期刊
ENDOCRINOLOGY
卷 156, 期 1, 页码 157-168出版社
OXFORD UNIV PRESS INC
DOI: 10.1210/en.2014-1354
关键词
-
资金
- Ministry of Oceans and Fisheries, Korea
- National Research Foundation Grant [NRF-2013R1A1A1007693]
Gallic acid [3,4,5-trihydroxybenzoic acid (GA)], a natural phytochemical, is known to have a variety of cellular functions including beneficial effects on metabolic syndromes. However, the molecular mechanism by which GA exerts its beneficial effects is not known. Here we report that GA plays its role through the activation of AMP-activated protein kinase (AMPK) and by regulating mitochondrial function via the activation of peroxisome proliferator-activated receptor-gamma coactivator1 alpha (PGC1 alpha). Sirtuin 1 (Sirt1) knockdown significantly blunted GA's effect on PGC1 alpha activation and downstream genes, suggesting a critical role of the AMPK/Sirt1/PGC1 alpha pathway in GA's action. Moreover, diet-induced obese mice treated with GA showed significantly improved glucose and insulin homeostasis. In addition, the administration of GA protected diet-induced body weight gain without a change in food intake. Biochemical analyses revealed a marked activation of AMPK in the liver, muscle, and interscapular brown adipose tissue of the GA-treated mice. Moreover, uncoupling protein 1 together with other genes related to energy expenditure was significantly elevated in the interscapular brown adipose tissue. Taken together, these results indicate that GA plays its beneficial metabolic roles by activating the AMPK/Sirt1/PGC1 alpha pathway and by changing the interscapular brown adipose tissue genes related to thermogenesis. Our study points out that targeting the activation of the AMPK/Sirt1/PGC1 alpha pathway by GA or its derivatives might be a potential therapeutic intervention for insulin resistance in metabolic diseases.
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