Affiliations 

  • 1 Department of Pharmacology and Therapeutics, Ahmadu Bello University, Zaria, Nigeria; School of Pharmacy Technician, Aminu Dabo College of Health Sciences and Technology, Kano State, Nigeria. Electronic address: mubarakhussainiahmad@gmail.com
  • 2 Department of Pharmacology and Therapeutics, Ahmadu Bello University, Zaria, Nigeria. Electronic address: zumar003@yahoo.com
  • 3 Department of Pharmacology and Therapeutics, Ahmadu Bello University, Zaria, Nigeria. Electronic address: sherifatanafi@yahoo.com
  • 4 Department of Pharmacology and Therapeutics, Ahmadu Bello University, Zaria, Nigeria. Electronic address: elzaky02@gmail.com
  • 5 Department of Clinical Pharmacy and Pharmacy Practice, Ahmadu Bello University, Zaria, Nigeria; School of Pharmaceutical Sciences, Universiti Sains, 11800, Pulau Penang, Malaysia. Electronic address: macreener88@gmail.com
  • 6 Department of Pharmacology and Therapeutics, Ahmadu Bello University, Zaria, Nigeria. Electronic address: danrakarabiu@gmail.com
J Ethnopharmacol, 2021 Apr 06;269:113750.
PMID: 33359856 DOI: 10.1016/j.jep.2020.113750

Abstract

ETHNOPHARMACOLOGICAL RELEVANCE: The plant Combretum hypopilinum Diels (Combretaceae) is used in traditional medicine for the treatment of diarrhoea and other diseases in Africa. Previously, the antidiarrhoeal activity of its methanol leaf extract was reported. However, the mechanism(s) responsible for this activity is yet to be evaluated.

AIM OF THE STUDY: This study aimed to elucidate the possible mechanism(s) of antidiarrhoeal activity of methanol leaf extract of Combretum hypopilinum (MECH) in mice.

MATERIALS AND METHODS: Phytochemical screening and acute toxicity study were conducted according to standard methods. Adult mice were orally (p.o) administered distilled water (10 ml/kg), MECH (1000 mg/kg) and loperamide (5 mg/kg). The probable mechanisms of antidiarrhoeal activity of MECH were investigated following pretreatment with naloxone (2 mg/kg, subcutaneously), prazosin (1 mg/kg, s.c), yohimbine (2 mg/kg, intraperitoneally), propranolol (1 mg/kg, i.p), pilocarpine (1 mg/kg, s.c) and isosorbide dinitrate (150 mg/kg, p.o) 30 min before administration of MECH (1000 mg/kg). The mice were then subjected to castor oil-induced intestinal motility test.

RESULTS: The oral median lethal dose (LD50) of MECH was found to be higher than 5000 mg/kg. There were significant (p 

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.