PREM) (<span class="html-italic">n =</span> 50) and control children (<span class="html-italic">n =</span> 123). Values are expressed as medians and interquartile ranges. * Median value was significantly different from that of the PREM group with <span class="html-italic">p</span> &lt; 0.05. ** Median value was significantly different from that of the CONTROL group with <span class="html-italic">p</span> &lt; 0.05 (Mann–Whitney <span class="html-italic">U</span> test). <span class="html-italic">p</span>, probability adjusted for gestational age, birth weight and length. Adiponectin: EUGR vs. PREM <span class="html-italic">p</span> &lt; 0.001, EUGR vs. CONTROL <span class="html-italic">p</span> &lt; 0.001; PREM vs. CONTROL <span class="html-italic">p</span> = 0.004. Leptin: EUGR vs. PREM <span class="html-italic">p</span> = 0.048, EUGR vs. CONTROL <span class="html-italic">p</span> = 0.214, PREM vs. CONTROL <span class="html-italic">p</span> = 0.029. Resistin: EUGR vs. PREM <span class="html-italic">p</span>= 0.007, EUGR vs. CONTROL <span class="html-italic">p</span> &lt; 0.001, PREM vs. CONTROL <span class="html-italic">p</span> &lt; 0.001.</p>
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13 pages, 588 KiB  
Article
Food Involvement, Eating Restrictions and Dietary Patterns in Polish Adults: Expected Effects of Their Relationships (LifeStyle Study)
by Marzena Jezewska-Zychowicz, Jerzy Gębski and Milena Kobylińska
Nutrients 2020, 12(4), 1200; https://doi.org/10.3390/nu12041200 - 24 Apr 2020
Cited by 22 | Viewed by 5506
Abstract
Understanding the factors that coexist with healthy and unhealthy eating behaviors is prevalent and important for public health. The aim of this study was to investigate the associations between food involvement, eating restrictions, and dietary patterns in a representative sample of Polish adults. [...] Read more.
Understanding the factors that coexist with healthy and unhealthy eating behaviors is prevalent and important for public health. The aim of this study was to investigate the associations between food involvement, eating restrictions, and dietary patterns in a representative sample of Polish adults. The study was conducted among a group of 1007 adults. Questions with the answers yes or no were used to obtain the data regarding eating restrictions. Data relating to food involvement were obtained with the Food Involvement Scale (FIS). Questions from the Beliefs and Eating Habits questionnaire were used to measure the frequency of consumption of different food groups. Five dietary patterns (DPs) were derived using principal component analysis (PCA), i.e., ‘Fruit and vegetables’, ‘Wholemeal food’, ‘Fast foods and sweets’, ‘Fruit and vegetable juices’ and “Meat and meat products’. In each of the DPs, three groups of participants were identified based on tertile distribution with the upper tertile denoting the most frequent consumption. Nearly two-thirds of the study sample declared some restrictions in food consumption. The probability of implementing restrictions in consumption of foods high in sugar, fat and high-fat foods increased in the upper tertile of ‘Fruit and vegetables’ and ‘Wholemeal’ DPs. Moreover, the probability of implementing restrictions in consumption of meat and high-starch products increased in ‘Wholemeal’ DP. The probability of using eating restrictions decreased in the upper tertile of ‘Fast foods and sweets’ and Meat and meat products’ DPs. In conclusion, individuals characterized by high food involvement were more inclined to use eating restrictions than individuals with lower food involvement. Their DPs were also healthier compared to those of individuals manifesting low food involvement. Therefore, promoting personal commitment to learning about and experiencing food may be an effective way of inducing a change of eating habits, and therefore a healthier diet. Full article
(This article belongs to the Special Issue Population-Based Nutrition Epidemiology)
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<p>Eating restrictions in the sample (%).</p>
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21 pages, 653 KiB  
Review
Microbial Adaptation Due to Gastric Bypass Surgery: The Nutritional Impact
by Silke Crommen, Alma Mattes and Marie-Christine Simon
Nutrients 2020, 12(4), 1199; https://doi.org/10.3390/nu12041199 - 24 Apr 2020
Cited by 15 | Viewed by 4926
Abstract
Bariatric surgery leads to sustained weight loss and the resolution of obesity-related comorbidities. Recent studies have suggested that changes in gut microbiota are associated with the weight loss induced by bariatric surgery. Several studies have observed major changes in the microbial composition following [...] Read more.
Bariatric surgery leads to sustained weight loss and the resolution of obesity-related comorbidities. Recent studies have suggested that changes in gut microbiota are associated with the weight loss induced by bariatric surgery. Several studies have observed major changes in the microbial composition following gastric bypass surgery. However, there are inconsistencies between the reported alterations in microbial compositions in different studies. Furthermore, it is well established that diet is an important factor shaping the composition and function of intestinal microbiota. However, most studies on gastric bypass have not assessed the impact of dietary intake on the microbiome composition in general, let alone the impact of restrictive diets prior to bariatric surgery, which are recommended for reducing liver fat content and size. Thus, the relative impact of bariatric surgery on weight loss and gut microbiota remains unclear. Therefore, this review aims to provide a deeper understanding of the current knowledge of the changes in intestinal microbiota induced by bariatric surgery considering pre-surgical nutritional changes. Full article
(This article belongs to the Section Clinical Nutrition)
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<p>Schematic Illustration Schematic illustration of the main gut microbial changes associated with successful (Responder) and poor (Non-Responder) weight loss after gastric bypass surgery and the possible impact of nutritional factors. Diet, physical activity, genes and gut microbiome composition are widely described factors leading to obesity. Following gastric bypass surgery, the individual response is affected by alterations in pH, bile flow, changes in gut hormones secretion, gut motility and medication usage. ↑—increase, ↓—decrease, ↔—unchanged.</p>
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19 pages, 2400 KiB  
Article
Kokumi Taste Active Peptides Modulate Salt and Umami Taste
by Mee-Ra Rhyu, Ah-Young Song, Eun-Young Kim, Hee-Jin Son, Yiseul Kim, Shobha Mummalaneni, Jie Qian, John R. Grider and Vijay Lyall
Nutrients 2020, 12(4), 1198; https://doi.org/10.3390/nu12041198 - 24 Apr 2020
Cited by 53 | Viewed by 7206
Abstract
Kokumi taste substances exemplified by γ-glutamyl peptides and Maillard Peptides modulate salt and umami tastes. However, the underlying mechanism for their action has not been delineated. Here, we investigated the effects of a kokumi taste active and inactive peptide fraction (500–10,000 Da) isolated [...] Read more.
Kokumi taste substances exemplified by γ-glutamyl peptides and Maillard Peptides modulate salt and umami tastes. However, the underlying mechanism for their action has not been delineated. Here, we investigated the effects of a kokumi taste active and inactive peptide fraction (500–10,000 Da) isolated from mature (FIIm) and immature (FIIim) Ganjang, a typical Korean soy sauce, on salt and umami taste responses in humans and rodents. Only FIIm (0.1–1.0%) produced a biphasic effect in rat chorda tympani (CT) taste nerve responses to lingual stimulation with 100 mM NaCl + 5 μM benzamil, a specific epithelial Na+ channel blocker. Both elevated temperature (42 °C) and FIIm produced synergistic effects on the NaCl + benzamil CT response. At 0.5% FIIm produced the maximum increase in rat CT response to NaCl + benzamil, and enhanced salt taste intensity in human subjects. At 2.5% FIIm enhanced rat CT response to glutamate that was equivalent to the enhancement observed with 1 mM IMP. In human subjects, 0.3% FIIm produced enhancement of umami taste. These results suggest that FIIm modulates amiloride-insensitive salt taste and umami taste at different concentration ranges in rats and humans. Full article
(This article belongs to the Special Issue Salt Taste, Nutrition, and Health)
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<p>Effect of FII<sub>im</sub> and FII<sub>m</sub> on the benzamil (Bz)-insensitive NaCl chorda tympani (CT) response. (<b>A</b>) Shows a representative trace in which the CT responses were monitored while the rat tongue was first superfused with a rinse solution (R) and then with a stimulating solution containing 100 mM NaCl + 5 μM Bz + FII<sub>m</sub> (0–1%) maintained at room temperature. The arrows represent the time periods when the rat tongue was superfused with R and the stimulating solutions. The data were normalized to the tonic response obtained with 0.3 M NH<sub>4</sub>Cl. (<b>B</b>) Shows the mean normalized tonic NaCl CT responses in different sets of 3 rats each while their tongues were first stimulated with R and then with NaCl + Bz solutions containing 0–1% of the FII<sub>m</sub> (●) or FII<sub>im</sub> (○) expressed in log units. The values are M ± SEM of 3 rats.</p>
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<p>Effect of resiniferatoxin (RTX), SB-377791 (SB), FII<sub>m</sub> and temperature on the benzamil (Bz)-insensitive NaCl chorda tympani (CT) response. (<b>A</b>) Shows a representative CT trace obtained while the rat tongue was first stimulated with rinse solution (R) and then with NaCl, NaCl + Bz, NaCl + Bz + 0.4% FII<sub>m</sub>, NaCl + Bz + 0.25 μM RTX, NaCl + Bz + 0.4% FII<sub>m</sub> + 0.25 μM RTX, NaCl + Bz + 1 μM SB and NaCl + Bz +SB + 0.4% FII<sub>m</sub> maintained at room temperature. The data were normalized to the tonic response obtained with 0.3 M NH<sub>4</sub>Cl. The arrows represent the time periods when the rat tongues were superfused with R and the stimulating solutions. (<b>B</b>) Shows a representative CT trace obtained while the rat tongue was first stimulated with R at 23 °C (R<sub>23</sub> <sub>°C</sub>) and then with NaCl + Bz (NaCl + Bz<sub>23</sub> <sub>°C</sub>), NaCl + Bz + 0.4% FII<sub>m</sub> at 23 °C (NaCl + Bz + FII<sub>m23</sub> <sub>°C</sub>), NaCl + Bz at 42 °C (NaCl + Bz<sub>42</sub> <sub>°C</sub>) and NaCl + Bz + 0.4% FII<sub>m</sub> at 42 °C (NaCl + Bz + FII<sub>m42</sub> <sub>°C</sub>). The trace also shows the CT response in the presence of NaCl + Bz + SB and NaCl + Bz + SB + 0.4% FII<sub>m</sub> maintained at 23 °C. The data were normalized to the tonic response obtained with 0.3 M NH<sub>4</sub>Cl. The arrows represent the time periods when the rat tongues were superfused with R and the stimulating solutions. (<b>C</b>) Shows the M ± SEM normalized rat tonic NaCl + Bz CT responses at 23 °C and 42 °C in the absence and presence of 0.4% FII<sub>m</sub>. All unpaired comparisons were made with respect to the normalized value of the tonic CT response to NaCl + Bz at 23 °C. * <span class="html-italic">p</span> = 0.0038; ** <span class="html-italic">p</span> = 0.0001; <span class="html-italic">n</span> = 3).</p>
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<p>Effects of FII<sub>m</sub> sub-fractions (FII<sub>m(a-d)</sub>) on the benzamil (Bz)-insensitive NaCl chorda tympani (CT) response. Representative CT responses showing the effect of adding varying concentrations of FII<sub>m</sub> sub-fractions FII<sub>ma</sub> (500–1000 Da) (<b>A</b>) and FII<sub>mc</sub> (1000–3000 Da) (<b>B</b>) on the rat CT responses to NaCl + Bz. The arrows represent the time period when the tongue was superfused with the rinse and stimulating solutions. In each rat the data were normalized to the tonic response obtained with 0.3M NH<sub>4</sub>Cl. (<b>C</b>) Shows the mean normalized tonic NaCl CT responses in different sets of 3 rats each while their tongues were first stimulated with R and then with NaCl + Bz solutions containing 0–1% of the four FII<sub>m</sub> sub-fractions in log units. The values are M ± SEM of 3 rats in each group. In each case the data were fitted to Equation (4).</p>
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<p>Effects of aromatic, neutral, acidic and basic FII<sub>m</sub> sub-fractions on the benzamil-insensitive NaCl chorda tympani (CT) response. (<b>A</b>) Shows the relationship between varying FII<sub>m</sub> sub-fraction concentrations expressed in log units and the mean normalized tonic NaCl CT response from 3 rats in each group for FII<sub>m</sub> (●), aromatic (○) and combined neutral, acidic and basic maillard reacted peptides (▲). (<b>B</b>) Shows the relationship between resiniferatoxin (RTX) concentrations expressed in log units and the mean normalized tonic NaCl CT responses from 3 rats (●). The values are M ± SEM of 3 rats in each group.</p>
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<p>Effect of i.p. injection of calcitonin gene related peptide (CGRP) on NaCl chorda tympani (CT) response. (<b>A</b>) Shows a representative CT trace obtained while the rat tongue was first stimulated with rinse solution (R) and then with 0.3M NH<sub>4</sub>Cl, 0.3M NaCl and 0.1M NaCl before and after i.p. injection of CGRP (68 μg/100 g BW in PBS). In each rat the data were normalized to the tonic response obtained with 0.3M NH<sub>4</sub>Cl. The values are M ± SEM of 3 rats in each group. (<b>B</b>) Shows summary of the data from 3 rats in each group injected with either 23 or 68 μg CGRP/100 g BW. Values are M ± SEM of 3 rats. * <span class="html-italic">p</span> = 0.017 (0.1M NaCl) and 0.009 (0.3M NaCl).</p>
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<p>Effect of amiloride and FII<sub>m</sub> on NaCl Preference in WT mice. (<b>A</b>) Shows NaCl Preference in WT mice when given a choice between H<sub>2</sub>O and varying concentrations of NaCl (3, 80, 100, 120, 150, 200 and 300 mM) in the absence (○) and presence of 10 µM amiloride (●). The values are presented as mean (M) ± SEM of <span class="html-italic">n</span>, where <span class="html-italic">n</span> = 7–10. * <span class="html-italic">p</span> = 0.02; ** <span class="html-italic">p</span> = 0.0134; *** <span class="html-italic">p</span> = 0.0024; **** <span class="html-italic">p</span> = 0.0001. (<b>B</b>) Shows NaCl Preference in WT mice when given a choice between H<sub>2</sub>O and 100 mM NaCl (○) or H<sub>2</sub>O and 100 mM NaCl + 10 µM amiloride (●) containing increasing concentrations of FII<sub>m</sub> (0.1 to 1%). * <span class="html-italic">p</span> = 0.0086; ** <span class="html-italic">p</span> = 0.0018; *** <span class="html-italic">p</span> = 0.0001 (<span class="html-italic">n</span> = 10). Dotted line represents the indifference value.</p>
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<p>Effect of FII<sub>m</sub> and FII<sub>im</sub> on human salt taste intensity. Shows the effect of varying concentrations (0.03 and 1.0%) of FII<sub>im</sub> (○) and FII<sub>m</sub> (●) expressed in log units on human salt taste intensity. R1 corresponds to the intensity (2.5) of 0.2% NaCl and R2 corresponds to the intensity (5.0) of 0.35% NaCl. FII<sub>m</sub> showed a significant (* <span class="html-italic">p</span> = 0.01) salt taste-enhancing activity at 0.003% and 0.005%. In contrast, no effect of FII<sub>im</sub> was observed on human salt taste intensity over the concentration range between 0.03 and 1.0%.</p>
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<p>Effect of FII<sub>m</sub> on the glutamate chorda tympani (CT) response and human umami taste sensory evaluation. (<b>A</b>) Shows a representative CT response in which the rat tongue was first rinsed with the rinse solution (R) and then with 100 mM MSG + 5 µM benzamil (Bz) + 1 µM SB-366791 (SB), MSG + Bz + SB +1 mM IMP, MSG + Bz + SB + 1% FII<sub>m</sub> and MSG + Bz + SB + 2.5% FII<sub>m</sub>. The arrows represent the time period when the tongue was superfused with the rinse and stimulating solutions. (<b>B</b>) Shows mean normalized tonic CT responses from 3 rats. In each rat the data were normalized to the tonic response obtained with 0.3 M NH<sub>4</sub>Cl. * <span class="html-italic">p</span> = 0.001. (<b>C</b>) Shows the effect of adding increasing concentrations of FII<sub>m</sub> (0.003 to 0.3%) to the 0.04% Fish Soup Base (open bars) or to H<sub>2</sub>O (filled bars). The values are presented as M ± SEM of n, where n represents the number of panel members tested. * <span class="html-italic">p</span> = 0.01.</p>
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15 pages, 267 KiB  
Article
Better Dietary Knowledge and Socioeconomic Status (SES), Better Body Mass Index? Evidence from China—An Unconditional Quantile Regression Approach
by Jie Yu, Xiao Han, Hongxing Wen, Jinzheng Ren and Lihong Qi
Nutrients 2020, 12(4), 1197; https://doi.org/10.3390/nu12041197 - 24 Apr 2020
Cited by 15 | Viewed by 5006
Abstract
Obesity is a rapidly growing public health threat in China. Improvement of dietary knowledge may potentially reduce the risk of obesity and being overweight. However, existing studies focus on measuring the mean effects of nutrition knowledge on body mass index (BMI). There is [...] Read more.
