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1.
Age (Dordr) ; 35(1): 69-81, 2013 Feb.
Article in English | MEDLINE | ID: mdl-22083438

ABSTRACT

Resveratrol, a polyphenolic compound, has been shown to extend lifespan in different organisms. Emerging evidence suggests that the prolongevity effect of resveratrol depends on dietary composition. However, the mechanisms underlying the interaction of resveratrol and dietary nutrients in modulating lifespan remain elusive. Here, we investigated the effect of resveratrol on lifespan of Drosophila melanogaster fed diets differing in the concentrations of sugar, yeast extract, and palmitic acid representing carbohydrate, protein, and fat, respectively. Resveratrol at up to 200 µM in diets did not affect lifespan of wild-type female flies fed a standard, restricted or high sugar-low protein diet, but extended lifespan of females fed a low sugar-high protein diet. Resveratrol at 400 µM extended lifespan of females fed a high-fat diet. Lifespan extension by resveratrol was associated with downregulation of genes in aging-related pathways, including antioxidant peroxiredoxins, insulin-like peptides involved in insulin-like signaling and several downstream genes in Jun-kinase signaling involved in oxidative stress response. Furthermore, resveratrol increased lifespan of superoxide dismutase 1 (sod1) knockdown mutant females fed a standard or high-fat diet. No lifespan extension by resveratrol was observed in wild-type and sod1 knockdown males under the culture conditions in this study. Our results suggest that the gender-specific prolongevity effect of resveratrol is influenced by dietary composition and resveratrol promotes the survival of flies by modulating genetic pathways that can reduce cellular damage. This study reveals the context-dependent effect of resveratrol on lifespan and suggests the importance of dietary nutrients in implementation of effective aging interventions using dietary supplements.


Subject(s)
Aging/drug effects , Caloric Restriction , Drosophila melanogaster/physiology , Longevity/drug effects , Oxidative Stress/physiology , Stilbenes/pharmacology , Aging/physiology , Animals , Antioxidants/pharmacology , Diet, High-Fat , Female , Male , Resveratrol , Ribonucleotide Reductases/antagonists & inhibitors , Signal Transduction
2.
Free Radic Biol Med ; 50(11): 1669-78, 2011 Jun 01.
Article in English | MEDLINE | ID: mdl-21406223

ABSTRACT

Fruits containing high antioxidant capacities and other bioactivities are ideal for promoting longevity and health span. However, few fruits are known to improve the survival and health span in animals, let alone the underlying mechanisms. Here we investigate the effects of nectarine, a globally consumed fruit, on life span and health span in Drosophila melanogaster. Wild-type flies were fed standard, dietary restriction (DR), or high-fat diet supplemented with 0-4% nectarine extract. We measured life span, food intake, locomotor activity, fecundity, gene expression changes, and oxidative damage indicated by the level of 4-hydroxynonenal-protein adduct in these flies. We also measured life span, locomotor activity, and oxidative damage in sod1 mutant flies on the standard diet supplemented with 0-4% nectarine. Supplementation with 4% nectarine extended life span, increased fecundity, and decreased expression of some metabolic genes, including a key gluconeogenesis gene, PEPCK, and oxidative stress-response genes, including peroxiredoxins, in female wild-type flies fed the standard, DR, or high-fat diet. Nectarine reduced oxidative damage in wild-type females fed the high-fat diet. Moreover, nectarine improved the survival of and reduced oxidative damage in female sod1 mutant flies. Together, these findings suggest that nectarine promotes longevity and health span partly by modulating glucose metabolism and reducing oxidative damage.


Subject(s)
Antioxidants/administration & dosage , Drosophila melanogaster/physiology , Fruit , Plant Extracts/administration & dosage , Superoxide Dismutase/metabolism , Animals , Animals, Genetically Modified , Diet , Female , Fertility/drug effects , Fertility/genetics , Gene Expression Regulation , Longevity/drug effects , Motor Activity/drug effects , Mutation/genetics , Oxidative Stress/drug effects , Oxidative Stress/genetics , Peroxiredoxins/genetics , Peroxiredoxins/metabolism , Phosphoenolpyruvate Carboxykinase (ATP)/genetics , Phosphoenolpyruvate Carboxykinase (ATP)/metabolism , Superoxide Dismutase/genetics , Superoxide Dismutase-1
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