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首页> 外文期刊>The Journal of Nutritional Biochemistry >Resveratrol regulates lipolysis via adipose triglyceride lipase.
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Resveratrol regulates lipolysis via adipose triglyceride lipase.

机译:白藜芦醇通过甘油三酸酯脂肪酶调节脂肪分解。

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摘要

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.
机译:据报道白藜芦醇可增加3T3-L1脂肪细胞中肾上腺素诱导的脂解。本工作的总体目的是获得更多关于反式白藜芦醇对脂质动员作用的见解。具体目的是评估两种主要脂肪酶:脂肪甘油三酸酯脂肪酶(ATGL)和激素敏感性脂肪酶(HSL)在此分子诱导的脂解激活中的参与。对于脂解实验,使用了3T3-L1和人SGBS脂肪细胞以及野生型,ATGL基因敲除和HSL基因敲除小鼠的脂肪组织。此外,分析了这些脂肪酶的基因和蛋白质表达。在SGBS脂肪细胞中,在基础和异丙肾上腺素刺激条件下以及在异丙肾上腺素刺激条件下,白藜芦醇诱导的游离脂肪酸在3T3-L1中释放但不释放甘油。当HSL被化合物76-0079阻断时,白藜芦醇仍可诱导游离脂肪酸释放。相反,在化合物C的存在下,该化合物C是腺苷单磷酸激活的蛋白激酶的抑制剂,白藜芦醇的作用完全减弱。白藜芦醇增加了ATGL基因和蛋白质的表达,这种作用在HSL中没有观察到。白藜芦醇增加了野生型和HSL基因敲除小鼠附睾脂肪组织中脂肪酸的释放,但ATGL基因敲除小鼠的脂肪组织中脂肪酸没有释放。总的来说,本发明结果提供了新的证据,白藜芦醇调节人和鼠脂肪细胞以及小鼠的白色脂肪组织中的脂解活性,主要在转录和转录后水平上作用于ATGL。似乎通过单磷酸腺苷活化的蛋白激酶诱导了酶的活化。

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