Bile acids induced hepatic lipid accumulation in mice by inhibiting mRNA expression of patatin-like phospholipase domain containing 3 and microsomal triglyceride transfer protein

Nutr Res. 2021 Aug:92:12-20. doi: 10.1016/j.nutres.2021.05.006. Epub 2021 May 26.

Abstract

Preliminary studies have shown that a lithogenic diet (LG), which contains cholesterol and cholic acid, induces gallstones and hepatic lipid accumulation (HLA), and reduction of blood triglyceride in mice. We hypothesized that an LG induces HLA by diminishing hepatic triglyceride excretion; however, there is no clear understanding of the mechanism of LG-induced HLA. This study aimed to investigate transcript expression related to the synthesis, expenditure, and efflux of hepatic triglyceride, in mice fed an LG for 4 weeks. Results showed lower plasma concentrations of triglyceride in the LG group than in the control group, but no symptoms of hepatic injury were observed. Hepatic mRNA expressions of patatin-like phospholipase domain containing 3 (Pnpla3), microsomal triglyceride transfer protein (Mttp), and acyl-CoA oxidase 1 (Acox1) were also reduced in the LG group. Deoxycholic acid and lithocholic acid promoted intracellular lipid accumulation, reduced triglyceride concentration in media, and suppressed expression of PNPLA3 and MTTP in HepG2 human hepatoma cells. These findings suggest that deoxycholic acid and lithocholic acid promote HLA by inhibiting the expression of PNPLA3, ACOX1, and MTTP that are involved in lipid metabolism.

Keywords: Bile acids; Cytochrome P450 family 2 subfamily E peptide 1; Hepatic lipid accumulation; Mice; Microsomal triglyceride transfer protein; Patatin-like phospholipase domain containing 3.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acyl-CoA Oxidase / metabolism
  • Animals
  • Bile Acids and Salts / adverse effects*
  • Bile Acids and Salts / metabolism
  • Carrier Proteins / genetics
  • Carrier Proteins / metabolism*
  • Cholesterol / metabolism
  • Diet / adverse effects
  • Hep G2 Cells
  • Humans
  • Lipase / genetics
  • Lipase / metabolism*
  • Lipid Metabolism / drug effects*
  • Lipid Metabolism / genetics
  • Liver / drug effects*
  • Liver / metabolism
  • Male
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism*
  • Mice
  • Mice, Inbred ICR
  • Non-alcoholic Fatty Liver Disease / etiology*
  • Non-alcoholic Fatty Liver Disease / genetics
  • Non-alcoholic Fatty Liver Disease / metabolism
  • Phospholipases
  • Phospholipases A2, Calcium-Independent / genetics
  • Phospholipases A2, Calcium-Independent / metabolism*
  • RNA, Messenger / metabolism
  • Triglycerides / metabolism

Substances

  • Bile Acids and Salts
  • Carrier Proteins
  • Membrane Proteins
  • RNA, Messenger
  • Triglycerides
  • microsomal triglyceride transfer protein
  • Cholesterol
  • ACOX1 protein, mouse
  • Acyl-CoA Oxidase
  • Phospholipases
  • Lipase
  • PNPLA3 protein, mouse
  • adiponutrin, human
  • Phospholipases A2, Calcium-Independent