Enhancing the Anti-Aging Potential of Green Tea Extracts Through Liquid-State Fermentation with Aspergillus niger RAF106.

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Microbial fermentation diversely modulates the bioactivity of green tea extracts (GTE), but its effects on anti-aging potential remain under-explored. This study investigated the effects of liquid-state fermentation by Aspergillus niger RAF106 on the anti-aging properties of GTE from Biluochun and identified its longevity-promoting metabolites. The unfermented GTE used herein showed no or limited effects, but the four-day fermented tea extracts (GTE-A4) significantly extended the mean lifespan in Caenorhabditis elegans, enhanced motility and stress resistance, and improved mitochondrial function and antioxidant properties, while reducing lipid accumulation and oxidative damage. The pro-longevity effect depended on insulin/IGF-1, MAPK, and p53 pathways and required transcription factors DAF-16 and HSF-1. Fermentation periods shorter or longer than 4 days led to reduced efficacy. Fermentation with RAF106 dynamically altered chemical composition and induced the enrichment of various longevity-promoting metabolites in GTE-A4, including proanthocyanidin A2, aromadendrin, and dalbergioidin-all newly identified as anti-aging agents. These findings demonstrate that RAF106 fermentation improves the anti-aging potential of green tea and provides a scientific basis for using precision fermentation to develop advanced anti-aging functional ingredients from tea extracts.

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The present study evaluated the antioxidant effect of green and black tea (Camellia sinensis L.) extracts in uncured pork sausages. The total polyphenol content in the green tea extract (GTE) was significantly higher (p < 0.05) than the black tea extract (BTE). DPPH assay showed significantly higher (p < 0.05) antioxidant activity in GTE compared to BTE. However, TBARS values of uncured pork sausages significantly reduced (p < 0.05) for all levels of concentrations of BTE (0.05%, 0.10%, 020%, and 0.30%) and GTE (0.05%, 0.10, 0.20%, and 0.30%) during the 5 days storage period. The reduction of TBARS values for the BTE 0.05% treated sausage sample was not, however, significantly different (p > 0.05) to the BHT 0.10% treated sausage sample on fifth day of the storage period. The sensory evaluation of pork sausages incorporated with a BTE of 0.05% and 0.30%, GTE of 0.05% and the control were not significantly differences (p < 0.05) in color, odor, texture, juiciness, taste, or overall acceptability. Practical applications In the present study, we evaluated the antioxidant effect of green and black tea (Camellia sinensis L.) extracts in uncured pork sausages. Adding of black tea extract 0.05%, 0.30%, and green tea extract 0.05% can reduce the TBARS value in uncured pork sausages without altering color, odor, texture, juiciness, or overall acceptability. Therefore, 0.05%, 0.30% black tea extract and 0.05% green tea extracts can be considered as potential antioxidants in uncured pork sausages.

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Chapter 46 - Green Tea Extract
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  • Research Article
  • Cite Count Icon 12
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English
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  • African Journal of Microbiology Research
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Green and black teas extracts are known for their antibacterial activity against many pathogenic microorganisms. These studies have been necessitated by the need to combat the recent rise of drug-resistant human pathogens which is becoming a common occurrence in the world making easily manageable infections to become life threatening illnesses. This study evaluated the antimicrobial activity of water soluble green and black tea extracts from a high quality Kenyan tea clone TRFK 6/8 against antibiotic resistant Escherichia coli ATCC 25922 and Staphylococcus aureusATCC 25923 using agar well diffusion method. Green and black tea extracts effectively inhibited the growth of both E. coli ATCC 25922 and S. aureus ATCC 25923 at concentrations of 0.1 and 0.05 mg/ml, respectively after 24 h. Green tea extracts and gentamicin showed greater zone of inhibition compared to penicillin G. In addition, the possible synergistic activity of water soluble green tea extract and antibiotics was also determined using agar well diffusion method. A combination of penicillin G and green tea extract inhibited the growth of E. coli ATCC 25922 and S. aureus ATCC 25923 compared to penicillin G alone while gentamicin exhibited an additive and antagonistic effect depending on tested bacteria. Green and black tea extracts can be used as an antimicrobial agent and also green tea extract can be used in combination with penicillin G to manage resistant pathogenic bacteria. Furthermore, tea which is a proven safe, cheap and readily available compound can be used in more ambitious trials to test the antimicrobial efficacy and chemo-preventive effects in animal and human models. &nbsp; Key words: Green tea, black tea, antimicrobial activity, synergistic activity, gentamicin, penicillin G.

