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22 pages, 2661 KiB  
Review
The Role of Antioxidant Plant Extracts’ Composition and Encapsulation in Dietary Supplements and Gemmo-Derivatives, as Safe Adjuvants in Metabolic and Age-Related Conditions: A Review
by Bogdan-Stefan Negreanu-Pirjol, Ticuta Negreanu-Pirjol, Florica Busuricu, Sanda Jurja, Oana Craciunescu, Ovidiu Oprea, Ludmila Motelica, Elena Iulia Oprita and Florentina Nicoleta Roncea
Pharmaceuticals 2024, 17(12), 1738; https://doi.org/10.3390/ph17121738 - 23 Dec 2024
Viewed by 1036
Abstract
Given the current global circumstances, marked by severe environmental pollution—including the contamination of food—along with daily stress and a sedentary lifestyle, many consumers choose to improve their quality of life by using, among others, minimally processed food, food supplements, and gemmo-derivatives. Recent lab [...] Read more.
Given the current global circumstances, marked by severe environmental pollution—including the contamination of food—along with daily stress and a sedentary lifestyle, many consumers choose to improve their quality of life by using, among others, minimally processed food, food supplements, and gemmo-derivatives. Recent lab and clinical studies have shown the positive impact of specific nutrients with antioxidant capacities in the treatment of several conditions generated by oxidative stress. This paper reviews antioxidant plant extracts utilized as components in various dietary supplements and gemmoderivatives, highlighting their chemical composition and biological properties in preventing diseases caused by oxidative stress. A modern approach to food science brings to the fore the concept of dietary supplements vs. functional food, nutraceuticals, and gemmo-derivatives. The definitions of these terms are not being unanimously regulated in this respect and describe each category of compound and product, also emphasizing the need to implement adequate nutrivigilance. In order to enhance the absorption and bioavailability of dietary supplements and gemmo-derivatives based on antioxidant plant extracts, some encapsulation techniques are outlined. Full article
(This article belongs to the Section Natural Products)
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<p>Biological activities of some dietary food supplements.</p>
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<p>Gemmotherapy depiction and its patterns of application.</p>
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<p>Conventional and green methods used for obtaining gemmotherapy extracts.</p>
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<p>Antioxidant mechanisms of plant extracts administered in form of dietary supplements and gemmo-derivatives.</p>
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<p>The microencapsulation of antioxidant bioactive compounds from fruits by spray drying, highlighting the variables of the process (adapted from [<a href="#B104-pharmaceuticals-17-01738" class="html-bibr">104</a>]).</p>
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<p>Obtaining lipid nanocarriers for antioxidant plant extracts’ encapsulation.</p>
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<p>Vacuum-assisted loading method of plant extract into mesoporous silica [<a href="#B112-pharmaceuticals-17-01738" class="html-bibr">112</a>].</p>
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<p>Antioxidant plant extract loaded onto nanoparticles by grinding in one-pot step.</p>
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17 pages, 1730 KiB  
Review
Complementary Practices in Pharmacy and Their Relation to Glaucoma—Classification, Definitions, and Limitations
by Tibor Rák and Adrienne Csutak
Sci. Pharm. 2024, 92(1), 16; https://doi.org/10.3390/scipharm92010016 - 14 Mar 2024
Cited by 3 | Viewed by 3201
Abstract
Background: Traditional and evidence-based medicines, as seen depicted throughout human history, reportedly first begin with the application of medicinal plants, animal products, or inorganic minerals as a basic framework towards effectively engineering the prototypes generally aligned to pharmaceuticals and medical nutrition. The growing [...] Read more.
Background: Traditional and evidence-based medicines, as seen depicted throughout human history, reportedly first begin with the application of medicinal plants, animal products, or inorganic minerals as a basic framework towards effectively engineering the prototypes generally aligned to pharmaceuticals and medical nutrition. The growing global trend of complementary treatments for glaucoma can be explained by the intraocular pressure (IOP)-independent mechanisms of the disease and its interpretation as a progressive neurodegenerative disorder. Unfortunately, the categorical positions of the major fields of applied popular complementary therapies and their relation to glaucoma are consistently neglected. Methods: In consideration of bibliographic resources, the most well-known online scientific databases were searched. Conclusion: The rising popularity and the trends of products coming onto the market cannot escape the attention of pharmacists and ophthalmologists, as their patients suffering from eye diseases are also increasingly looking for such medicinal products. Most of them still lack knowledge of the appropriate evidence and side effect profiles. Our proposed systematic charts demonstrate the position of each mainstream complementary therapy throughout the applied medical sciences and are distinctively unique; we could not find any similar relevant illustration or resource among the published international literature. Full article
(This article belongs to the Special Issue Feature Papers in Scientia Pharmaceutica)
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Graphical abstract

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<p>Summarized chart representing the “Aroma-sciences”. The recent scientific literature and databases lack an official description regarding “Aroma-sciences”; therefore, for this purpose, we summarize them in a self-made chart.</p>
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<p>Classification and illustration of products used in apitherapy. (Self-edited and photographed image. The central image is of <span class="html-italic">Apis mellifera</span> L., courtesy of the photographer, Dr. Gina Vágó, Bőszénfa, Hungary, 2020.).</p>
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<p>Positions of plant-based therapy systems and their frontier areas in contemporary medicine—self-edited chart. Applied human and veterinary medicine systems holistically consist of the subdivisions “Western” or “Allopathic” EBM and complementary medicinal systems (TCM, Ayurvedic medicine, Tibetan–Mongolian medicine, anthroposophic medicine, etc.).</p>
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31 pages, 2045 KiB  
Article
Specific Antimicrobial Activities Revealed by Comparative Evaluation of Selected Gemmotherapy Extracts
by Melinda Héjja, Emőke Mihok, Amina Alaya, Maria Jolji, Éva György, Noemi Meszaros, Violeta Turcus, Neli Kinga Oláh and Endre Máthé
Antibiotics 2024, 13(2), 181; https://doi.org/10.3390/antibiotics13020181 - 13 Feb 2024
Cited by 1 | Viewed by 4117
Abstract
Nowadays, unprecedented health challenges are urging novel solutions to address antimicrobial resistance as multidrug-resistant strains of bacteria, yeasts and moulds are emerging. Such microorganisms can cause food and feed spoilage, food poisoning and even more severe diseases, resulting in human death. In order [...] Read more.