Obesity is a rapidly growing public health threat in China. Improvement of dietary knowledge may potentially reduce the risk of obesity and being overweight. However, existing studies focus on measuring the mean effects of nutrition knowledge on body mass index (BMI). There is a lack of literature on the effect of dietary knowledge on BMI, and the potential heterogeneity of the effect across the whole BMI distribution and across socioeconomic status (SES) groups. This study aims to investigate the heterogeneous nature of the relationship between dietary knowledge, SES, and BMI, using data from the China Health and Nutrition Survey (CHNS) in 2015. We employed unconditional quantile regression (UQR) to assess how the relationship between dietary knowledge, SES, and BMI varies across the whole BMI distribution, and conducted subgroup analyses using different socio-economic subsamples. Results indicate that dietary knowledge had no statistically significant impact on BMI across the BMI distribution. There was a large degree of heterogeneity in the SES effect across the BMI distribution as well as a major gender difference in the SES effect on BMI. Education had a significant and inverse association with BMI across the BMI distribution, greater at higher BMI quantiles. Income growth had a larger effect on the 50th quantile of BMI for males in the middle-income group, but was not significant for females. As income increased, males without college educations had higher BMI while females with college or higher education generally had lower BMI. The findings of this study reveal the heterogeneous nature of the relationship between SES, gender, and obesity across the entire BMI distribution, suggesting that quantile regressions might offer a valuable framework for exploring the complex relationship of dietary knowledge, demographic, and socio-economic factors on obesity. Full article
(This article belongs to the Section Nutrition and Public Health)
15 pages, 586 KiB  
Article
Proinflammatory Dietary Intake is Associated with Increased Risk of Metabolic Syndrome and Its Components: Results from the Population-Based Prospective Study
by Imran Khan, Minji Kwon, Nitin Shivappa, James R. Hébert and Mi Kyung Kim
Nutrients 2020, 12(4), 1196; https://doi.org/10.3390/nu12041196 - 24 Apr 2020
Cited by 26 | Viewed by 4391
Abstract
Metabolic syndrome (MetS) is a major public health challenge throughout the world, although studies on its association with the inflammatory potential of diet are inconsistent. The aim of this prospective study was to assess the association between the Dietary Inflammatory Index (DII® [...] Read more.
Metabolic syndrome (MetS) is a major public health challenge throughout the world, although studies on its association with the inflammatory potential of diet are inconsistent. The aim of this prospective study was to assess the association between the Dietary Inflammatory Index (DII®) and the risk of MetS and its components in a Korean population. Data from 157,812 Korean adults (mean age 52.8 years; 53,304 men and 104,508 women with mean follow-up of 7.4 years) collected by members of the Korean Genome and Epidemiology Study form the basis for this report. DII scores were calculated based on Semi-Quantitative Food-Frequency Questionnaire data. Multivariable-adjusted Cox proportional hazard models were used to estimate the association between DII scores and MetS. In women, higher DII scores (pro-inflammatory diet) increased the risk of MetS (hazard ratio [HR]quintile5 v. 1 1.43; 95% confidence interval (CI) 1.21–1.69; p for trend ≤ 0.0001) and its five components. A positive association was observed for postmenopausal women, with a 50% higher risk of developing MetS (HRquintile5 v. 1 1.50; 95% CI 1.23–1.83; p for trend = 0.0008) after fully adjusting for potential confounders. Irrespective of the menopausal status of women, higher DII (=Q5) scores were positively associated with all 5 components of MetS (p < 0.05). In men, higher DII scores significantly increased the risk of low HDL cholesterol [HR]quintile5 v. 1 1.59 (1.27–1.99); p for trend = 0.0001], elevated waist circumferences [HR]quintile5 v. 1 1.28 (1.08–1.52); p for trend = 0.01], and high blood pressure [HR]quintile5 v. 1 1.17 (1.03–1.32); p for trend = 0.05]. These results indicate that diet with pro-inflammatory potential, as represented by higher DII scores, is prospectively associated with increased risk of MetS, and the relationship is stronger in women than in men. Full article
(This article belongs to the Special Issue Dietary Inflammatory Index and Non-communicable Disease Risk)
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<p>Flowchart of Korean Genome and Epidemiological Studies Health Examination (KoGES_HEXA) cohort participants included in the main analysis. MetS: Metabolic Syndrome.</p>
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9 pages, 477 KiB  
Review
Does ENaC Work as Sodium Taste Receptor in Humans?
by Albertino Bigiani
Nutrients 2020, 12(4), 1195; https://doi.org/10.3390/nu12041195 - 24 Apr 2020
Cited by 47 | Viewed by 6324
Abstract
Taste reception is fundamental for the proper selection of food and beverages. Among the several chemicals recognized by the human taste system, sodium ions (Na+) are of particular relevance. Na+ represents the main extracellular cation and is a key factor [...] Read more.
Taste reception is fundamental for the proper selection of food and beverages. Among the several chemicals recognized by the human taste system, sodium ions (Na+) are of particular relevance. Na+ represents the main extracellular cation and is a key factor in many physiological processes. Na+ elicits a specific sensation, called salty taste, and low-medium concentrations of table salt (NaCl, the common sodium-containing chemical we use to season foods) are perceived as pleasant and appetitive. How we detect this cation in foodstuffs is scarcely understood. In animal models, such as the mouse and the rat, the epithelial sodium channel (ENaC) has been proposed as a key protein for recognizing Na+ and for mediating preference responses to low-medium salt concentrations. Here, I will review our current understanding regarding the possible involvement of ENaC in the detection of food Na+ by the human taste system. Full article
(This article belongs to the Special Issue Salt Taste, Nutrition, and Health)
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<p>Structure of L-arginine (top) and amiloride (bottom). Both chemicals bear a guanidinium group (red), which is protonated in physiological conditions. This group is believed to interact with the ENaC channel pore from the extracellular space.</p>
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24 pages, 850 KiB  
Review
Mechanisms of Lifespan Regulation by Calorie Restriction and Intermittent Fasting in Model Organisms
by Dae-Sung Hwangbo, Hye-Yeon Lee, Leen Suleiman Abozaid and Kyung-Jin Min
Nutrients 2020, 12(4), 1194; https://doi.org/10.3390/nu12041194 - 24 Apr 2020
Cited by 112 | Viewed by 22607
Abstract
Genetic and pharmacological interventions have successfully extended healthspan and lifespan in animals, but their genetic interventions are not appropriate options for human applications and pharmacological intervention needs more solid clinical evidence. Consequently, dietary manipulations are the only practical and probable strategies to promote [...] Read more.
Genetic and pharmacological interventions have successfully extended healthspan and lifespan in animals, but their genetic interventions are not appropriate options for human applications and pharmacological intervention needs more solid clinical evidence. Consequently, dietary manipulations are the only practical and probable strategies to promote health and longevity in humans. Caloric restriction (CR), reduction of calorie intake to a level that does not compromise overall health, has been considered as being one of the most promising dietary interventions to extend lifespan in humans. Although it is straightforward, continuous reduction of calorie or food intake is not easy to practice in real lives of humans. Recently, fasting-related interventions such as intermittent fasting (IF) and time-restricted feeding (TRF) have emerged as alternatives of CR. Here, we review the history of CR and fasting-related strategies in animal models, discuss the molecular mechanisms underlying these interventions, and propose future directions that can fill the missing gaps in the current understanding of these dietary interventions. CR and fasting appear to extend lifespan by both partially overlapping common mechanisms such as the target of rapamycin (TOR) pathway and circadian clock, and distinct independent mechanisms that remain to be discovered. We propose that a systems approach combining global transcriptomic, metabolomic, and proteomic analyses followed by genetic perturbation studies targeting multiple candidate pathways will allow us to better understand how CR and fasting interact with each other to promote longevity. Full article
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<p>Possible anti-aging mechanisms of caloric restriction (CR) and intermittent fasting (IF). Different dietary interventions by CR and IF result in similar molecular and physiological changes that promote longevity in model organisms. Patterns of individual dietary, metabolic, molecular, and physiological parameters can be different depending on the types of CR and IF as well as the animal models. See the main text for details.</p>
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17 pages, 2308 KiB  
Perspective
A Novel Combination of Vitamin C, Curcumin and Glycyrrhizic Acid Potentially Regulates Immune and Inflammatory Response Associated with Coronavirus Infections: A Perspective from System Biology Analysis
by Liang Chen, Chun Hu, Molly Hood, Xue Zhang, Lu Zhang, Juntao Kan and Jun Du
Nutrients 2020, 12(4), 1193; https://doi.org/10.3390/nu12041193 - 24 Apr 2020
Cited by 112 | Viewed by 14887
Abstract
Novel coronaviruses (CoV) have emerged periodically around the world in recent years. The recurrent spreading of CoVs imposes an ongoing threat to global health and the economy. Since no specific therapy for these CoVs is available, any beneficial approach (including nutritional and dietary [...] Read more.
Novel coronaviruses (CoV) have emerged periodically around the world in recent years. The recurrent spreading of CoVs imposes an ongoing threat to global health and the economy. Since no specific therapy for these CoVs is available, any beneficial approach (including nutritional and dietary approach) is worth investigation. Based on recent advances in nutrients and phytonutrients research, a novel combination of vitamin C, curcumin and glycyrrhizic acid (VCG Plus) was developed that has potential against CoV infection. System biology tools were applied to explore the potential of VCG Plus in modulating targets and pathways relevant to immune and inflammation responses. Gene target acquisition, gene ontology and Kyoto encyclopedia of genes and genomes (KEGG) pathway enrichment were conducted consecutively along with network analysis. The results show that VCG Plus can act on 88 hub targets which are closely connected and associated with immune and inflammatory responses. Specifically, VCG Plus has the potential to regulate innate immune response by acting on NOD-like and Toll-like signaling pathways to promote interferons production, activate and balance T-cells, and regulate the inflammatory response by inhibiting PI3K/AKT, NF-κB and MAPK signaling pathways. All these biological processes and pathways have been well documented in CoV infections studies. Therefore, our findings suggest that VCG Plus may be helpful in regulating immune response to combat CoV infections and inhibit excessive inflammatory responses to prevent the onset of cytokine storm. However, further in vitro and in vivo experiments are warranted to validate the current findings with system biology tools. Our current approach provides a new strategy in predicting formulation rationale when developing new dietary supplements. Full article
(This article belongs to the Section Phytochemicals and Human Health)
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<p>Hub target analysis of VCG Plus. A Venn diagram of hub target distribution in VC, CC and GA, respectively (<b>A</b>). PPI network of 88 hub targets of VCG Plus (<b>B</b>). OmicsBean (<a href="http://www.omicsbean.cn/" target="_blank">http://www.omicsbean.cn/</a>) was employed to draw <a href="#nutrients-12-01193-f001" class="html-fig">Figure 1</a>A. Cytoscape software (Version 3.6.1) was employed to draw <a href="#nutrients-12-01193-f001" class="html-fig">Figure 1</a>B. In <a href="#nutrients-12-01193-f001" class="html-fig">Figure 1</a>B, all the targets are represented by nodes, whereas the interaction between the targets are represented by edges. The node size is proportional to the node degree. The intersect targets of VC, CC and GA are represented by green. VCG Plus, the combination of vitamin C, curcumin and glycyrrhizic acid. VC, vitamin C (group1); CC, curcumin (group 2); GA, glycyrrhizic acid (group 3). PPI, protein-protein interaction.</p>
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<p>Distribution analysis of targets in tissues and systems. The bubble plots were made using JMP software 14.2.0 (SAS institute Inc. USA). Distribution of targets of VCG Plus in system (<b>A</b>), distribution of targets of VC, CC and GA in tissues (<b>B</b>). In <a href="#nutrients-12-01193-f002" class="html-fig">Figure 2</a>A, the bubble size is proportional to the targets number, and the shade of bubble is inversely proportional to the <span class="html-italic">p</span>-value. In <a href="#nutrients-12-01193-f002" class="html-fig">Figure 2</a>B, the bubble size is proportional to the targets number. The targets distribution of VC is represented by blue bubble, CC is represented by red bubble, and GA are represented by green bubble. VC, vitamin C; CC, curcumin; GA, glycyrrhizic acid.</p>
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<p>Top 10 gene ontology (GO) terms of biologic process, molecular function and cellular component, respectively. The bubble plot was made using JMP software 14.2.0 (SAS institute Inc. USA). The bubble size is proportional to the targets number, and the shade of bubble is inversely proportional to the <span class="html-italic">p</span>-value.</p>
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<p>Target immune-related biologic process network. The network was constructed by ClueGo (Latest Version 2.5.6), integrating immune process EBI-Uniport GO annotation database. Only pathways with <span class="html-italic">p</span> &lt; 0.05 are shown. The targets and biologic processes are represented by nodes while the interactions among them are represented by edges. Contribution of VC (vitamin c) in targets and pathways is represented by red, while CC (curcumin) is represented by blue, and GA (glycyrrhizic acid) is represented by green.</p>
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<p>Target KEGG pathways network of VCG Plus. The network was constructed by ClueGo (Latest Version 2.5.6), integrating the latest KEGG pathway database. The targets and pathways are represented by nodes while the interactions among them are represented by edges. Contribution of VC (vitamin c) in targets and pathways is represented by red, while CC (curcumin) is represented by blue, and GA (glycyrrhizic acid) is represented by green.</p>
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19 pages, 3119 KiB  
Article
Bus Stops Near Schools Advertising Junk Food and Sugary Drinks
by Donna Huang, Amanda Brien, Lima Omari, Angela Culpin, Melody Smith and Victoria Egli
Nutrients 2020, 12(4), 1192; https://doi.org/10.3390/nu12041192 - 24 Apr 2020
Cited by 24 | Viewed by 10480
Abstract
Children rarely understand the full extent of the persuasive purpose of advertising on their eating behaviours. Addressing the obesogenic environments in which children live, through a quantification of outdoor advertising, is essential in informing policy changes and enforcing stricter regulations. This research explores [...] Read more.
