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24 pages, 3196 KiB  
Article
Dietary Tannic Acid Promotes Growth Performance and Resistance Against Aeromonas hydrophila Infection by Improving the Antioxidative Capacity and Intestinal Health in the Chinese Soft-Shelled Turtle (Pelodiscus sinensis)
by Liqin Ji, Yisen Shangguan, Chen Chen, Chengqing Wei, Junxian Zhu, Xiaoyou Hong, Xiaoli Liu, Xinping Zhu and Wei Li
Antioxidants 2025, 14(1), 112; https://doi.org/10.3390/antiox14010112 (registering DOI) - 20 Jan 2025
Abstract
To investigate the effect of tannic acid (TA) on the growth, disease resistance, and intestinal health of Chinese soft-shelled turtles, individual turtles were fed with 0 g/kg (CG), 0.5 g/kg, 1 g/kg, 2 g/kg, and 4 g/kg TA diets for 98 days. Afterwards, [...] Read more.
To investigate the effect of tannic acid (TA) on the growth, disease resistance, and intestinal health of Chinese soft-shelled turtles, individual turtles were fed with 0 g/kg (CG), 0.5 g/kg, 1 g/kg, 2 g/kg, and 4 g/kg TA diets for 98 days. Afterwards, the turtles’ disease resistance was tested using Aeromonas hydrophila. The results showed that 0.5–4 g/kg of dietary TA increased the growth performance and feed utilization (p < 0.05), with 2.38 g/kg being the optimal level for the specific growth rate (SGR). The addition of 0.5–4 g/kg of TA in diets increased the mucosal fold height and submucosa thickness of the small intestine, which reached a maximum of 2 g/kg. The addition of 0.5–2 g/kg of TA effectively reduced the cumulative mortality that had been induced by A. hydrophila, with the 2 g/kg dosage leading to the lowest mortality. Additionally, 1–4 g/kg of TA improved the T-SOD, CAT, and GSH-Px activities during infection, while 2 g/kg of dietary TA enhanced the richness and diversity of the microbiota, for example, by increasing Actinobacteria but inhibiting Firmicutes. The transcriptome demonstrated that the predominant differentially expressed genes (DEGs) in TA2 were mainly enriched in the PPAR signaling pathway (Acsl5, Apoa2, Apoa5, Fabp1, Fabp2, and Fabp6); in glycine, serine, and threonine metabolism (Chdh, Gatm, and Shmt1); and in steroid biosynthesis (Cel, Hsd17b7, Soat2, and Sqle). The main differentially expressed metabolites (DEMs) that were discovered by means of metabolome analysis included cholylhistidine, calcipotriol, 13-O-tetradecanoylphorbol 12-acetate, and hexahomomethionine in CG vs. TA2. Integrative analyses of two omics revealed that 2 g/kg of TA mitigated inflammation by activating the PPAR signaling pathway and regulating the lipid metabolism via multiple pathways, such as steroid biosynthesis and α-linolenic acid metabolism. In general, the inclusion of 2 g/kg of TA in turtle diets can optimally promote growth and bacterial resistance by maintaining intestinal health and improving antioxidant capacity. Full article
(This article belongs to the Special Issue Novel Antioxidants for Animal Nutrition—2nd Edition)
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Figure 1
<p>Experimental flowchart. CG indicates the control group. TA0.5 indicates the group supplemented with 0.5 g/kg TA. TA1 indicates the group supplemented with 1 g/kg TA. TA2 indicates the group supplemented with 2 g/kg TA. TA4 indicates the group supplemented with 4 g/kg TA.</p>
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<p>Quadratic regression analysis of the SGR (<b>A</b>) and WGR (<b>B</b>) of Chinese soft-shelled turtles who were fed a diet with graded levels of TA for 98 days. (<b>C</b>) The cumulative mortality of Chinese soft-shelled turtles who were infected with <span class="html-italic">Aeromonas hydrophila</span>. Different letters indicate significant differences among groups at the same point (<span class="html-italic">p</span> &lt; 0.05). CG indicates the control group. TA0.5 indicates the group supplemented with 0.5 g/kg TA. TA1 indicates the group supplemented with 1 g/kg TA. TA2 indicates the group supplemented with 2 g/kg TA. TA4 indicates the group supplemented with 4 g/kg TA.</p>
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<p>The effect of TA on plasma T-SOD (<b>A</b>), CAT (<b>B</b>), GSH-Px (<b>C</b>), ACP (<b>D</b>), and ALP (<b>E</b>) activities. All data are represented as mean ± SE (n = 3). Different letters indicate significant differences among groups at the same point (<span class="html-italic">p</span> &lt; 0.05). T-SOD, total superoxide dismutase; CAT, catalase; GSH-Px, glutathione peroxidase; ACP, acid phosphatase; ALP, alkaline phosphatase. CG indicates the control group. TA0.5 indicates the group supplemented with 0.5 g/kg TA. TA1 indicates the group supplemented with 1 g/kg TA. TA2 indicates the group supplemented with 2 g/kg TA. TA4 indicates the group supplemented with 4 g/kg TA. The x-axis represents the number of hours post-infection with <span class="html-italic">Aeromonas hydrophila</span>.</p>
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<p>Images of the small intestinal morphology, observed using an optical microscope, in Chinese soft-shelled turtles after the 98-day feeding experiment. CG (<b>A</b>,<b>F</b>) indicates the control group. TA0.5 (<b>B</b>,<b>G</b>) indicates the group supplemented with 0.5 g/kg TA. TA1 (<b>C</b>,<b>H</b>) indicates the group supplemented with 1 g/kg TA. TA2 (<b>D</b>,<b>I</b>) indicates the group supplemented with 2 g/kg TA. TA4 (<b>E</b>,<b>J</b>) indicates the group supplemented with 4 g/kg TA. Scale bar = 500 μm (<b>A</b>–<b>E</b>). Scale bar = 50 μm (<b>F</b>–<b>J</b>). MH indicates the mucosal fold height, MW represents the mucosal fold width, LP denotes the lamin propria width, and SM denotes the submucosa.</p>
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<p>Analyses of the intestinal microbiome. (<b>A</b>) Venn diagram showing the number of OTUs that were identified in the CG and TA2 groups. (<b>B</b>) Comparison of the Shannon indexes of the CG and TA2 groups using Student’s <span class="html-italic">t</span>-test. (<b>C</b>) PCoA analysis of the intestinal microflora of the CG vs. the TA2 group. Intestinal microflora at the OTU (<b>D</b>) and species (<b>E</b>) levels. (<b>F</b>) LEfSe multilevel species hierarchy tree in the CG vs. the TA2 group. (<b>G</b>) A comparative KEGG pathway enrichment analysis of the microbial functional abundance in the CG and TA2 groups with PICRUSt2. <span class="html-italic">p</span> &lt; 0.05 indicates a significant difference in the Shannon index. “CG” indicates the control group. “TA2” indicates the group supplemented with 2 g/kg TA.</p>
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<p>Overview of the DEGs from the transcriptome in the CG vs. TA2 group comparison. (<b>A</b>) The results of the PCA demonstrating the difference in gene expression patterns between the CG and TA2 groups. (<b>B</b>) A correlation heatmap of all the gene expression patterns in the three replicates of the CG and TA2 groups. (<b>C</b>) A volcano plot of the DEGs in the CG vs. TA2 group comparison. (<b>D</b>) A KEGG enrichment analysis of the DEGs in the CG and TA2 group comparison. (<b>E</b>) A GO enrichment analysis of the DEGs in the CG and TA2 group comparison. “CG” indicates the control group. “TA2” indicates the group supplemented with 2 g/kg TA.</p>
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<p>Identification of the DEMs and signaling pathways from the metabolome in the CG vs. TA2 group comparison. The cross-validation (<b>A</b>) and permutation test (<b>B</b>) of the metabolite profiles were carried out using orthogonal projection to latent structures–discriminant analysis (OPLS-DA). (<b>C</b>) The number of DEMs, filtered based on |log2 (FoldChange)| &gt; 1 and an adjusted <span class="html-italic">p</span>-value &lt; 0.05 in the CG vs. TA2 group comparisons. (<b>D</b>) Z-score plots exhibiting the top-30 DEMs from the CG vs. TA2 comparison. (<b>E</b>) The differential abundance score based on a pathway analysis of the metabolic changes in the CG vs. TA2 group comparison.</p>
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<p>Joint analysis of the DEGs and DEMs in the CG vs. TA2 group comparison for the small intestine. (<b>A</b>) A nine-quadrant diagram indicating the correlation of the DEGs and DEMs in the CG vs. TA2 group comparison. The DEGs and DEMs with the absolute value of fold change ≧ 2 were marked with red color, which, with the absolute value of fold change &lt; 2, were marked with yellow color. (<b>B</b>) A chord diagram exhibiting the significant association of DEGs with DEMs in the CG vs. TA2 group comparison. (<b>C</b>) Conjoint analyses of the DEG and DEM-enriched KEGG pathways. (<b>D</b>) The interactive networks of the DEGs and DEMs in the dominant KEGG pathways. “CG” indicates the control group. “TA2” indicates the group supplemented with 2 g/kg TA.</p>
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14 pages, 1041 KiB  
Article
Exploitation of the Nutraceutical Potential of the Infesting Seaweed Chaetomorpha linum as a Yellow Mealworms’ Feed: Focus on Nutrients and Antioxidant Activity
by Annalaura Brai, Edoardo Brogi, Franca Tarchi, Federica Poggialini, Chiara Vagaggini, Sauro Simoni, Valeria Francardi and Elena Dreassi
Foods 2025, 14(2), 325; https://doi.org/10.3390/foods14020325 (registering DOI) - 20 Jan 2025
Viewed by 96
Abstract
According to the Sustainable Blue Economy Communication, the Farm to Fork Strategy, and the European Green Deal, novel business models supporting the use of resources from oceans and seas are of primary importance. Interestingly, several infesting seaweeds are consumed as foods in Asia [...] Read more.