Nowadays, unprecedented health challenges are urging novel solutions to address antimicrobial resistance as multidrug-resistant strains of bacteria, yeasts and moulds are emerging. Such microorganisms can cause food and feed spoilage, food poisoning and even more severe diseases, resulting in human death. In order to overcome this phenomenon, it is essential to identify novel antimicrobials that are naturally occurring, biologically effective and increasingly safe for human use. The development of gemmotherapy extracts (GTEs) using plant parts such as buds and young shoots has emerged as a novel approach to treat/prevent human conditions due to their associated antidiabetic, anti-inflammatory and/or antimicrobial properties that all require careful evaluations. Seven GTEs obtained from plant species like the olive (Olea europaea L.), almond (Prunus amygdalus L.), black mulberry (Morus nigra L.), walnut (Juglans regia L.), blackberry (Rubus fruticosus L.), blackcurrant (Ribes nigrum L.) and bilberry (Vaccinium myrtillus L.) were tested for their antimicrobial efficiency via agar diffusion and microbroth dilution methods. The antimicrobial activity was assessed for eight bacterial (Bacillus cereus, Staphylococcus aureus, Salmonella enterica subsp. enterica, Proteus vulgaris, Enterococcus faecalis, Escherichia coli, Pseudomonas aeruginosa and Listeria monocytogenes), five moulds (Aspergillus flavus, Aspergillus niger, Aspergillus ochraceus, Penicillium citrinum, Penicillium expansum) and one yeast strain (Saccharomyces cerevisiae). The agar diffusion method revealed the blackberry GTE as the most effective since it inhibited the growth of three bacterial, four moulds and one yeast species, having considered the total number of affected microorganism species. Next to the blackberry, the olive GTE appeared to be the second most efficient, suppressing five bacterial strains but no moulds or yeasts. The minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) were then determined for each GTE and the microorganisms tested. Noticeably, the olive GTE appeared to feature the strongest bacteriostatic and bactericidal outcome, displaying specificity for S. aureus, E. faecalis and L. monocytogenes. The other GTEs, such as blueberry, walnut, black mulberry and almond (the list indicates relative strength), were more effective at suppressing microbial growth than inducing microbial death. However, some species specificities were also evident, while the blackcurrant GTE had no significant antimicrobial activity. Having seen the antimicrobial properties of the analysed GTEs, especially the olive and black mulberry GTEs, these could be envisioned as potential antimicrobials that might enhance antibiotic therapies efficiency, while the blackberry GTE would act as an antifungal agent. Some of the GTE mixtures analysed have shown interesting antimicrobial synergies, and all the antimicrobial effects observed argue for extending these studies to include pathological microorganisms. Full article
(This article belongs to the Special Issue Antimicrobial Activity of Natural Products and Plants Extracts)
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<p>The different sizes of the inhibition zones induced by the GTEs on some microorganisms: (<b>a</b>) <span class="html-italic">L. monocytogenes</span>—<span class="html-italic">Juglans regia</span> 100% GTE; (<b>b</b>) <span class="html-italic">P. vulgaris</span>—<span class="html-italic">Vaccinium myrtillus</span> 100% GTE; and (<b>c</b>) <span class="html-italic">L. monocytogenes</span>—<span class="html-italic">Rubus fruticosus</span> 100% GTE.</p>
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<p>Picture of a microtiter plate with the various concentrations of GTEs and the microorganism in broth culture. Pink to red colour indicates bacterial growth. (N.C.—negative control, P.C.—positive control).</p>
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<p>Olive GTE concentration with specific <span class="html-italic">Salmonella enterica</span> colony numbers.</p>
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<p>Inhibition zone size comparison for <span class="html-italic">Olea europaea.</span> Values with different letters (<sup>a–e</sup>) are statistically different at <span class="html-italic">p</span> &lt; 0.05, according to Tukey’s test.</p>
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<p>The mobile phase gradient.</p>
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17 pages, 1898 KiB  
Article
Influence of Maceration Solvent on Chemical Composition of Gemmotherapy Macerates—A Case Study on Olea europaea Young Shoots
by Dimitri Bréard, Hélène Esselin, Lucie Bugeia, Séverine Boisard, David Guilet, Pascal Richomme, Anne-Marie Le Ray and Christophe Ripoll
Nutraceuticals 2023, 3(4), 574-590; https://doi.org/10.3390/nutraceuticals3040041 - 1 Dec 2023
Cited by 1 | Viewed by 1795
Abstract
Gemmotherapy, a natural therapy based on bud macerates, has recently gained importance in the field of food supplements. However, two coexisting extraction methods employ a glycerin-based solvent, either in a binary or ternary solvent mixture. The absence of an official method for bud [...] Read more.
Gemmotherapy, a natural therapy based on bud macerates, has recently gained importance in the field of food supplements. However, two coexisting extraction methods employ a glycerin-based solvent, either in a binary or ternary solvent mixture. The absence of an official method for bud preparation leads to non-standardized bud macerates. Given this context, this study aimed to (i) assess the influence of solvent composition on the chemical profile of olive young shoot macerates obtained using glycerin-based solvents or using different solvent extractions and (ii) to compare the two coexisting traditional bud extraction methods described by Dr Pol Henry and by the European Pharmacopoeia. A comprehensive phytochemical analysis of all macerates was conducted using HPLC-DAD-ELSD-MS2, identifying 50 metabolites divided into 7 classes through dereplication. The extracts obtained with the solvent described by the European Pharmacopoeia (ethanol/glycerin) and by Dr Pol Henry (water/ethanol/glycerin) appeared to be the most diversified in terms of metabolite distribution and possessed higher rates of secondary metabolites. These observations reinforce the interest in a glycerin-based solvent mixture for bud extraction in gemmotherapy. In addition, the difference in composition between the two traditional solvents was highlighted. Indeed, iridoids were predominant in both macerates, representing about 50% of the chemical composition, but differences were observed from one macerate to another regarding the proportions of the other chemical classes. This emphasizes the necessity for standardized gemmotherapy macerates. Full article
(This article belongs to the Topic Applied Sciences in Functional Foods - 2nd Volume)
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<p>Metabolite repartition (% ELSD) of the different extracts. Primary metabolites and chlorophylls (hatched bar plots); secondary metabolites (full bar plots).</p>
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<p>HPLC-ELSD profiles of the different extracts.</p>
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<p>Principal iridoid contents (mg/g DW) in the different solvent systems extracts (sample <b>g</b> is not shown because it does not contain any iridoids).</p>
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<p>Metabolites repartition (% ELSD) of <b>w</b>/<b>e</b>/<b>g</b> (internal circle) and <b>e</b>/<b>g</b> (external circle) extracts (organic acids were not present in these extracts).</p>
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<p>HPLC-ELSD profiles of <b>w</b>/<b>e</b>/<b>g</b> (green) and <b>fresh w/e/g</b> (black) extracts.</p>
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<p>Metabolites repartition (% ELSD) of <b>w</b>/<b>e</b>/<b>g</b> (internal circle) and <b>fresh w/e/g</b> (external circle) extracts (organic acids and chlorophylls were not present in these extracts).</p>
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<p>Iridoids (<b>a</b>), flavonoids (<b>b</b>), and other (sugar and phenylethanoid) (<b>c</b>) contents (mg/g DW) for <b>w</b>/<b>e</b>/<b>g</b> and <b>fresh w/e/g</b> extracts.</p>
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<p>Iridoids (<b>a</b>), flavonoids (<b>b</b>), and other (sugar and phenylethanoid) (<b>c</b>) contents (mg/g DW) for <b>w</b>/<b>e</b>/<b>g</b> and <b>fresh w/e/g</b> extracts.</p>
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25 pages, 6114 KiB  
Article
Phytochemical Profile and Biological Activities of Extracts Obtained from Young Shoots of Blackcurrant (Ribes nigrum L.), European Blueberry (Vaccinium myrtillus L.), and Mountain Cranberry (Vaccinium vitis-idaea L.)
