Modulatory Effect of Methanol Extract of Piper guineense in CCl₄-Induced Hepatotoxicity in Male Rats

Int J Environ Res Public Health. 2017 Aug 24;14(9):955. doi: 10.3390/ijerph14090955.

Abstract

This study seeks to investigate the possible protective role of the methanol extract of Piper guineense seeds against CCl₄-induced hepatotoxicity in an animal model. Hepatotoxicity was induced by administering oral doses of CCl₄ (1.2 g/kg bw) three times a week for three weeks. Group 1 (Control) and Group 2 (CCl₄) were left untreated; Piper guineense (PG; 400 mg/kg bw) was administered to Group 3 (T₁) by oral gavage for 14 days prior to the administration of CCl₄ and simultaneously with CCl₄; PG (400 mg/kg bw) was administered simultaneously with CCl₄ in Group 4 (T₂); and Livolin forte (20 mg/kg bw) was administered simultaneously with CCl₄ in Group 5 (T₃), the standard drug group. The administration of CCl₄ induces histopathological alteration in the liver, with concomitant increased activities of serum hepatic marker enzymes associated with increased levels of lipid peroxidation. Similarly, there was decrease in non-enzymatic (reduced glutathione) and enzymatic antioxidants (glutathione S-transferase), superoxide dismutase, and catalase. An elevation in serum triglyceride and total cholesterol levels was noticed along with decreased levels of serum total protein. Treatment with PG 400 mg/kg bw exhibited excellent modulatory activity with respect to the different parameters studied by reversing all the above-mentioned biochemical changes significantly in the experimental animals. These results suggest that PG offered protection comparable to that of Livolin forte with better efficacy when pre-treated with 400 mg/kg bw 14 days prior to CCl₄-exposure.

Keywords: Piper guineense; antioxidant enzymes; carbon tetrachloride; lipid peroxidation; liver toxicity.

MeSH terms

  • Administration, Oral
  • Animals
  • Carbon Tetrachloride / toxicity*
  • Liver / drug effects*
  • Male
  • Oxidative Stress / drug effects*
  • Piper / chemistry*
  • Plant Extracts / pharmacology*
  • Protective Agents / pharmacology*
  • Rats
  • Rats, Wistar

Substances

  • Plant Extracts
  • Protective Agents
  • Carbon Tetrachloride