According to the Sustainable Blue Economy Communication, the Farm to Fork Strategy, and the European Green Deal, novel business models supporting the use of resources from oceans and seas are of primary importance. Interestingly, several infesting seaweeds are consumed as foods in Asia and are fundamental ingredients in several traditional dishes. Herein, according to the circular economy approach, we investigate the use of Chaetomorpha linum (CL) as a Tenebrio molitor larvae feed in different percentages: 20%, 50%, and 100%, respectively. We analyzed the effects of CL on the survival and biometric parameters of larvae. The survival rate remained comparable to the control, while the mean weight was inversely proportional to the CL%. The nutrient composition was substantially different from the control, showing increased protein and reduced fat content. Analysis of the secondary metabolites revealed a better fatty acid composition, rich in PUFA, with lipid nutritional indexes comparable to seaweeds and crabs. The simulated gastrointestinal digestion highlights the increased content of essential amino acids, and a two times higher antioxidant activity with respect to the control. Taken together, our results confirm that CL can be used as a TML supplement, with beneficial effects in protein content and fat quality. Full article
(This article belongs to the Section Nutraceuticals, Functional Foods, and Novel Foods)
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<p>Design of the trial. Three plastic trays containing 50 larvae/each, were fed with a standard diet (CTRL); three containers were fed with a diet containing 20% <span class="html-italic">Chaetomorpha linum</span> (CL20%); three containers were fed with a diet containing 50% <span class="html-italic">Chaetomorpha linum</span> (CL50%); and three containers were fed with a diet containing 100% <span class="html-italic">Chaetomorpha linum</span> (CL100%). At various time points (7, 15, 21, 28, 34, 42, and 48 days) survival and biometrical measurements were made. Nutrients and secondary metabolites were analyzed after 15, 30, and 48 days.</p>
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<p>(<b>A</b>) Kaplan–Meier curve of <span class="html-italic">Tenebrio molitor</span> larvae fed on a standard diet (CTRL) or a standard diet supplemented with <span class="html-italic">Chaetomorpha linum</span> (CL). Larvae supplemented with 20% (<span class="html-italic">w</span>/<span class="html-italic">w</span>) CL, 50% (<span class="html-italic">w</span>/<span class="html-italic">w</span>) CL (CL50%), or 100% (<span class="html-italic">w</span>/<span class="html-italic">w</span>) CL (CL100%). Curve comparison has been analyzed with the Mantel–Cox test (χ<sup>2</sup> = 2.677, df = 3, and <span class="html-italic">p</span>-value = 0.4441). (<b>B</b>) Mean body weight over time. Statistical analysis was performed with two-way ANOVA with different diets and time of rearing (15, 28, and 48 days) as fixed factors and Tukey’s posthoc test. a, b, c, d, e, f, g, h and i values without a common superscript are significantly different (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Fat (g of fat/100 g of TML) quantification of <span class="html-italic">Tenebrio molitor</span> larvae fed on a standard diet (CTRL) or a standard diet supplemented with <span class="html-italic">Chaetomorpha linum</span> (CL) 20% (<span class="html-italic">w</span>/<span class="html-italic">w</span>) CL, 50% (<span class="html-italic">w</span>/<span class="html-italic">w</span>) CL (CL50%), or 100% (<span class="html-italic">w</span>/<span class="html-italic">w</span>) CL (CL100%) over time. The results represent the mean ± SD of three experiments. Statistical analysis was performed with two-way ANOVA with different diets and time of rearing (15, 30, and 45 days) as fixed factors and Tukey’s post hoc test. a, b, c, d and e values without a common superscript are significantly different (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Trolox equivalent antioxidant capacity (TEAC) analysis before gastric digestion (GD), after gastric digestion (GD), and after gastrointestinal digestion (GID). <span class="html-italic">Tenebrio molitor</span> larvae were fed on a standard diet (CTRL) or a standard diet supplemented with <span class="html-italic">Chaetomorpha linum</span> (CL). The results represent the mean ± SD of three experiments. Larvae supplemented with 20% (<span class="html-italic">w</span>/<span class="html-italic">w</span>) CL, 50% (<span class="html-italic">w</span>/<span class="html-italic">w</span>) CL (CL50%), or 100% (<span class="html-italic">w</span>/<span class="html-italic">w</span>) CL (CL100%). Statistical analysis was performed with two-way ANOVA with different diets and digestion steps as fixed factors and Tukey’s post hoc test. a, b, c and d values without a common superscript are significantly different (<span class="html-italic">p</span> &lt; 0.05).</p>
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14 pages, 1006 KiB  
Article
Oil and Biodiesel Production from Mortierella isabellina Biomass by a Direct Near-Critical Fluid Extraction and Transesterification Method
by Daniela Sallet, Gustavo Andrade Ugalde, Marcus Vinícius Tres, Marcio Antonio Mazutti, Giovani Leone Zabot and Raquel Cristine Kuhn
Biomass 2025, 5(1), 6; https://doi.org/10.3390/biomass5010006 (registering DOI) - 19 Jan 2025
Viewed by 446
Abstract
Oil and biodiesel produced from lipidic microorganisms are gaining attention in the scientific area. However, intracellular oil needs additional steps for its recovery for transesterification, which generally uses catalysts. In this context, thermal processes that do not use catalysts demand to be investigated. [...] Read more.
Oil and biodiesel produced from lipidic microorganisms are gaining attention in the scientific area. However, intracellular oil needs additional steps for its recovery for transesterification, which generally uses catalysts. In this context, thermal processes that do not use catalysts demand to be investigated. Therefore, the objective was to produce oil and biodiesel from Mortierella isabellina biomass by direct transformation of dry microbial biomass without using a catalyst. Near-critical fluid extraction (nCFE) of lipids followed by direct transesterification was carried out with the same equipment, as an intensification process. A central composite design was used to evaluate the influence of temperature, pressure, and solvent mass-to-feed mass ratio on the extraction yield. Microbial lipids produced by submerged fermentation and extracted by nCFE with ethanol were used for biodiesel production. The highest total extraction yield (55.4 wt%) and biodiesel conversion (22.2%) were obtained at 300 °C and 20 MPa with 30 g of ethanol/g of fungal biomass. The other conditions yielded extraction yields and biodiesel conversions ranging from 9.7 to 46.0% and from 1.5 to 22.0%, respectively. The interaction between temperature and pressure was significant (p < 0.05), with a positive correlation, indicating that higher temperatures and pressures yielded higher biodiesel conversion rates. The process intensification is advantageous because it is developed sequentially in one step and uses only ethanol as a solvent/reagent, without catalysts. Therefore, the direct extraction and transesterification of Mortierella isabellina lipids demonstrated to be technically feasible and an environmentally friendly technology for the production of fungal oil and biodiesel. The oil can be used in the food and cosmetic industries because it has nutrients that regulate physiological mechanisms promoting human health, while biodiesel can be used in the transport sector and in stationary engines. Full article
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<p>Schematic illustration of the homemade equipment: 1—pump for the liquid; 2—pre-heating bath; 3—reactor A; 4—reactor B; 5—temperature control system; 6—cooling bath; 7—micrometering valve; 8—sample flask.</p>
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<p>Kinetic yields of extracted compounds obtained from <span class="html-italic">Mortierella isabellina</span>; top graphic: assays 1—4; middle graphic: assays 5—8; bottom graphic: assays 9—11.</p>
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<p>Standardized Pareto chart for effect estimate of process variables on total extraction yields and biodiesel conversion.</p>
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<p>Example of mass balance for oil plus biodiesel production from <span class="html-italic">Mortierella isabellina</span> biomass by a direct extraction and transesterification method with the process conditions defined in Assay 1.</p>
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14 pages, 659 KiB  
Article
County-Level Food Insecurity and Hepatocellular Carcinoma Risk: A Cross-Sectional Analysis
by Rebecca D. Kehm, Chrystelle L. Vilfranc, Jasmine A. McDonald and Hui-Chen Wu
Int. J. Environ. Res. Public Health 2025, 22(1), 120; https://doi.org/10.3390/ijerph22010120 - 18 Jan 2025
Viewed by 288
Abstract
Food insecurity (FI) is associated with several known hepatocellular carcinoma (HCC) risk factors, but few studies have directly examined FI in association with HCC risk. We aimed to investigate whether county-level FI is associated with HCC risk. We used data from 21 registries [...] Read more.