by Maria-Beatrice Solcan, Ionel Fizeșan, Laurian Vlase, Ana-Maria Vlase, Marius Emil Rusu, Letiția Mateș, Andreea-Elena Petru, Ionuț-Valentin Creștin, Ioan Tomuțǎ and Daniela-Saveta Popa
Horticulturae 2023, 9(11), 1163; https://doi.org/10.3390/horticulturae9111163 - 24 Oct 2023
Cited by 8 | Viewed by 2213
Abstract
This study explores the bioactive potential of young shoots from blackcurrant, European blueberry, and mountain cranberry, widely employed in gemmotherapy and phytotherapy, as rich sources of antioxidants, antimicrobial agents, and anti-inflammatory components. The primary aims of this study were to enhance the extraction [...] Read more.
This study explores the bioactive potential of young shoots from blackcurrant, European blueberry, and mountain cranberry, widely employed in gemmotherapy and phytotherapy, as rich sources of antioxidants, antimicrobial agents, and anti-inflammatory components. The primary aims of this study were to enhance the extraction conditions for bioactive compounds from blackcurrant young shoots using Modde software for experimental design, to conduct a comprehensive phytochemical analysis of blackcurrant, European blueberry, and mountain cranberry young shoot extracts through LC–MS analysis, and to evaluate the in vitro biological activities of these optimized extracts. The experimental design comprised multiple variables: extraction techniques, solvent type, extraction time, apparent pH, and the solvent-to-vegetal product ratio. The responses included total phenolic content, total flavonoid content, condensed tannin content, and total antioxidant activity determined through the DPPH assay. Furthermore, the antioxidant potential of the extracts was validated through in vitro cell culture experiments, in addition to the cytotoxicity assessments conducted on both normal and cancer cell lines. Extracts obtained through Ultra-Turrax extraction using 70% acetone displayed high levels of polyphenolic compounds and enhanced antioxidant potential, regardless of young shoots origin. LC–MS analysis revealed the predominant occurrence of chlorogenic acid, hyperoside, and isoquercitrin in all examined samples. The optimized extracts also displayed significant biological potential when evaluated in vitro on cell lines. These results provide valuable insights into the potent bioactive components present in these young shoot extracts, paving the way for further exploration in therapeutic applications. Full article
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<p>The fitting parameters for the evaluated output variables.</p>
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<p>The influence of working conditions on TPC, TFC, CTC, and TAA by DPPH assay upon <span class="html-italic">R. nigrum</span> L. extract during the screening step, depicted as scaled and centered coefficient plots. X<sub>1</sub>—extraction method; X<sub>2</sub>—stirring time; X<sub>3</sub>—extraction solvent; X<sub>4</sub>—solvent apparent pH; X<sub>5</sub>—solvent (mL):vegetal product (g) ratio.</p>
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<p>The influence of working conditions on TPC, TFC, CTC, and TAA by DPPH assay upon <span class="html-italic">R. nigrum</span> L. extract during the screening step, depicted as scaled and centered coefficient plots. X<sub>1</sub>—extraction method; X<sub>2</sub>—stirring time; X<sub>3</sub>—extraction solvent; X<sub>4</sub>—solvent apparent pH; X<sub>5</sub>—solvent (mL):vegetal product (g) ratio.</p>
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<p>Response surface for predicting the bioactive compounds recovery from RNYS extract with respect to X<sub>1</sub>—extraction method; X<sub>2</sub>—stirring time; X<sub>3</sub>—extraction solvent; X<sub>4</sub>—solvent apparent pH; X<sub>5</sub>—solvent (mL):vegetal product (g) ratio. The red areas on the graphics depict the extraction parameter ranges that ensure the highest extraction yield for the bioactive compounds under evaluation and maximum outcome for the evaluated dependent variables.</p>
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<p>Cytotoxicity of VMYSs, RNYSs, and VVIYSs on A549 cell line, Caco-2 cell line, and BJ cell line evaluated using Alamar Blue assay after a 24 h exposure. The results were expressed as the mean ± SD (n = 3) and as relative values compared to the negative control (NC) (100%). * <span class="html-italic">p</span> &lt; 0.05 vs. NC (ANOVA + post hoc Holm–Šídák test).</p>
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<p>Antioxidant effects of VMYSs (<b>A</b>), RNYSs (<b>B</b>), and VVIYSs (<b>C</b>), evaluated using DCFH-DA assay on Caco-2 cell line. Cells were incubated with the extracts at three noncytotoxic concentrations or NAC (20 mM) for 24 h and further loaded with 50 µM DCFH-DA. The antioxidant potential was measured in stimulated/non-stimulated conditions after a 3 h exposure in the presence and absence of 250 µM H<sub>2</sub>O<sub>2</sub>. Data are expressed as means ± SD (n = 3). All values are expressed as relative values compared to the negative control (100%). Different letters (a–d in non-stimulated conditions, and A–E in stimulated conditions) show statistically significant differences (ANOVA + Holm–Šídák post hoc test at <span class="html-italic">p</span> &lt; 0.05).</p>
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36 pages, 6430 KiB  
Article
Phytoconstituent Profiles Associated with Relevant Antioxidant Potential and Variable Nutritive Effects of the Olive, Sweet Almond, and Black Mulberry Gemmotherapy Extracts
by Amina Aleya, Emőke Mihok, Bence Pecsenye, Maria Jolji, Attila Kertész, Péter Bársony, Szabolcs Vígh, Zoltán Cziaky, Anna-Beáta Máthé, Ramona Flavia Burtescu, Neli-Kinga Oláh, Andreea-Adriana Neamțu, Violeta Turcuș and Endre Máthé
Antioxidants 2023, 12(9), 1717; https://doi.org/10.3390/antiox12091717 - 4 Sep 2023
Cited by 3 | Viewed by 2869
Abstract
The extracts of whole plants or specific organs from different plant species are gaining increasing attention for their phytotherapy applications. Accordingly, we prepared standardized gemmotherapy extracts (GTEs) from young shoots/buds of olive (Olea europaea), sweet almond (Prunus amygdalus), and [...] Read more.