Children rarely understand the full extent of the persuasive purpose of advertising on their eating behaviours. Addressing the obesogenic environments in which children live, through a quantification of outdoor advertising, is essential in informing policy changes and enforcing stricter regulations. This research explores the proportion of bus stop advertisements promoting non-core food and beverages within walking distance (500 m) from schools in Auckland, New Zealand while using Google Street View. Information was collected on: school type, decile, address, Walk Score®, and Transit Score for all 573 schools in the Auckland region. Ground-truthing was conducted on 10% of schools and showed an alignment of 87.8%. The majority of advertisements on bus shelters were for non-food items or services (n = 541, 64.3%). Of the advertisements that were for food and/or beverages, the majority were for non-core foods (n = 108, 50.2%). There was no statistically significant difference between the variables core and non-core food and beverages and School decile (tertiles), Walk Score (quintiles), and Transit Score (quintiles). 12.8% of all bus stop advertisements in this study promoted non-core dietary options; highlighting an opportunity for implementing stricter regulations and policies preventing advertising unhealthy food and drink to children in New Zealand. Full article
(This article belongs to the Special Issue Food Marketing and Dietary Behaviors among Children)
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<p>Child standing next to a typical bus stop.</p>
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<p>Flow Chart of Data Collection Processes.</p>
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<p>Image Capture Date Example.</p>
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<p>Map Tool Example.</p>
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<p>Distance on Foot Example.</p>
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19 pages, 1832 KiB  
Article
Spirulina Enhances Bone Modeling in Growing Male Rats by Regulating Growth-Related Hormones
by Jin Ah Cho, Seong Yeon Baek, Sun Hee Cheong and Mee Ree Kim
Nutrients 2020, 12(4), 1187; https://doi.org/10.3390/nu12041187 - 24 Apr 2020
Cited by 19 | Viewed by 5654
Abstract
In recent years, growth hormone deficiency in children has been treated with hormone therapy despite the possible significant side effects. Therefore, it was deemed beneficial to develop functional foods or dietary supplements for safely improving children’s growth. Spirulina platensis is known for its [...] Read more.
In recent years, growth hormone deficiency in children has been treated with hormone therapy despite the possible significant side effects. Therefore, it was deemed beneficial to develop functional foods or dietary supplements for safely improving children’s growth. Spirulina platensis is known for its high antioxidant, anti-aging, anti-cancer, and immunity-enhancing properties, as well as its high digestibility and high protein content, but little has been reported about its influence on bone development in children with a normal supply of protein. In this study, we evaluated the effects of spirulina on the bone metabolism and antioxidant profiles of three-week-old growing male rats. The animals were divided into four groups (n = 17 per group) and were fed AIN93G diets with 0% (control), 30% (SP30), 50% (SP50), and 70% (SP70) of casein protein replaced by spirulina, respectively, for seven weeks. We observed that spirulina enhanced bone growth and bone strength by stimulating parathyroid hormone and growth hormone activities, as well its increased antioxidant activity. These results indicate that spirulina provides a suitable dietary supplement and alternative protein source with antioxidant benefits for growth improvement in early developmental stages. Full article
(This article belongs to the Section Nutrition and Public Health)
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<p>Effect of spirulina on the weight of body, organs, and fat tissues. Weights of (<b>A</b>) body, (<b>B</b>) liver (g/100 g BW), (<b>C</b>) kidney (g/100 g BW), (<b>D</b>) heart (g/100 g BW), (<b>E</b>) mesenteric fat (g/100 g BW), (<b>F</b>) retroperitoneal fat (g/100 g BW), (<b>G</b>) epididymal fat (g/100 g BW), and (<b>H</b>) total fat (g/100 g BW) were measured in growing male rats over the 7-week course of the study. Data are mean ± SEM values. Significant differences were determined using <span class="html-italic">t</span>-tests or one-way ANOVA with post hoc Duncan’s multiple-range test comparisons. *** <span class="html-italic">p</span> &lt; 0.001 between weeks within a group and <sup>#</sup> <span class="html-italic">p</span> &lt; 0.05, <sup>##</sup> <span class="html-italic">p</span> &lt; 0.01, or <sup>###</sup> <span class="html-italic">p</span>&lt; 0.001 between groups in the same week. Control: AIN 93G diet; SP30: 30% of protein source replaced with spirulina; SP50: 50% of protein source replaced with spirulina; SP70: 70% of protein source replaced with spirulina. The week of the treatment is represented by O: 0 weeks; ■: 3 weeks; ▲: 7 weeks in each group.</p>
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<p>Effect of spirulina on bone growth, bone strength, and bone mineral content (BMC). (<b>A</b>) Femur length, (<b>B</b>) femur weight, (<b>C</b>) lumbar spine length, (<b>D</b>) lumbar spine weight, (<b>E</b>) breaking force of femur, (<b>F</b>) Ca content of femur, (<b>G</b>) Mg content of femur, and (<b>H</b>) phosphate content of femur were measured in growing male rats over the 7-week course of the study. Data are mean ± SEM values. Significant differences were determined using <span class="html-italic">t</span>-tests or one-way ANOVA with post hoc Duncan’s multiple-range test comparisons. <sup>#</sup> <span class="html-italic">p</span> &lt; 0.05, <sup>##</sup> <span class="html-italic">p</span> &lt; 0.01, or <sup>###</sup> <span class="html-italic">p</span> &lt; 0.001 between groups in the same week. Control: AIN 93G diet; SP30: 30% of protein source replaced with spirulina; SP50: 50% of protein source replaced with spirulina; SP70: 70% of protein source replaced with spirulina. The week of the treatment is represented by O: 0 weeks; ■: 3 weeks; ▲: 7 weeks in each group.</p>
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<p>Effect of spirulina on growth hormones and related hormones in blood. Plasma (<b>A</b>) Growth hormone (GH), (<b>B</b>) insulin-like growth factor 1 (IGF-1), (<b>C</b>) insulin-like growth factor binding protein 3 (IGFBP-3), (<b>D</b>) osteocalcin, (<b>E</b>) free calcium, (<b>F</b>) free phosphate, and (<b>G</b>) parathyroid hormones (PTHs) were measured in growing male rats over the 7-week course of study. Data are mean ± SEM values. Significant differences were determined using <span class="html-italic">t</span>-tests or one-way ANOVA with post hoc Duncan’s multiple-range test comparisons. * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01 between weeks within a group and <sup>#</sup> <span class="html-italic">p</span> &lt; 0.05, <sup>##</sup> <span class="html-italic">p</span> &lt; 0.01, or <sup>###</sup> <span class="html-italic">p</span> &lt; 0.001 between groups in the same week. Control: AIN 93G diet; SP30: 30% of protein source replaced with spirulina; SP50: 50% of protein source replaced with spirulina; SP70: 70% of protein source replaced with spirulina. The week of the treatment is represented by O: 0 weeks; ■: 3 weeks; ▲: 7 weeks in each group. White bar: 0 weeks; black bar: 7 weeks.</p>
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<p>Effect of spirulina on antioxidant activities and lipid peroxidation. (<b>A</b>) quinone reductase (QR) in liver, (<b>B</b>) glutathione (GSH) in liver, (<b>C</b>) GSH in plasma, (<b>D</b>) glutathione <span class="html-italic">S</span>-transferase (GST) in liver, (<b>E</b>) glutathione reductase (GR) in liver, (<b>F</b>) thiobar–bituric acid reactive substance (TBARS) in liver, (<b>G</b>) TBARS in heart, (<b>H</b>) TBARS in kidney, and (<b>I</b>) TBARS in plasma were measured in growing male rats fed with control, SP30, SP50, and SP70 diet over the 7-week course of the study. Data are mean ± SEM values. Significant differences were determined using one-way ANOVA with post hoc Duncan’s multiple-range test comparisons. <sup>#</sup> <span class="html-italic">p</span> &lt; 0.05, <sup>##</sup> <span class="html-italic">p</span> &lt; 0.01, or <sup>###</sup> <span class="html-italic">p</span> &lt; 0.001 between groups in the same week. Control: AIN 93G diet; SP30: 30% of protein source replaced with spirulina; SP50: 50% of protein source replaced with spirulina; SP70: 70% of protein source replaced with spirulina. The week of the treatment is represented by O: 0 weeks; ■: 3 weeks; ▲: 7 weeks in each group. White bar: 0 weeks; black bar: 7 weeks.</p>
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<p>Effect of spirulina on antioxidant activities and lipid peroxidation. (<b>A</b>) quinone reductase (QR) in liver, (<b>B</b>) glutathione (GSH) in liver, (<b>C</b>) GSH in plasma, (<b>D</b>) glutathione <span class="html-italic">S</span>-transferase (GST) in liver, (<b>E</b>) glutathione reductase (GR) in liver, (<b>F</b>) thiobar–bituric acid reactive substance (TBARS) in liver, (<b>G</b>) TBARS in heart, (<b>H</b>) TBARS in kidney, and (<b>I</b>) TBARS in plasma were measured in growing male rats fed with control, SP30, SP50, and SP70 diet over the 7-week course of the study. Data are mean ± SEM values. Significant differences were determined using one-way ANOVA with post hoc Duncan’s multiple-range test comparisons. <sup>#</sup> <span class="html-italic">p</span> &lt; 0.05, <sup>##</sup> <span class="html-italic">p</span> &lt; 0.01, or <sup>###</sup> <span class="html-italic">p</span> &lt; 0.001 between groups in the same week. Control: AIN 93G diet; SP30: 30% of protein source replaced with spirulina; SP50: 50% of protein source replaced with spirulina; SP70: 70% of protein source replaced with spirulina. The week of the treatment is represented by O: 0 weeks; ■: 3 weeks; ▲: 7 weeks in each group. White bar: 0 weeks; black bar: 7 weeks.</p>
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17 pages, 2662 KiB  
Article
Effect of Increased Daily Water Intake and Hydration on Health in Japanese Adults
by Yumi Nakamura, Hiroshi Watanabe, Aiko Tanaka, Masato Yasui, Jun Nishihira and Norihito Murayama
Nutrients 2020, 12(4), 1191; https://doi.org/10.3390/nu12041191 - 23 Apr 2020
Cited by 30 | Viewed by 25931
Abstract
Increased hydration is recommended as healthy habit with several merits. However, supportive data are sparse. To assess the efficacy of increased daily water intake, we tested the effect of water supplementation on biomarkers in blood, urine, and saliva. Twenty-four healthy Japanese men and [...] Read more.
