Acute and Subchronic Toxicity Studies of Aqueous Extract of Desmodium adscendens (Sw) DC

J Evid Based Complementary Altern Med. 2017 Oct;22(4):753-759. doi: 10.1177/2156587217736587. Epub 2017 Nov 7.

Abstract

Extracts of Desmodium adscendens (Sw) DC are used for the treatment of various diseases but limited toxicological evaluations have been done on the medicinal plant. This study investigates toxicity effects of the leave extract of D adscendens, and the possibility of drug-drug interaction of the plant extract when co-administered with other drugs. Oral administrations of leaf extract of D adscendens to white Wistar rats in an acute toxicity studies allowed the estimation of an LD50 (median lethal dose) value of 1122 mg/kg body weight. In a subchronic toxicity studies, the plant extract caused a decrease in zoxazolamine paralysis time and prevented thiopentone from causing sleep in test animals compared to controls. Overall, the results are consistent with the plant extract being safe at the doses administered in humans. However, the induction of the CYP enzymes is an indication of a possible drug interaction when the plant extract is co-administered with other drugs.

Keywords: Desmodium adscendens (Sw) DC; acute toxicity; cytochrome P450 xenobiotic-metabolizing enzymes; drug metabolism; subchronic toxicity.

MeSH terms

  • Animals
  • Anticonvulsants / pharmacology
  • Dose-Response Relationship, Drug
  • Ethnopharmacology / methods
  • Fabaceae*
  • Ghana
  • Herb-Drug Interactions
  • Humans
  • Lethal Dose 50
  • Male
  • Muscle Relaxants, Central / pharmacology
  • Plant Extracts* / pharmacology
  • Plant Extracts* / toxicity
  • Plants, Medicinal / toxicity
  • Rats
  • Rats, Wistar
  • Thiopental / pharmacology*
  • Zoxazolamine / pharmacology*

Substances

  • Anticonvulsants
  • Muscle Relaxants, Central
  • Plant Extracts
  • Zoxazolamine
  • Thiopental