In Vitro and In Vivo Toxicity Studies on Cymbopogon giganteus Chiov. Leaves Essential Oil from Benin

Author:

Toukourou Habib12ORCID,Uwambayinema Francine3,Yakoub Yousof3,Mertens Birgit4,Laleye Anatole5,Lison Dominique3,Quetin-Leclercq Joelle2,Gbaguidi Fernand1

Affiliation:

1. Laboratoire de Chimie Pharmaceutique Organique, Ecole de Pharmacie, Faculté des Sciences de la Santé, Université d’Abomey-Calavi, Campus du champ de Foire, 01BP 188 Cotonou, Benin

2. Pharmacognosy Research Group, Louvain Drug Research Institute, Université Catholique de Louvain, B1 7203 Av. E. Mounier 72, B-1200 Brussels, Belgium

3. Louvain Centre for Toxicology and Applied Pharmacology, Institut de Recherche Expérimentale et Clinique, Université catholique de Louvain, B1.57.06 Av. Hippocrate 57, B-1200 Brussels, Belgium

4. Scientific Direction of Chemical and Physical Health Risks, Sciensano, Juliette Wytsmanstraat 14, 1050 Brussels, Belgium

5. Unité de Biologie Humaine, Laboratoire de Cytogénétique et de Biologie Moléculaire, Faculté des Sciences de Santé, Université d’Abomey-Calavi, Campus du champ de Foire, 01BP 188 Cotonou, Benin

Abstract

Cymbopogon giganteus Chiov. (Poaceae) is a medicinal plant used to treat various diseases in traditional medicine in several African countries. The present study aims to evaluate the oral and inhalation toxicity as well as the mutagenic effects of the essential oil of Cymbopogon giganteus leaves (EOCG) from a sample collected in Benin. Mutagenic potential was assessed by the Ames test using Salmonella typhimurium strains TA98 and TA100. Oral acute toxicity was carried out by administration of a single dose of 2000 mg/kg b.w. to Wistar rats while oral subacute toxicity was assessed by daily administration of 50 and 500 mg/kg of EOCG for 28 days. Finally, inhalation toxicity was assessed by administration of a single dose of 0.125%, 0.5%, 2% or 5% v/v of EOCG emulsions in 0.05% v/v lecithin solution in sterile water for the first experiment, and in a second one by administration of single dose of 0.125% or 0.5% v/v. A broncho-alveolar lavage was performed after 3 h or 24 h, respectively. The results show that EOCG is not mutagenic on Salmonella typhimurium strains at the highest concentration tested (200 μg/plate). In the acute oral toxicity study, EOCG induce neither mortality nor toxicity, showing that the LD50 is greater than 2000 mg/kg. The subacute oral toxicity study at both doses did not show any significant difference in body weight, relative organ weight, hematological and/or biochemical parameters or histopathology as compared to the control group. EOCG induced mortality and inflammation in lungs 3 h after administration of a single dose of 5% or 2% v/v. Single doses of 0.125% or 0.5% v/v did not induce inflammation, cell recruitment nor cytotoxicity in lungs 3 h or 24 h after administration, suggesting safety at these concentrations. This first report on the in vivo toxicity will be useful to guide safe uses of EOCG.

Funder

ARES-CCD

Publisher

Hindawi Limited

Subject

Pharmacology,Toxicology

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