Antioxidant and hepatoprotective activity of Piper retrofractum against Paracetamol-induced hepatotoxicity in Sprague-Dawley rat

Nat Prod Res. 2020 Nov;34(22):3219-3225. doi: 10.1080/14786419.2018.1550768. Epub 2019 Jan 19.

Abstract

The ethanol extracts of Piper retrofractum were investigated for antioxidant and hepatoprotective activity. Hepatoprotective activity against paracetamol-induced acute hepatotoxicity was estimated in Sprague-Dawley rat. In DPPH free radical assay the root and stem extracts showed IC50 values at 133 and 91 µg/mL, respectively, while ascorbic acid at 14 µg/mL. Extracts also exhibited hydroxyl radical scavenging activity and reducing power. HPLC-DAD analysis indicated the presence of some polyphenolic compounds. Treatment of extracts significantly reduced the elevated serum levels of GPT (P < 0.01), GOT (P < 0.01) and bilirubin (P < 0.001). Both extracts restored the reduced level of total proteins and albumin. A significant increase in HDL-c but decrease in LDL-c level was observed compared to induced control. In histopathological study of liver sections, both extracts showed minimal to mild multifocal and diffuse granular degeneration and mild to moderate lobular disarray compared to control group. Results suggest that both extracts can prevent paracetamol induced hepatotoxicity.

Keywords: HPLC-DAD; Hepatic markers; Sprague-Dawley strain rat; liver histopathology; serum lipid profile; total proteins.

MeSH terms

  • Acetaminophen / adverse effects*
  • Animals
  • Antioxidants / pharmacology*
  • Chemical and Drug Induced Liver Injury / drug therapy*
  • Chemical and Drug Induced Liver Injury / pathology
  • Cholesterol, HDL / blood
  • Liver / drug effects
  • Liver / metabolism
  • Male
  • Piper / chemistry*
  • Plant Extracts / chemistry
  • Plant Extracts / pharmacology*
  • Polyphenols / analysis
  • Protective Agents / pharmacology*
  • Rats, Sprague-Dawley

Substances

  • Antioxidants
  • Cholesterol, HDL
  • Plant Extracts
  • Polyphenols
  • Protective Agents
  • Acetaminophen