Food insecurity (FI) is associated with several known hepatocellular carcinoma (HCC) risk factors, but few studies have directly examined FI in association with HCC risk. We aimed to investigate whether county-level FI is associated with HCC risk. We used data from 21 registries in the Surveillance Epidemiology and End Results database to obtain county-level counts of HCC cases from 2018 to 2021. We obtained the county-level FI rates for 2018–2021 from Feeding America’s Map the Meal Gap. We used multi-level Poisson regression models with robust standard errors to calculate incidence rate ratios (IRRs) and 95% confidence intervals (CIs). Overall, a one-standard-deviation (SD) increase in county-level FI was associated with an 8% increase in HCC risk in the fully adjusted model (IRR = 1.08, 95% CI = 1.06, 1.10). When stratified by age at diagnosis, a one-SD increase in county-level FI was associated with a 2% higher risk of HCC in the ≥65 age group (IRR = 1.02, 95% CI = 1.00, 1.05) and a 15% higher risk in the <65 age group (IRR = 1.15, 95% CI = 1.11, 1.19; interaction p-value < 0.001). If confirmed in other studies, these findings support the need for interventions and policies addressing FI in populations at increased risk for HCC. Full article
(This article belongs to the Section Global Health)
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<p>(<b>a</b>) County-level food insecurity rates and (<b>b</b>) county-level hepatocellular carcinoma incidence rates for the timeframe of 2018–2021 for each county within Surveillance, Epidemiology, and End Results catchment areas in the contiguous United States. The values in the heatmaps reflect rates per 100,000, with the lowest rates illustrated in dark purple and the highest rates illustrated in yellow.</p>
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<p>Association between county-level food insecurity tertiles and hepatocellular carcinoma risk stratified by age group at diagnosis and estimated from multi-level Poisson regression models, 21 SEER Registries, 2018–2021. Legend: Estimates are adjusted for sex, race, ethnicity, county-level rates of binge drinking, tobacco smoking, and obesity. County-level food insecurity is modeled as a categorical variable with three levels: low (≤11%), medium (&gt; 1% to &lt;14.5%), and high (≥14.5%). Interaction term <span class="html-italic">p</span>-value &lt; 0.001.</p>
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16 pages, 1811 KiB  
Article
Short- But Not Long-Term Effects of Creep Feeding Provided to Suckling Piglets
by María Romero, Ana Heras-Molina, María Muñoz, Luis Calvo, José Ignacio Morales, Ana Isabel Rodríguez, Rosa Escudero, Clemente López-Bote, Cristina Óvilo and Álvaro Olivares
Animals 2025, 15(2), 253; https://doi.org/10.3390/ani15020253 - 17 Jan 2025
Viewed by 289
Abstract
Fifty-eight litters (16 from primiparous gilts and 42 from multiparous sows) were used, with a total number of 750 piglets involved in the study. Birth weight was stratified into three groups: low (<1.02 kg; LBW), normal (1.02–1.62 kg; NBW), and high (>1.62 kg; [...] Read more.
Fifty-eight litters (16 from primiparous gilts and 42 from multiparous sows) were used, with a total number of 750 piglets involved in the study. Birth weight was stratified into three groups: low (<1.02 kg; LBW), normal (1.02–1.62 kg; NBW), and high (>1.62 kg; HBW). A creep feeding diet was offered to piglets in a creep feeder in 29 litters from day 7 until their weaning. Piglet mortality was recorded daily. Traceability was ensured up to the point of carcass splitting and subsequent meat analysis. Each carcass was eviscerated and weighed individually. Sixty-nine piglets were selected for the microbiome analysis (35 from the control group and 34 from the creep feeding group). Feces samples from the rectum were obtained at three time points (three days prior weaning, a week after weaning, and before the slaughtering of the pigs). Mortality during lactation was influenced by birth weight, with LBW piglets exhibiting a six-fold higher mortality rate than HBW. Creep feeding did not impact piglet mortality. Heavier piglets demonstrated greater weight gain when subjected to creep feeding, while the growth potential of lighter piglets was reduced. Variation in creep feeding consumption based on birth weight also affected microbiome composition, with high-birth-weight piglets displaying higher alpha diversity than low- and normal-birth-weight piglets seven days after lactation. Alpha diversity is indicative of gut health, with higher values suggesting greater stability and adaptability to different feed sources. In conclusion, the immediate impacts of creep feeding appear to be most prominent during lactation and potentially early postweaning. These short-term effects are modulated by birth weight, with HBW piglets demonstrating the greatest benefits from the implementation of creep-feeding practices. Full article
(This article belongs to the Section Pigs)
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<p>Relationship between birth weight (BW) and daily weight gain (g/d) along lactation because of the presence (CF, dotted line) or absence (Ctr, filled line) of creep feeding. Daily gain in CT group = 87.5 (±19.7) + 54.9 (±13.7) × BW (kg); <span class="html-italic">p</span> &lt; 0.0001; R<sup>2</sup> = 0.16; daily gain in CF group (g/d) = 42.5 (±14.3) + 94.1 (±10.5) × BW; <span class="html-italic">p</span> &lt; 0.0001; R<sup>2</sup> = 0.25. Slopes were different (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Observed richness according to treatment and birth weight after weaning. CF = creep feeding. Low: weight equal to or less than 1.02 kg; normal: weight between 1.02 and 1.62 kg; high: weight over 1.62 kg.</p>
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<p>Treatment and time effects in Bray–Curtis’s beta diversity dissimilarity index in rectal samples from pigs 3 days before weaning (T1) and a week after weaning (T2). CF = creep feeding.</p>
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<p>Alpha-diversity analyses (observed richness and Shannon index) three days prior weaning (T1) and before slaughtering (T3) in pigs that underwent creep feeding treatment (CF) or not (control) separated by birth weight (low: weight equal to or less than 1.02 kg; normal: weight between 1.02 and 1.62 kg; high: weight over 1.62 kg).</p>
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<p>Time effect in Bray–Curtis beta diversity dissimilarity index in rectal samples from pigs 3 days before weaning (T1) and before slaughtering (T3).</p>
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18 pages, 11389 KiB  
Article
Artemia Nauplii Enriched with Soybean Lecithin Enhances Growth Performance, Intestine Morphology, and Desiccation Stress Resistance in Yellow Drum (Nibea albiflora) Larvae
by Zhenya Zhou, Pian Zhang, Peng Tan, Ruiyi Chen, Weihua Hu, Ligai Wang, Yuming Zhang and Dongdong Xu
Metabolites 2025, 15(1), 63; https://doi.org/10.3390/metabo15010063 - 17 Jan 2025
Viewed by 395
Abstract
The inherent deficiency of phospholipids in Artemia limits its nutritional value as live prey for marine fish larvae. In our previous study, we optimized a phospholipid enrichment method by incubating Artemia nauplii with 10 g of soybean lecithin per m3 of seawater [...] Read more.