Increased hydration is recommended as healthy habit with several merits. However, supportive data are sparse. To assess the efficacy of increased daily water intake, we tested the effect of water supplementation on biomarkers in blood, urine, and saliva. Twenty-four healthy Japanese men and 31 healthy Japanese women with fasting blood glucose levels ranging from 90–125 mg/dL were included. An open-label, two-arm, randomized controlled trial was conducted for 12 weeks. Two additional 550 mL bottles of water on top of habitual fluid intake were consumed in the intervention group. The subjects drank one bottle of water (550 mL) within 2 h of waking, and one bottle (550 mL) 2 h before bedtime. Subjects increased mean fluid intake from 1.3 L/day to 2.0 L/day, without changes in total energy intake. Total body water rate increased with associated water supplementation. There were no significant changes in fasting blood glucose and arginine vasopressin levels, but systolic blood pressure was significantly decreased in the intervention group. Furthermore, water supplementation increased body temperature, reduced blood urea nitrogen concentration, and suppressed estimated glomerular filtration rate reduction. Additionally, existence of an intestinal microbiome correlated with decreased systolic blood pressure and increased body temperature. Habitual water supplementation after waking up and before bedtime in healthy subjects with slightly elevated fasting blood glucose levels is not effective in lowering these levels. However, it represents a safe and promising intervention with the potential for lowering blood pressure, increasing body temperature, diluting blood waste materials, and protecting kidney function. Thus, increasing daily water intake could provide several health benefits. Full article
(This article belongs to the Section Nutrition and Metabolism)
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<p>Flow diagram for the involvement of subjects during the trial.</p>
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<p>Daily fluid intake. Total daily fluid intake from the pre-observation period to the end of the test period. The dotted line indicates the control group. The solid line shows the intervention group. Mean ± SEM (<b>a</b>). The mean amount of each kind of fluid intake during the pre-observation period and the test period (Week 0 to Week 12) (<b>b</b>).</p>
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<p>Total body water (TBW) rate and extra-cellular water (ECW)/TBW. The actual level (upper) and changes (lower) in the TBW rates (<b>a</b>). The actual level (upper) and changes (lower) in ECW/TBW (<b>b</b>). The dotted line is the control group. The solid line is the intervention group. Mean ± SEM. The <span class="html-italic">P</span> value is the difference between the groups for the change from Week 0 to Week 12. Two-way analysis of variance was performed. Paired <span class="html-italic">t</span>-test adjusted by the Bonferroni method was performed for intragroup comparisons from Week 0. * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.001.</p>
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<p>Fasting blood glucose level and arginine vasopressin (AVP). The actual level (upper) and changes (lower) in the fasting blood glucose level (<b>a</b>). The actual level (upper) and changes (lower) in AVP (<b>b</b>). The dotted line is the control group. The solid line is the intervention group. Mean ± SEM. The <span class="html-italic">p</span> value is the difference between the groups for the change from Week 0 to Week 12. Two-way analysis of variance was performed. Paired <span class="html-italic">t</span>-test adjusted by the Bonferroni method was performed for intragroup comparisons from Week 0. There was no significant difference.</p>
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<p>Systolic blood pressure (SBP), diastolic blood pressure (DBP), and body temperature. The actual level (upper) and changes (lower) in SBP (<b>a</b>). The actual level (upper) and changes (lower) in DBP (<b>b</b>). Body temperature. The actual level (upper) and changes (lower) in body temperature. The dotted line is the control group (<b>c</b>). The dotted line is the control group. The solid line is the intervention group. Mean ± SEM. The <span class="html-italic">P</span> value is the difference between the groups for the change from Week 0 to Week 12. Two-way analysis of variance was performed. * Paired <span class="html-italic">t</span>-test adjusted by the Bonferroni method was performed for intragroup comparisons from Week 0. * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.001.</p>
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<p>Renal functions, plasma osmotic pressure, and urine aquaporin2/creatinine (AQP2/CRE). The actual level (upper) and changes (lower) in blood urea nitrogen (BUN) (<b>a</b>). The actual level (upper) and changes (lower) in the estimated glomerular filtration rate (eGFR) (<b>b</b>). The actual level (upper) and changes (lower) in plasma osmotic pressure (<b>c</b>). The actual level (upper) and changes (lower) in urine AQP2/CRE (<b>d</b>). The dotted line is the control group. The solid line is the intervention group. Mean ± SEM. The <span class="html-italic">P</span> value is the difference between the groups for the change from Week 0 to Week 12. Two-way analysis of variance was performed. * Paired <span class="html-italic">t</span>-test adjusted by the Bonferroni method was performed for intragroup comparisons from Week 0. * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.001, ## <span class="html-italic">p</span> &lt; 0.001.</p>
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<p>Correlation between the change in systolic blood pressure (SBP) and changes in intestinal bacteria. The actual level (upper) and changes (lower) in the OTU of Psudoflavoniflactor capillosus. The dotted line is the control group. The solid line is the intervention group. Mean±SEM (<b>a</b>). # <span class="html-italic">t</span>-test of two independent samples, for comparison between groups at each time point, # <span class="html-italic">p</span> &lt; 0.05. A correlation diagram between the changes in OTU of Psudoflavoniflactor capillosus, and changes in SBP between Weeks 0 and 12, in the intervention group (<b>b</b>). R = Correlation coefficient.</p>
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<p>Correlation between changes in body temperature and changes in intestinal bacteria. The actual level (upper), changes (middle), and correlation between changes (lower) in the operational taxonomic unit (OTU) of Kineothrix xp. (<b>a</b>), Feacalibacterium prausnizzii (<b>b</b>), and Ruminococcaceae (<b>c</b>). The dotted line is the control group. The solid line is intervention group. Mean ± SEM. * Paired <span class="html-italic">t</span>-test was performed for intragroup comparisons from Week 0. * <span class="html-italic">p</span> &lt; 0.05. # <span class="html-italic">t</span>-test of two independent samples, for comparison between groups at each time point, # <span class="html-italic">p</span> &lt; 0.05.</p>
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17 pages, 2842 KiB  
Article
Kaempferide Enhances Chemosensitivity of Human Lung Adenocarcinoma A549 Cells Mediated by the Decrease in Phosphorylation of Akt and Claudin-2 Expression
by Hiroaki Eguchi, Toshiyuki Matsunaga, Satoshi Endo, Kenji Ichihara and Akira Ikari
Nutrients 2020, 12(4), 1190; https://doi.org/10.3390/nu12041190 - 23 Apr 2020
Cited by 23 | Viewed by 3979
Abstract
Claudins (CLDNs) play crucial roles in the formation of tight junctions. We have reported that abnormal expression of CLDN2 confers chemoresistance in the spheroids of human lung adenocarcinoma A549 cells. A food composition, which can reduce CLDN2 expression, may function to prevent the [...] Read more.
Claudins (CLDNs) play crucial roles in the formation of tight junctions. We have reported that abnormal expression of CLDN2 confers chemoresistance in the spheroids of human lung adenocarcinoma A549 cells. A food composition, which can reduce CLDN2 expression, may function to prevent the malignant progression. Here, we found that ethanol extract of Brazilian green propolis (EBGP) and kaempferide, a major component of EBGP, decrease CLDN2 expression. In the two-dimensional culture model, EBGP decreased the tight junctional localization of CLDN2 without affecting that of zonula occludens-1, an adaptor protein, and enhanced paracellular permeability to doxorubicin, a cytotoxic anticancer drug. EBGP reduced hypoxic stress, and enhanced the accumulation and sensitivity of doxorubicin in the spheroid of A549 cells. Kaempferide dose-dependently decreased CLDN2 expression, although dihydrokaempferide and pinocembrin did not. The phosphorylation of Akt, a regulatory factor of CLDN2 expression, was inhibited by kaempferide but not by dihydrokaempferide. The 2,3-double bond in the C ring may be important to inhibit Akt. Kaempferide decreased the mRNA level and promoter activity of CLDN2, indicating that it inhibits the transcription of CLDN2. In accordance with EBGP, kaempferide decreased the tight junctional localization of CLDN2 and increased a paracellular permeability to doxorubicin, suggesting that it diminished the paracellular barrier to small molecules. In addition, kaempferide reduced hypoxic stress, and enhanced the accumulation and sensitivity of doxorubicin in the spheroids. In contrast, dihydrokaempferide did not improve the sensitivity to doxorubicin. Further study is needed using an animal model, but we suggest that natural foods abundantly containing kaempferide are candidates for the prevention of the chemoresistance of lung adenocarcinoma. Full article
(This article belongs to the Section Nutrition and Metabolism)
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Figure 1

Figure 1
<p>Effect of ethanol extract of Brazilian green propolis (EBGP) on the viability and expression of claudin-2 (CLDN2) in A549 cells. (<b>A</b>) Cells were incubated with 0, 10, and 50 μg EBGP for 24 h, followed by incubation with 4-[3-[4-iodophenyl]-2-4(4-nitrophenyl)-2<span class="html-italic">H</span>-5-tetrazolio-1,3-benzene disulfonate] (WST-1) reagent. Cell viability is represented as a percentage relative to 0 μg/mL. (<b>B</b>,<b>C</b>) The cell lysates were immunoblotted with anti-CLDN2 and anti-β-actin antibodies. The protein level of CLDN2 is represented as a percentage relative to 0 μg (<b>D</b>). The mRNA level of CLDN2 was determined by quantitative real-time PCR, and is represented as a percentage relative to 0 μg/mL. <span class="html-italic">n</span> = 3–4. ** <span class="html-italic">p</span> &lt; 0.01 and NS <span class="html-italic">p</span> &gt; 0.05 compared with 0 μg/mL (one-way analysis). Protein (F<sub>3,8</sub> = 201.24, <span class="html-italic">p</span> &lt; 0.0001), viability (F<sub>6,9</sub> = 0.05, <span class="html-italic">p</span> = 0.953646), and mRNA (F<sub>3,8</sub> = 28.31, <span class="html-italic">p</span> = 0.00023).</p>
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<p>Effect of EBGP on cellular localization of CLDN2 and barrier function. (<b>A</b>) Cells cultured on cover glasses were incubated in the absence (control) and presence of 50 μg/mL EBGP for 24 h. The cells were stained with anti-CLDN2 (red) and anti-zonula occludens-1 (ZO-1) (green) antibodies. Images were taken using the confocal laser microscope equipped with × 100 objective lens. Merged images are shown on the right. Scale bar represents 10 μm. (<b>B</b>,<b>C</b>) Cells cultured on transwell inserts were incubated in the absence and presence of 50 μg/mL EBGP for 24 h. TER was measured using a volt ohmmeter. Doxorubicin (10 μM) was added to the apical compartment. After incubation at 4 °C for 60 min, the solution in the basal compartment was collected, followed by measurement of the fluorescence intensity using an Infinite F200 Pro microplate reader. <span class="html-italic">n</span> = 4. ** <span class="html-italic">p</span> &lt; 0.01 compared with control (Student’s <span class="html-italic">t</span> test).</p>
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<p>Effect of EBGP on the sensitivity to doxorubicin in the spheroids. (<b>A</b>) The spheroids were incubated in the absence and presence of 50 μg of EBGP for 24 h. Spheroid size, fluorescence intensity of a hypoxia probe solution (LOX-1), and cell viability are represented as a percentage relative to 0 μg/mL. ** <span class="html-italic">p</span> &lt; 0.01, * <span class="html-italic">p</span> &lt; 0.05, and NS <span class="html-italic">p</span> &gt; 0.05 compared with 0 μg/mL EBGP (Student’s <span class="html-italic">t</span> test). (<b>B</b>) The spheroids were pre-incubated with 50 μg of EBGP for 24 h, followed by incubation with doxorubicin for 60 min. The fluorescence intensity of doxorubicin in the spheroids was examined using a BZ-X800 fluorescence microscopy. (<b>C</b>) After incubation of the spheroids with doxorubicin in the absence and presence of 50 μg/mL of EBGP for 24 h, cell viability was measured using a CellTiter-Glo 3D Cell Viability Assay kit. The fluorescence intensity of doxorubicin and cell viability are represented as a percentage relative to 0 μM doxorubicin. <span class="html-italic">n</span> = 3–6. ** <span class="html-italic">p</span> &lt; 0.01 compared with 0 μg/mL EBGP. <sup>##</sup> <span class="html-italic">p</span> &lt; 0.01 compared with control. NS <span class="html-italic">p</span> &gt; 0.05 compared with 0 μg/mL EBGP or control (Two-way analysis). Fluorescence intensity (F<sub>1,31</sub> = 145.43, <span class="html-italic">p</span> &lt; 0.0001) and cytotoxicity (F<sub>1,23</sub> = 57.45.45, <span class="html-italic">p</span> &lt; 0.0001).</p>
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<p>Decrease in CLDN2 expression by kaempferol and kaempferide. (<b>A</b>) Structures of kaempferol and kaempferide. (<b>B</b>,<b>C</b>) Cells were incubated with 0, 1, 10, and 50 μM kaempferol or kaempferide for 24 h. Cell viability was assessed by the WST-1 assay and represented as a percentage relative to 0 μM. The protein level of CLDN2 was examined by Western blotting and represented as a percentage relative to 0 μM. β-Actin was used as an internal control. <span class="html-italic">n</span> = 3–8. ** <span class="html-italic">p</span> &lt; 0.01 and NS <span class="html-italic">p</span> &gt; 0.05 compared with 0 μM (one-way analysis). Viability (F<sub>6,22</sub> = 5.19, <span class="html-italic">p</span> = 0.00184), protein in kaempferol (F<sub>3,8</sub> = 52.71, <span class="html-italic">p</span> &lt; 0.0001), and protein in kaempferide (F<sub>3,8</sub> = 490.69, <span class="html-italic">p</span> &lt; 0.0001).</p>
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<p>Effects of dihydrokaempferide derivatives on viability and CLDN2 expression. Cells were incubated with 0, 1, 10, and 50 μM dihydrokaempferol (<b>A</b>), dihydrokaempferide (<b>B</b>), or pinocembrin (<b>C</b>) for 24 h. The structures of these derivatives are shown in the left. Cell viability was assessed by WST-1 assay and represented as a percentage relative to 0 μM. The protein level of CLDN2 was examined by Western blotting and represented as a percentage relative to 0 μM. <span class="html-italic">n</span> = 3–8. ** <span class="html-italic">p</span> &lt; 0.01 and NS <span class="html-italic">p</span> &gt; 0.05 compared with 0 μM (One-way analysis). Viability in dihydrokaempferol (F<sub>6,11</sub> = 4.72, <span class="html-italic">p</span> = 0.02357), viability in dihydrokaempferide (F<sub>6,16</sub> = 17.65, <span class="html-italic">p</span> &lt; 0.0001), viability in pinocembrin (F<sub>6,11</sub> = 9.43, <span class="html-italic">p</span> = 0.00892), protein in dihydrokaempferol (F<sub>3,11</sub> = 0.11, <span class="html-italic">p</span> = 0.95341), protein in dihydrokaempferide (F<sub>3,11</sub> = 1.31, <span class="html-italic">p</span> = 0.3379), protein in pinocembrin (F<sub>3,11</sub> = 2.34, <span class="html-italic">p</span> = 0.14872).</p>
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<p>Inhibition of phosphorylation of Akt by EBGP and kaempferide. Cells were incubated with 10 μM kaempferide for 0, 1, and 2 h (<b>A</b>), or 10 μM dihydrokaempferide (<b>B</b>) and 50 μg/mL EBGP for 2 h (<b>C</b>). The protein levels of p-Akt, Akt, p-PDK1, and PDK1 were examined by Western blotting and represented as a percentage relative to 0 h, 0 μM, or 0 μg/mL. <span class="html-italic">n</span> = 3–4. ** <span class="html-italic">p</span> &lt; 0.01, * <span class="html-italic">p</span> &lt; 0.05, and NS <span class="html-italic">p</span> &gt; 0.05 compared with 0 h (one-way analysis), 0 μM, or 0 μg/mL (Student’s <span class="html-italic">t</span> test). Time course (F<sub>3,6</sub> = 10.47, <span class="html-italic">p</span> = 0.01106).</p>
