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15-甲氧基松苓酸通过抑制 PPARγ 活性抑制脂肪细胞分化。

Suppression of adipocyte differentiation by 15-methoxypinusolidic acid through inhibition of PPARγ activity.

机构信息

Center for Cell Signaling & Drug Discovery Research, Ewha Womans University, Seoul, Korea.

出版信息

Arch Pharm Res. 2010 Jul;33(7):1035-41. doi: 10.1007/s12272-010-0709-0. Epub 2010 Jul 27.

Abstract

Pinusolide and its derivative, 15-methoxypinusolidic acid (15-MPA) are diterpenoid compounds isolated from Biota orientalis, which has been used as a Korean folk medicine for treating inflammatory disorders. Pinusolide and 15-MPA suppress nitric oxide generation by suppressing inducible nitric oxide synthase and exerted anti-inflammatory functions, whereas other functions and regulatory mechanisms are largely unknown. In this study, we investigated whether pinusolide and 15-MPA modulate adipocyte differentiation from pre-adipocytes 3T3-L1 cells. We found that 15-MPA, not pinusolide, suppressed adipocyte differentiation in a dose-dependent manner, as revealed by lipid droplet formation and expression of adipogenic genes such as adiponectin and aP2. 15-MPA did not affect mRNA and protein levels of PPARgamma, a key adipogenic transcription factor, whereas transcriptional activity of PPARgamma was significantly attenuated by 15-MPA. While aP2 promoter activity was increased by ectopic overexpression of PPARgamma or by rosiglitazone-induced endogenous PPARgamma activation, PPARgamma-induced aP2 promoter activity was inhibited in the presence of 15-MPA. These results suggest that 15-MPA suppresses adipocyte differentiation through the inhibition of PPARgamma-dependent adipogenic gene expression.

摘要

松萝酸及其衍生物 15-甲氧基松萝酸(15-MPA)是从东方被孢霉中分离得到的二萜类化合物,被韩国民间用作治疗炎症性疾病的药物。松萝酸和 15-MPA 通过抑制诱导型一氧化氮合酶来抑制一氧化氮的产生,并发挥抗炎作用,而其他功能和调节机制在很大程度上尚不清楚。在这项研究中,我们研究了松萝酸和 15-MPA 是否调节前脂肪细胞 3T3-L1 细胞向脂肪细胞的分化。我们发现,15-MPA 而非松萝酸以剂量依赖性方式抑制脂肪细胞分化,这表现在脂滴形成和脂联素和 aP2 等脂肪生成基因的表达上。15-MPA 不影响关键脂肪生成转录因子 PPARγ的 mRNA 和蛋白水平,而 PPARγ 的转录活性则被 15-MPA 显著抑制。虽然 aP2 启动子活性可通过过表达 PPARγ或罗格列酮诱导的内源性 PPARγ激活而增加,但在存在 15-MPA 的情况下,PPARγ 诱导的 aP2 启动子活性受到抑制。这些结果表明,15-MPA 通过抑制 PPARγ 依赖性脂肪生成基因表达来抑制脂肪细胞分化。

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