Volume 16, Issue 3 pp. 244-247
Research Article

Toxicity of chloroform extract of Prunus africana stem bark in rats: gross and histological lesions

P. K. Gathumbi

Corresponding Author

P. K. Gathumbi

Department of Veterinary Pathology and Microbiology, University of Nairobi, PO Box 29053, Nairobi, Kenya

Department of Veterinary, Pathology and Microbiology, University of Nairobi, PO Box 29053, Nairobi, KenyaSearch for more papers by this author
J. W. Mwangi

J. W. Mwangi

Department of Pharmacology and Pharmacognosy, University of Nairobi, PO Box 30197, Nairobi, Kenya

Search for more papers by this author
G. M. Mugera

G. M. Mugera

Department of Veterinary Pathology and Microbiology, University of Nairobi, PO Box 29053, Nairobi, Kenya

Search for more papers by this author
S. M. Njiro

S. M. Njiro

Department of Veterinary Pathology and Microbiology, University of Nairobi, PO Box 29053, Nairobi, Kenya

Search for more papers by this author
First published: 15 May 2002
Citations: 15

Abstract

Chloroform extract of Prunus africana (Hook f. (Rosaceae) did not cause clinical signs or pathology in rats at daily oral doses of up to 1000 mg/kg for 8 weeks. The extract caused marked clinical signs, organ damage and a 50% mortality rate at a dose of 3.3 g/kg for 6 days. The main lesions observed at this dose were marked centrilobular hepatocellular degeneration and necrosis, diffuse nephrosis, myocardial degeneration, lymphocytic necrosis and neuronal degeneration.

The morphological damage in these tissues caused a corresponding rise in blood biochemical parameters namely, aspartate aminotransferase, alanine aminotransferase, alkaline phosphatase, lactate dehydrogenase, creatine kinase and blood urea nitrogen. The target organs of toxicity of this extract are the liver, kidney and heart. Overt toxicity occurred only after the administration of multiple doses of 3.3 g/kg body weight. These findings confirm the suitability of this extract for therapeutic use, since the doses used in the therapy of prostate gland are much lower than those used in this study and would therefore not be expected to cause pathological changes. Copyright © 2002 John Wiley & Sons, Ltd.

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.