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<p>Effect of kaempferide on the transcriptional activity of CLDN2. (<b>A</b>) Cells were incubated with 10 μM kaempferide or 10 μM dihydrokaempferide for 6 h. The mRNA level of CLDN2 was examined by real-time PCR, and represented as a percentage relative to the control. (<b>B</b>) Cells were transfected with reporter vector of human CLDN2 and pRL-TK, an internal control. After treatment with 10 μg/mL EBGP, 10 μM kaempferide, or 10 μM dihydrokaempferide for 6 h, the reporter activity was measured by the Dual-Luciferase Reporter Assay System and represented as a percentage relative to control. <span class="html-italic">n</span> = 4–5. ** <span class="html-italic">p</span> &lt; 0.01 and NS <span class="html-italic">p</span> &gt; 0.05 compared with control (One-way analysis). mRNA (F<sub>4,9</sub> = 18.16, <span class="html-italic">p</span> = 0.00069) and reporter activity (F<sub>4,15</sub> = 24.45, <span class="html-italic">p</span> &lt; 0.0001).</p>
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<p>Effect of kaempferide on cellular localization of CLDN2 and barrier function. (<b>A</b>) Cells cultured on cover glasses were incubated in the absence and presence of 10 μM kaempferide or 10 μM dihydrokaempferide for 24 h. The cells were stained with anti-CLDN2 (red) and anti-ZO-1 (green) antibodies. Images were taken using the confocal laser microscope equipped with × 100 objective lens. Merged images are shown on the right. Scale bar represents 10 μm. (<b>B</b>,<b>C</b>) Cells cultured on transwell inserts were incubated in the absence and presence of 10 μM kaempferide or 10 μM dihydrokaempferide for 24 h. TER was measured using a volt ohmmeter. doxorubicin (10 μM) was added to the apical compartment. After incubation at 4 °C for 60 min, the solution in the basal compartment was collected, followed by measurement of fluorescence intensity. <span class="html-italic">n</span> = 4–8. ** <span class="html-italic">p</span> &lt; 0.01 and NS <span class="html-italic">p</span> &gt; 0.05 compared with control (One-way analysis). TER (F<sub>4,9</sub> = 27.02, <span class="html-italic">p</span> = 0.0016) and paracellular flux (F<sub>4,14</sub> = 13.90, <span class="html-italic">p</span> = 0.00047).</p>
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<p>Increase in the sensitivity of spheroid cells to doxorubicin by kaempferide. (<b>A</b>) The spheroids were incubated in the absence (control) and presence of 10 μM kaempferide or 10 μM dihydrokaempferide for 24 h. Spheroid size, fluorescence intensity of LOX-1, and cell viability are represented as a percentage relative to the control. ** <span class="html-italic">p</span> &lt; 0.01, * <span class="html-italic">p</span> &lt; 0.05, and NS <span class="html-italic">p</span> &gt; 0.05 compared with the control (one-way analysis). Spheroid size (F<sub>2,16</sub> = 1.71, <span class="html-italic">p</span> = 0.21639), LOX-1 (F<sub>2,11</sub> = 8.31, <span class="html-italic">p</span> = 0.00902), and cytotoxicity (F<sub>2,10</sub> = 6.28, <span class="html-italic">p</span> = 0.02293). (<b>B</b>) The spheroids were pre-incubated with 10 μM kaempferide or 10 μM dihydrokaempferide for 24 h, followed by incubation with doxorubicin for 60 min. The fluorescence intensity of doxorubicin in the spheroids was examined using a BZ-X800 fluorescence microscopy. (<b>C</b>) After incubation of the spheroids with doxorubicin in the absence and presence of 10 μM kaempferide or 10 μM dihydrokaempferide for 24 h, cell viability was measured using a CellTiter-Glo 3D Cell Viability Assay kit. The fluorescence intensity of doxorubicin and cell viability are represented as a percentage relative to 0 μM doxorubicin. <span class="html-italic">n</span> = 4–6. ** <span class="html-italic">p</span> &lt; 0.01, * <span class="html-italic">p</span> &lt; 0.05, and NS <span class="html-italic">p</span> &gt; 0.05 compared with 0 μM. <sup>##</sup> <span class="html-italic">p</span> &lt; 0.01 and <sup>#</sup> <span class="html-italic">p</span> &lt; 0.05 compared with control (Two-way analysis). Fluorescence intensity (F<sub>2,59</sub> = 4.54, <span class="html-italic">p</span> = 0.01563) and cytotoxicity (F<sub>2,35</sub> = 9.27, <span class="html-italic">p</span> = 0.00212).</p>
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<p>Elevation of chemoresistance by overexpression of CLDN2. (<b>A</b>) The spheroid cells were transfected with mock or CLDN2 expression vector followed by incubation with 10 μM kaempferide for 24 h. (<b>A</b>) The cells were incubation with doxorubicin for 60 min. The fluorescence intensity of doxorubicin in the spheroids was examined using a BZ-X800 fluorescence microscopy. (<b>B</b>) Cell viability was measured using a CellTiter-Glo 3D Cell Viability Assay kit. The fluorescence intensity of doxorubicin and cell viability are represented as a percentage relative to 0 μM doxorubicin. <span class="html-italic">n</span> = 5–8. ** <span class="html-italic">p</span> &lt; 0.01 compared with 0 μM doxorubicin. <sup>##</sup> <span class="html-italic">p</span> &lt; 0.01, <sup>#</sup> <span class="html-italic">p</span> &lt; 0.05, and <span class="html-italic">NS p</span> &gt; 0.05 compared with control (Two-way analysis). Fluorescence intensity (F<sub>2,59</sub> = 22.07, <span class="html-italic">p</span> &lt; 0.0001) and cytotoxicity (F<sub>2,47</sub> = 42.71, <span class="html-italic">p</span> &lt; 0.0001).</p>
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19 pages, 4315 KiB  
Article
A Dietary Combination of Forskolin with Homotaurine, Spearmint and B Vitamins Protects Injured Retinal Ganglion Cells in a Rodent Model of Hypertensive Glaucoma
by Maurizio Cammalleri, Massimo Dal Monte, Rosario Amato, Paola Bagnoli and Dario Rusciano
Nutrients 2020, 12(4), 1189; https://doi.org/10.3390/nu12041189 - 23 Apr 2020
Cited by 32 | Viewed by 5786
Abstract
There is indication that nutritional supplements protect retinal cells from degeneration. In a previous study, we demonstrated that dietary supplementation with an association of forskolin, homotaurine, spearmint extract and B vitamins efficiently counteracts retinal dysfunction associated with retinal ganglion cell (RGC) death caused [...] Read more.
There is indication that nutritional supplements protect retinal cells from degeneration. In a previous study, we demonstrated that dietary supplementation with an association of forskolin, homotaurine, spearmint extract and B vitamins efficiently counteracts retinal dysfunction associated with retinal ganglion cell (RGC) death caused by optic nerve crush. We extended our investigation on the efficacy of dietary supplementation with the use of a mouse model in which RGC degeneration depends as closely as possible on intraocular pressure (IOP) elevation. In this model, injecting the anterior chamber of the eye with methylcellulose (MCE) causes IOP elevation leading to RGC dysfunction. The MCE model was characterized in terms of IOP elevation, retinal dysfunction as determined by electrophysiological recordings, RGC loss as determined by brain-specific homeobox/POU domain protein 3A immunoreactivity and dysregulated levels of inflammatory and apoptotic markers. Except for IOP elevation, dysfunctional retinal parameters were all recovered by dietary supplementation indicating the involvement of non-IOP-related neuroprotective mechanisms of action. Our hypothesis is that the diet supplement may be used to counteract the inflammatory processes triggered by glial cell activation, thus leading to spared RGC loss and the preservation of visual dysfunction. In this respect, the present compound may be viewed as a potential remedy to be added to the currently approved drug therapies for improving RGC protection. Full article
(This article belongs to the Special Issue Nutrition for Eye Health)
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Graphical abstract

Graphical abstract
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<p>Dietary supplementation did not affect intraocular pressure (IOP). The injection of methylcellulose (MCE) in the anterior chamber at day 0 (arrow) resulted in a significant elevation in the intraocular pressure. Both the vehicle and diet supplement did not affect IOP in mice receiving MCE. Data are shown as mean ± SEM (<span class="html-italic">n</span> = 11 for each group). Black circles and line: control mice; red squares and line: mice intraocularly injected with MCE fed with vehicle; red triangles and line: mice intraocularly injected with MCE fed with diet supplement.</p>
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<p>Effects of dietary supplementation on retinal function as evaluated by scotopic and photopic full-field electroretinogram (ERG). Representative ERG traces showing scotopic a- and b-waves (<b>A</b>) or photopic b-waves with photopic negative response (PhNR; (<b>B</b>)) in control mice and in mice that received intraocular MCE injection fed with either vehicle or diet supplement. (<b>C</b>) Mean amplitudes of ERG responses evaluated as changes from baseline, normalized to the amplitude measured in control mice. MCE did not affect the amplitude of the scotopic a-wave, scotopic b-wave and photopic b-wave, while it reduced the amplitude of PhNR. Dietary supplementation partially prevented the reduction in PhNR amplitude. Data are shown as mean ± SEM (<span class="html-italic">n</span> = 6 for each group). * <span class="html-italic">p</span> &lt; 0.01 and ** <span class="html-italic">p</span> &lt; 0.001 versus control; <sup>§</sup> <span class="html-italic">p</span> &lt; 0.001 versus MCE mice fed with vehicle (one-way ANOVA followed by the Newman–Keuls multiple comparison post-hoc test). Black bars: mice intraocularly injected with MCE fed with vehicle; grey bars: mice intraocularly injected with MCE fed with diet supplement.</p>
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<p>Effects of dietary supplementation on retinal function as evaluated by pattern ERG (PERG). (<b>A</b>) Representative PERG traces showing the two negative peaks (N35 and N95) and the positive peak P50 in control mice and in mice injected with MCE fed with either vehicle or diet supplement. (<b>B</b>) Mean amplitudes of the N35–P50 and P50–N95 waves. MCE reduced the amplitude of both waves, an effect that was partially prevented by dietary supplementation. (<b>C</b>) Mean implicit time of the P50 and N95 peaks was increased by MCE, an effect that was abolished by dietary supplementation. Data are shown as mean ± SEM (<span class="html-italic">n</span> = 6 for each group). * <span class="html-italic">p</span> &lt; 0.01 and ** <span class="html-italic">p</span> &lt; 0.001 versus control; <sup>§</sup> <span class="html-italic">p</span> &lt; 0.001 versus MCE mice fed with vehicle (one-way ANOVA followed by the Newman–Keuls multiple comparison post-hoc test).</p>
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<p>Effects of dietary supplementation on retinal ganglion cell (RGC) number. (<b>A</b>–<b>C</b>) Representative images of retinal whole mounts immunostained for brain-specific homeobox/POU domain protein 3A (Brn3a) in control mice (<b>A</b>) and in mice that received MCE either fed with either vehicle (<b>B</b>) or diet supplement (<b>C</b>) (<span class="html-italic">n</span> = 5 for each experimental group). (<b>D</b>–<b>F</b>) High magnification of the boxed areas in A–C. Scale bars: 1 mm (<b>A</b>–<b>C</b>) or 250 µm (<b>D</b>–<b>F</b>). (<b>G</b>) A count of Brn3a-labeled RGCs. MCE reduced RGC number, an effect that was partially prevented by dietary supplementation. Data are shown as mean ± SEM (<span class="html-italic">n</span> = 5 for each group). * <span class="html-italic">p</span> &lt; 0.001 versus control; <sup>§</sup> <span class="html-italic">p</span> &lt; 0.001 versus MCE mice fed with vehicle (one-way ANOVA followed by the Newman–Keuls multiple comparison post-hoc test).</p>
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<p>Effects of dietary supplementation on glial activation. (<b>A</b>) Representative Western blots from retinal homogenates of control mice or mice that received MCE fed with either vehicle or diet supplement. (<b>B</b>,<b>C</b>) Densitometric analysis of ionized calcium binding adaptor molecule 1 (Iba1; (<b>B</b>)) or glial fibrillary acidic protein (GFAP; <b>C</b>) levels. MCE resulted in increased levels of both Iba1 and GFAP. Dietary supplementation prevented the upregulation of Iba1 and GFAP (<span class="html-italic">n</span> = 6 for each group). * <span class="html-italic">p</span> &lt; 0.001 versus control; <sup>§</sup> <span class="html-italic">p</span> &lt; 0.001 versus MCE mice fed with vehicle (one-way ANOVA followed by the Newman–Keuls multiple comparison post-hoc test).</p>
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<p>Effects of dietary supplementation on inflammatory markers. (<b>A</b>) Representative Western blots from retinal homogenates of control mice or mice that received MCE fed with either vehicle or diet supplement. (<b>B</b>–<b>E</b>) Densitometric analysis of the levels of phosphorylated form of nuclear factor kappa-light-chain-enhancer of activated B cells (NF-kB), tumor necrosis factor (TNF)-α, interleukin (IL)-6 and IL-10. MCE resulted in increased levels of the phosphorylated form of NF-kB, TNF-α and IL-6, while IL-10 levels were decreased, effects that were almost completely prevented by dietary supplementation (<span class="html-italic">n</span> = 6 for each group). * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01 and *** <span class="html-italic">p</span> &lt; 0.001 versus control; <sup>§</sup> <span class="html-italic">p</span> &lt; 0.05 and <sup>§§</sup> <span class="html-italic">p</span> &lt; 0.001 versus MCE mice fed with vehicle (one-way ANOVA followed by the Newman–Keuls multiple comparison post-hoc test).</p>
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<p>Effects of dietary supplementation on apoptotic markers. (<b>A</b>) Representative Western blots from retinal homogenates of control mice or mice that received MCE fed with either vehicle or diet supplement. (<b>B</b>,<b>C</b>) Densitometric analysis of the levels of Bax/Bcl-2 (<b>B</b>) and active caspase 3 (<b>C</b>). MCE resulted in increased levels of both Bax and active caspase 3 without altering Bcl-2 levels. Dietary supplementation prevented the upregulation of both Bax and the active form of caspase 3 (<span class="html-italic">n</span> = 6 for each group). * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01 and *** <span class="html-italic">p</span> &lt; 0.001 versus control; <sup>§</sup> <span class="html-italic">p</span> &lt; 0.001 versus MCE mice fed with vehicle (one-way ANOVA followed by the Newman–Keuls multiple comparison post-hoc test).</p>
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<p>Schematic diagram showing possible mechanisms through which the diet supplement counteracts RGC death thus preserving, at least in part, retinal function. MCE leads to IOP elevation that, in turn, generates a downstream cascade that, through the induction of gliosis and inflammation, triggers RGC degeneration by apoptosis and visual dysfunction. The diet supplement, acting as a direct neuroprotectant, reduces gliosis, inflammation and apoptotic processes thus sparing RGCs from death and counteracting visual dysfunction.</p>
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17 pages, 1349 KiB  
Article
Plasma Metabolome Alterations Associated with Extrauterine Growth Restriction
by Danuta Dudzik, Isabel Iglesias Platas, Montserrat Izquierdo Renau, Carla Balcells Esponera, Beatriz del Rey Hurtado de Mendoza, Carles Lerin, Marta Ramón-Krauel and Coral Barbas
Nutrients 2020, 12(4), 1188; https://doi.org/10.3390/nu12041188 - 23 Apr 2020
Cited by 8 | Viewed by 4304
Abstract
Very preterm infants (VPI, born at or before 32 weeks of gestation) are at risk of adverse health outcomes, from which they might be partially protected with appropriate postnatal nutrition and growth. Metabolic processes or biochemical markers associated to extrauterine growth restriction (EUGR) [...] Read more.