The extracts of whole plants or specific organs from different plant species are gaining increasing attention for their phytotherapy applications. Accordingly, we prepared standardized gemmotherapy extracts (GTEs) from young shoots/buds of olive (Olea europaea), sweet almond (Prunus amygdalus), and black mulberry (Morus nigra), and analyzed the corresponding phytonutrient profiles. We identified 42, 103, and 109 phytonutrients in the olive, almond, and black mulberry GTEs, respectively, containing amino acids, vitamins, polyphenols, flavonoids, coumarins, alkaloids, iridoids, carboxylic acids, lignans, terpenoids, and others. In order to assess the physiological effects generated by the GTEs, we developed a translational nutrition model based on Drosophila melanogaster and Cyprinus carpio. The results indicate that GTEs could influence, to a variable extent, viability and ATP synthesis, even though both are dependent on the specific carbohydrate load of the applied diet and the amino acid and polyphenol pools provided by the GTEs. It seems, therefore, likely that the complex chemical composition of the GTEs offers nutritional properties that cannot be separated from the health-promoting mechanisms that ultimately increase viability and survival. Such an approach sets the paves the way for the nutritional genomic descriptions regarding GTE-associated health-promoting effects. Full article
(This article belongs to the Special Issue Olive Tree Products and Antioxidants)
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<p>Phytonutrient profiles of GTEs.</p>
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<p>Evaluation of fruit fly viability in the 0N diet. Viability assessment of the larvae (<b>A</b>) and pupae (<b>B</b>) at the applied concentrations of GTEs.</p>
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<p>Images of w<sup>m4h</sup> newly hatched adults raised at NM (control) and 0 M dietary conditions.</p>
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<p>Assessment of w<sup>m4h</sup> newly hatched adults for their body length (blue) and ATP content (red), raised in NM (control) and 0 M dietary conditions.</p>
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<p>Developmental timing of fruit fly lifecycle on NS versus HS diet. The viability assessment of the larvae and pupae (<span class="html-fig-inline" id="antioxidants-12-01717-i001"><img alt="Antioxidants 12 01717 i001" src="/antioxidants/antioxidants-12-01717/article_deploy/html/images/antioxidants-12-01717-i001.png"/></span>) respectively adults (<span class="html-fig-inline" id="antioxidants-12-01717-i002"><img alt="Antioxidants 12 01717 i002" src="/antioxidants/antioxidants-12-01717/article_deploy/html/images/antioxidants-12-01717-i002.png"/></span>) in the context of the duration of development in NM- and HS-dietary conditions. The blue curves are for normal sugar media respectively the orange one for high sugar media.</p>
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<p>Comparison of larval and adult viability in NM- and HS-dietary conditions.</p>
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<p>The fruit flies’ viability in NM- and HS-dietary conditions with O-GTE. Where NM means normal media and HS high sugar media.</p>
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<p>The fruit flies’ viability in NM- and HS-dietary conditions with SA-GTE.</p>
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<p>The fruit flies’ viability in NM- and HS-dietary conditions with BM-GTE.</p>
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<p>Assessment of carp viability. (<b>A</b>) Fertilized eggs during embryogenesis; (<b>B</b>) Eggs that completed embryogenesis with visible larvae; (<b>C</b>) Larvae at the time of hatching; (<b>D</b>) Non-feeding larvae at day 1 after hatching, also called pre-feeding larvae; (<b>E</b>) Feeding larvae, day 3 after hatching (green arrow indicates the swim bladder); (<b>F</b>) Feeding larvae at day 7 after hatching, fed with GTE; (<b>G</b>) Feeding larva at day 7, fed with brine shrimp (red arrow).</p>
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<p>Fish feed-induced ATP synthesis in carp larvae. The colors indicate the fish feed: green—O-GTE; red—control, i.e., brine shrimp (<span class="html-italic">Artemia salina</span>); brown—SA-GTE; purple—BM-GTE.</p>
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<p>The quantitatively assessed selected polyphenol distribution in O-GTE.</p>
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<p>The quantitatively assessed selected polyphenol distribution in SA-GTE.</p>
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<p>The quantitatively assessed selected polyphenol distribution in BM-GTE.</p>
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17 pages, 8291 KiB  
Article
Phytochemical Profiling and Anti-Fibrotic Activities of the Gemmotherapy Bud Extract of Corylus avellana in a Model of Liver Fibrosis on Diabetic Mice
by Cornel Balta, Hildegard Herman, Alina Ciceu, Bianca Mladin, Marcel Rosu, Alciona Sasu, Victor Eduard Peteu, Sorina Nicoleta Voicu, Mihaela Balas, Mihaela Gherghiceanu, Anca Dinischiotu, Neli Kinga Olah and Anca Hermenean
Biomedicines 2023, 11(6), 1771; https://doi.org/10.3390/biomedicines11061771 - 20 Jun 2023
Cited by 2 | Viewed by 2319
Abstract
In this study, we aimed to explore the hepatoprotective effects of the gemmotherapy bud extract of Corylus avellana in a model of liver fibrosis on diabetic mice. An evaluation of total flavonoids and polyphenols contents and LC/MS analyses were performed. Experimental fibrosis was [...] Read more.
