The molecular targets of resveratrol

被引:410
作者
Kulkarni, Sameer S. [1 ]
Canto, Carles [1 ]
机构
[1] Nestle Inst Hlth Sci, CH-1015 Lausanne, Switzerland
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE | 2015年 / 1852卷 / 06期
关键词
Resveratrol; SIRT1; AMPK; Metabolism; Mitochondria; ACTIVATED PROTEIN-KINASE; NF-KAPPA-B; COACTIVATOR-1-ALPHA PGC-1-ALPHA DEACETYLATION; REGULATES ENERGY-METABOLISM; EXTENDS LIFE-SPAN; SKELETAL-MUSCLE; MITOCHONDRIAL BIOGENESIS; CALORIE RESTRICTION; GLUCOSE-UPTAKE; INSULIN SENSITIVITY;
D O I
10.1016/j.bbadis.2014.10.005
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Resveratrol has emerged in recent years as a compound conferring strong protection against metabolic, cardiovascular and other age-related complications, including neurodegeneration and cancer. This has generated the notion that resveratrol treatment acts as a calorie-restriction mimetic, based on the many overlapping health benefits observed upon both interventions in diverse organisms, including yeast, worms, flies and rodents. Though studied for over a decade, the molecular mechanisms governing the therapeutic properties of resveratrol still remain elusive. Elucidating how resveratrol exerts its effects would provide not only new insights in its fundamental biological actions but also new avenues for the design and development of more potent drugs to efficiently manage metabolic disorders. In this review we will cover the most recent advances in the field, with special focus on the metabolic actions of resveratrol and the potential role of SIRT1 and AMPK. This article is part of a Special Issue entitled: Resveratrol: Challenges in translating pre-clinical findings to improved patient outcomes. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:1114 / 1123
页数:10
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