Very preterm infants (VPI, born at or before 32 weeks of gestation) are at risk of adverse health outcomes, from which they might be partially protected with appropriate postnatal nutrition and growth. Metabolic processes or biochemical markers associated to extrauterine growth restriction (EUGR) have not been identified. We applied untargeted metabolomics to plasma samples of VPI with adequate weight for gestational age at birth and with different growth trajectories (29 well-grown, 22 EUGR) at the time of hospital discharge. A multivariate analysis showed significantly higher levels of amino-acids in well-grown patients. Other metabolites were also identified as statistically significant in the comparison between groups. Relevant differences (with corrections for multiple comparison) were found in levels of glycerophospholipids, sphingolipids and other lipids. Levels of many of the biochemical species decreased progressively as the level of growth restriction increased in severity. In conclusion, an untargeted metabolomic approach uncovered previously unknown differences in the levels of a range of plasma metabolites between well grown and EUGR infants at the time of discharge. Our findings open speculation about pathways involved in growth failure in preterm infants and the long-term relevance of this metabolic differences, as well as helping in the definition of potential biomarkers. Full article
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<p>OPLS-DA scores plot (<b>A</b>) capillary electrophoresis-mass spectrometry, (R2 = 0.66, Q2 = 0.2, CV-ANOVA <span class="html-italic">p</span> = 0.026); (<b>B</b>) gas chromatography-mass spectrometry, (R2 = 0.63, Q2 = 0.034, CV- ANOVA <span class="html-italic">p</span> = 0.036); (<b>C</b>) liquid chromatography-mass spectrometry/ESI+,(R2 = 0.48, Q2 = -0.006, CV- ANOVA, <span class="html-italic">p</span> = 1.000); and (<b>D</b>) liquid chromatography-mass spectrometry /ESI- (R2 = 0.62, Q2 = −0.00006, CV- ANOVA <span class="html-italic">p</span> = 0.046). R2 = coefficient for variance explained; Q2 = coefficient for variance predicted. <span style="color:green">▲</span> non-EUGR, <span style="color:#C00000">●</span> EUGR.</p>
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<p>(<b>A</b>) Panel A. Pie chart representing the distribution of metabolites identified from multiplatform metabolomic analysis that were significantly different between EUGR and non EUGR individuals. (<b>B</b>) Panel B. A hierarchical clustering with heatmap using Euclidean distance measure and Ward clustering algorithm has been applied for statistically significant metabolites, illustrating the differences in the metabolite abundance between non-EUGR, EUGR-mod and EUGR-sev cases. Each colored cell corresponds to an abundance value, where blue indicates the lowest and red the highest value.</p>
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<p>The scaled relative abundance of statistically significant amino acids reflecting the differences between non-EUGR and EUGR, together with stratification for moderate and severe EUGR cases.</p>
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14 pages, 493 KiB  
Article
Association of Basal Metabolic Rate and Nutrients Oxidation with Cardiometabolic Risk Factors and Insulin Sensitivity in Sedentary Middle-Aged Adults
by Francisco J. Amaro-Gahete, Lucas Jurado-Fasoli, Jonatan R. Ruiz and Manuel J. Castillo
Nutrients 2020, 12(4), 1186; https://doi.org/10.3390/nu12041186 - 23 Apr 2020
Cited by 8 | Viewed by 4490
Abstract
This cross-sectional study aimed to examine the association of basal metabolic rate (BMR) and basal fat and carbohydrate oxidation (BFox and BCHox, respectively) with cardiometabolic risk factors and insulin sensitivity in sedentary middle-aged adults. A total of 71 healthy sedentary adults (37 women) [...] Read more.
This cross-sectional study aimed to examine the association of basal metabolic rate (BMR) and basal fat and carbohydrate oxidation (BFox and BCHox, respectively) with cardiometabolic risk factors and insulin sensitivity in sedentary middle-aged adults. A total of 71 healthy sedentary adults (37 women) aged 40–65 years participated in the current study. Data were collected during the baseline assessments of the FIT-AGEING randomized controlled trial. BMR was measured via indirect calorimetry, and BFox and BCHox estimated by stoichiometric equations. Blood pressure, glucose, insulin, total cholesterol, high-density lipoprotein cholesterol, low-density lipoprotein cholesterol, and triglycerides plasma levels were selected as cardiometabolic risk factors and assessed following standard procedures. We observed positive associations of BMR with plasma insulin and the homeostatic model assessment of insulin resistance index (HOMA; all p < 0.05) which were attenuated or disappeared after controlling by sex, age, and/or lean mass. There were positive associations between BFox and the quantitative insulin sensitivity check index (QUICKI; p < 0.015), while negative associations were noted between BFox and plasma insulin and HOMA (p < 0.015). There was a significant negative association between BCHox with QUICKI (p < 0.01), whereas significant positive relationships were obtained when BCHox was associated with plasma insulin and HOMA (p < 0.01). These associations persisted in almost all cases when controlling by sex, age and/or lean mass. No further relationships were found when BMR, BFox, and BCHox were associated with other cardiometabolic risk factors. In conclusion, our study findings support that greater BFox and lower BCHox are related to improved insulin sensitivity, whereas BMR seems to be not associated with neither cardiometabolic risk nor insulin sensitivity in sedentary middle-aged adults. Further intervention studies are necessary to well-understand the physiological mechanism implied in this relationship. Full article
(This article belongs to the Section Nutrition and Metabolism)
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<p>(<b>A</b>) Basal metabolic rate (BMR), (<b>B</b>,<b>C</b>) basal fat oxidation, and (<b>D</b>,<b>E</b>) basal carbohydrate oxidation in metabolically healthy normal-weight (MHNW), metabolically unhealthy normal–weight (MUNW), metabolically healthy overweight–obese (MHOO), and metabolically unhealthy overweight–obese (MHOO) participants. <span class="html-italic">P</span> from analysis of variance (Model 0) and analysis of covariance (Model 1: adjusting by sex; Model 2: adjusting by age; Model 3: adjusting by lean mass).</p>
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18 pages, 912 KiB  
Review
Intestinal Permeability, Inflammation and the Role of Nutrients
by Ricard Farré, Marcello Fiorani, Saeed Abdu Rahiman and Gianluca Matteoli
Nutrients 2020, 12(4), 1185; https://doi.org/10.3390/nu12041185 - 23 Apr 2020
Cited by 166 | Viewed by 26207
Abstract
The interaction between host and external environment mainly occurs in the gastrointestinal tract, where the mucosal barrier has a critical role in many physiologic functions ranging from digestion, absorption, and metabolism. This barrier allows the passage and absorption of nutrients, but at the [...] Read more.
The interaction between host and external environment mainly occurs in the gastrointestinal tract, where the mucosal barrier has a critical role in many physiologic functions ranging from digestion, absorption, and metabolism. This barrier allows the passage and absorption of nutrients, but at the same time, it must regulate the contact between luminal antigens and the immune system, confining undesirable products to the lumen. Diet is an important regulator of the mucosal barrier, and the cross-talk among dietary factors, the immune system, and microbiota is crucial for the modulation of intestinal permeability and for the maintenance of gastrointestinal tract (GI) homeostasis. In the present review, we will discuss the role of a number of dietary nutrients that have been proposed as regulators of inflammation and epithelial barrier function. We will also consider the metabolic function of the microbiota, which is capable of elaborating the diverse nutrients and synthesizing products of great interest. Better knowledge of the influence of dietary nutrients on inflammation and barrier function can be important for the future development of new therapeutic approaches for patients with mucosal barrier dysfunction, a critical factor in the pathogenesis of many GI and non-GI diseases. Full article
(This article belongs to the Special Issue The Relationship between Nutrition and Digestive Diseases)
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<p>Summary of the different components of the mucosal barrier in the gastrointestinal tract (GI) tract. The physical elements include the (1) mucus layer, (2) intestinal epithelium, and (3) commensal microbiota. The immunological elements consist of (4) antimicrobial peptides secreted by Paneth cells and enterocytes, (5) cellular immunity. AMPs: antimicrobial peptides.</p>
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3 pages, 207 KiB  
Reply
Reply to “Limitations of the Digestible Indispensable Amino Acid Score (DIAAS) and Choice of Statistical Reporting. Comment on “A Comparison of Dietary Protein Digestibility, Based on DIAAS Scoring, in Vegetarian and Non-Vegetarian Athletes.” Nutrients 2019, 11, 3106”
by Carol S. Johnston, Heidi Lynch and Christopher Wharton
Nutrients 2020, 12(4), 1184; https://doi.org/10.3390/nu12041184 - 23 Apr 2020
Viewed by 3613
Abstract
We appreciate the critique of our paper (Ciuris et al [...] Full article
2 pages, 184 KiB  
Comment
Limitations of the Digestible Indispensable Amino Acid Score (DIAAS) and Choice of Statistical Reporting. Comment on “A Comparison of Dietary Protein Digestibility, Based on DIAAS Scoring, in Vegetarian and Non-Vegetarian Athletes. Nutrients 2019, 11, 3106”
by Angela Genoni, Joel C Craddock and Emma F Strutt
Nutrients 2020, 12(4), 1183; https://doi.org/10.3390/nu12041183 - 23 Apr 2020
Cited by 4 | Viewed by 5337
Abstract
Dear Editor, [...] Full article
17 pages, 3168 KiB  
Article
Consumption of Cooked Black Beans Stimulates a Cluster of Some Clostridia Class Bacteria Decreasing Inflammatory Response and Improving Insulin Sensitivity
by Mónica Sánchez-Tapia, Irma Hernández-Velázquez, Edgar Pichardo-Ontiveros, Omar Granados-Portillo, Amanda Gálvez, Armando R Tovar and Nimbe Torres
Nutrients 2020, 12(4), 1182; https://doi.org/10.3390/nu12041182 - 23 Apr 2020
Cited by 28 | Viewed by 11979
Abstract
There is limited information on the effect of black beans (BB) as a source of protein and resistant starch on the intestinal microbiota. The purpose of the present work was to study the effect of cooked black beans with and without high fat [...] Read more.
There is limited information on the effect of black beans (BB) as a source of protein and resistant starch on the intestinal microbiota. The purpose of the present work was to study the effect of cooked black beans with and without high fat and sugar (HF + S) in the diet on body composition, energy expenditure, gut microbiota, short-chain fatty acids, NF-κB, occluding and insulin signaling in a rat model and the area under the curve for glucose, insulin and incretins in healthy subjects. The consumption of BB reduced the percentage of body fat, the area under the curve of glucose, serum leptin, LPS, glucose and insulin concentrations and increased energy expenditure even in the presence of HF + S. These results could be mediated in part by modification of the gut microbiota, by increasing a cluster of bacteria in the Clostridia class, mainly R. bromii, C. eutactus, R. callidus, R. flavefaciens and B. pullicaecorum and by an increase in the concentration of fecal butyrate. In conclusion, the consumption of BB can be recommended to prevent insulin resistance and metabolic endotoxemia by modifying the gut microbiota. Finally, the groups fed BB showed lower abundance of hepatic FMO-3, even with a high-fat diet protecting against the production of TMAO and obesity. Full article
(This article belongs to the Section Nutrition and Metabolism)
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<p>Black bean maintains lean mass and reduces body fat by increasing energy expenditure. (<b>A</b>) Weight gain after the consumption of casein (<b>C</b>), black bean (BB), C + high-fat + 5% sucrose (HF + S) (C + HF + S), BB + HF + S for 2 months. Inset: final body weight. (<b>B</b>), body fat, (<b>C</b>), lean body mass. (<b>D</b>) oxygen consumption, (<b>E</b>) correlation between lean mass and oxygen consumption, (<b>F</b>) respiratory exchange ratio (RER), <span class="html-italic">n</span> = 8 per group.</p>
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<p>Black bean downregulates leptin and insulin concentration, decreasing glucose intolerance. (<b>A</b>) Glucose tolerance test after 2 months of dietary treatment with casein (<b>C</b>), black bean (BB), C + high-fat + 5%sucrose (C + HF + S), BB + HF + S. (<b>B</b>) Area under the curve (AUC), (<b>C</b>) fasting serum glucose, (<b>D</b>) fasting serum insulin, (<b>E</b>) fasting serum leptin, (<b>F</b>) correlation between leptin an fat mass, <span class="html-italic">n</span> = 8 per group.</p>
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<p>Black bean increases α-diversity and a cluster of bacterias of the Clostridia family and decreases metabolic endotoxemia and glucose concentration. (<b>A</b>) α-diversity after 2 months of dietary treatment with casein (<b>C</b>), black bean (BB), C + high-fat + 5% sucrose (C + HF + S), BB + HF + S. (<b>B</b>) Principal components analysis of the C, BB, C + HF + S, BB + HF + S groups, <span class="html-italic">n</span> = 6 per group. (<b>C</b>) relative abundance of the main phyla, (<b>D</b>) relative abundance of gut microbiota at the class level, (<b>E</b>) and at the genus level, (<b>F</b>) linear discriminat analysis (LDA), (<b>G</b>) serum LPS concentration, (<b>H</b>) correlation between <span class="html-italic">R. bromii</span> abundance and serum glucose concentration, <span class="html-italic">n</span> = 6 per group.</p>
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<p>Consumption of black bean increases butyrate and decreases NF-κB protein abundance in the colon. (<b>A</b>) Fecal butyrate concentration, (<b>B</b>) Western blot analysis of G protein-coupled receptor (GPR) 41 and 43, occludin, NF-κB, P-NF-κB, (<b>C</b>–<b>E</b>) and densitometric analysis of GPR41, GPR43 and occludin after 2 months of dietary treatments with casein [C], black bean [BB], Casein + high-fat + S 5% [C + HF + S], BB + HF + S. (<b>F</b>) Correlation between occludin and butyrate, (<b>G</b>) correlation between NF-κB and butyrate, (<b>H</b>) correlation between LPS and GPR43. (<b>I</b>) correlation between VO2 and fecal butyrate concentration.</p>
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<p>Black bean consumption maintains intestinal integrity and insulin signaling after an acute metabolic challenge with glucose. (<b>A</b>) Western blot analysis of small intestinal G-protein-coupled receptors (GPR43 and GPR41) and occludin. (<b>B</b>) Intestinal GIP, GLP-1, (<b>C</b>) skeletal muscle IRS, phosphorylation of IRS-1 at Tyr<sup>896</sup>, AKT, phosphorylation of AKT at Ser<sup>473</sup> (<b>D</b>) Hepatic flavin monooxygenase 3 (FM03) after 2 months of dietary treatments with casein [C], black bean [BB], Casein + high-fat + S 5% [C + HF + S], BB + HF + S. Four rats of each group were injected with 2 g/kg body weight of glucose and killed 30 min later.</p>
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<p>The consumption of 25 g of available carbohydrates from black bean attenuates serum glucose and postprandial insulin peaks. After consumption of 25 g of glucose or 25 g of available carbohydrates from black bean, blood samples were taken at different times over 2 h. (<b>A</b>) Serum glucose, (<b>B</b>) serum insulin, (<b>C</b>) total plasma GIP and (<b>D</b>) total serum GLP-1 in eight healthy subjects. For each graph, the area under the curve (AUC) was calculated and showed as an inset in each panel. Data are shown as mean ± SEM. Significant differences were considered with <span class="html-italic">p</span> &lt; 0.005.</p>
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10 pages, 244 KiB  
Review
Optimal Nutritional Status for a Well-Functioning Immune System Is an Important Factor to Protect against Viral Infections
by Philip C. Calder, Anitra C. Carr, Adrian F. Gombart and Manfred Eggersdorfer
Nutrients 2020, 12(4), 1181; https://doi.org/10.3390/nu12041181 - 23 Apr 2020
Cited by 600 | Viewed by 124182
Abstract
Public health practices including handwashing and vaccinations help reduce the spread and impact of infections. Nevertheless, the global burden of infection is high, and additional measures are necessary. Acute respiratory tract infections, for example, were responsible for approximately 2.38 million deaths worldwide in [...] Read more.