In this study, we aimed to explore the hepatoprotective effects of the gemmotherapy bud extract of Corylus avellana in a model of liver fibrosis on diabetic mice. An evaluation of total flavonoids and polyphenols contents and LC/MS analyses were performed. Experimental fibrosis was induced with CCl4 (2 mL/kg by i.p. injections twice a week for 7 weeks) in streptozotocin-induced diabetic mice. Our results showed a content of 6–7% flavonoids, while hyperoside and chlorogenic acids were highlighted in the bud extract. Toxic administration of CCl4 increased oxidative stress, mRNA expression of the transforming growth factor-β1 (TGF-β1) and Smad 2/3, and reduced Smad 7 expression. Furthermore, up-regulation of α-smooth muscle actin (α-SMA) revealed an activation of hepatic stellate cells (HSCs), while collagen I (Col I) up-regulation and matrix metalloproteinases (MMPs) unbalance led to an altered extracellular matrix enriched in collagen, confirmed as well by a trichrome stain and electron microscopy analysis. Treatment with gemmotherapy extract significantly restored the liver architecture and the antioxidant balance, and significantly decreased collagen deposits in the liver and improved the liver function. Our results suggest that Corylus avellana gemmotherapy extract may have anti-fibrotic effects and could be useful in the prevention and treatment of liver fibrosis. The hepatoprotective mechanism is based on HSC inhibition, a reduction in oxidative stress and liver damage, a downregulation of the TGF-β1/Smad signaling pathway and a MMPs/TIMP rebalance. Full article
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<p><span class="html-italic">Corylus avellana</span> gemmotherapy extract improves biochemical parameters and hepatic structure and ultrastructure of the fibrosis livers in diabetic mice. (<b>A</b>) Biochemical parameters of aspartate-amino-transferase (AST); alanine-amino-transferase (ALT); Values are expressed as mean ± SD (n = 10). *** <span class="html-italic">p</span> &lt; 0.001 compared to control; ** <span class="html-italic">p</span> &lt; 0.01 compared to control; * <span class="html-italic">p</span> &lt; 0.05 compared to control; <sup>###</sup> <span class="html-italic">p</span> &lt; 0.001 compared to DF; Legend: Control; <span class="html-italic">DF</span>—liver fibrosis in diabetic mice; <span class="html-italic">DFR</span>—self-recovery of liver fibrosis (positive control) in diabetic mice; <span class="html-italic">DCA</span>—<span class="html-italic">Corylus avellana</span> treatment of liver fibrosis in diabetic mice. (<b>B</b>) Representative light microscopy micrographs of liver histology in H&amp;E stain, (<b>a</b>) control; (<b>b</b>) DF; (<b>c</b>) DFR, (<b>d</b>) DCA, Scale bar: 50 μm; Fibrosis (arrowhead), foam hepatocyte (*), inflammatory infiltrate (arrow). (<b>C</b>) Representative electron microscopy micrographs of the liver for the experimental groups; (<b>a</b>) control; (<b>b</b>–<b>d</b>) DF; (<b>e</b>) DFR; (<b>f</b>) DCA. N—hepatocyte’s nuclei; HSC—hepatocyte stellate cells; lipids (arrowhead); collagen (*); glycogen (G).</p>
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<p>The effect induced by <span class="html-italic">Corylus avellana</span> gemmotherapy extract on reduction of collagen deposition in fibrotic livers of diabetic mice. (<b>A</b>) RT–PCR analysis of collagen 1 (Col 1) gene levels. Legend: Control, <span class="html-italic">DF</span>—liver fibrosis in diabetic mice; <span class="html-italic">DFR</span>—self-recovery of liver fibrosis (positive control) in diabetic mice; <span class="html-italic">DCA—Corylus avellana</span> treatment of liver fibrosis in diabetic mice; *** <span class="html-italic">p</span> &lt; 0.001 compared to control; <sup>###</sup> <span class="html-italic">p</span> &lt; 0.001 compared to <span class="html-italic">DF</span>; ^^^ <span class="html-italic">p</span> &lt; 0.001 compared to <span class="html-italic">DFR</span>; (<b>B</b>) Collagen staining with Gomori’s trichrome kit. (<b>a</b>) Control group: no significant collagen deposition; (<b>b</b>) <span class="html-italic">DF</span> group: significant collagen deposition with pseudo-lobular separation (arrows); (<b>c</b>) <span class="html-italic">DFR</span> group: aspect almost similar to the LF-DIA group (arrows); (<b>d</b>) <span class="html-italic">DCA</span> less collagen deposition (isolated islands) compared to <span class="html-italic">DF</span> and <span class="html-italic">DFR</span> (arrows).</p>
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<p><span class="html-italic">Corylus avellana</span> gemmotherapy extract <span class="html-italic">inhibits</span> activation and proliferation of HSCs. (<b>A</b>) RT–PCR analysis of α-SMA gene level. Legend: Control, <span class="html-italic">DF</span>—liver fibrosis in diabetic mice; <span class="html-italic">DFR</span>—self-recovery of liver fibrosis (positive control) in diabetic mice; <span class="html-italic">DCA</span>—<span class="html-italic">Corylus avellana</span> treatment of liver fibrosis in diabetic mice; *** <span class="html-italic">p</span> &lt; 0.001 compared to control; <sup>###</sup> <span class="html-italic">p</span> &lt; 0.001 compared to DF; ^^^ <span class="html-italic">p</span> &lt; 0.001 compared to DFR; (<b>B</b>) Immunohistochemical expression of α-SMA in experimental livers: (<b>a</b>) Control; (<b>b</b>) <span class="html-italic">DF</span>—liver fibrosis in diabetic mice—strong α-SMA immunopositivity; (<b>c</b>) <span class="html-italic">DFR</span>—self-recovery of liver fibrosis (positive control) in diabetic mice—α-SMA immunopositivity almost similar to DF group; (<b>d</b>) <span class="html-italic">DCA</span>—<span class="html-italic">Corylus avellana</span> treatment of liver fibrosis in diabetic mice; Scale bar: 200 μm. (<b>C</b>) Electron microscopy micrographs of the hepatic stellate cells; Legend: (<b>a</b>) Control; (<b>b</b>) <span class="html-italic">DF</span>—liver fibrosis in diabetic mice; (<b>c</b>) <span class="html-italic">DFR</span>—self-recovery of liver fibrosis (positive control) in diabetic mice; (<b>d</b>) <span class="html-italic">DCA</span>—<span class="html-italic">Corylus avellana</span> treatment of liver fibrosis in diabetic mice; hepatic stellate cells (arrowhead), lipids (L), collagen (*).</p>
