Hepatoprotective and anti-oxidant activities of Glossogyne tenuifolia against acetaminophen-induced hepatotoxicity in mice

Am J Chin Med. 2014;42(6):1385-98. doi: 10.1142/S0192415X14500876.

Abstract

The present study investigated the anti-oxidative and hepatoprotective effects of Glossogyne tenuifolia (GT) Cassini, against acetaminophen-induced acute liver injury in BALB/c mice. The extracts of GT by various solvents (hot water, 50% ethanol and 95% ethanol) were compared for their 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical scavenging activity, reducing power, total phenolic content, and total anti-oxidant capacity. The results showed that hot water (HW) extracts of GT contained high levels of phenolics and exerted an excellent anti-oxidative capacity; thus, these were used in the animal experiment. The male BALB/c mice were randomly divided into control group, acetaminophen (APAP) group, positive control group and two GT groups at low (GT-L) and high (GT-H) dosages. The results showed that mice treated with GT had significantly decreased serum levels of alanine aminotransferase (ALT) and aspartate aminotransferase (AST). GT-H increased glutathione levels and the ratios of reduced glutathione and oxidized glutathione (GSH/GSSG) in the liver, and inhibited serum and lipid peroxidation. This experiment was the first to determine phenolic compounds, chlorogenic acid and luteolin-7-glucoside in HW extract of GT. In conclusion, HW extract of GT may have potential anti-oxidant capacity and show hepatoprotective capacities in APAP-induced liver damaged mice.

Keywords: Acetaminophen; Anti-oxidative; Glossogyne tenuifolia; Hepatoprotective; Mice.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetaminophen / poisoning*
  • Alanine Transaminase / blood
  • Analgesics, Non-Narcotic / poisoning*
  • Animals
  • Antioxidants*
  • Antipyretics / poisoning*
  • Aspartate Aminotransferases / blood
  • Asteraceae / chemistry*
  • Biomarkers / blood
  • Chemical and Drug Induced Liver Injury / diagnosis
  • Chemical and Drug Induced Liver Injury / drug therapy*
  • Dose-Response Relationship, Drug
  • Drug Overdose
  • Glutathione / metabolism
  • Glutathione Disulfide / metabolism
  • Lipid Peroxidation / drug effects
  • Liver / metabolism
  • Male
  • Mice, Inbred BALB C
  • Phytotherapy*
  • Plant Extracts / chemistry
  • Plant Extracts / pharmacology*
  • Plant Extracts / therapeutic use*

Substances

  • Analgesics, Non-Narcotic
  • Antioxidants
  • Antipyretics
  • Biomarkers
  • Plant Extracts
  • Acetaminophen
  • Aspartate Aminotransferases
  • Alanine Transaminase
  • Glutathione
  • Glutathione Disulfide