1. Academic Validation
  2. Alisol A attenuates high-fat-diet-induced obesity and metabolic disorders via the AMPK/ACC/SREBP-1c pathway

Alisol A attenuates high-fat-diet-induced obesity and metabolic disorders via the AMPK/ACC/SREBP-1c pathway

  • J Cell Mol Med. 2019 Aug;23(8):5108-5118. doi: 10.1111/jcmm.14380.
Chiakang Ho 1 Ya Gao 1 Danning Zheng 1 Yanjun Liu 1 Shengzhou Shan 1 Bin Fang 1 Yixuan Zhao 1 Dingzhong Song 2 Yifan Zhang 1 Qingfeng Li 1
Affiliations

Affiliations

  • 1 Department of Plastic & Reconstructive Surgery, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
  • 2 China State Institute of Pharmaceutical Industry, National Pharmaceutical Engineering Research Center, Shanghai, China.
Abstract

Obesity and its associated metabolic disorders such as diabetes, hepatic steatosis and chronic heart diseases are affecting billions of individuals. However there is no satisfactory drug to treat such diseases. In this study, we found that alisol A, a major active triterpene isolated from the Chinese traditional medicine Rhizoma Alismatis, could significantly attenuate high-fat-diet-induced obesity. Our biochemical detection demonstrated that alisol A remarkably decreased lipid levels, alleviated glucose metabolism disorders and Insulin resistance in high-fat-diet-induced obese mice. We also found that alisol A reduced hepatic steatosis and improved liver function in the obese mice model.In addition, protein expression investigation revealed that alisol A had an active effect on AMPK/ACC/SREBP-1c pathway. As suggested by the molecular docking study, such bioactivity of alisol A may result from its selective binding to the catalytic region of AMPK.Therefore, we believe that Alisol A could serve as a promising agent for treatment of obesity and its related metabolic diseases.

Keywords

AMPK/ACC/SREBP-1c; alisol A; hepatic steatosis; metabolism dysfunction; obesity.

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