The inherent deficiency of phospholipids in Artemia limits its nutritional value as live prey for marine fish larvae. In our previous study, we optimized a phospholipid enrichment method by incubating Artemia nauplii with 10 g of soybean lecithin per m3 of seawater for 12 h, significantly enhancing their phospholipid content. Purpose: The present study evaluated the impact of this enrichment on yellow drum (Nibea albiflora) larvae, focusing on growth performance, intestinal morphology, body composition, weaning success, and desiccation stress resistance. Methods: The larvae (12 days post-hatching, dph) were fed either soybean lecithin-enriched (SL group) or newly hatched (NH group) Artemia nauplii for 10 days. Results: By the end of the experiment, the SL group exhibited a markedly greater body weight and standard length compared to the NH group (p < 0.05). This growth improvement was due to enhanced intestinal morphology, characterized by a significantly higher mucosal fold height, microvillus density, and microvillus length (p < 0.05). Intestinal RNA sequencing identified 160 upregulated and 447 downregulated differentially expressed genes (DEGs) in the SL group compared to the NH group. Soybean lecithin enrichment reduced the expression of lipogenesis-related genes (fasn, scd, elovl1) while upregulating lipid catabolism genes (ppara, cpt1, cpt2), indicating increased lipid breakdown and energy production. After a 5-day weaning period onto a commercial microdiet, the SL group continued to show significantly superior growth performance. In an afterward desiccation stress test, larvae from the SL group demonstrated significantly higher survival rates, potentially due to the decreased expression of intestinal cytokine genes (ccl13, mhc1, mhc2) observed in the RNA-seq analysis. Conclusion: This study highlights that feeding soybean lecithin-enriched Artemia nauplii enhances growth performance and desiccation stress in yellow drum larvae by promoting lipid catabolism, improving intestinal structure, and regulating immune responses. Full article
(This article belongs to the Special Issue Metabolism and Nutrition in Fish)
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<p>General workflow of the present study. The 12 post-hatching (dph) larvae were fed either soybean lecithin-enriched <span class="html-italic">Artemia</span> nauplii (SL) or newly hatched <span class="html-italic">Artemia</span> nauplii (NH). At the end of feeding stage 1 (17 dph), growth performance was analyzed using 10 larvae per tank (<span class="html-italic">n</span> = 6). By the end of feeding stage 2 (22 dph), larvae from three tanks per group were sampled to assess growth performance, body nutrient composition, and intestinal tissue morphology. Transcriptome analysis was performed to uncover the molecular mechanisms driving the observed outcomes. A weaning experiment was subsequently performed over five days, during which the proportion of <span class="html-italic">Artemia</span> nauplii was reduced by 20% daily, while microdiet quantities were adjusted based on larval consumption. Finally, a desiccation stress resistance test was conducted to evaluate larval stress tolerance. Avg. SL refers to the average standard length (SL) of larvae, while Avg. BW represents the average body weight (BW) of larvae.</p>
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<p>Survival, growth performance, nutrient composition in yellow drum larvae. (<b>A</b>) Larval survival rate at the end of feeding stage 1 (17 dph), feeding stage 2 (22 dph), and after weaning experiment (27 dph). (<b>B</b>) Larval body weight and standard length. (<b>C</b>) Crude lipid crude protein and phospholipid content (%, dry weight) of larvae at the end of feeding stage 2 (22 dph) and after weaning experiment (27 dph). * <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>Desiccation stress challenge. (<b>A</b>) Survival rate of larvae after the desiccation stress challenge. (<b>B</b>) Comparison of body weight and standard length between surviving and dead larvae. *** <span class="html-italic">p</span> &lt; 0.001.</p>
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<p>Intestinal tissue morphology and ultrastructure analysis. Violin plots illustrate the perimeter ratio, muscular thickness, and mucosal fold height of intestinal tissues. Scanning electron microscopy (SEM) images reveal the surface ultrastructure of intestinal tissues, while transmission electron microscopy (TEM) images display microvillus morphology, including quantified microvillus density and length. * <span class="html-italic">p</span> &lt; 0.05, *** <span class="html-italic">p</span> &lt; 0.001; otherwise, differences were not significant (<span class="html-italic">p</span> &gt; 0.05).</p>
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<p>Transcriptome analysis of larval intestine tissues. (<b>A</b>) Pearson’s correlation matrix of intestinal tissue samples. (<b>B</b>) Volcano plot depicting DEGs between groups. (<b>C</b>) Enrichment analysis of DEGs for Kyoto Encyclopedia of Genes and Genomes (KEGGs) pathways. (<b>D</b>) Enrichment analysis of DEGs for Gene Ontology (GO) terms.</p>
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<p>Transcriptome analysis of larval intestine tissues. (<b>A</b>) Pearson’s correlation matrix of intestinal tissue samples. (<b>B</b>) Volcano plot depicting DEGs between groups. (<b>C</b>) Enrichment analysis of DEGs for Kyoto Encyclopedia of Genes and Genomes (KEGGs) pathways. (<b>D</b>) Enrichment analysis of DEGs for Gene Ontology (GO) terms.</p>
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<p>DEGs encoding protein–protein interaction (PPI) networks. (<b>A</b>) Validation of RNA-seq results using qRT-PCR for selected DEGs. (<b>B</b>) Heatmap of selected DEGs between treatments. (<b>C</b>) Network of DEGs related to lipid metabolism and immunity pathways in intestinal tissue.</p>
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15 pages, 547 KiB  
Review
Heat Stress in Dairy Cows: Impacts, Identification, and Mitigation Strategies—A Review
by Charles Paranhos Oliveira, Fernanda Campos de Sousa, Alex Lopes da Silva, Érica Beatriz Schultz, Roger Iván Valderrama Londoño and Pedro Antônio Reinoso de Souza
Animals 2025, 15(2), 249; https://doi.org/10.3390/ani15020249 - 17 Jan 2025
Viewed by 359
Abstract
Heat stress in animals affects productivity, health, and reproduction, with particularly pronounced effects in dairy cows. Identifying heat stress requires understanding both physiological and environmental indicators, such as increased heart rate, respiratory rate, and rectal temperature, which reflect the animal’s thermal condition within [...] Read more.
Heat stress in animals affects productivity, health, and reproduction, with particularly pronounced effects in dairy cows. Identifying heat stress requires understanding both physiological and environmental indicators, such as increased heart rate, respiratory rate, and rectal temperature, which reflect the animal’s thermal condition within its environment. Thermoregulation in cows involves behavioral and physiological adjustments to maintain homeothermy, aiming to stabilize their internal thermal state. To assess the thermal condition of animals, machine learning models have been developed, leveraging both environmental and physiological indicators for more accurate stress detection. Among the various indices of thermal environment, the Temperature and Humidity Index (THI) is the most widely used. Cooling strategies for animals and their environments are essential to mitigate the effects of heat stress. One effective approach involves the use of evaporative adiabatic cooling combined with forced ventilation systems in feeding alleys and pre-milking holding areas. This method enhances evaporative exchanges and facilitates heat dissipation between the animal and its surroundings, thereby alleviating heat stress and improving both the welfare and productivity of dairy cows. Full article
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<p>Schematic representation of animal comfort, homeothermic, and survival zones. Where T.C.Z. é the thermal comfort zone, L.C.T is the lower critical temperature, and U.C.T. is the upper critical temperature.</p>
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17 pages, 1266 KiB  
Article
Analysis of the Surface Quality Characteristics in Hard Turning Under a Minimal Cutting Fluid Environment
by Sandip Mane, Rajkumar Bhimgonda Patil, Anindita Roy, Pritesh Shah and Ravi Sekhar
Appl. Mech. 2025, 6(1), 5; https://doi.org/10.3390/applmech6010005 - 17 Jan 2025
Viewed by 356
Abstract
This paper analyzes the surface quality characteristics, such as arithmetic average roughness (Ra), maximum peak-to-valley height (Rt), and average peak-to-valley height (Rz), in hard turning of AISI 52100 steel using a (TiN/TiCN/Al2O3) coated carbide insert under a minimal cutting [...] Read more.
This paper analyzes the surface quality characteristics, such as arithmetic average roughness (Ra), maximum peak-to-valley height (Rt), and average peak-to-valley height (Rz), in hard turning of AISI 52100 steel using a (TiN/TiCN/Al2O3) coated carbide insert under a minimal cutting fluid environment (MCFA). MCFA, a sustainable high-velocity pulsed jet technique, reduces harmful effects on human health and the environment while improving machining performance. Taguchi’s L27 orthogonal array was used to conduct the experiments. The findings showed that surface roughness increases with feed rate, identified as the most influential parameter, while the depth of cut shows a negligible effect. The main effects plot of signal-to-noise (S/N) ratios for the combined response of Ra, Rt, and Rz revealed the optimal cutting conditions: cutting speed of 140 m/min, feed rate of 0.05 mm/rev, and depth of cut of 0.3 mm. Feed rate ranked highest in influence, followed by cutting speed and depth of cut. The lower values of surface roughness parameters were observed in the ranges of Ra ≈ 0.248–0.309 µm, Rt ≈ 2.013–2.186 µm, and Rz ≈ 1.566 µm at a feed rate of 0.05–0.07 mm/rev. MCFA-assisted hard turning reduces surface roughness by 35–40% compared to dry hard turning and 10% to 24% when compared to the MQL technique. Moreover, this study emphasizes the significant environmental benefits of MCFA, as it incorporates minimal eco-friendly cutting fluids that minimize ecological impact while enhancing surface finish. Full article
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<p>Experimental setup of minimal cutting fluid application (Mane et al., 2020) [<a href="#B27-applmech-06-00005" class="html-bibr">27</a>]. (1) AC Motor, (2) Fluid Pump, (3) Variable Frequency Device, (4) Cutting Fluid Tank, (5) Cutting Fluid High-Pressure Line, (6) Nozzle, (7) Dynamometer, (8) Digital Display unit, (9) Infrared Thermometer, (10) Thermocouple Cable.</p>
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<p>Main effects plot for S/N ratios for the combined response of Ra, Rt, and Rz.</p>
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<p>Contour plot of (<b>a</b>) Ra, (<b>b</b>) Rt, and (<b>c</b>) Rz for cutting speed vs. feed rate.</p>
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<p>Contour plot of (<b>a</b>) Ra, (<b>b</b>) Rt, and (<b>c</b>) Rz for depth of cut vs. feed rate.</p>
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21 pages, 5551 KiB  
Article
Effects of Chinese Herbal Medicines on Growth Performance, Antioxidant Capacity, and Liver and Intestinal Health of Hybrid Snakehead (Channa maculata ♀ × Channa. argus ♂)
by Jiamin Kang, Shuzhan Fei, Junhao Zhang, Haiyang Liu, Qing Luo, Mi Ou, Langjun Cui, Tao Li and Jian Zhao
Fishes 2025, 10(1), 33; https://doi.org/10.3390/fishes10010033 - 16 Jan 2025
Viewed by 505
Abstract
Chinese herbal medicines have become a new green feed additive in the aquaculture industry. The aim of this study is to investigate the effects of traditional Chinese herbal medicines (Isatidis radix, Forsythia suspensa, and Schisandra chinensis) on the growth [...] Read more.