Public health practices including handwashing and vaccinations help reduce the spread and impact of infections. Nevertheless, the global burden of infection is high, and additional measures are necessary. Acute respiratory tract infections, for example, were responsible for approximately 2.38 million deaths worldwide in 2016. The role nutrition plays in supporting the immune system is well-established. A wealth of mechanistic and clinical data show that vitamins, including vitamins A, B6, B12, C, D, E, and folate; trace elements, including zinc, iron, selenium, magnesium, and copper; and the omega-3 fatty acids eicosapentaenoic acid and docosahexaenoic acid play important and complementary roles in supporting the immune system. Inadequate intake and status of these nutrients are widespread, leading to a decrease in resistance to infections and as a consequence an increase in disease burden. Against this background the following conclusions are made: (1) supplementation with the above micronutrients and omega-3 fatty acids is a safe, effective, and low-cost strategy to help support optimal immune function; (2) supplementation above the Recommended Dietary Allowance (RDA), but within recommended upper safety limits, for specific nutrients such as vitamins C and D is warranted; and (3) public health officials are encouraged to include nutritional strategies in their recommendations to improve public health. Full article
(This article belongs to the Special Issue Vitamins C and D: Global and Population Health Perspectives)
18 pages, 572 KiB  
Article
Effect of a 12-Week Almond-Enriched Diet on Biomarkers of Cognitive Performance, Mood, and Cardiometabolic Health in Older Overweight Adults
by Alison Mary Coates, Samantha Morgillo, Catherine Yandell, Andrew Scholey, Jonathan David Buckley, Kathryn Ann Dyer and Alison Marie Hill
Nutrients 2020, 12(4), 1180; https://doi.org/10.3390/nu12041180 - 23 Apr 2020
Cited by 34 | Viewed by 7403
Abstract
Long term nut consumption is associated with reduced risk of coronary heart disease and better cognitive function. This study examined supplementing habitual diets with almonds or carbohydrate-rich snack foods (providing 15% energy) on biomarkers of cardiovascular and metabolic health, mood and cognitive performance. [...] Read more.
Long term nut consumption is associated with reduced risk of coronary heart disease and better cognitive function. This study examined supplementing habitual diets with almonds or carbohydrate-rich snack foods (providing 15% energy) on biomarkers of cardiovascular and metabolic health, mood and cognitive performance. Participants (overweight/obese, 50–80 years) were randomised to an almond-enriched diet (AED) or isocaloric nut-free diet (NFD) for 12 weeks. Body weight, blood lipids, glucose, insulin, blood pressure (BP), arterial stiffness, cell adhesions molecules, C reactive protein (CRP), mood, and cognitive performance (working memory primary outcome), dietary profiles and energy intake/expenditure were measured at baseline and Week 12 in 128 participants (n = 63 AED, n = 65 NFD). Compared with NFD, AED was associated with altered macro and micronutrient profiles, but no differences in energy intake or expenditure. The AED significantly reduced triglycerides and SBP but there were no other changes in cardiometabolic biomarkers, mood, or cognitive performance. The inclusion of almonds in the diet improves aspects of cardiometabolic health without affecting cognitive performance or mood in overweight/obese adults. Full article
(This article belongs to the Special Issue Nuts Intake and Human Health)
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<p>Consort diagram showing the flow of participants through the study.</p>
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26 pages, 3276 KiB  
Article
Omega-3 Fatty Acids and Eye Health: Opinions and Self-Reported Practice Behaviors of Optometrists in Australia and New Zealand
by Alexis Ceecee Zhang, Sumeer Singh, Jennifer P. Craig and Laura E. Downie
Nutrients 2020, 12(4), 1179; https://doi.org/10.3390/nu12041179 - 22 Apr 2020
Cited by 20 | Viewed by 9174
Abstract
This study investigated optometrists’ attitudes and self-reported practice behaviors towards omega-3 fatty acids for eye health, and knowledge and understanding of their potential risks and benefits. An anonymous online survey was distributed to optometrists in Australia and New Zealand. Questions included practitioner demographics [...] Read more.
This study investigated optometrists’ attitudes and self-reported practice behaviors towards omega-3 fatty acids for eye health, and knowledge and understanding of their potential risks and benefits. An anonymous online survey was distributed to optometrists in Australia and New Zealand. Questions included practitioner demographics and practice modality; self-reported practices and recommendations relating to diet, nutritional supplements, and omega-3 fatty acids for age-related macular degeneration (AMD) and dry eye disease (DED); and practitioner knowledge about omega-3 fatty acids. Of 206 included surveys, most respondents (79%) indicated recommending for their patients to consume omega-3 fatty acids to improve their eye health. Sixty-eight percent of respondents indicated recommending omega-3-rich foods for AMD management, while 62% indicated recommending omega-3 supplements. Most respondents (78%) indicated recommending omega-3-rich foods or supplements for DED. For DED, recommended omega-3 supplement dosages were (median [inter-quartile range, IQR]) 2000 mg [1000–2750 mg] per day. The main sources of information reported by respondents to guide their clinical decision making were continuing education articles and conferences. In conclusion, optometrists routinely make clinical recommendations about diet and omega-3 fatty acids. Future education could target improving optometrists’ knowledge of differences in the evidence for whole-food versus supplement sources of omega-3 fatty acids in AMD. Further research is needed to address uncertainties in the evidence regarding optimal omega-3 dosage and formulation composition in DED. Full article
(This article belongs to the Special Issue Nutrition Education in Medicine)
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<p>Survey structure.</p>
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<p>Optometrists’ self-reported clinical practices as related to diet and nutritional supplementation. Percentage (%) of respondents, from <span class="html-italic">n =</span> 206, who selected each frequency of practice, on a five-step Likert scale.</p>
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<p>Optometrists’ self-reported clinical practices as related to omega-3 fatty acid intake as a component of AMD management. (<b>A</b>) Self-reported frequency of recommending omega-3-rich foods and nutritional supplements. Percentage of respondents shown from <span class="html-italic">n =</span> 162 who indicated recommending omega-3 fatty acids for AMD. (<b>B</b>) Omega-3 food sources(s) recommended by respondents. Percentage shown from <span class="html-italic">n =</span> 140 who indicated recommending omega-3-rich foods. (<b>C</b>) Recommended ideal frequency for patients to consume marine-based (long-chain) omega-3-containing foods. Percentage shown from <span class="html-italic">n =</span> 133 who indicated recommending fish or seafood as omega-3 food sources in (<b>B</b>). (<b>D</b>) Word-cloud representation of specific recommendations for omega-3 supplementation (based on <span class="html-italic">n =</span> 80 responses from the 132 participants who indicated recommending omega-3 supplements).</p>
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<p>Optometrists’ self-reported clinical practices as related to omega-3 fatty acids for managing DED. (<b>A</b>) Self-reported frequency of recommending omega-3-rich foods and nutritional supplements. Percentage of respondents shown from <span class="html-italic">n =</span> 162 who indicated recommending omega-3 fatty acids for DED, (<b>B</b>) DED subtypes, and (<b>C</b>) severities that participants self-reported making recommendations for omega-3 fatty acids (in either food or supplement forms). Percentages shown from <span class="html-italic">n =</span> 162. (<b>D</b>) Type of omega-3 food source(s) recommended. Percentage shown from <span class="html-italic">n =</span> 159 who indicated recommending omega-3-rich foods. (<b>E</b>) Recommended ideal frequency for patients to consume marine-based (long-chain) omega-3-rich foods. Percentages shown from <span class="html-italic">n =</span> 154 who indicated recommending fish or seafood as omega-3 food sources in (e). (<b>F</b>) Type of oral omega-3 supplements recommended. Percentages shown from <span class="html-italic">n =</span> 160 who indicated recommending omega-3 supplements. (<b>G</b>) Word-cloud representation of specific recommendations for omega-3 supplementation (based on <span class="html-italic">n =</span> 105 responses from the 160 participants who indicated recommending omega-3 supplementation).</p>
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<p>Percentage of optometrists who selected each information and/or evidence source (with no limit on the number of sources able to be selected) as informing their clinical decision-making regarding omega-3 fatty acids. CE, continuing education.</p>
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1 pages, 158 KiB  
Retraction
RETRACTED: Nassef et al. The Impact of Aerobic Exercise and Badminton on HDL Cholesterol Levels in Adult Taiwanese. Nutrients 2019, 11, 515
by Nutrients Editorial Office
Nutrients 2020, 12(4), 1178; https://doi.org/10.3390/nu12041178 - 22 Apr 2020
Cited by 1 | Viewed by 3081
Abstract
The published article [...] Full article
10 pages, 886 KiB  
Article
Acute Effect of the Timing of Resistance Exercise and Nutrient Intake on Muscle Protein Breakdown
by Wataru Kume, Jun Yasuda and Takeshi Hashimoto
Nutrients 2020, 12(4), 1177; https://doi.org/10.3390/nu12041177 - 22 Apr 2020
Cited by 5 | Viewed by 7525
Abstract
Background: Combining resistance exercise (RE) with nutrient intake stimulates muscle protein net balance. However, it is still unclear whether the optimal timing of nutrient intake is before or after RE, especially on muscle protein breakdown (MPB) for an augmented muscle anabolic response. The [...] Read more.
Background: Combining resistance exercise (RE) with nutrient intake stimulates muscle protein net balance. However, it is still unclear whether the optimal timing of nutrient intake is before or after RE, especially on muscle protein breakdown (MPB) for an augmented muscle anabolic response. The aim of this study was to investigate the effect of a substantial mixed meal (i.e., nutrient- and protein-dense whole foods) before or after RE, compared with RE without a meal on the acute response of MPB in a crossover-design study. Methods: Eight healthy young men performed three trials: (1) meal intake before RE (Pre), (2) meal intake after RE (Post), and (3) RE without meal intake (No). Plasma insulin and 3-methylhistidine (3-MH), an MPB marker, were measured. Results: Time course change in plasma insulin level after RE was significantly higher in the Post condition than in the Pre and No conditions. The area under the curve of 3-MH concentration was significantly lower in the Post condition than in the Pre and No conditions. Conclusions: These results suggest that a substantial mixed meal immediately after RE may effectively suppress MPB in the morning. Full article
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<p>Experimental protocol. RE, resistance exercise; M, meal; Pre, meal intake before RE; Post, meal intake after RE; No, RE without meal intake.</p>
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<p>Time course change in plasma insulin. *; <span class="html-italic">p</span> = 0.043 Post vs. Pre, #; <span class="html-italic">p</span> = 0.023 Pre vs. No, †; <span class="html-italic">p</span> = 0.015 Post vs. No, **; <span class="html-italic">p</span> = 0.001 Post vs. Pre, ## <span class="html-italic">p</span> = 0.001 Pre vs. No, ††; <span class="html-italic">p</span> &lt; 0.001 Post vs. No. RE: resistance exercise; Post: meal intake after RE; Pre: meal intake before RE; No: RE without meal intake.</p>
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<p>Time course change in plasma 3-MH concentration (<b>A</b>), the area under the curve of plasma 3-MH concentration (7:00–15:00) (<b>B</b>), time course change in plasma 3-MH/LBM levels (<b>C</b>), the area under the curve of plasma 3-MH/LBM levels (7:00–15:00) (<b>D</b>). * <span class="html-italic">p</span> = 0.016, † <span class="html-italic">p</span> = 0.007 (<b>B</b>), * <span class="html-italic">p</span> = 0.020, † <span class="html-italic">p</span> = 0.007 (<b>D</b>). RE: resistance exercise; Post: meal intake after RE; Pre: meal intake before RE; No: RE without meal intake; 3-MH: 3-methylhistidine; LBM: lean body mass.</p>
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11 pages, 764 KiB  
Article
Acute Ingestion of a Novel Nitrate-Rich Dietary Supplement Significantly Increases Plasma Nitrate/Nitrite in Physically Active Men and Women
by Richard J. Bloomer, Matthew Butawan, Brandon Pigg and Keith R. Martin
Nutrients 2020, 12(4), 1176; https://doi.org/10.3390/nu12041176 - 22 Apr 2020
Cited by 5 | Viewed by 6586
Abstract
Background: Dietary supplements purported to increase circulating nitric oxide are very popular among consumers. We determined the acute impact of two novel dietary supplements on plasma nitrate/nitrite (NOx) and nitrite alone. Methods: 20 men and women (age: 24 ± 5 years) ingested two [...] Read more.
