Resveratrol in high doses has been shown to extend lifespan in some
studies in invertebrates and to prevent early mortality in mice fed a
high-fat diet. We fed mice from middle age (14-months) to old age
(30-months) either a control diet, a low dose of resveratrol (4.9 mg kg
−1 day
−1),
or a calorie restricted (CR) diet and examined genome-wide
transcriptional profiles. We report a striking transcriptional overlap
of CR and resveratrol in heart, skeletal muscle and brain. Both dietary
interventions inhibit gene expression profiles associated with cardiac
and skeletal muscle aging, and prevent age-related cardiac dysfunction.
Dietary resveratrol also mimics the effects of CR in insulin mediated
glucose uptake in muscle. Gene expression profiling suggests that both
CR and resveratrol may retard some aspects of aging through alterations
in chromatin structure and transcription. Resveratrol, at doses that
can be readily achieved in humans, fulfills the definition of a dietary
compound that mimics some aspects of CR.
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