Chinese herbal medicines have become a new green feed additive in the aquaculture industry. The aim of this study is to investigate the effects of traditional Chinese herbal medicines (Isatidis radix, Forsythia suspensa, and Schisandra chinensis) on the growth performance, antioxidant capacity, and intestinal microbiota of hybrid snakehead (Channa maculata× Channa argus ♂). A total of 600 fish (mean weight: 15.85 ± 0.15 g) were randomly assigned to five groups, including the control group (CG), I. radix extract group (IRE), F. suspensa extract group (FSE), S. chinensis extract group (SCE), and the Chinese herbal medicine mixture group (CHMM; a mixture of extracts of I. radix, F. suspensa, and S. chinensis at the ratio of 1:1:1) for 6 weeks. The results show that the IRE-supplemented diet improved the survival rate (SR), feed efficiency ratio (FE), and condition factor (CF) compared to others. Compared to the control group, the activity of superoxide dismutase (SOD) in plasma and intestine was significantly increased in the FSE and CHMM groups, whereas the content of malondialdehyde (MDA) in plasma and liver was significantly reduced in the SCE group. A 16s rRNA analysis indicates that dietary supplementation with FSE significantly promoted the proliferation of Fusobacteriota, while IRE supplementation increased the alpha diversity of intestinal bacteria. In conclusion, the addition of I. radix to the diet of hybrid snakehead improves growth, antioxidant capacity, and liver and intestine health, and modulates the intestinal microbiota of snakehead positively. Full article
(This article belongs to the Special Issue Impacts of Dietary Supplements on Fish Growth and Health)
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<p>(<b>A</b>) Effects of dietary supplementation with CHM extracts on liver histology of hybrid snakehead. (<b>B</b>) Relative contents of liver lipid droplets in each experimental group. Values are expressed as means ± S.E. Values not sharing same letters are significantly different (<span class="html-italic">p</span> &lt; 0.05). N and black arrow: nucleus; V and red arrow: fat vacuoles; red circles indicate nuclei offset by cell vacuolization; black circles indicate the accumulation of fat droplets.</p>
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<p>Effects of dietary supplementation with CHM extracts on intestinal histology of hybrid snakehead (HE). The MT indicates the muscular thickness, the VH indicates the villi heights, the VW indicates the villi width, and the GC indicates the goblet cells. The circles represent intestinal mucous membrane shedding. The triangles represent intestinal villi fall-off. The pentagram represents intestinal villus adhesion.</p>
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<p>The intestinal microscopic structure parameters of hybrid snakehead. (<b>A</b>) The intestinal villi heights of hybrid snakehead; (<b>B</b>) The intestinal villi width of hybrid snakehead; (<b>C</b>) The intestinal muscular thickness of hybrid snakehead; (<b>D</b>) The intestinal goblet cells of hybrid snakehead. Values are expressed as means ± S.E. Values not sharing same letters are significantly different (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Effects of dietary supplementation with CHM extracts on antioxidant performance in plasma (<b>A</b>–<b>C</b>), liver (<b>D</b>–<b>F</b>), and intestine (<b>G</b>–<b>I</b>) of hybrid snakehead. Values are expressed as means ± S.E. (n = 6), and values not sharing same letters are significantly different (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Effect of dietary supplementation with CHM on the relative expression of immune-related genes and antioxidant genes in the liver (<b>A</b>) and (<b>B</b>) intestine of hybrid snakehead. Values are expressed as means ± S.E., and values not sharing same letters are significantly different (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>PCoA analysis of intestinal microflora in hybrid snakehead at the OTU level. (<b>A</b>) Venn diagram; (<b>B</b>) Venn diagram showing the OTUs between different groups and the OTUs shared between groups in the intestinal microbiota in hybrid snakehead.</p>
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<p>The relative abundance of intestine microbiota composition in hybrid snakehead at the (<b>A</b>) phylum level and (<b>B</b>) genus level.</p>
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<p>Pearson correlation between intestinal microbial community and growth indexes, inflammatory genes, and antioxidant indexes. (<b>A</b>) The relationship between the abundance of intestinal contents at phylum level with inflammatory genes, growth performance, and antioxidant indexes. (<b>B</b>) The relationship between the abundance of intestinal contents at genus level with inflammatory genes, growth performance, and antioxidant indexes. *: values differ significantly (<span class="html-italic">p</span> &lt; 0.05); **: values differ extremely significantly (<span class="html-italic">p</span> &lt; 0.01).</p>
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23 pages, 7326 KiB  
Article
Significance of Tool Coating Properties and Compacted Graphite Iron Microstructure for Tool Selection in Extreme Machining
by Anna Maria Esposito, Qianxi He, Jose M. DePaiva and Stephen C. Veldhuis
Nanomaterials 2025, 15(2), 130; https://doi.org/10.3390/nano15020130 - 16 Jan 2025
Viewed by 380
Abstract
This study aims to determine the extent to which coating composition and workpiece properties impact machinability and tool selection when turning Compacted Graphite Iron (CGI) under extreme roughing conditions. Two CGI workpieces, differing in pearlite content and graphite nodularity, were machined at a [...] Read more.
This study aims to determine the extent to which coating composition and workpiece properties impact machinability and tool selection when turning Compacted Graphite Iron (CGI) under extreme roughing conditions. Two CGI workpieces, differing in pearlite content and graphite nodularity, were machined at a cutting speed of 180 m/min, feed rate of 0.18 mm/rev, and depth of cut of 3 mm. To assess the impact of tool properties across a wide range of commercially available tools, four diverse multilayered cemented carbide tools were evaluated: Tool A and Tool B with a thin AlTiSiN PVD coating, Tool C with a thick Al2O3-TiCN CVD coating, and Tool D with a thin Al2O3-TiC PVD coating. The machinability of CGI and wear mechanisms were analyzed using pre-cutting characterization, in-process optical microscopy, and post-test SEM analysis. The results revealed that CGI microstructural variations only affected tool life for Tool A, with a 110% increase in tool life between machining CGI Grade B and Grade A, but that the effects were negligible for all other tools. Tool C had a 250% and 70% longer tool life compared to the next best performance (Tool A) for CGI Grade A and CGI Grade B, respectively. With its thick CVD-coating, Tool C consistently outperformed the others due to its superior protection of the flank face and cutting edge under high-stress conditions. The cutting-induced stresses played a more significant role in the tool wear process than minor differences in workpiece microstructure or tool properties, and a thick CVD coating was most effective in addressing the tool wear effects for the extreme roughing conditions. However, differences in tool life for Tool A showed that tool behavior cannot be predicted based on a single system parameter, even for extreme conditions. Instead, tool properties, workpiece properties, cutting conditions, and their interactions should be considered collectively to evaluate the extent that an individual parameter impacts machinability. This research demonstrates that a comprehensive approach such as this can allow for more effective tool selection and thus lead to significant cost savings and more efficient manufacturing operations. Full article
(This article belongs to the Special Issue Mechanical Properties and Applications for Nanostructured Alloys)
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<p>CGI workpiece microstructure at two different magnifications.</p>
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<p>SEM/EDS coating and substrate cross-section for (<b>a</b>,<b>a’</b>) Tool A; (<b>b</b>,<b>b’</b>) Tool B; (<b>c</b>,<b>c’</b>) Tool C; and (<b>d</b>,<b>d’</b>) Tool D.</p>
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<p>SEM tool surface images for (<b>a</b>) Tool A; (<b>b</b>) Tool B; (<b>c</b>) Tool C; and (<b>d</b>) Tool D.</p>
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<p>SEM/EDS substrate microstructure for (<b>a</b>,<b>a’</b>) Tool A; (<b>b</b>,<b>b’</b>) Tool B; (<b>c</b>,<b>c’</b>) Tool C; and (<b>d</b>,<b>d’</b>) Tool D.</p>
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<p>Scratch test images for (<b>a</b>) Tool A; (<b>b</b>) Tool B; (<b>c</b>) Tool C; and (<b>d</b>) Tool D.</p>
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<p>Tool life curves for (<b>a</b>) CGI Grade A at S = 180 m/min; (<b>b</b>) CGI Grade B at S = 180 m/min; and (<b>c</b>) CGI Grade A at S = 250 m/min.</p>
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<p>Average Pass 1 cutting forces for (<b>a</b>) CGI Grade A and (<b>b</b>) CGI Grade B.</p>
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<p>Undersurface of Pass 1 chips.</p>
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<p>Shear bands of Pass 1 chips.</p>
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<p>Tool A end-of-life SEM images.</p>
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<p>Tool A rapid wear progression.</p>
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<p>Tool B end-of-life SEM images.</p>
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<p>Tool B rapid wear progression.</p>
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<p>Tool C end-of-life SEM images.</p>
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<p>Tool C rapid wear progression.</p>
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<p>Tool D end-of-life SEM images.</p>
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<p>Tool D rapid wear progression.</p>
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16 pages, 3456 KiB  
Article
Effects of Bile Acids on Growth Performance, Hepatopancreatic Antioxidant Capacity, Intestinal Immune-Related Gene Expression, and Gut Microbiota of Penaeus vannamei
by Yun Zhao, Duanduan Chen and Hui Wang
Animals 2025, 15(2), 240; https://doi.org/10.3390/ani15020240 - 16 Jan 2025
Viewed by 229
Abstract
This study aimed to examine the impact of varying concentrations of bile acids (BA) added to the feed on several aspects of Penaeus vannamei. The purity of BA was 25.29%, and its main components were 5.74% chenodeoxycholic acid, 6.27% allocholic acid, 3.20% [...] Read more.
