Resveratrol as a calorie restriction mimetic: therapeutic implications

被引:186
作者
Chung, Jay H. [1 ]
Manganiello, Vincent [2 ]
Dyck, Jason R. B. [3 ]
机构
[1] NHLBI, Lab Obes & Aging Res, Genet & Dev Biol Ctr, NIH, Bethesda, MD 20892 USA
[2] NHLBI, Cardiovasc Pulm Branch, NIH, Bethesda, MD 20892 USA
[3] Univ Alberta, Dept Pediat, Mazankowski Alberta Heart Inst, Cardiovasc Res Ctr, Edmonton, AB T6G 2S2, Canada
基金
加拿大健康研究院; 美国国家卫生研究院;
关键词
PDE; AMPK; Sirt1; calorie restriction; diabetes; ACTIVATED PROTEIN-KINASE; SIRT1 TRANSGENIC MICE; LIFE-SPAN; MITOCHONDRIAL-FUNCTION; ISCHEMIA-REPERFUSION; METABOLIC DISEASE; LIPID-METABOLISM; AMPK; PHOSPHODIESTERASE; SIRTUINS;
D O I
10.1016/j.tcb.2012.07.004
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
It is widely believed that calorie restriction (CR) can extend the lifespan of model organisms and protect against aging-related diseases. A potential CR mimetic is resveratrol, which may have beneficial effects against numerous diseases such as type 2 diabetes, cardiovascular diseases, and cancer in tissue culture and animal models. However, resveratrol in its current form is not ideal as therapy, because even at very high doses it has modest efficacy and many downstream effects. Identifying the cellular targets responsible for the effects of resveratrol and developing target-specific therapies will be helpful in increasing the efficacy of this drug without increasing its potential adverse effects. A recent discovery suggests that the metabolic effects of resveratrol may be mediated by inhibiting cAMP phosphodiesterases (PDEs), particularly PDE4. Here, we review the current literature on the metabolic and cardiovascular effects of resveratrol and attempt to shed light on the controversies surrounding its action.
引用
收藏
页码:546 / 554
页数:9
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