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反式10,顺式12-共轭亚油酸通过作为过氧化物酶体增殖物激活受体γ(PPARγ)调节剂来防止脂肪细胞中三酰甘油的积累。

Trans10, cis12-conjugated linoleic acid prevents triacylglycerol accumulation in adipocytes by acting as a PPARgamma modulator.

作者信息

Granlund Linda, Juvet Lene K, Pedersen Jan I, Nebb Hilde I

机构信息

Institute for Nutrition Research, University of Oslo, N-0316 Oslo, Norway.

出版信息

J Lipid Res. 2003 Aug;44(8):1441-52. doi: 10.1194/jlr.M300120-JLR200. Epub 2003 May 16.

Abstract

A group of polyunsaturated fatty acids called conjugated linoleic acids (CLAs) are found in ruminant products, where the most common isomers are cis9, trans11 (c 9,t11) and trans10, cis12 (t10,c12) CLA. A crude mixture of these isomers has been shown in animal studies to alter body composition by a reduction in body fat mass as well as an increase in lean body mass, with the t10,c12 isomer having the most pronounced effect. The objective of this study was to establish the molecular mechanisms by which t10,c12 CLA affects lipid accumulation in adipocytes. We have shown that t10,c12 CLA prevents lipid accumulation in human and mouse adipocytes at concentrations as low as 5 microM and 25 microM, respectively. t10,c12 CLA fails to activate peroxisome proliferator-activated receptor gamma (PPARgamma) but selectively inhibits thiazolidinedione-induced PPARgamma activation in 3T3-L1 adipocytes. Treatment of mature adipocytes with t10,c12 CLA alone or in combination with Darglitazone down-regulates the mRNA expression of PPARgamma as well as its target genes, fatty acid binding protein (aP2) and liver X receptor alpha (LXRalpha). Taken together, our results suggest that the trans10, cis12 CLA isomer prevents lipid accumulation in adipocytes by acting as a PPARgamma modulator.

摘要

一类称为共轭亚油酸(CLA)的多不饱和脂肪酸存在于反刍动物产品中,其中最常见的异构体是顺式9,反式11(c9,t11)和反式10,顺式12(t10,c12)CLA。在动物研究中已表明,这些异构体的粗混合物可通过减少体脂量以及增加瘦体重来改变身体组成,其中t10,c12异构体的作用最为明显。本研究的目的是确定t10,c12 CLA影响脂肪细胞脂质积累的分子机制。我们已经表明,t10,c12 CLA分别在低至5 microM和25 microM的浓度下可防止人和小鼠脂肪细胞中的脂质积累。t10,c12 CLA未能激活过氧化物酶体增殖物激活受体γ(PPARγ),但在3T3-L1脂肪细胞中选择性抑制噻唑烷二酮诱导的PPARγ激活。单独用t10,c12 CLA或与达格列净联合处理成熟脂肪细胞可下调PPARγ及其靶基因脂肪酸结合蛋白(aP2)和肝X受体α(LXRα)的mRNA表达。综上所述,我们的结果表明反式10,顺式12 CLA异构体通过作为PPARγ调节剂来防止脂肪细胞中的脂质积累。

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