This study aimed to examine the impact of varying concentrations of bile acids (BA) added to the feed on several aspects of Penaeus vannamei. The purity of BA was 25.29%, and its main components were 5.74% chenodeoxycholic acid, 6.27% allocholic acid, 3.20% cholic acid, 5.79% hyodeoxycholic acid, and 2.31% hyocholic acid. The experiment was designed with four groups: CT, BA1, BA2, and BA3, where BA were added to the shrimp basal diet at concentrations of 0.0 mg/kg, 0.1 mg/kg, 1.0 mg/kg, and 10.0 mg/kg, respectively. After 60 days of farming P. vannamei (initial body weight: 1.21 ± 0.05 g), the results showed that BA supplementation significantly improved growth performance, and BA2 group was the most significant, which increased the final weight (FBW) by 18.6%, weight gain rate (WGR) by 19.5%, and survival rate (SR) by 5.8% compared with the CT group (p < 0.05). Additionally, the activities of trypsin and lipase in gut tissue were significantly increased (p < 0.05). Furthermore, BA supplementation increased the activity of antioxidant-related enzymes in the hepatopancreas and enhanced the mRNA expression levels of gut-associated immune genes. In addition, the supplementation of 0.1 mg/kg BA significantly altered the gut microbial composition, reducing the proportion of harmful Proteobacteria while enhancing the relative abundance of beneficial microorganisms such as Firmicutes and Bacteroides. In conclusion, 1.0 mg/kg and 10.0 mg/kg BA supplementation significantly improved the growth performance, digestive capacity, and antioxidant capacity of shrimp, among which 1.0 mg/kg supplementation had the most significant effect and improved the intestinal microbial composition of shrimp. Full article
(This article belongs to the Section Aquatic Animals)
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<p>The effect of BA on the activity of digestive enzymes in the intestine of <span class="html-italic">P. vannamei</span>. Data were presented as mean ± SD, n = 3. <sup>a–c</sup> The values in the same row sharing different superscript letters are significantly different, as determined by one-way ANOVA and Turkey’s test (<span class="html-italic">p</span> &lt; 0.05). CT—basal diet; BA1—basal diet supplemented with 0.1 mg/kg BA; BA2—basal diet supplemented with 1.0 mg/kg BA; BA3—basal diet supplemented with 10.0 mg/kg BA.</p>
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<p>The effects of BA on antioxidant enzyme activity in hepatopancreas of <span class="html-italic">P. vannamei</span>. The data were presented as mean ± SD, n = 3. <sup>a–c</sup> Values in the same row sharing different superscript letters are significantly different, as determined by one-way ANOVA and Turkey’s test (<span class="html-italic">p</span> &lt; 0.05). CT—basal diet; BA1—basal diet supplemented with 0.1 mg/kg BA; BA2—basal diet supplemented with 1.0 mg/kg BA; BA3—basal diet supplemented with 10.0 mg/kg BA.</p>
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<p>The effects of BA on gut immune-related gene expression in <span class="html-italic">P. vannamei</span>. The data were presented as mean ± SD, n = 3. <sup>a,b</sup> The values in the same row sharing different superscript letters are significantly different, as determined by one-way ANOVA and Turkey’s test (<span class="html-italic">p</span> &lt; 0.05). CT—basal diet; BA1—basal diet supplemented with 0.1 mg/kg BA; BA2—basal diet supplemented with 1.0 mg/kg BA; BA3—basal diet supplemented with 10.0 mg/kg BA.</p>
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<p>LEfSe analysis (LDA &gt; 4). The data were presentedas mean ± SD, n = 3. <sup>a,b</sup> The values in the same row sharing different superscript letters are significantly different, as determined by one-way ANOVA and Turkey’s test (<span class="html-italic">p</span> &lt; 0.05). CT—basal diet; BA2—BA, basal diet supplemented with 1.0 mg/kg BA.</p>
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<p>Differential analysis of dominant flora in the BA2 group. The data were presentedas mean ± SD, n = 3. CT—basal diet; BA2—BA, basal diet supplemented with 1.0 mg/kg BA.</p>
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23 pages, 2327 KiB  
Article
Metabolic Performance of Mealworms and Black Soldier Fly Larvae Reared on Food and Agricultural Waste and By-Products
by Frederik Kjær Nielsen, Rasmus Juhl Hansen, Asmus Toftkær Muurmann, Simon Bahrndorff and Niels Thomas Eriksen
Animals 2025, 15(2), 233; https://doi.org/10.3390/ani15020233 - 16 Jan 2025
Viewed by 382
Abstract
Mealworms and black soldier fly (BSF) larvae are two of the most reared insects at an industrial scale. Both may feed on by-products from agricultural and food industries. Feed efficiency is one of the most important aspects of such processes and varies between [...] Read more.
