Pioglitazone prevents early-phase hepatic fibrogenesis caused by carbon tetrachloride

Biochem Biophys Res Commun. 2002 Feb 15;291(1):55-61. doi: 10.1006/bbrc.2002.6385.

Abstract

Here we investigated the effect of pioglitazone, a peroxisome proliferator-activated receptor (PPAR)-gamma ligand, on early-phase hepatic fibrogenesis in vivo caused by acute carbon tetrachloride (CCl(4)) administration in the rat. Pioglitazone (1 mg/kg BW) prevented pericentral fibrosis and induction of alpha-smooth muscle actin (SMA) 72 h after CCl(4) administration (1 ml/kg BW). CCl(4) induction of alpha1(I)procollagen mRNA in the liver was blunted by pioglitazone to the levels almost 2/3 of CCl(4) alone. Pioglitazone also prevented CCl(4)-induced hepatic inflammation and necrosis, as well as increases in serum tumor necrosis factor-alpha levels. Further, pioglitazone inhibited the induction of alphaSMA and type I collagen in primary cultured hepatic stellate cells in a dose-dependent manner. In conclusion, pioglitazone inhibits both hepatic inflammation and activation of hepatic stellate cells, thereby ameliorating early-phase fibrogenesis in the liver following acute CCl(4).

MeSH terms

  • Actins / genetics
  • Actins / metabolism
  • Animals
  • Carbon Tetrachloride*
  • Cells, Cultured
  • Collagen Type I / genetics
  • Collagen Type I / metabolism
  • Dose-Response Relationship, Drug
  • Female
  • Gene Expression Regulation / drug effects
  • Hypoglycemic Agents / pharmacology*
  • Inflammation / pathology
  • Inflammation / prevention & control
  • Liver / drug effects
  • Liver / metabolism
  • Liver / pathology
  • Liver Cirrhosis / chemically induced*
  • Liver Cirrhosis / pathology
  • Liver Cirrhosis / prevention & control*
  • Necrosis
  • Pioglitazone
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Wistar
  • Receptors, Cytoplasmic and Nuclear / metabolism
  • Thiazoles / pharmacology*
  • Thiazolidinediones*
  • Transcription Factors / metabolism

Substances

  • Actins
  • Collagen Type I
  • Hypoglycemic Agents
  • RNA, Messenger
  • Receptors, Cytoplasmic and Nuclear
  • Thiazoles
  • Thiazolidinediones
  • Transcription Factors
  • Carbon Tetrachloride
  • Pioglitazone