Paeoniflorin attenuates ANIT-induced cholestasis by inhibiting apoptosis in vivo via mitochondria-dependent pathway

Biomed Pharmacother. 2017 May:89:696-704. doi: 10.1016/j.biopha.2017.02.084. Epub 2017 Mar 6.

Abstract

Apoptosis induced by the bile acids in the liver is considered to play a pivotal role in the pathogenesis of cholestatic disease. Increasing evidence has demonstrated that Paeoniflorin (PF) exerts therapeutic effect on severe cholestatic liver diseases. However, whether PF could protect against alpha-naphthylisothiocyanate (ANIT)-induced cholestasis by inhibiting apoptosis remains unclear. In this study, we mainly investigated the effect and anti-apoptosis mechanism of PF on cholestasis. Experimental results indicated that PF pretreatment could attenuate liver damage and cholestasis by ANIT in rats, lift the biliary excretion in addition to decrease serum indices (ALT, AST, DBIL, TBIL, TBA, ALP and ϒ-GT) and conspicuous neutrophil infiltration and cell apoptosis in liver evidenced by TUNEL staining. Furthermore, the pro-apoptosis genes expression of Bax, Caspase-9 and Caspase-3 increased by ANIT were prominently reduced after PF treatment. The increase of anti-apoptosis gene and main regulator Bcl-2 in mitochondria by ANIT was largely reversed by PF pre-treatment. In summary, our study demonstrated that PF pre-treatment not only significantly attenuated ANIT-induced cholestasis and liver injury, but also largely reduced cell apoptosis in liver, thus may act as a potential therapeutic agent for cholestasis disease.

Keywords: ANIT; Apoptosis; Cholestasis; Mitochondria signaling pathway; Peaoniflorin.

MeSH terms

  • 1-Naphthylisothiocyanate / antagonists & inhibitors*
  • 1-Naphthylisothiocyanate / toxicity
  • Animals
  • Apoptosis / drug effects*
  • Apoptosis Regulatory Proteins / drug effects
  • Apoptosis Regulatory Proteins / genetics
  • Biomarkers / blood
  • Chemical and Drug Induced Liver Injury / pathology
  • Chemical and Drug Induced Liver Injury / prevention & control
  • Cholestasis / chemically induced
  • Cholestasis / prevention & control*
  • Cytokines / metabolism
  • Genes, bcl-2 / drug effects
  • Glucosides / pharmacology*
  • Liver / pathology
  • Mitochondria / drug effects*
  • Monoterpenes / pharmacology*
  • Neutrophil Infiltration / drug effects
  • Rats
  • Rats, Wistar
  • Signal Transduction / drug effects*

Substances

  • Apoptosis Regulatory Proteins
  • Biomarkers
  • Cytokines
  • Glucosides
  • Monoterpenes
  • peoniflorin
  • 1-Naphthylisothiocyanate