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<p><span class="html-italic">Corylus avellana</span> gemmotherapy extract inhibits pro-fibrotic TGF-β1/Smad signaling. (<b>A</b>) RT–PCR analysis of Smad 2, 3 and 7 gene levels. Legend: Control; <span class="html-italic">DF</span>—liver fibrosis in diabetic mice; <span class="html-italic">DFR</span>—self-recovery of liver fibrosis (positive control) in diabetic mice; <span class="html-italic">DCA</span>—<span class="html-italic">Corylus avellana</span> treatment of liver fibrosis in diabetic mice; *** <span class="html-italic">p</span> &lt; 0.001 compared to control; * <span class="html-italic">p</span> &lt; 0.05 compared to control; <sup>###</sup> <span class="html-italic">p</span> &lt; 0.001 compared to DF; ^^^ <span class="html-italic">p</span> &lt; 0.001 compared to DFR; (<b>B</b>) RT–PCR analysis of TGF-β1 gene level. Legend: Control; <span class="html-italic">DF</span>—liver fibrosis in diabetic mice; <span class="html-italic">DFR</span>—self-recovery of liver fibrosis (positive control) in diabetic mice; <span class="html-italic">DCA</span>—<span class="html-italic">Corylus avellana</span> treatment of liver fibrosis in diabetic mice; *** <span class="html-italic">p</span> &lt; 0.001 compared to control; <sup>###</sup> <span class="html-italic">p</span> &lt; 0.001 compared to DF; ^^^ <span class="html-italic">p</span> &lt; 0.001 compared to DFR; (<b>C</b>) Immunohistochemical expression of TGF-β1 in experimental livers. Legend: (<b>a</b>) Control; (<b>b</b>) <span class="html-italic">DF</span>—liver fibrosis in diabetic mice; (<b>c</b>) <span class="html-italic">DFR</span>—self-recovery of liver fibrosis (positive control) in diabetic mice; (<b>d</b>) <span class="html-italic">DCA</span>—<span class="html-italic">Corylus avellana</span> treatment of liver fibrosis in diabetic mice.</p>
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<p>Effects of <span class="html-italic">Corylus avellana</span> gemmotherapy buds extract on tissue inhibitors of metalloproteinase (TIMP)-1/matrix metalloproteinase (MMP) pathway regulation. RT–PCR analysis of MMP1 (<b>A</b>), Timp-1 (<b>B</b>), MMP2 (<b>C</b>), MMP3 (<b>D</b>), MMP9 (<b>E</b>) gene expression levels. (<b>F</b>) Effects of on MMPs expression and enzymatic activity. (<b>a</b>) Images of gelatin zymography (pro-MMP-2, MMP-2, and MMP-9); (<b>b</b>) enzymatic activity of the metalloproteinases pro-MMP-2, MMP-2, and MMP-9, as well as (<b>c</b>) profile of MMP-2 and MMP-9 blots; (<b>d</b>) the expression of metalloproteinases MMP-2 and MMP-9 obtained following in vivo treatment of CA gemmotherapy extract. Legend: Control; <span class="html-italic">DF</span>—liver fibrosis in diabetic mice; <span class="html-italic">DFR</span>—self-recovery of liver fibrosis (positive control) in diabetic mice; <span class="html-italic">DCA—Corylus avellana</span> treatment of liver fibrosis in diabetic mice; *** <span class="html-italic">p</span> &lt; 0.001 compared to control; * <span class="html-italic">p</span> &lt; 0.05 compared to control; ** <span class="html-italic">p</span> &lt; 0.01 compared to control; <sup>###</sup> <span class="html-italic">p</span> &lt; 0.001; <sup>##</sup> <span class="html-italic">p</span> &lt; 0.01; ^^^ <span class="html-italic">p</span> &lt; 0.001 compared to <span class="html-italic">DFR</span>; ^ <span class="html-italic">p</span> &lt; 0.05 compared to <span class="html-italic">DFR</span>.</p>
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<p>Effects of <span class="html-italic">Corylus avellana</span> (CA) extract on oxidative stress parameters. (<b>A</b>) The level of malondialdehyde (MDA), (<b>B</b>) the concentration of reduced glutathione (GSH), and (<b>C</b>) the products of advanced oxidation of proteins (AOPP) obtained after the in vivo administration of <span class="html-italic">Corylus avellana</span> (DCA) extract; <span class="html-italic">DF</span>—liver fibrosis in diabetic mice; <span class="html-italic">DFR</span>—self-recovery of liver fibrosis (positive control) in diabetic mice; <span class="html-italic">DCA—Corylus avellana</span> treatment of liver fibrosis in diabetic mice. # <span class="html-italic">p</span> &lt; 0.05; (*)—group versus DF group; (#)—group versus DFR group.</p>
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<p>Effects of <span class="html-italic">Corylus avellana</span> (CA) extract on Ub-Nrf2 and HO-1 protein expression. (<b>A</b>) Protein bands on blot membrane; (<b>B</b>) expression of ubiquitinylated Nrf2 (Ub-Nrf2) protein, and (<b>C</b>) expression of heme oxygenase (HO-1) proteins after in vivo treatment of the <span class="html-italic">Corylus avellana</span> extract. DF–liver fibrosis in diabetic mice; DFR–self-recovery of liver fibrosis (positive control) in diabetic mice; DCA-<span class="html-italic">Corylus avellana</span> treatment of liver fibrosis in diabetic mice. ** <span class="html-italic">p</span> &lt; 0.01; *** <span class="html-italic">p</span> &lt; 0.001; <sup>##</sup> <span class="html-italic">p</span> &lt; 0.01, <sup>#</sup> <span class="html-italic">p</span> &lt; 0.05; (*)—group versus DF group; (#)—group versus DFR group.</p>
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17 pages, 1667 KiB  
Communication
The Flavonoid Rich Black Currant (Ribes nigrum) Ethanolic Gemmotherapy Extract Elicits Neuroprotective Effect by Preventing Microglial Body Swelling in Hippocampus and Reduces Serum TNF-α Level: Pilot Study
by Tímea Téglás, Emőke Mihok, Zoltán Cziáky, Neli-Kinga Oláh, Csaba Nyakas and Endre Máthé
Molecules 2023, 28(8), 3571; https://doi.org/10.3390/molecules28083571 - 19 Apr 2023
Cited by 5 | Viewed by 2722
Abstract
Many plant-derived flavonoids are known for their anti-neuroinflammatory and anti-neurodegenerative effects. The fruits and leaves of the black currant (BC, Ribes nigrum) contain these phytochemicals with therapeutic benefits. The current study presents a report on a standardized BC gemmotherapy extract (BC-GTE) that [...] Read more.