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  • F1000Research
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Background: Insulin resistance has been independently associated with cardiac diseases. Free fatty acids are recently known to induce cardiac insulin resistance due to low-grade inflammation. Therefore, the improvement of free fatty acid levels can also improve cardiac insulin resistance. This study investigated the combination of green tea and decaffeinated-light roasted green coffee extract in the improvement of free fatty acid-induced cardiac insulin resistance by improving the adiponectin/FAS pathways. Methods: This study used 25 males Sprague-Dawley rats induced by a high-fat high sucrose diet and injection of low dose streptozotocin to make a metabolic syndrome (MS) rat model and standard chow as healthy control rats. The MS rats were treated with green tea (200 mg/ b. w.), decaffeinated-light roasted green coffee (300 mg/ b. w.), and the combination of both extracts in 9 weeks. Experimental groups in this study were divided into 5 groups: 1) MS (HFHS diet + STZ) group, 2) NC (normal chow) group, 3) GT (green tea extract) group, 4) GC (decaffeinated-light roasted green coffee extract), 5) CM (combination of both extracts) group. Adiponectin and HOMA-IR level was analysed using ELISA, and the gene expression of Adipo-R1, FAS, PI3K, PDK1, Akt, GLUT4 was measured by RT-PCR. Results: The combination of green tea and decaffeinated-light roasted green coffee showed synergistic effects in improving FFA levels. The adiponectin/FAS pathways was attenuated in the CM group. Moreover, the combination also showed improvement in cardiac insulin resistance markers such as IRS1/2, PI3K, PDK1, Akt, and GLUT4. Conclusions: The combination of green tea and decaffeinated-light roasted green coffee extract improved cardiac insulin resistance better than green tea and green coffee extract administration alone by reducing free fatty acids levels through adiponectin/FAS pathways modulation.

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  • Research Article
  • Cite Count Icon 1
  • 10.12688/f1000research.55470.1
Green Tea and Decaffeinated Light Roasted Green Coffee Extract Combination Improved Cardiac Insulin Resistance through Free Fatty Acids and Adiponectin/FAS Pathway Amelioration in Metabolic Syndrome Rat Model
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  • F1000Research
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An Appraisal of Drug-Drug Interactions with Green Tea (Camellia sinensis)
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This review summarizes published in vitro, animal, and clinical studies investigating the effects of green tea (Camellia sinensis) extract and associated catechins on drug-metabolizing enzymes and drug transporters. In vitro studies suggest that green tea extract and its main catechin, (-)-epigallocatechin-3-gallate, to varying degrees, inhibit the activity of CYP1A1, CYP1A2, CYP2B6, CYP2C8, CYP2C9, CYP2D6, and CYP3A4. UGT1A1 and UGT1A4 isoforms were also inhibited by (-)-epigallocatechin-3-gallate. Animal studies suggest green tea extract and/or (-)-epigallocatechin-3-gallate significantly increase the bioavailability of diltazem, verapamil, tamoxifen simvastatin, 5-fluorouracil, and nicardipine. Conversely, green tea extract and/or (-)-epigallocatechin-3-gallate reduce the bioavailability of quetiapine, sunitinib, clozapine, and nadolol. Of the few clinical studies available for review, it appears neither green tea extract nor (-)-epigallocatechin-3-gallate inhibit any major cytochrome P450 enzyme. Regarding drug transporters, in vitro studies indicate P-glycoprotein, organic anion transporting polypeptide 1A1, organic anion transporting polypeptide 1B1, organic anion transporting polypeptide 1B3, organic anion transporting polypeptide 2B1, organic cation transporter 1, organic cation transporter 2, multidrug and toxin extrusion 1, and multidrug and toxin extrusion 2-K are potentially inhibited by green tea extract. A clinical study indicates the organic anion transporting polypeptide 1A1 transporter is inhibited by (-)-epigallocatechin-3-gallate while P-glycoprotein is unaffected. In conclusion, the ingestion of green tea extract or its associated catechins is not expected to result in clinically significant influences on major cytochrome P450 or uridine 5'-diphospho-glucuronosyltransferase enzyme substrates or drugs serving as substrates of P-glycoprotein. However, some caution is advised in the consumption of significant amounts of green tea beverages or green tea extract in patients prescribed known substrates of organic anion transporting polypeptide, particularly those with a narrow therapeutic index.

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Comparison of the Antimicrobial Efficacy of Green and Black Tea Extracts Against E.Coli: In Vitro and In Vivo Study -
  • Mar 24, 2021
  • Systematic Reviews in Pharmacy
  • Sawsan Mohammed Sorchee + 2 more

Green and black tea is one of the most popular beverages consumed worldwide. Moreover, during the last two decades it has received much attention in regard to its beneficial effects on various human health problems .This study aimed to investigate the antibacterial effect of hot and cold extracts of green tea and black tea separately against E. coli and after infecting the burned skin rat with them, also to screen the effect of both types of tea on rat liver and kidney. Sixteen male rats divided into four Groups (4 animals each), Group 1: untreated rat (control). Group 2: burn rats infected with E.coli(1.5×108 bacteria /ml). Group 3: burn treated by Green tea aqueous extract (1000 µg/ml) for E.coli bacteria. Group 4: burn treated by black tea extract (800 µg/ml) for E.coli bacteria. The tea extracts antimicrobial activity was analyzed by agar diffusion inhibition assay and minimum inhibitory concentration. Results exhibited that E. coli in particular, have high levels of resistance against 13 antimicrobial and response only to Imepeneme and Meropenem . Hot watery green tea extract is more effective against bacterial type than cold once. Based on assessment of inhibition zones. E. coli was more sensitive black tea extraction, according to the inhibitions zone. Depending on MIC, we concluded that hot extract from two types of teas have the best antibacterial effect than cold extract demonstrated that the best MIC against E.coli is hot green tea extract (400 µg/ml) then hot black tea extract (600 µg/ml) followed by cold green tea extract (800 µg/ml) and less activity is cold black tea extract (1000 µg/ml). Infected rats showed inflammation and hemorrhage. While treating rats with tea extracts dermally approximately restored kidney normal histological architecture and liver became nearly normal in histological structure. Black tea extract showed greater effectiveness in tissue recovery than green once.

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