Curcumin regulates endogenous and exogenous metabolism via Nrf2-FXR-LXR pathway in NAFLD mice

Biomed Pharmacother. 2018 Sep:105:274-281. doi: 10.1016/j.biopha.2018.05.135. Epub 2018 May 31.

Abstract

Background: Curcumin is a natural polyphenol with beneficial effects on NAFLD patients and NAFLD is accompanied by metabolism decompensation.

Methods: This study was focused on the effect of curcumin on the relationship between endogenous bile acids metabolism pathway and exogenous xenobiotics metabolism pathway in C57BL/6 mice of non-alcoholic fatty liver disease induced by high-fat and high-fructose diet (HFHFr) and in cultured mice hepatocytes.

Results: Our results showed curcumin treatment apparently attenuated the hepatic steatosis and reversed the abnormalities of serum biochemical parameters in HFHFr-fed mice. Curcumin effectively reversed the expression of CYP3A and CYP7A in fatty liver status to restore metabolism capability. In the meantime, lipid synthesis has been controlled by curcumin, evidenced by the expression of CD36, SREBP-1c and FAS. Further, FXR, SHP and Nrf2 expressions were remarkably dropped in HFHFr-fed mice and LXRα expression was significantly enhanced, while curcumin treatment was quite effective to restore this pathway. In addition, LXRα antagonist GGPP pretreatment weakened the curcumin effects on CYP3A, CYP7A and SREBP-1c.

Conclusions: These findings indicate that the Nrf2/FXR/LXRα pathway might synergistically regulate both endogenous and exogenous metabolism in NAFLD mice and LXRα may be a novel therapeutic target of curcumin for the prevention and treatment of NAFLD.

Keywords: CYP3A; CYP7A; Curcumin; Endogenous metabolism; Exogenous metabolism; Metabolic regulation.

MeSH terms

  • Animals
  • Curcumin / pharmacology*
  • Cytochrome P-450 Enzyme System / metabolism
  • Diet, High-Fat
  • Fructose
  • Hepatocytes / drug effects
  • Hepatocytes / metabolism
  • Hepatocytes / pathology
  • Lipids / biosynthesis
  • Liver / drug effects
  • Liver / enzymology
  • Liver / pathology
  • Liver X Receptors / metabolism*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • NF-E2-Related Factor 2 / metabolism*
  • Non-alcoholic Fatty Liver Disease / metabolism*
  • Non-alcoholic Fatty Liver Disease / pathology
  • Polyisoprenyl Phosphates / pharmacology
  • Protective Agents / pharmacology
  • Protective Agents / therapeutic use
  • Receptors, Cytoplasmic and Nuclear / metabolism*
  • Signal Transduction*
  • Sterol Regulatory Element Binding Protein 1 / metabolism

Substances

  • Lipids
  • Liver X Receptors
  • NF-E2-Related Factor 2
  • Polyisoprenyl Phosphates
  • Protective Agents
  • Receptors, Cytoplasmic and Nuclear
  • Sterol Regulatory Element Binding Protein 1
  • farnesoid X-activated receptor
  • Fructose
  • Cytochrome P-450 Enzyme System
  • Curcumin
  • geranylgeranyl pyrophosphate