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1.
Food Funct ; 9(7): 3798-3806, 2018 Jul 17.
Artículo en Inglés | MEDLINE | ID: mdl-29932178

RESUMEN

Here we identified that BTE (black tea extract), within the studied concentration range, is more effective than GTE (green tea extract) in protecting C. elegans against hypertonic stress, by enhancing survival after exposure to various salts, and alleviating suffered motility loss and body shrinkage. The mechanism of such protection may be due to the ability of black tea to induce the conserved WNK/GCK signaling pathway and down-regulation of the expression levels of nlp-29. Intriguingly, black tea does not relieve hypertonicity-induced protein damage. The findings implicate the potential health benefits of black tea consumed worldwide.


Asunto(s)
Caenorhabditis elegans/efectos de los fármacos , Caenorhabditis elegans/fisiología , Camellia sinensis/química , Presión Osmótica/efectos de los fármacos , Extractos Vegetales/farmacología , Animales , Caenorhabditis elegans/genética , Proteínas de Caenorhabditis elegans/genética , Proteínas de Caenorhabditis elegans/metabolismo , Extractos Vegetales/química , Transducción de Señal/efectos de los fármacos
2.
Redox Biol ; 14: 305-315, 2018 04.
Artículo en Inglés | MEDLINE | ID: mdl-28992589

RESUMEN

The green tea polyphenol epigallocatechin-3-gallate (EGCG) is widely consumed as a dietary supplement. Its potential properties include slowing aging and extending lifespan, although how exactly this is achieved remains unclear. Here, we report that EGCG promoted healthy lifespan in Caenorhabditis elegans when administered throughout or only at early-to-mid adulthood. Specifically, EGCG extended lifespan in an inverted U-shaped dose-response manner. The life-extending mechanism was stimulated by EGCG-induced production of reactive oxygen species (ROS). Additionally, EGCG triggered mitochondrial biogenesis to restore mitochondrial function. The EGCG-induced increase in lifespan depends on known energy sensors such as AMPK/AAK-2, as well as SIRT1/SIR-2.1 and FOXO/DAF-16. Interestingly, aging decreased the response to EGCG and progressively neutralized its beneficial effects on longevity. Collectively, our findings link EGCG to the process of mitohormesis and suggest an inducible, AMPK/SIRT1/FOXO-dependent redox signaling module that could be invoked in different contexts to extend healthy lifespan. Its effectiveness is higher in younger adults and declines with age.


Asunto(s)
Caenorhabditis elegans/efectos de los fármacos , Catequina/análogos & derivados , Longevidad/efectos de los fármacos , Envejecimiento/efectos de los fármacos , Animales , Caenorhabditis elegans/fisiología , Catequina/química , Catequina/farmacología , Mitocondrias/efectos de los fármacos , Mitocondrias/metabolismo , Biogénesis de Organelos , Especies Reactivas de Oxígeno/metabolismo , Té/química
3.
Food Chem ; 217: 196-204, 2017 Feb 15.
Artículo en Inglés | MEDLINE | ID: mdl-27664626

RESUMEN

The antibacterial effects of tea polyphenol epigallocatechin gallate (EGCG), a common phytochemical with a number of potential health benefits, are well known. However, the mechanism of its bactericidal action remains unclear. Using E. coli as a model organism, it is argued here that H2O2 synthesis by EGCG is not attributed to its inhibitory effects. In contrast, the bactericidal action of EGCG was a result of increased intracellular reactive oxygen species and blunted adaptive oxidative stress response in E. coli due to the co-administration of antioxidant N-acetylcysteine, and not on account of exogenous catalase. Furthermore, we noted a synergistic bactericidal effect for EGCG when combined with paraquat. However, under anaerobic conditions, the inhibitory effect of EGCG was prevented. In conclusion, EGCG caused an increase in endogenous oxidative stress in E. coli, thereby inhibiting its growth, and hence the use of EGCG as a prooxidant is supported by this study.


Asunto(s)
Catequina/análogos & derivados , Escherichia coli/efectos de los fármacos , Estrés Oxidativo/efectos de los fármacos , Polifenoles/farmacología , Té/química , Acetilcisteína/farmacología , Antioxidantes/farmacología , Catalasa/metabolismo , Catequina/farmacología , Peróxido de Hidrógeno/química , Especies Reactivas de Oxígeno/metabolismo
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