Background: Dietary supplements purported to increase circulating nitric oxide are very popular among consumers. We determined the acute impact of two novel dietary supplements on plasma nitrate/nitrite (NOx) and nitrite alone. Methods: 20 men and women (age: 24 ± 5 years) ingested two different nitrate-rich supplements (Resync Recovery Blend at 7.5 g and 15 g; Resync Collagen Blend at 21 g), or placebo, on four different days. Fasting blood samples were obtained before and 75 min following ingestion and analyzed for NOx and nitrite. Results: Nitrite was not differently impacted by treatment (p > 0.05). The NOx response for men and women was very similar, with no sex interactions noted (p > 0.05). Condition (p < 0.0001), time (p < 0.0001), and condition x time (p < 0.0001) effects were noted for NOx. Values increased from baseline to post-ingestion for the Resync Recovery Blend at 7.5 g (11 ± 9 to 101 ± 48 µM) and at 15 g (9 ± 5 to 176 ± 91 µM), as well as for the Resync Collagen Blend (9 ± 9 to 46 ± 21 µM), while values for placebo remained stable (9 ± 7 to 8 ± 5 µM). Conclusion: While nitrite alone was not impacted by treatment, both Resync products result in an increase in plasma NOx, with the increase proportionate to the quantity of “nitric oxide blend” ingredients contained within each product. Future studies are needed to determine the physiological implications of the increased NOx, as pertaining to exercise performance and recovery, in addition to other aspects of human health. Full article
(This article belongs to the Section Sports Nutrition)
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<p>Heart rate before and 75 min after ingestion of Resync or placebo. Values are the mean ± SD. No differences of statistical significance were noted (<span class="html-italic">p</span> &gt; 0.05). Note: Resync Recovery 1 = 1 serving; Resync Recovery 2 = 2 servings.</p>
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<p>Systolic blood pressure before and 75 min after ingestion of Resync or placebo. Values are the mean ± SD. No differences of statistical significance were noted (<span class="html-italic">p</span> &gt; 0.05). Note: Resync Recovery 1 = 1 serving; Resync Recovery 2 = 2 servings.</p>
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<p>Diastolic blood pressure before and 75 min after ingestion of Resync or placebo. Values are the mean ± SD. No differences of statistical significance were noted (<span class="html-italic">p</span> &gt; 0.05). Note: Resync Recovery 1 = 1 serving; Resync Recovery 2 = 2 servings.</p>
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<p>Nitrate/nitrite before and 75 min after ingestion of Resync or placebo. Values are the mean ± SD; total nitrate+nitrite. * Statistical significance from pre- to post-ingestion noted for Resync Recovery 1 (<span class="html-italic">p</span> &lt; 0.0001), Resync Recovery 2 (<span class="html-italic">p</span> &lt; 0.0001), and Resync Collagen (<span class="html-italic">p</span> = 0.002); ** post-ingestion Resync values are greater than post-ingestion placebo values (<span class="html-italic">p</span> &lt; 0.05); no differences noted for pre-ingestion values between conditions (<span class="html-italic">p</span> &gt; 0.05). Note: Resync Recovery 1 = 1 serving; Resync Recovery 2 = 2 servings.</p>
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18 pages, 2493 KiB  
Article
Glycomacropeptide Prevents Iron/Ascorbate-Induced Oxidative Stress, Inflammation and Insulin Sensitivity with an Impact on Lipoprotein Production in Intestinal Caco-2/15 Cells
by Mathilde Foisy-Sauvé, Lena Ahmarani, Edgard Delvin, Alain T. Sané, Schohraya Spahis and Emile Levy
Nutrients 2020, 12(4), 1175; https://doi.org/10.3390/nu12041175 - 22 Apr 2020
Cited by 15 | Viewed by 4308
Abstract
Background. Metabolic Syndrome (MetS), a major worldwide concern for the public health system, refers to a cluster of key metabolic components, and represents a risk factor for diabetes and cardiovascular diseases. As oxidative stress (OxS) and inflammation are the major triggers of insulin [...] Read more.
Background. Metabolic Syndrome (MetS), a major worldwide concern for the public health system, refers to a cluster of key metabolic components, and represents a risk factor for diabetes and cardiovascular diseases. As oxidative stress (OxS) and inflammation are the major triggers of insulin sensitivity (IS), a cardinal MetS feature, the principal aim of the present work is to determine whether glycomacropeptide (GMP), a milk-derived bioactive peptide, exerts beneficial effects on their expression. Methods. Fully differentiated intestinal Caco-2/15 cells are used to evaluate the preventive action of 2 mg/mL GMP against OxS and inflammation induced by the mixture iron-ascorbate (Fe/Asc) (200 μM:2 mM). The potency of GMP of decreasing the production of lipoproteins, including chylomicrons (CM), very-low-density lipoproteins (VLDL) and low-density lipoproteins (LDL) is also assessed. Results. The administration of GMP significantly reduces malondialdehyde, a biomarker of lipid peroxidation, and raises superoxide dismutase 2 and glutathione peroxidase via the induction of the nuclear factor erythroid 2–related factor 2, a transcription factor, which orchestrates cellular antioxidant defenses. Similarly, GMP markedly lowers the inflammatory agents tumor necrosis factor-α and cyclooxygenase-2 via abrogation of the nuclear transcription factor-kB. Moreover, GMP-treated cells show a down-regulation of Fe/Asc-induced mitogen activated protein kinase pathway, suggesting greater IS. Finally, GMP decreases the production of CM, VLDL, and LDL. Conclusions. Our results highlight the effectiveness of GMP in attenuating OxS, inflammation and lipoprotein biogenesis, as well as improving IS, the key components of MetS. Further investigation is needed to elucidate the mechanisms mediating the preventive action of GMP. Full article
(This article belongs to the Section Nutrition and Metabolism)
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<p>Effects of treatments on cell integrity in Caco-2/15 cells. Integrity of the cell monolayer was evaluated by cell viability, differentiation, and tight junction assays using fully differentiated Caco-2/15 cells. Different doses (0.5, 1, and 2 mg/mL) of purified glycomacropeptide (GMP) powder were added to Caco-2/15 cells 18 h before incubation with Fe/Asc (200 µM/2 mM) for 6 h at 37 °C for the (<b>A</b>) MTT assay. A dose of 2 mg/mL was selected for the assessment of (<b>B</b>) villin and (<b>C</b>) occludin protein expression as well as (<b>D</b>) transepithelial electrical resistance (TEER). Results represent the means ± SEM of <span class="html-italic">n</span> = 3 independent experiments in triplicate.</p>
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<p>Effects of GMP on lipid peroxidation and antioxidant defense in Caco-2/15 cells. Caco-2/15 cells were pre-incubated for 18 h before treatment with Fe/Asc (200 µM/2 mM) +/− GMP (2 mg/mL) for 6 h at 37 °C as described in Materials and Methods. (<b>A</b>) Levels of malondialdehyde (MDA), a biomarker of lipid peroxidation, were measured in cell lysates. Protein expression of the anti-oxidative markers (<b>B</b>) superoxide dismutase 2 (SOD2), (<b>C</b>) glutathione peroxidase (GPx), and (<b>D</b>) nuclear factor erythroid 2–related factor 2 (Nrf2) was determined by Western blot. Results represent the means ± SEM of <span class="html-italic">n</span> = 3 independent experiments in triplicate. * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01, *** <span class="html-italic">p</span> &lt; 0.001 vs. controls (Ctrl). <sup>#</sup> <span class="html-italic">p</span> &lt; 0.05, <sup>##</sup> <span class="html-italic">p</span> &lt; 0.01, <sup>###</sup> <span class="html-italic">p</span> &lt; 0.001 vs. Fe/Asc-treated cells.</p>
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<p>Effects of GMP on inflammation in Caco-2/15 cells. Caco-2/15 cells were pre-incubated for 18 h before treatment with Fe/Asc (200 µM/2 mM) +/− GMP (2 mg/mL) for 6 h at 37°C as described in Materials and Methods. Protein expression of the inflammatory biomarkers (<b>A</b>) Tumor necrosis factor alpha (TNF-α), (<b>B</b>) Cyclooxygenase-2 (COX-2), (<b>C</b>) Nuclear transcription factor-kappa B (NF-κB), and (<b>D</b>) Inhibitor of kappa B (IκB) was determined by Western blot. (<b>E</b>) The NF-κB/IκB ratio was calculated. Results represent the means ± SEM of <span class="html-italic">n</span> = 3 independent experiments in triplicate. * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01 vs. controls (Ctrl). <sup>#</sup> <span class="html-italic">p</span> &lt; 0.05, <sup>##</sup> <span class="html-italic">p</span> &lt;0.01 vs Fe/Asc-treated cells.</p>
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<p>Effects of GMP on insulin sensitivity in Caco-2/15 cells. Caco-2/15 cells were pre-incubated for 18 h before treatment with Fe/Asc (200 µM/2 mM) +/− GMP (2 mg/mL) for 6 h at 37 °C. Two hours before the end of the six hour-incubation with Fe/Asc, insulin (100 nM) was added to evaluate insulin sensitivity as described in Materials and Methods. Protein expression of (<b>A</b>) p38-MAPK, (<b>B</b>) phospho-p38-MAPK, (<b>D</b>) AKT and (<b>E</b>) phospho-Akt was determined by Western blot. (<b>C</b>) Phospho p38-MAP/p38-MAPK and (<b>F</b>) phospho-Akt/AKT ratios were calculated. Results represent the means ± SEM of <span class="html-italic">n</span> = 3 independent experiments in triplicate. ** <span class="html-italic">p</span> &lt; 0.01, *** <span class="html-italic">p</span> &lt; 0.001 vs. Controls (Ctr); <sup>#</sup> <span class="html-italic">p</span> &lt; 0.05 vs. Fe/Asc Caco-2 cells treated with insulin.</p>
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<p>Effects of GMP on insulin signaling in Caco-2/15 cells. Caco-2/15 cells were pre-incubated for 18 h before treatment with Fe/Asc (200 µM/2 mM) +/− GMP (2 mg/mL) for 6 h at 37 °C. Two hours before the end of the six hours incubation with Fe/Asc, insulin (100 nM) was added to evaluate insulin signaling as described in Materials and Methods. Protein expression of (<b>A</b>) PI3K, (<b>B</b>) phospho-PI3K, (<b>D</b>) AMPKα and (<b>E</b>) phospho-AMPKα was determined by Western blot. (<b>C</b>) Phospho-PI3K/PI3K and (<b>F</b>) phospho-AMPKα/AMPKα ratios were calculated. Results represent the means ± SEM of <span class="html-italic">n</span> = 3 independent experiments in triplicate. *<span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01, *** <span class="html-italic">p</span> &lt; 0.001 vs. controls (Ctrl). <sup>#</sup> <span class="html-italic">p</span> &lt; 0.05, <sup>###</sup> <span class="html-italic">p</span> &lt; 0.001 vs. Fe/Asc Caco-2 cells treated with insulin.</p>
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<p>Effects of GMP on lipoprotein production in Caco-2/15 cells. Caco-2/15 cells were pre-incubated for 18 h with serum-free Eagle’s minimal essential medium (EMEM) containing BSA/oleic acid +/− GMP (2 mg/mL). After 18 h, medium was discarded and replaced with fresh EMEM and radiolabeled [<sup>14</sup>C]-oleic acid +/− GMP (2 mg/mL). After 24 h incubation, apical and basolateral media were collected. Lipoprotein production was assessed by quantification of (<b>A</b>) chylomicrons, (<b>B</b>) very low-density lipoproteins (VLDL), and (<b>C</b>) low-density lipoproteins (LDL) in basolateral medium. Results represent the means ± SEM of <span class="html-italic">n</span> = 3 independent experiments in triplicate. ** <span class="html-italic">p</span> &lt; 0.01 vs. control (Ctrl) cells.</p>
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13 pages, 1156 KiB  
Article
Facial EMG Correlates of Subjective Hedonic Responses During Food Consumption
by Wataru Sato, Kazusa Minemoto, Akira Ikegami, Makoto Nakauma, Takahiro Funami and Tohru Fushiki
Nutrients 2020, 12(4), 1174; https://doi.org/10.3390/nu12041174 - 22 Apr 2020
Cited by 25 | Viewed by 4536
Abstract
An exploration of physiological correlates of subjective hedonic responses while eating food has practical and theoretical significance. Previous psychophysiological studies have suggested that some physiological measures, including facial electromyography (EMG), may correspond to hedonic responses while viewing food images or drinking liquids. However, [...] Read more.
An exploration of physiological correlates of subjective hedonic responses while eating food has practical and theoretical significance. Previous psychophysiological studies have suggested that some physiological measures, including facial electromyography (EMG), may correspond to hedonic responses while viewing food images or drinking liquids. However, whether consuming solid food could produce such subjective–physiological concordance remains untested. To investigate this issue, we assessed participants’ subjective ratings of liking, wanting, valence, and arousal while they consumed gel-type food stimuli of various flavors and textures. We additionally measured their physiological signals, including facial EMG from the corrugator supercilii. The results showed that liking, wanting, and valence ratings were negatively correlated with corrugator supercilii EMG activity. Only the liking rating maintained a negative association with corrugator supercilii activity when the other ratings were partialed out. These data suggest that the subjective hedonic experience, specifically the liking state, during food consumption can be objectively assessed using facial EMG signals and may be influenced by such somatic signals. Full article
(This article belongs to the Section Nutrition Methodology & Assessment)
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<p>Schematic illustrations of the stimuli (left) and experimental setups (right): The bite-sized gel-type food stimuli were placed on disposable plastic spoons in a row.</p>
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<p>Schematic illustrations of electrode placement for electromyography recording of the corrugator supercilii, zygomatic major, masseter, and suprahyoid muscles.</p>
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<p>Mean (with standard error) intraindividual correlation coefficients between subjective ratings and physiological responses across stimuli: Corrugator = corrugator supercilii; Zygomatic = zygomatic major; SPL = skin potential level; HR = heart rate. ***, <span class="html-italic">p</span> &lt; 0.001; **, <span class="html-italic">p</span> &lt; 0.005.</p>
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<p>Group-mean (with standard error) values and regression lines of subjective ratings (liking, wanting, and valence) and corrugator supercilii electromyography activity (standardized within each individual).</p>
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<p>Mean (with standard error) intraindividual partial correlation coefficients between subjective ratings and corrugator supercilii electromyography activity, controlling for the other two ratings. * <span class="html-italic">p</span> &lt; 0.05.</p>
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