Many plant-derived flavonoids are known for their anti-neuroinflammatory and anti-neurodegenerative effects. The fruits and leaves of the black currant (BC, Ribes nigrum) contain these phytochemicals with therapeutic benefits. The current study presents a report on a standardized BC gemmotherapy extract (BC-GTE) that is prepared from fresh buds. It provides details about the phytoconstituent profile specific to the extract as well as the associated antioxidant and anti-neuroinflammatory properties. The reported BC-GTE was found to contain approximately 133 phytonutrients, making it unique in its composition. Furthermore, this is the first report to quantify the presence of significant flavonoids such as luteolin, quercetin, apigenin, and kaempferol. Drosophila melanogaster-based tests revealed no cytotoxic but nutritive effects. We also demonstrated that adult male Wistar rats, pretreated with the analyzed BC-GTE and assessed after lipopolysaccharide (LPS) injection, did not show any apparent increase in body size in the microglial cells located in the hippocampal CA1 region, while in control experiments, the activation of microglia was evident. Moreover, no elevated levels of serum-specific TNF-α were observed under the LPS-induced neuroinflammatory condition. The analyzed BC-GTE’s specific flavonoid content, along with the experimental data based on an LPS-induced inflammatory model, suggest that it possesses anti-neuroinflammatory/neuroprotective properties. This indicates that the studied BC-GTE has the potential to be used as a GTE-based complementary therapeutic approach. Full article
(This article belongs to the Section Chemical Biology)
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Graphical abstract

Graphical abstract
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<p>The HPLC chromatogram of BC-GTE. 1 = quercetine, 2 = luteolin, 3 = kaempferol, 4 = apigenin.</p>
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<p>Effects of exposure to different concentrations of BC-GTE on the survival of <span class="html-italic">Drosophila melanogaster.</span> Abbreviations: 0M-zero media, NM-normal media; (****) <span class="html-italic">p</span> &lt; 0.0001 zero media vs. normal media group. The values are mean ± SEM, n = 1000.</p>
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<p>Experimental data presenting the physiological effects of BC-GTE on LPS-induced adult rats. The microglial cell body swelling (B, C). Abbreviations: BC-GTE—extract treated animal group; (***) <span class="html-italic">p</span> &lt; 0.001 control vs. BC-GTE group; (<sup>#</sup>) <span class="html-italic">p</span> &lt; 0.01 control vs. saline group. The values are mean ± SEM, n = 30–60. Scale bar: 10 µm.</p>
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<p>Experimental data presenting the serum <span class="html-italic">TNF-α</span> levels of BC-GTE on LPS-induced adult rats. Abbreviations: BC-GTE—extract treated animal group; ND—not detected. (***) <span class="html-italic">p</span> &lt; 0.001 control vs. BC-GTE group. The values are mean ± SEM, n = 6.</p>
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15 pages, 4285 KiB  
Article
A Descriptive Chemical Composition of Concentrated Bud Macerates through an Optimized SPE-HPLC-UV-MS2 Method—Application to Alnus glutinosa, Ribes nigrum, Rosa canina, Rosmarinus officinalis and Tilia tomentosa
by Thomas Charpentier, Séverine Boisard, Anne-Marie Le Ray, Dimitri Bréard, Amélie Chabrier, Hélène Esselin, David Guilet, Christophe Ripoll and Pascal Richomme
Plants 2022, 11(2), 144; https://doi.org/10.3390/plants11020144 - 6 Jan 2022
Cited by 9 | Viewed by 3010
Abstract
Concentrated bud macerates (CBMs) are obtained from meristematic tissues such as buds and young shoots by maceration in a solvent composed of glycerin, water and ethanol (1/1/1/, v/v). Their traditional utilization in gemmotherapy has gained interest in the past years, [...] Read more.
Concentrated bud macerates (CBMs) are obtained from meristematic tissues such as buds and young shoots by maceration in a solvent composed of glycerin, water and ethanol (1/1/1/, v/v). Their traditional utilization in gemmotherapy has gained interest in the past years, and the knowledge of their chemical characterization can provide commercial arguments, particularly to secure their quality control. Therefore, an optimized method for phytochemical analysis including glycerol removal by a preliminary solid phase extraction (SPE) followed by compound identification using high performance liquid chromatography coupled with ultra-violet and tandem mass detectors (HPLC-UV-MS2) was developed. This method was applied on 5 CBMs obtained from Alnus glutinosa, Ribesnigrum, Rosmarinus officinalis, Rosa canina and Tilia tomentosa in order to determinate their chemical composition. Their antioxidant effects were also investigated by radical scavenging activity assays (DPPH and ORAC). Glycerol removal improved the resolution of HPLC chemical profiles and allowed us to perform TLC antioxidant screening. Our approach permitted the identification of 57 compounds distributed in eight major classes, three of them being common to all macerates including nucleosides, phenolic acids and glycosylated flavonoids. Quantification of the later class as a rutin equivalent (RE) showed a great disparity between Rosa canina macerate (809 mg RE/L), and the other ones (from 175 to 470 mg RE/L). DPPH and ORAC assays confirmed the great activity of Rosa canina (4857 and 6479 μmol TE/g of dry matter, respectively). Finally, phytochemical and antioxidant analysis of CBMs strengthened their phytomedicinal interest in the gemmotherapy field. Full article
(This article belongs to the Special Issue Structural and Functional Analysis of Extracts in Plants II)
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<p>HPLC-ELSD profile of <span class="html-italic">Rosa canina</span> concentrated bud macerate before (<b>a</b>) and after (<b>b</b>) solid phase extraction (SPE).</p>
