Article

Bavachin protects against diet-induced hepatic steatosis and obesity in mice

Xiang Wei1,2, Li Lin1, Qian-qian Yuan1, Xiu-yun Wang1, Qing Zhang1, Xiao-min Zhang1, Ke-chao Tang1, Man-yu Guo1, Ting-yu Dong3, Wei Han4, Da-ke Huang5, Yin-liang Qi2, Mei Zhang6, Hua-bing Zhang1,7
1 Department of Biochemistry and Molecular Biology, Metabolic Disease Research Center, School of Basic Medicine, Anhui Medical University, Hefei 230032, China
2 Department of Hyperbaric Oxygen, The Second People’s Hospital of Hefei, Hefei Hospital Affiliated to Anhui Medical University, Hefei 230011, China
3 The Second Clinical Medical College of Anhui Medical University, Hefei 230032, China
4 Department of Gastroenterology, The First Affiliated Hospital of Anhui Medical University, Hefei 230022, China
5 Synthetic Laboratory of School of Basic Medicine Sciences, Anhui Medical University, Hefei 230032, China
6 Health Management Center, The First Affiliated Hospital of the University of Sciences and Technology of China (Anhui Provincial Hospital), Hefei 230001, China
7 The Affiliated Chuzhou Hospital of Anhui Medical University (The First People’s Hospital of Chuzhou), Chuzhou 239001, China
DOI: 10.1038/s41401-023-01056-z
Received: 8 September 2022
Accepted: 13 January 2023
Advance online: 31 January 2023

Abstract

Non-alcoholic fatty liver disease (NAFLD) is a major health concern worldwide, and the incidence of metabolic disorders associated with NAFLD is rapidly increasing because of the obesity epidemic. There are currently no approved drugs that prevent or treat NAFLD. Recent evidence shows that bavachin, a flavonoid isolated from the seeds and fruits of Psoralea corylifolia L., increases the transcriptional activity of PPARγ and insulin sensitivity during preadipocyte differentiation, but the effect of bavachin on glucose and lipid metabolism remains unclear. In the current study we investigated the effects of bavachin on obesity-associated NAFLD in vivo and in vitro. In mouse primary hepatocytes and Huh7 cells, treatment with bavachin (20 μM) significantly suppressed PA/OA or high glucose/high insulin-induced increases in the expression of fatty acid synthesis-related genes and the number and size of lipid droplets. Furthermore, bavachin treatment markedly elevated the phosphorylation levels of AKT and GSK-3β, improving the insulin signaling activity in the cells. In HFD-induced obese mice, administration of bavachin (30 mg/kg, i.p. every other day for 8 weeks) efficiently attenuated the increases in body weight, liver weight, blood glucose, and liver and serum triglyceride contents. Moreover, bavachin administration significantly alleviated hepatic inflammation and ameliorated HFD-induced glucose intolerance and insulin resistance. We demonstrated that bavachin protected against HFD-induced obesity by inducing fat thermogenesis and browning subcutaneous white adipose tissue (subWAT). We revealed that bavachin repressed the expression of lipid synthesis genes in the liver of obese mice, while promoting the expression of thermogenesis, browning, and mitochondrial respiration- related genes in subWAT and brown adipose tissue (BAT) in the mice. In conclusion, bavachin attenuates hepatic steatosis and obesity by repressing de novo lipogenesis, inducing fat thermogenesis and browning subWAT, suggesting that bavachin is a potential drug for NAFLD therapy.
Keywords: non-alcoholic fatty liver disease; obesity; bavachin; lipogenesis; insulin sensitivity; AKT; GSK-3β; thermogenesis; subcutaneous white adipose tissue; mouse primary hepatocytes

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