Paeoniflorin alleviates liver fibrosis by inhibiting HIF-1α through mTOR-dependent pathway

Fitoterapia. 2014 Dec:99:318-27. doi: 10.1016/j.fitote.2014.10.009. Epub 2014 Oct 16.

Abstract

HIF-1α/mTOR signaling pathway is considered to play a crucial role in genesis and progress of tissue fibrosis. The elevation of HIF-1α and mTOR is relevant to CCl4 induced liver fibrotic rats. Paeoniflorin has been consistently shown to exhibit multiple pharmacological effects in liver disease. However, so far, no research demonstrates the relationship between paeoniflorin and HIF-1α/mTOR fibrogenesis pathway in liver fibrosis. In this study, the liver fibrosis was performed by CCl4 rats and HSC-T6 cell line. The data demonstrated that paeoniflorin treatment could attenuate liver fibrosis and inhibit the activation of HSC. Moreover, paeoniflorin significantly enhanced hepatic function by decreasing serum level of ALT, AST and ALP, and increasing level of ALB, TP. Meanwhile, ECM degradation was modulated by paeoniflorin treated rats with a remarkable reduce of α-SMA and collagen III mRNA expression. Moreover, the alleviation effect of liver fibrosis was relevant to inhibiting HIF-1α and phosphor-mTOR. Our data indicate that paeoniflorin alleviates liver fibrosis by inhibiting HIF-1α expression partly through mTOR pathway and paeoniflorin may be a potential therapeutic agent for liver fibrosis.

Keywords: Carbon tetrachloride; Hypoxia inducible factor; Liver fibrosis; Paeoniflorin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line
  • Glucosides / pharmacology*
  • Hepatic Stellate Cells / drug effects
  • Hypoxia-Inducible Factor 1, alpha Subunit / metabolism*
  • Liver / drug effects
  • Liver / pathology
  • Liver Cirrhosis / drug therapy*
  • Male
  • Monoterpenes / pharmacology*
  • Rats, Sprague-Dawley
  • Signal Transduction / drug effects
  • TOR Serine-Threonine Kinases / metabolism*

Substances

  • Glucosides
  • Hif1a protein, rat
  • Hypoxia-Inducible Factor 1, alpha Subunit
  • Monoterpenes
  • peoniflorin
  • mTOR protein, rat
  • TOR Serine-Threonine Kinases