Shugan Xiaozhi Decoction Attenuates Nonalcoholic Steatohepatitis by Enhancing PPARα and L-FABP Expressions in High-Fat-Fed Rats.
Yu-Feng XingZhen ZhangWen-Jun FuDa-Qiao ZhouAilsa Chui-Ying YuenDaniel Kam-Wah MokChi-On ChanGuang-Dong TongPublished in: Evidence-based complementary and alternative medicine : eCAM (2016)
This study aimed to investigate the effects of Shugan Xiaozhi decoction (SX) on nonalcoholic steatohepatitis (NASH) induced by high-fat diet in rats. The rats were randomly divided into 6 groups, namely, control, model, fenofibrate, and three different dosage of SX (10, 20, and 40 g/kg/day, p.o.). After establishing the NASH model, at 8 weeks of the experiment, treatments were administrated intragastrically to the fenofibrate and SX groups. All rats were killed after 4 weeks of treatment. Compared with the model group, alanine aminotransferase (ALT), aspartate aminotransferase (AST), free fatty acid (FFA), total cholesterol (TC), triacylglycerol (TG), and low-density lipoprotein cholesterol (LDL) serum in the serum were significantly reduced in all SX treatment groups in a dose-dependent manner. Evidence showed that SX could protect the liver by upregulating the gene and protein expressions of peroxisome proliferator-activated receptor alpha (PPARα) and liver fatty acid binding protein (L-FABP) in a dose-dependent manner. Chemical constituents of SX were further analyzed by ultraperformance liquid chromatography coupled with electrospray ionization mass spectrometry (UPLC-ESI-MS) and 30 chemicals in the ethanolic extract were tentatively identified. To conclude, our results clearly indicated that SX could protect liver functions and relieve hepatic steatosis and inflammation.
Keyphrases
- binding protein
- mass spectrometry
- fatty acid
- high fat diet
- liquid chromatography
- insulin resistance
- oxidative stress
- ms ms
- adipose tissue
- high resolution
- multiple sclerosis
- simultaneous determination
- high performance liquid chromatography
- high resolution mass spectrometry
- skeletal muscle
- genome wide
- low density lipoprotein
- copy number
- tandem mass spectrometry
- gene expression
- combination therapy
- gas chromatography
- amino acid
- anti inflammatory
- solid phase extraction
- genome wide analysis