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二十碳五烯酸诱导过氧化物酶体增殖物激活受体γ的mRNA表达。

Eicosapentaenoic acid induces mRNA expression of peroxisome proliferator-activated receptor gamma.

作者信息

Chambrier Cécile, Bastard Jean-Philippe, Rieusset Jennifer, Chevillotte Emmanuel, Bonnefont-Rousselot Dominique, Therond Patrice, Hainque Bernard, Riou Jean-Paul, Laville Martine, Vidal Hubert

机构信息

INSERM U449 and Human Nutrition Research Center of Lyon, R. Laennec Faculty of Medicine, Claude Bernard Lyon-1 University, France.

出版信息

Obes Res. 2002 Jun;10(6):518-25. doi: 10.1038/oby.2002.70.

Abstract

OBJECTIVE

To verify whether polyunsaturated fatty acids (PUFAs) can regulate the expression of the nuclear receptor peroxisome proliferator-activated receptor gamma (PPARgamma) in human adipose tissue.

RESEARCH METHODS AND PROCEDURES

The effect of various PUFAS on PPARgamma1 and -gamma2 mRNA expression was investigated in freshly isolated adipocytes prepared from fat samples obtained during surgery. PPARgamma mRNA levels were also determined in subcutaneous adipose tissue biopsies of 11 obese women, in the fasting state, to search for in vivo associations between PPARgamma expression and plasma PUFA concentrations. PPARgamma mRNA levels were determined by reverse-transcription competitive polymerase chain reaction.

RESULTS

Eicosapentaenoic acid (EPA) significantly increased PPARgamma1 mRNA levels in isolated adipocytes, without affecting the expression of PPARgamma2. The other tested fatty acids (linolenic acid, docosahexaenoic acid and omega-6 PUFAs) had no effect. The effect of EPA was dependent on the concentration (maximal effect after 6 hours with 50 microM) and was not reproduced by activators of the different members of the PPAR family. In addition, a strong positive correlation was found between plasma EPA concentrations and PPARgamma mRNA levels in adipose tissue of obese subjects.

DISCUSSION

Our results demonstrate that adipose tissue PPARgamma1 mRNA concentration is positively regulated by EPA, suggesting that the composition of dietary lipids may affect PPARgamma gene expression in vivo in humans. These data also suggest that an induction of the expression of this nuclear receptor isoform might be involved in the mechanism of action of EPA and in some of its beneficial effects.

摘要

目的

验证多不饱和脂肪酸(PUFAs)是否能调节人类脂肪组织中核受体过氧化物酶体增殖物激活受体γ(PPARγ)的表达。

研究方法与步骤

在从手术中获取的脂肪样本制备的新鲜分离脂肪细胞中,研究各种PUFAs对PPARγ1和 -γ2 mRNA表达的影响。还测定了11名肥胖女性在空腹状态下皮下脂肪组织活检样本中的PPARγ mRNA水平,以寻找PPARγ表达与血浆PUFA浓度之间的体内关联。通过逆转录竞争聚合酶链反应测定PPARγ mRNA水平。

结果

二十碳五烯酸(EPA)显著增加分离脂肪细胞中PPARγ1 mRNA水平,而不影响PPARγ2的表达。其他测试脂肪酸(亚麻酸、二十二碳六烯酸和ω-6 PUFAs)无此作用。EPA的作用取决于浓度(50 microM作用6小时后达到最大效应),且不能被PPAR家族不同成员的激活剂复制。此外,在肥胖受试者的脂肪组织中,血浆EPA浓度与PPARγ mRNA水平之间发现有很强的正相关性。

讨论

我们的结果表明,脂肪组织中PPARγ1 mRNA浓度受EPA正向调节,这表明饮食脂质的组成可能在体内影响人类PPARγ基因表达。这些数据还表明,这种核受体亚型表达的诱导可能参与EPA的作用机制及其一些有益作用。

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