Mealworms and black soldier fly (BSF) larvae are two of the most reared insects at an industrial scale. Both may feed on by-products from agricultural and food industries. Feed efficiency is one of the most important aspects of such processes and varies between species and feed substrates and depends on the metabolic performance of the larvae. Compared to each other, both species may hold advantageous capabilities affecting their feed efficiency, likely depending on the feed substrate. We reared mealworms and BSF larvae on a diverse selection of by-products from agricultural and food industries, quantified major metabolic rates across their life spans, and compared their performances. The type of feed substrates had stronger effects on the growth of mealworms than on black soldier fly larvae. Generally, BSF larvae were advantageous in terms of the highest maximal specific growth rate (0.50–0.77 day−1) and feed assimilation rate (0.81–1.16 day−1) and shortest development period (23–25 days) but disadvantageous in terms of metabolic maintenance cost (0.07–0.21 day−1). In mealworms, the maximal specific growth rates were 0.02–0.11 day−1, the highest feed assimilation rates were 0.16–0.37 day−1, and the development period was at least 65–93 days, while maintenance was only 0.02–0.05 day−1. In contrast to the BSF larvae, the specific maintenance rate was weight dependent in the mealworms and lowest in the largest individuals. The combined outcome of these metabolic rates resulted in an average carbon net growth efficiency, NGE*avg of 0.16–0.40 in mealworms and 0.33–0.56 in BSF larvae across their life span. It thus seems that BSF larvae are more versatile and somewhat more efficient at converting diverse feed substrates into growth than mealworms. Differences in NGE*avg affected the substrate conversion efficiencies (i.e., the ratio of the weight gain of the larvae to the reduced weight of feed substrates) and may thus impact the overall outcome of insect farming. Full article
(This article belongs to the Section Animal Nutrition)
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Graphical abstract
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<p>Growth and CO<sub>2</sub> production rates of mealworms reared on (<b>A</b>–<b>C</b>) wheat bran, (<b>D</b>–<b>F</b>) rapeseed cake, (<b>G</b>–<b>I</b>) brewers’ spent grain, and (<b>J</b>–<b>L</b>) deproteinized grass. Left panels show the larval dry weight, <span class="html-italic">X<sub>DW</sub></span> (●, solid curves predicted by Equation (2)), and specific growth rate, <span class="html-italic">μ</span> (dotted curves predicted by Equation (3)). Center panels show the CO<sub>2</sub> production rates per individual larvae, <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>r</mi> </mrow> <mrow> <mi>C</mi> <mi>O</mi> <mn>2</mn> </mrow> </msub> </mrow> </semantics></math> (♦, solid curves predicted by Equation (5)), specific CO<sub>2</sub> production rate (<span class="html-fig-inline" id="animals-15-00233-i001"><img alt="Animals 15 00233 i001" src="/animals/animals-15-00233/article_deploy/html/images/animals-15-00233-i001.png"/></span>, dashed curves predicted by Equation (6)), and specific feed assimilation rate, <span class="html-italic">a</span> (dashed curves, grey scale predicted by Equation (8)). Right panels compare the specific CO<sub>2</sub> production rate to specific growth rate (curve predicted by Equations (2)–(8)). Data points represent averages of 5 replicate cultures ± standard deviation. Extinction of individual larval cultures indicated by †.</p>
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<p>(<b>A</b>) Individual CO<sub>2</sub> production rate, <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>r</mi> </mrow> <mrow> <mi>C</mi> <mi>O</mi> <mn>2</mn> </mrow> </msub> </mrow> </semantics></math>. (<b>B</b>) Specific CO<sub>2</sub> production rate (measured in carbon equivalents), <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>q</mi> </mrow> <mrow> <mi>C</mi> <mi>O</mi> <mn>2</mn> </mrow> </msub> </mrow> </semantics></math>. (<b>C</b>) NGE* of mealworms reared on wheat bran (●, solid curve), rapeseed cake (○, dashed curve), or brewers’ spent grain (<span class="html-fig-inline" id="animals-15-00233-i001"><img alt="Animals 15 00233 i001" src="/animals/animals-15-00233/article_deploy/html/images/animals-15-00233-i001.png"/></span>). Insets in panels (<b>B</b>,<b>C</b>) show the <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>q</mi> </mrow> <mrow> <mi>C</mi> <mi>O</mi> <mn>2</mn> </mrow> </msub> </mrow> </semantics></math> and NGE* on brewers’ spent grain on expanded scales. Data points represent average values of 5 replicate cultures (standard deviations indicated in <a href="#animals-15-00233-f001" class="html-fig">Figure 1</a>). Curves are model predictions from <a href="#animals-15-00233-f001" class="html-fig">Figure 1</a>.</p>
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<p>Growth and CO<sub>2</sub> production rates of BSF larvae reared on (<b>A</b>–<b>C</b>) chicken feed, (<b>D</b>–<b>F</b>) rapeseed cake, (<b>G</b>–<b>I</b>) brewers’ spent grain, (<b>J</b>–<b>L</b>) deproteinized grass, and (<b>M</b>–<b>O</b>) biopulp. Left panels show the larval dry weight, <span class="html-italic">X<sub>DW</sub></span> (●, solid curves predicted by Equation (2)), and specific growth rate, <span class="html-italic">μ</span> (dotted curves predicted by Equation (3)). Center panels show the CO<sub>2</sub> production rates per individual larvae, <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>r</mi> </mrow> <mrow> <mi>C</mi> <mi>O</mi> <mn>2</mn> </mrow> </msub> </mrow> </semantics></math> (♦, solid curves predicted by Equation (5)), specific CO<sub>2</sub> production rate (<span class="html-fig-inline" id="animals-15-00233-i001"><img alt="Animals 15 00233 i001" src="/animals/animals-15-00233/article_deploy/html/images/animals-15-00233-i001.png"/></span>, dashed curves predicted by Equation (6)), and specific feed assimilation rate, <span class="html-italic">a</span> (dashed curves, grey scale predicted by Equation (8)). Right panels compare the specific CO<sub>2</sub> production rate to specific growth rate (curve predicted by Equations (2)–(8)). Data points represent averages of 5 replicate cultures ± standard deviation.</p>
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<p>(<b>A</b>) Individual CO<sub>2</sub> production rate, <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>r</mi> </mrow> <mrow> <mi>C</mi> <mi>O</mi> <mn>2</mn> </mrow> </msub> </mrow> </semantics></math>. (<b>B</b>) Specific CO<sub>2</sub> production rate (measured in carbon equivalents), <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>q</mi> </mrow> <mrow> <mi>C</mi> <mi>O</mi> <mn>2</mn> </mrow> </msub> </mrow> </semantics></math>. (<b>C</b>) NGE* of BSF larvae reared on wheat bran (●, solid curve), rapeseed cake (○, dashed curve), brewers’ spent grain (<span class="html-fig-inline" id="animals-15-00233-i001"><img alt="Animals 15 00233 i001" src="/animals/animals-15-00233/article_deploy/html/images/animals-15-00233-i001.png"/></span>, solid curve), deproteinized grass (♦, dashed curve), and biopulp (Δ, dotted curve). Data points represent average values of 5 replicate cultures (standard deviation indicated in <a href="#animals-15-00233-f003" class="html-fig">Figure 3</a>). Curves are model predictions from <a href="#animals-15-00233-f003" class="html-fig">Figure 3</a>.</p>
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<p>Net growth efficiency based on mass, NGE*<sub>DW,avg</sub>, black bars, and substrate conversion efficiency, SCE, grey bars of (<b>A</b>) mealworms and (<b>B</b>) BSF larvae reared on different feed substrates. Error bars indicate standard deviations of 5 replicate experiments.</p>
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17 pages, 2294 KiB  
Article
Tuning the Shape of Spray-Dried Pullulan Particles Through Feed Rheological Behavior
by Francesca Selmin, Francesco Cilurzo and Francesco Briatico Vangosa
Polysaccharides 2025, 6(1), 7; https://doi.org/10.3390/polysaccharides6010007 - 16 Jan 2025
Viewed by 308
Abstract
Pullulan is a natural polysaccharide used in many health products, including dry powders for oral and pulmonary administration. In these cases, the control of the shape and dimensions of particles is crucial for obtaining the desired functionality. Different from other polysaccharides, pullulan cannot [...] Read more.
Pullulan is a natural polysaccharide used in many health products, including dry powders for oral and pulmonary administration. In these cases, the control of the shape and dimensions of particles is crucial for obtaining the desired functionality. Different from other polysaccharides, pullulan cannot be easily shaped without chemical modifications or adjuvants’ addition. This work aims to systematically investigate the impact of the solvent composition and polymer concentration on the possibility of tuning the pullulan particle shape by spray drying. The results revealed that the microparticle-to-fiber transition can be induced using a hydro-alcoholic solution since ethanol increased the relaxation time and reduced the evaporation rate. Furthermore, a high Péclet number during drying favors the formation of wrinkled surfaces at all feed compositions. Overall, these data evidenced the possibility of tuning the spray-dried product morphology without any processing aids, paving the way for new applications of pullulan, especially in the pharmaceutical field. Full article
(This article belongs to the Collection Bioactive Polysaccharides)
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<p>Schematic representation of a CaBER experiment. The liquid sample is placed between two parallel plates positioned at a certain distance (initial gap, L<sub>0</sub>). The plates are then pulled apart quickly to the final gap distance, L<sub>f</sub>. Due to the generated curvature, surface tension acts as a pinching force that causes the evolution of the liquid into a filament that thins out to rupture at t<sub>B</sub>.</p>
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<p>Effect of the concentration on the viscosity of PUL aqueous and hydro-alcoholic solutions. Filled points refer to solutions prepared from Batch 1; empty points refer to solutions from Batch 2.</p>
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<p>Effect of the solution concentration on the longest relaxation time for (<b>a</b>) PUL aqueous and hydro-alcoholic solutions prepared using PUL from Batch 1. The concentration is the final PUL concentration. (<b>b</b>) PUL aqueous solutions prepared using PUL from Batch 1 or Batch 2. The concentration reported on the x-axis is expressed as the aqueous solution concentration before dilution with ethanol.</p>
