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大黄素通过激活AMP活化蛋白激酶α抑制脂肪生成并诱导产热。

Chrysophanic Acid Suppresses Adipogenesis and Induces Thermogenesis by Activating AMP-Activated Protein Kinase Alpha and .

作者信息

Lim Hara, Park Jinbong, Kim Hye-Lin, Kang JongWook, Jeong Mi-Young, Youn Dong-Hyun, Jung Yunu, Kim Yong-Il, Kim Hyun-Ju, Ahn Kwang Seok, Kim Su-Jin, Choe Seong-Kyu, Hong Seung-Heon, Um Jae-Young

机构信息

College of Korean Medicine, Basic Research Laboratory for Comorbidity Regulation Kyung Hee University, Seoul, South Korea.

Department of Microbiology and Center for Metabolic Function Regulation, School of Medicine, Wonkwang University Iksan, South Korea.

出版信息

Front Pharmacol. 2016 Dec 8;7:476. doi: 10.3389/fphar.2016.00476. eCollection 2016.

Abstract

Chrysophanic acid (CA) is a member of the anthraquinone family abundant in rhubarb, a widely used herb for obesity treatment in Traditional Korean Medicine. Though several studies have indicated numerous features of CA, no study has yet reported the effect of CA on obesity. In this study, we tried to identify the anti-obesity effects of CA. By using 3T3-L1 adipocytes and primary cultured brown adipocytes as models, high-fat diet (HFD)-induced obese mice, and zebrafish as models, we determined the anti-obesity effects of CA. CA reduced weight gain in HFD-induced obese mice. They also decreased lipid accumulation and the expressions of adipogenesis factors including peroxisome proliferator-activated receptor gamma (PPARγ) and CCAAT/enhancer-binding protein alpha (C/EBPα) in 3T3-L1 adipocytes. In addition, uncoupling protein 1 (UCP1) and peroxisome proliferator-activated receptor gamma coactivator 1-alpha (PGC1α), the brown fat specific thermogenic genes, were up-regulated in brown adipocytes by CA treatment. Furthermore, when co-treated with Compound C, the AMP-activated protein kinase (AMPK) inhibitor, the action of CA on AMPKα was nullified in both types of adipocytes, indicating the multi-controlling effect of CA was partially via the AMPKα pathway. Given all together, these results indicate that CA can ameliorate obesity by controlling the adipogenic and thermogenic pathway at the same time. On these bases, we suggest the new potential of CA as an anti-obese pharmacotherapy.

摘要

大黄酸(CA)是蒽醌家族的一员,在大黄中含量丰富,大黄是韩国传统医学中广泛用于治疗肥胖症的草药。尽管多项研究表明了CA的多种特性,但尚无研究报道CA对肥胖症的影响。在本研究中,我们试图确定CA的抗肥胖作用。通过使用3T3-L1脂肪细胞和原代培养的棕色脂肪细胞作为模型、高脂饮食(HFD)诱导的肥胖小鼠以及斑马鱼作为模型,我们确定了CA的抗肥胖作用。CA减少了HFD诱导的肥胖小鼠的体重增加。它们还减少了3T3-L1脂肪细胞中的脂质积累以及包括过氧化物酶体增殖物激活受体γ(PPARγ)和CCAAT/增强子结合蛋白α(C/EBPα)在内的脂肪生成因子的表达。此外,棕色脂肪特异性产热基因解偶联蛋白1(UCP1)和过氧化物酶体增殖物激活受体γ共激活因子1α(PGC1α)在棕色脂肪细胞中通过CA处理而上调。此外,当与AMP激活的蛋白激酶(AMPK)抑制剂Compound C共同处理时,CA对AMPKα的作用在两种类型的脂肪细胞中均被消除,表明CA的多重控制作用部分是通过AMPKα途径实现的。综上所述,这些结果表明CA可以通过同时控制脂肪生成和产热途径来改善肥胖症。基于这些依据,我们提出了CA作为抗肥胖药物治疗的新潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd7b/5143616/a123f6005769/fphar-07-00476-g001.jpg

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