Qushi Huayu decoction attenuated hepatic lipid accumulation via JAK2/STAT3/CPT-1A-related fatty acid β-oxidation in mice with non-alcoholic steatohepatitis

Pharm Biol. 2022 Dec;60(1):2124-2133. doi: 10.1080/13880209.2022.2134898.

Abstract

Context: Qushi Huayu decoction (QHD) has been clinically used for treating non-alcoholic steatohepatits (NASH). However, little is known about the effect of QHD on fatty acid β-oxidation (FAO)-dependent lipid consumption.

Objective: To investigate the mechanism of QHD on FAO-related hepatic lipid accumulation.

Materials and methods: Male C57BL/6J mice were randomly divided into 5 groups (n = 8): normal diet and drinking water (CON), high-fat and high-carbohydrate diet (HFHC), QHD-L (2.875 g/kg), QHD-H (11.5 g/kg) and obeticholic acid (OCA) (10 mg/kg/day) groups. All mice freely consumed an appropriate diet for 18 weeks, and QHD was orally administered in the last 6 weeks. Measurements of general condition, hepatic histopathology, and JAK2/STAT3 signalling pathway were taken.

Results: QHD significantly improved NASH in mice, as reflected by improving serum glucolipid metabolism, decreasing enzymes activities, reducing hepatic triglyceride (HFHC: 70.07 ± 2.81 mg/g; QHD-H: 34.06 ± 5.74 mg/g) and ameliorating hepatic steatosis, inflammation in pathology. Further, both the mRNA and protein level of hepatic CPT-1A (p < 0.05), a rate-limiting enzyme of FAO, increased drastically following QHD treatment. Meanwhile, the content of hepatic ATP (p < 0.05) increased significantly after treatment with QHD. Further mechanistic results revealed that both the total protein and nuclear p-STAT3 in the liver were significantly down-regulated after QHD treatment. The protein level of hepatic p-JAK2 was significantly inhibited by QHD (p < 0.05 or p < 0.01).

Conclusions: QHD could attenuate lipid accumulation by increasing JAK2/STAT3/CPT-1A-related FAO, which provides a scientific basis for the clinical application of QHD in treating NASH.

Keywords: NASH; hepatic steatohepatitis; lipid metabolism; traditional Chinese medicine.

MeSH terms

  • Animals
  • Diet, High-Fat / adverse effects
  • Fatty Acids / pharmacology
  • Liver
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Non-alcoholic Fatty Liver Disease* / pathology
  • Triglycerides

Substances

  • qushi huayu
  • Triglycerides
  • Fatty Acids

Grants and funding

This work was supported by the National Natural Science Foundation of China (No. 82174040 to Q. F; No. 82174186 to YY.H; No. 81973456 to XT.T), the National Science & Technology Major Project “Key New Drug Creation and Manufacturing Program,” China (No. 2019ZX09201001-001-002 to Q.F), the Shanghai Science and Technology Development Funds (No. 18401933100 to Q.F), and the Innovative Projects of Shanghai University of Traditional Chinese Medicine (No. Y2021081 to QM. S).