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<p>TGA experiments on PUL solutions. (<b>a</b>) Solvent mass loss and (<b>b</b>) mass transfer coefficient for aqueous solutions with different concentrations; (<b>c</b>) solvent mass loss; and (<b>d</b>) mass transfer coefficient for hydro-alcoholic solutions with different PUL concentrations. In the case of hydro-alcoholic solutions, the PUL concentration reported is that of the aqueous solution before dilution with EtOH.</p>
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<p>TGA experiments on PUL solutions. (<b>a</b>) Solvent mass loss and (<b>b</b>) mass transfer coefficient for aqueous solutions with different concentrations; (<b>c</b>) solvent mass loss; and (<b>d</b>) mass transfer coefficient for hydro-alcoholic solutions with different PUL concentrations. In the case of hydro-alcoholic solutions, the PUL concentration reported is that of the aqueous solution before dilution with EtOH.</p>
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<p>TGA experiments on PUL solutions. (<b>a</b>) Solvent mass loss and (<b>b</b>) mass transfer coefficient for aqueous solutions with different concentrations; (<b>c</b>) solvent mass loss; and (<b>d</b>) mass transfer coefficient for hydro-alcoholic solutions with different PUL concentrations. In the case of hydro-alcoholic solutions, the PUL concentration reported is that of the aqueous solution before dilution with EtOH.</p>
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<p>SE microphotographs of spray-dried particles obtained from (<b>a</b>,<b>b</b>) aqueous and (<b>c</b>,<b>d</b>) hydro-alcoholic PUL solutions. PUL concentrations before dilution are 7.5%<span class="html-italic">w</span>/<span class="html-italic">w</span> in (<b>a</b>,<b>c</b>) and 5%<span class="html-italic">w</span>/<span class="html-italic">w</span> in (<b>b</b>,<b>d</b>).</p>
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<p>SE microphotographs of spray-dried particles obtained from (<b>a</b>,<b>b</b>) aqueous and (<b>c</b>,<b>d</b>) hydro-alcoholic PUL solutions. PUL concentrations before dilution are 7.5%<span class="html-italic">w</span>/<span class="html-italic">w</span> in (<b>a</b>,<b>c</b>) and 5%<span class="html-italic">w</span>/<span class="html-italic">w</span> in (<b>b</b>,<b>d</b>).</p>
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<p>Diameter distribution of spheroidal particles obtained from spray drying of (<b>a</b>) Batch 1 PUL 7.5%<span class="html-italic">w</span>/<span class="html-italic">w</span> aqueous solution diluted with ethanol and spray-dried immediately after dilution; (<b>b</b>) Batch 2 PUL 5.5%<span class="html-italic">w</span>/<span class="html-italic">w</span> aqueous solution diluted with ethanol and spray-dried immediately after dilution; (<b>c</b>) Batch 1 PUL 5.5%<span class="html-italic">w</span>/<span class="html-italic">w</span> aqueous solution diluted with ethanol and spray-dried 24 h after dilution.</p>
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<p>Diameter distribution of spheroidal particles obtained from spray drying of (<b>a</b>) Batch 1 PUL 7.5%<span class="html-italic">w</span>/<span class="html-italic">w</span> aqueous solution diluted with ethanol and spray-dried immediately after dilution; (<b>b</b>) Batch 2 PUL 5.5%<span class="html-italic">w</span>/<span class="html-italic">w</span> aqueous solution diluted with ethanol and spray-dried immediately after dilution; (<b>c</b>) Batch 1 PUL 5.5%<span class="html-italic">w</span>/<span class="html-italic">w</span> aqueous solution diluted with ethanol and spray-dried 24 h after dilution.</p>
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13 pages, 560 KiB  
Article
The Effect of Drinking Ionized Water on the Productive Performance, Physiological Status, and Carcass Characteristics of Broiler Chicks
by Abdullah Mohamed, Mohamed Khalil, Farid Soliman and Karim El-Sabrout
Animals 2025, 15(2), 229; https://doi.org/10.3390/ani15020229 - 16 Jan 2025
Viewed by 394
Abstract
Water treatment technologies have received great attention recently, as water is the most important nutritional element, and animals consume it daily in larger quantities than those of food. The ideal water treatment affects the chemical composition and physical properties of water, having a [...] Read more.
Water treatment technologies have received great attention recently, as water is the most important nutritional element, and animals consume it daily in larger quantities than those of food. The ideal water treatment affects the chemical composition and physical properties of water, having a significant positive impact on the animal’s physiology, productivity, and welfare. Studies conducted on water ionization devices for broiler chickens remain limited; therefore, this study was planned to investigate the effect of ionized drinking water on the productive performance, physiological status, and carcass characteristics of broiler chicks. A total of 900 one-day-old broiler chicks were randomly and equally assigned to three groups, each with six replicates (50 birds/replicate). The first group (C) received tap drinking water and served as a control, while the second group (T1) received ionized drinking water from an ionizing device that worked for 1 h/100 L. The third group (T2) received ionized drinking water from an ionizing device that worked for 2 h/100 L. Water analysis for each treatment was performed. Productive traits, such as weekly body weight, feed intake, and water intake, were recorded. Hematological parameters and biochemical constituents were measured according to the reference’s description. Furthermore, carcass characteristics, such as carcass weight and dressing percentage, and bacterial count of the intestine, such as Lactobacilli and Coliform counts, were determined. From the results, ionized water (T1 and T2) had a negative ORP, which is often desirable as it suggests the presence of antioxidant properties and lower total dissolved solids (TDSs), heterotrophic plate count (HPC), and algal total count (ATC) than in tap water. The treated chicks showed higher final body weights and better feed conversion rates than the control. Ionized water also improved carcass quality characteristics, such as carcass weight and dressing percentage. T1 and T2 chicks exhibited higher hemoglobin, total protein, globulin, G and M immunoglobulin, and total antioxidant capacity (TAC) levels, as well as lower malondialdehyde (MDA) and low-density lipoprotein (LDL) levels than the control. Furthermore, they had lower pathogenic bacteria counts. Therefore, it is recommended to employ the ionizing approach for broiler chicken drinking water, particularly a 2 h/100 L ionization application, for better animal productivity, health, and welfare. Full article
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<p>The water ionizing device.</p>
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16 pages, 899 KiB  
Article
An Assessment of Intermittent and Continuous Enteral Feeding in Critically Ill Children
by Merve Misirlioglu, Dincer Yildizdas, Faruk Ekinci, Nihal Akcay, Ilyas Bingol, Ebru Sahin, Fatih Varol, Muhterem Duyu, Ayse Asik, Fatih Durak, Leyla Atman, Suleyman Bayraktar, Mehmet Alakaya, Ali Ertug Arslankoylu, Gurkan Bozan, Eylem Kiral, Ozden Ozgur Horoz, Hasan Ali Telefon, Abdullah Akkus, Abdullah Yazar, Ozlem Sandal, Hasan Agin, Alper Koker, Nazan Ulgen Tekerek, Nurettin Onur Kutlu, Mehmet Arda Kilinc, Ali Korulmaz, Hatice Feray Ari, Mutlu Uysal Yazici, Esra Sevketoglu, Mehmet Emin Menentoglu, Ebru Kacmaz, Mehmet Nur Talay, Ozhan Orhan, Berna Egehan Oruncu, Selman Kesici, Caglar Odek, Didar Arslan, Pinar Hepduman, Gultac Evren, Hatice Elif Kinik Kaya, Nazik Yener, Emrah Gun, Ilkem Gardiyanoglu, Muhammed Udurgucu, Sinan Yavuz, Ali Avci, Murat Ozkale, Yasemin Ozkale, Damla Pinar Yavas Kocaoglu, Sahin Sincar and Yasemin Cobanadd Show full author list remove Hide full author list
Nutrients 2025, 17(2), 301; https://doi.org/10.3390/nu17020301 - 15 Jan 2025
Viewed by 439
Abstract
Background: The inability to ensure adequate nutrition for patients, and failure to provide adequate calorie and protein intake, result in malnutrition, leading to increased morbidity and mortality. The present study assesses the two approaches to enteral nutrition—intermittent and continuous enteral feeding—in critically ill [...] Read more.
Background: The inability to ensure adequate nutrition for patients, and failure to provide adequate calorie and protein intake, result in malnutrition, leading to increased morbidity and mortality. The present study assesses the two approaches to enteral nutrition—intermittent and continuous enteral feeding—in critically ill pediatric patients in Türkiye to determine the superiority of one method over the other. Methods: Included in this multicenter prospective study were patients receiving enteral nutrition via a tube who were followed up over a 3-month period. Anthropometric data, calorie and protein intake, and signs of feeding intolerance were evaluated in a comparison of the different feeding methods. Results: A total of 510 patients were examined. In the continuous enteral feeding (CEF) group, 20.2% of patients developed metabolic abnormalities, and 49.5% experienced enteral nutrition intolerance, both of which were higher than in the intermittent enteral feeding (IEF) group, and the differences were statistically significant. No significant differences were observed between the two feeding methods in terms of reaching the target calorie intake on days 2 and 7 (p > 0.05). On day 7, there were significant differences between the two feeding methods in terms of calorie and protein intake (p = 0.023 and 0.014, respectively). Conclusions: In the present study, assessing the IEF and CEF approaches to enteral nutrition, critically ill pediatric patients receiving intermittent feeding exhibited lower rates of enteral nutrition intolerance and metabolic abnormalities. Furthermore, the calorie and protein intake on day 7 were noted to be higher in the IEF group than in the CEF group. Further randomized controlled trials are needed to confirm the findings of the present study. Full article
(This article belongs to the Section Pediatric Nutrition)
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<p>Algorithm used for the determination of the enteral feeding method [<a href="#B4-nutrients-17-00301" class="html-bibr">4</a>]. GIT: gastrointestinal tract, N/G: nasogastric, O/G: orogastric.</p>
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<p>Feeding protocol [<a href="#B4-nutrients-17-00301" class="html-bibr">4</a>,<a href="#B13-nutrients-17-00301" class="html-bibr">13</a>,<a href="#B14-nutrients-17-00301" class="html-bibr">14</a>].</p>
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