4.7 Article

Resveratrol regulates lipolysis via adipose triglyceride lipase

期刊

JOURNAL OF NUTRITIONAL BIOCHEMISTRY
卷 23, 期 4, 页码 379-384

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.jnutbio.2010.12.014

关键词

Resveratrol; Adipose triglyceride lipase; Hormone-sensitive lipase; 3T3-L1

资金

  1. Ministerio de Ciencia e Innovacion [AGL2008-01005-ALI]
  2. Basque Government [IT386-10]
  3. SFB Lipotox [F30-02. A]
  4. Ministerio de Educacion y Ciencia
  5. Austrian Science Fund (FWF) [F 3002, W 901, Z 136] Funding Source: researchfish

向作者/读者索取更多资源

Resveratrol has been reported to increase adrenaline-induced lipolysis in 3T3-L1 adipocytes. The general aim of the present work was to gain more insight concerning the effects of trans-resveratrol on lipid mobilization. The specific purpose was to assess the involvement of the two main lipases: adipose triglyceride lipase (ATGL) and hormone-sensitive lipase (HSL), in the activation of lipolysis induced by this molecule. For lipolysis experiments, 3T3-L1 and human SGBS adipocytes as well as adipose tissue from wild-type, ATGL knockout and HSL knockout mice were used. Moreover, gene and protein expressions of these lipases were analyzed. Resveratrol-induced free fatty acids release but not glycerol release in 3T3-L1 under basal and isoproterenol-stimulating conditions and under isoproterenol-stimulating conditions in SGBS adipocytes. When HSL was blocked by compound 76-0079, free fatty acid release was still induced by resveratrol. By contrast, in the presence of the compound C, an inhibitor of adenosine monophosphate-activated protein kinase, resveratrol effect was totally blunted. Resveratrol increased ATGL gene and protein expressions, an effect that was not observed for HSL Resveratrol increased fatty acids release in epididymal adipose tissue from wild-type and HSL knockout mice but not in that adipose tissue from ATGL knockout mice. Taking as a whole, the present results provide novel evidence that resveratrol regulates lipolytic activity in human and murine adipocytes, as well as in white adipose tissue from mice, acting mainly on ATGL at transcriptional and posttranscriptional levels. Enzyme activation seems to be induced via adenosine monophosphate-activated protein kinase. (C) 2012 Elsevier Inc. All rights reserved.

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