Protective effects of protopanaxatriol on acute liver injury induced by concanavalin A

Naunyn Schmiedebergs Arch Pharmacol. 2019 Jan;392(1):81-87. doi: 10.1007/s00210-018-1567-4. Epub 2018 Sep 30.

Abstract

The purpose of this study was to explore the protective effect of protopanaxatriol (PPT) on acute liver injury induced by concanavalin A (ConA). In this study, mice were randomly separated into four groups. The first group received PBS (i.v.). The second group was given PPT (50 mg/kg body weight, i.p.) for 3 days before PBS (i.v.) injection. The third group received ConA (15 mg/kg body weight, i.v.). The fourth group was administered PPT (50 mg/kg body weight, i.p.) for 3 days before ConA (i.v.) injection. The serum levels of ALT and AST were detected after 20 h of ConA injection. The pathological changes of liver were observed by H/E staining. The expression of inflammatory factors was measured by ELISA and qRTPCR, and the changes of the signaling pathway were detected by western blot. Histopathological changes and blood transaminase elevation indicated significant liver injury after ConA injection. However, PPT pretreatment obviously reversed these changes. The ELISA and qRT-PCR results indicated that PPT preconditioning significantly inhibited the production of inflammatory factors. In addition, this inhibitory effect of PPT was mainly mediated by regulation of the nuclear factor-κB (NF-κB) signaling pathway. The active ingredient of ginseng, PPT, exerts an obvious protective effect on acute liver injury caused by ConA through inhibiting the inflammatory response.

Keywords: ConA; Liver injury; NF-κB; Protopanaxitriol.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Chemical and Drug Induced Liver Injury / drug therapy*
  • Chemical and Drug Induced Liver Injury / pathology
  • Concanavalin A
  • Liver / drug effects
  • Liver / pathology
  • Male
  • Mice, Inbred C57BL
  • Protective Agents / therapeutic use*
  • Sapogenins / therapeutic use*

Substances

  • Protective Agents
  • Sapogenins
  • Concanavalin A
  • protopanaxatriol