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脱氢表雄酮下调脂肪细胞中过氧化物酶体增殖物激活受体γ的表达。

Dehydroepiandrosterone down-regulates the expression of peroxisome proliferator-activated receptor gamma in adipocytes.

作者信息

Kajita Kazuo, Ishizuka Tatsuo, Mune Tomoatsu, Miura Atsushi, Ishizawa Masayoshi, Kanoh Yoshinori, Kawai Yasunori, Natsume Yoshiyuki, Yasuda Keigo

机构信息

The Third Department of Internal Medicine, Gifu University School of Medicine, Tsukasa-machi 40, Gifu 500-8705, Japan.

出版信息

Endocrinology. 2003 Jan;144(1):253-9. doi: 10.1210/en.2002-220039.

Abstract

Dehydroepiandrosterone (DHEA) is expected to have a weight-reducing effect. In this study, we evaluated the effect of DHEA on genetically obese Otsuka Long Evans Fatty rats (OLETF) compared with Long-Evans Tokushima rats (LETO) as control. Feeding with 0.4% DHEA-containing food for 2 wk reduced the weight of sc, epididymal, and perirenal adipose tissue in association with decreased plasma leptin levels in OLETF. Adipose tissue from OLETF showed increased expression of peroxisome proliferator-activated receptor gamma (PPARgamma) protein, which was prevented by DHEA treatment. Further, we examined the effect of DHEA on PPARgamma in primary cultured adipocytes and monolayer adipocytes differentiated from rat preadipocytes. PPARgamma protein level was decreased in a time- and concentration-dependent manner, and DHEA significantly reduced mRNA levels of PPARgamma, adipocyte lipid-binding protein, and sterol regulatory element-binding protein, but not CCAAT/enhancer binding protein alpha. DHEA-sulfate also reduced the PPARgamma protein, but dexamethasone, testosterone, or androstenedione did not alter its expression. In addition, treatment with DHEA for 5 d reduced the triglyceride content in monolayer adipocytes. These results suggest that DHEA down-regulates adiposity through the reduction of PPARgamma in adipocytes.

摘要

脱氢表雄酮(DHEA)有望具有减肥作用。在本研究中,我们评估了DHEA对遗传性肥胖的大冢长- Evans肥胖大鼠(OLETF)的影响,并将其与作为对照的长- Evans德岛大鼠(LETO)进行比较。给OLETF喂食含0.4% DHEA的食物2周,可减轻皮下、附睾和肾周脂肪组织的重量,同时血浆瘦素水平降低。OLETF的脂肪组织显示过氧化物酶体增殖物激活受体γ(PPARγ)蛋白表达增加,而DHEA治疗可阻止这种增加。此外,我们研究了DHEA对原代培养脂肪细胞以及从大鼠前脂肪细胞分化而来的单层脂肪细胞中PPARγ的影响。PPARγ蛋白水平呈时间和浓度依赖性降低,DHEA显著降低了PPARγ、脂肪细胞脂质结合蛋白和固醇调节元件结合蛋白的mRNA水平,但对CCAAT/增强子结合蛋白α没有影响。硫酸脱氢表雄酮也降低了PPARγ蛋白水平,但地塞米松、睾酮或雄烯二酮并未改变其表达。此外,用DHEA处理5天可降低单层脂肪细胞中的甘油三酯含量。这些结果表明,DHEA通过降低脂肪细胞中的PPARγ来下调肥胖程度。

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