Hepatoprotective effect of the ethanol extract of Polygonum orientale on carbon tetrachloride-induced acute liver injury in mice

J Food Drug Anal. 2018 Jan;26(1):369-379. doi: 10.1016/j.jfda.2017.04.007. Epub 2017 May 31.

Abstract

Polygonum orientale L. (Polygonaceae) fruits have various medicinal uses, but their hepatoprotective effects have not yet been studied. This study investigated the hepatoprotective activity of the ethanolic extract of P. orientale (POE) fruits against carbon tetrachloride (CCl4)-induced acute liver injury (ALI). Mice were pretreated with POE (0.1, 0.5, and 1.0 g/kg) or silymarin (0.2 g/kg) for 5 consecutive days and administered a dose of 0.175% CCl4 (ip) on the 5th day to induce ALI. Blood and liver samples were collected to measure antioxidative activity and cytokines. The bioactive components of POE were identified through high-performance liquid chromatography (HPLC). Acute toxicity testing indicated that the LD50 of POE exceeded 10 g/kg in mice. Mice pretreated with POE (0.5, 1.0 g/kg) experienced a significant reduction in their serum aspartate aminotransferase (AST), serum alanine aminotransferase (ALT), and alkaline phosphatase (ALP) levels and reduction in the extent of liver lesions. POE reduced the malondialdehyde (MDA), nitric oxide (NO), tumor necrosis factor-α (TNF-α), interleukin-1β (IL-1β), and interleukin-6 (IL-6) levels, and increased the activity of superoxide dismutase (SOD), glutathione peroxidase (GPx), and glutathione reductase (GRd) in liver. HPLC revealed peaks at 11.28, 19.55, and 39.40 min for protocatechuic acid, taxifolin, and quercetin, respectively. In summary, the hepatoprotective effect of POE against CCl4-induced ALI was seemingly associated with its antioxidant and anti-proinflammatory activities.

Keywords: Carbon tetrachloride; Hepatoprotective activity; Polygonum orientale.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biomarkers
  • Biopsy
  • Carbon Tetrachloride / adverse effects*
  • Chemical and Drug Induced Liver Injury / drug therapy
  • Chemical and Drug Induced Liver Injury / metabolism*
  • Chemical and Drug Induced Liver Injury / pathology*
  • Chromatography, High Pressure Liquid
  • Cytokines / blood
  • Disease Models, Animal
  • Inflammation Mediators / blood
  • Liver / drug effects*
  • Liver / metabolism
  • Liver / pathology
  • Liver Function Tests
  • Mice
  • Oxidation-Reduction / drug effects
  • Plant Extracts / chemistry
  • Plant Extracts / pharmacology*
  • Polygonum / chemistry*
  • Protective Agents / chemistry
  • Protective Agents / pharmacology*
  • Reactive Oxygen Species / metabolism
  • Toxicity Tests, Acute

Substances

  • Biomarkers
  • Cytokines
  • Inflammation Mediators
  • Plant Extracts
  • Protective Agents
  • Reactive Oxygen Species
  • Carbon Tetrachloride

Grants and funding

This study was supported by the Ministry of Health and Welfare program (MOHW104-CMAP-M-114-000423), Taiwan, R.O.C.