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<p>HPLC-DAD profiles of (<b>a</b>) <span class="html-italic">Alnus glutinosa</span>, (<b>b</b>) <span class="html-italic">Ribes nigrum</span>, (<b>c</b>) <span class="html-italic">Rosa canina</span>, (<b>d</b>) <span class="html-italic">Rosmarinus officinalis</span> and (<b>e</b>) <span class="html-italic">Tilia tomentosa</span> concentrated bud macerates (λ 254 nm): <b>1</b> cytidine (1-β-D-ribofuranosyl-cytosine), <b>2</b> uridine (1-β-D-Ribofuranosyluracil), <b>3</b> guanosine (2-Amino-9-(β-D-ribofuranosyl)-3,9-dihydro-6H-purin-6-on), <b>4</b> thymidine (1-(2-Deoxy-β-D-ribofuranosyl)-5-methyluracil), <b>5</b> 3-O-caffeoylquinic acid (neochlorogenic acid), <b>6</b> methyl-galloyl glucose, <b>7</b> <span class="html-italic">p</span>-coumaroylquinic acid, <b>8</b> digalloylquinic acid 1, <b>9</b> trigalloylglucose, <b>10</b> digalloylquinic acid 2, <b>11</b> 4-O-caffeoylquinic acid (crypto-chlorogenic acid), <b>12</b> 5-O-caffeoylquinic acid (chlorogenic acid), <b>13</b> medioresinol, <b>14</b> gallotannin, <b>15</b> (E)-p-coumaric acid, <b>16</b> myricetin-3-O-hexoside, <b>17</b> apigenin pentosyl hexoside, <b>18</b> hesperetin-7-O-rutinoside (hesperidin), <b>19</b> phloretin-2′-O-glucoside (phloridzin), <b>20</b> quercetin rhamnosyl hexoside, <b>21</b> rosmarinic acid, <b>22</b> hispidulin-7-b-glucoside (homoplantaginin/tectoridin), <b>23</b> quercetin glucuronide, <b>24</b> quercetin-3-O-glucoside (isoquercetin), <b>25</b> quercetin-3-O-galactoside (hyperoside), <b>26</b> quercetin-3-O-rutinoside (rutin), <b>27</b> isorhamnetin-3-O-hexoside, <b>28</b> kaempferol rhamnosyl hexoside, <b>29</b> caffeic acid ethylester ((E)-ethyl caffeate), <b>30</b> quercetin-3,7-O-dirhamnoside, <b>31</b> quercetin 3-glucosyl-(1-&gt;2)-glucoronide, <b>32</b> apigenin-7-O-glucoside (apigetrin), <b>33</b> quercetin pentoside, <b>34</b> galloyl quercetin glycoside, <b>35</b> apigenin 7-O-glucoronide, <b>36</b> quercetin 3-O-rhamnoside (quercitrin), <b>37</b> kaempferol hexoside, <b>38</b> kaempferol glucuronide, <b>39</b> isorhamnetin hexoside, <b>40</b> kaempferol rhamnosyl-hexoside, <b>41</b> kaempferol-3,7-O-dirhamnoside (kaempferitrin), <b>42</b> isorhamnetin rutinoside 1, <b>43</b> quercetin hexoside, <b>44</b> galloyl kaempferol hexoside or hexoside derivative, <b>45</b> kaempferol pentoside, <b>46</b> luteolin-7-O-glucoronide, <b>47</b> kaempferol rhamnoside, <b>48</b> quercetin, <b>49</b> acacetin 7-O-rutinoside (linarin/acaciin), <b>50</b> isorhamnetin, <b>51</b> kaempferol-3-O-(coumaroyl)-glucoside (trans-tiliroside), <b>52</b> isorhamnetin-rutinoside 2, <b>53</b> centaureidin, <b>54</b> dihydroxy-dimethoxyflavone 1, <b>55</b> rosmanol quinone, <b>56</b> dihydroxy-dimethoxyflavone 2 and <b>57</b> rosmanol isomer (epiisorosmanol).</p>
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<p>TLC profiles of the five CBMs respectively with Neu reagent and DPPH solution before SPE (<b>a</b>,<b>b</b>) and after SPE (<b>c</b>,<b>d</b>) (<span class="html-italic">Ag</span>: <span class="html-italic">Alnus glutinosa</span>, <span class="html-italic">Rn</span>: <span class="html-italic">Ribes nigrum</span>, <span class="html-italic">Rc</span>: <span class="html-italic">Rosa canina</span>, <span class="html-italic">Ro</span>: <span class="html-italic">Rosmarinus officinalis</span>, <span class="html-italic">Tt</span>: <span class="html-italic">Tilia tomentosa</span>, Ru: rutin as standard).</p>
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13 pages, 899 KiB  
Article
The Influence of Locality on Phenolic Profile and Antioxidant Capacity of Bud Extracts
by Zuzana Kovalikova, Jan Lnenicka and Rudolf Andrys
Foods 2021, 10(7), 1608; https://doi.org/10.3390/foods10071608 - 12 Jul 2021
Cited by 12 | Viewed by 2373
Abstract
Gemmotherapy represents the most recent therapeutic technique that uses the properties of extracts from fresh meristematic plant tissues, mainly buds and sprouts, by macerating them in ethanol and glycerol. The harvesting time and the location can significantly affect the chemical composition of the [...] Read more.
Gemmotherapy represents the most recent therapeutic technique that uses the properties of extracts from fresh meristematic plant tissues, mainly buds and sprouts, by macerating them in ethanol and glycerol. The harvesting time and the location can significantly affect the chemical composition of the buds. Therefore, this work aimed to point out the possible variability in the phenolic content and the antioxidant potential of extracts prepared from commonly grown trees in the Czech Republic. Extracts from buds collected during autumn and spring in three different localities were analysed using UHPLC-MS (ultra-high-pressure liquid chromatography) for the phenols profile. Five tests assays were used for the evaluation of the extract antioxidant potential. The sampling time positively affected the content of total phenols, flavonoids, and phenolic acids. The increased levels of total phenols and flavonoids in localities with high and medium pollution may be the result of the higher levels of NO and SO2, the main air pollutants. However, surprisingly, the content of phenolic acid showed the highest values in the area with the lowest pollution. The results of antioxidant tests did not completely correlate with the levels of phenolic metabolites, which may be due to the involvement of other active molecules (e.g., ascorbate, tocopherol, or proline) in the antioxidant machinery. Full article
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<p>Buds of individual trees collected in April 2020; (<b>a</b>). <span class="html-italic">Acer pseudoplatanus</span>, (<b>b</b>). <span class="html-italic">Betula pendula</span>, (<b>c</b>). <span class="html-italic">Quercus robur</span>.</p>
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<p>Representative chromatogram of measured phenolic acids. 1. gallic acid; 2. protocatechuic acid; 3. chlorogenic acid; 4. salicylic acid; 5. <span class="html-italic">p</span>-hydroxycbenzoic acid; 6. vanillic acid; 7. caffeic acid; 8. syringic acid; 9. benzoic acid; 10. <span class="html-italic">p</span>-coumaric acid; 11. ferulic acid; 12. cinnamic acid.</p>
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<p>The content of total phenols (mg g<sup>−1</sup> FW) and flavonoids (mg g<sup>−1</sup> FW) in spring bud extracts of <span class="html-italic">Acer pseudoplatanus</span>, <span class="html-italic">Betula pendula</span>, and <span class="html-italic">Quercur robur</span>. J, Jičín; HK, Hradec Králové; O, Opatovice n. Labem; N, Naděje; RA, Rabštejnská Apatyka. Data are as mean ± SDs (<span class="html-italic">n</span> = 6). Values within column followed by the same letter(s), are not significantly different according to Tukey’s test (<span class="html-italic">p</span> &lt; 0.05). The same type of letters shows a significant difference between the values of individual tree.</p>
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2 pages, 212 KiB  
Extended Abstract
Gemmotherapy—Modern Medicine
by Anca-Daniela Raiciu
Proceedings 2019, 29(1), 117; https://doi.org/10.3390/proceedings20190290117 - 18 Oct 2019
Cited by 1 | Viewed by 2070
Abstract
Gemmotherapy, also known as phytoembryotherapy, is a modern homeopathic method of biotherapeutic drainage using the extracts of various trees and shrubs. [...] Full article
(This article belongs to the Proceedings of Priorities of Chemistry for a Sustainable Development-PRIOCHEM)
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