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Weingand, K., Brown, G., Hall, R., Davies, D., Gossett, K., Neptun, D., Waner, T., Matsuzama, T., Salemink, P., Froelke, W., Provost, J.P., Negro, G., Batchelor, J., Nomura, M., Groetsch, H., Boink, A., Woodman, D., York, M. and Melloni, E. (1996) Harmonization of Animal Clinical Pathology Testing in Toxicity and Safety Studies. Fundamental and Applied Toxicology, 29, 198-201.
https://doi.org/10.1093/toxsci/29.2.198

has been cited by the following article:

• TITLE: Acute and Sub-Chronic Toxicity Evaluation of the Crude Methanolic Bark Extract of Bridelia micrantha (Hochst.) Baill. (Phyllanthaceae) and Its Fraction

  AUTHORS: Colette Elysée Aboudi Etono, Landry Lienou Lienou, Fabrice Fabien Dongho Dongmo, Aristide Laurel Mokale Kognou, Raphael Tchientcheu, Rebecca Madeleine Ebelle Etame, Rosalie Anne Ngono Ngane

  KEYWORDS: Bridelia micrantha, Acute Toxicity, Sub-Chronic Toxicity, Biochemical Parameters, Hematological Parameters

  JOURNAL NAME: Journal of Biosciences and Medicines, Vol.11 No.10, October 12, 2023

  ABSTRACT: Bridelia micrantha, commonly known as coastal golden leaf, is a member of the family Phyllanthaceae. In preliminary studies nine fractions, named F1 - F9, were obtained by fractionating the crude methanol extract of the stem bark of Bridelia micrantha using column chromatographic techniques. The fraction F6 was the most active when tested for antibacterial activity. Thus, toxicity of this fraction was investigated for further use. The present study evaluated the acute and sub-chronic toxicity of the crude methanolic bark extract of Bridelia micrantha and its fraction. The acute toxicity was carried out according to the experimental protocol of Organization for Economic Co-operation and Development (OECD). The plant extract or the fraction F6 was administered orally to female mice at a single dose of 2000 mg/kg and the animals were observed for any behavioral changes or mortality for 14 days. In the sub-chronic toxicity study, the extract and fraction were administered orally at 200, 400 and 800 mg/kg bw/day for 28 days to healthy Wistar rats. The general behavior and body weight of the rats were recorded daily. At the end of the experimental period, hematological and biochemical analyses, changes in vital organ weight (liver, lung, heart, spleen and kidney), and histopathological examination of the liver and kidney were performed. No mortality or adverse effects were noted at the 2000 mg/kg dose during the oral acute toxicity test. In the sub-chronic study, the crude methanolic bark extract of Bridelia micrantha and the fraction F6 induced no mortality or treatment-related adverse effects on body weight, general behavior, relative organ weights, hematological and biochemical parameters. Histopathological examination of the liver and kidney showed normal architecture suggesting no morphological alterations. In conclusion, the oral administration of the crude methanolic bark extract of Bridelia micrantha and the fraction F6 for 28 days at a dosage of up to 800 mg/kg did not induce toxicological damage in rats. From acute toxicity study, the median lethal dose (LD50) of the crude methanolic bark extract of Bridelia micrantha and the fraction F6 was estimated to be more than 2000 mg/kg.