2015International Journal of Pharmacology and ToxicologyOpen access

Subchronic toxicity of aqueous extract of Alstonia boonei de wild. (apocynaceae) stem bark in normal rats

Barnabé Lucien Nkono Ya Nkono, Sélestin Dongmo Sokeng, Paul Désiré Djomeni Dzeufiet, Frida Longo, Pièrre Kamtchouing

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Abstract

Methodology: Wistar rats were randomly assigned into eight groups of five animals each: four male groups and four female groups. Each sex group had a control group receiving distilled water and three test groups receiving 200, 500 and 1000mg/kg respectively. Animal’s body weights were recorded on the first day and once a week for the four experiment weeks. The hematological analysis included total WBC count, total RBC count, Hb, %HCT, MCV, MCH and MCHC. Biochemical/serum profile studies include TG, TC, ALT, AST, urea and TP. Tissue specimens of the liver, kidney and lung were subjected to histological examination using standard hematoxylin-eosin staining.Results: In male rats, aqueous extract showed significant decreases in relative weight of liver with extreme significance P<0.001 at a dose of 200mg/kg (vs. control group), P<0.001 of lung at all the doses, P<0.05 (200 and 500mg/kg) and P<0.01 (1000mg/kg) in heart weight. In relative kidney weight, only the dose of 1000mg/kg showed a significant increase vs. normal control male rats. Unlike male rats, only relative kidney weight in female rats was significantly different from the control group in a dose-dependent manner. The aqueous extract treated male groups showed significant increases P<0.001 (1000mg/kg) of total WBC count and MCHC, significant decreases of %HTC (dose response manner), P<0.05 total RBC count (at doses of 500 and 1000mg/kg) and Hb P<0.01 (500mg/kg) vs. normal male rats. In female rats, the haematological study showed significant increase P<0.01 of total WBC count (at the doses of 500 and 1000mg/kg), significant decreases P<0.05 and P<0.01 of total RBC respectively at the doses of 200 and 1000mg/kg, significant decrease of Hb with extreme significance P<0.001 at the dose 1000mg/kg, %HTC also decrease dose response manner vs. control female rats. Biochemical study showed in male rats significant decreases in level of TG P<0.001 (at the doses of 200 and 500mg/kg) and urea, although it showed any dose-dependent effect vs. control male rats. AST also decreases (P<0.05) in male rats at the dose of 200mg/kg but significantly increase P<0.001 at the dose of 500mg/kg. In the female rats, biochemical study revealed significant increases in level of TG P<0.001 and urea P<0.01 at the dose of 200mg/kg and significant decreases in level of TG P<0.01, AST P<0.05 and urea P<0.05 at the dose of 500mg/kg (vs. control female rats). Microscopically, there were mild hepatic and renal tissue injuries supporting the hematological analysis.Conclusion: The results indicated that aqueous extract of Alstonia boonei De Wild is toxic in high doses.

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Methodology: Wistar rats were randomly assigned into eight groups of five animals each: four male groups and four female groups. Each sex group had a control group receiving distilled water and three test groups receiving 200, 500 and 1000mg/kg respectively. Animal’s body weights were recorded on the first day and once a week for the four experiment weeks. The hematological analysis included total WBC count, total RBC count, Hb, %HCT, MCV, MCH and MCHC. Biochemical/serum profile studies include TG, TC, ALT, AST, urea and TP. Tissue specimens of the liver, kidney and lung were subjected to histological examination using standard hematoxylin-eosin staining.Results: In male rats, aqueous extract showed significant decreases in relative weight of liver with extreme significance P<0.001 at a dose of 200mg/kg (vs. control group), P<0.001 of lung at all the doses, P<0.05 (200 and 500mg/kg) and P<0.01 (1000mg/kg) in heart weight. In relative kidney weight, only the dose of 1000mg/kg showed a significant increase vs. normal control male rats. Unlike male rats, only relative kidney weight in female rats was significantly different from the control group in a dose-dependent manner. The aqueous extract treated male groups showed significant increases P<0.001 (1000mg/kg) of total WBC count and MCHC, significant decreases of %HTC (dose response manner), P<0.05 total RBC count (at doses of 500 and 1000mg/kg) and Hb P<0.01 (500mg/kg) vs. normal male rats. In female rats, the haematological study showed significant increase P<0.01 of total WBC count (at the doses of 500 and 1000mg/kg), significant decreases P<0.05 and P<0.01 of total RBC respectively at the doses of 200 and 1000mg/kg, significant decrease of Hb with extreme significance P<0.001 at the dose 1000mg/kg, %HTC also decrease dose response manner vs. control female rats. Biochemical study showed in male rats significant decreases in level of TG P<0.001 (at the doses of 200 and 500mg/kg) and urea, although it showed any dose-dependent effect vs. control male rats. AST also decreases (P<0.05) in male rats at the dose of 200mg/kg but significantly increase P<0.001 at the dose of 500mg/kg. In the female rats, biochemical study revealed significant increases in level of TG P<0.001 and urea P<0.01 at the dose of 200mg/kg and significant decreases in level of TG P<0.01, AST P<0.05 and urea P<0.05 at the dose of 500mg/kg (vs. control female rats). Microscopically, there were mild hepatic and renal tissue injuries supporting the hematological analysis.Conclusion: The results indicated that aqueous extract of Alstonia boonei De Wild is toxic in high doses.

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Available abstract

Methodology: Wistar rats were randomly assigned into eight groups of five animals each: four male groups and four female groups. Each sex group had a control group receiving distilled water and three test groups receiving 200, 500 and 1000mg/kg respectively. Animal’s body weights were recorded on the first day and once a week for the four experiment weeks. The hematological analysis included total WBC count, total RBC count, Hb, %HCT, MCV, MCH and MCHC. Biochemical/serum profile studies include TG, TC, ALT, AST, urea and TP. Tissue specimens of the liver, kidney and lung were subjected to histological examination using standard hematoxylin-eosin staining.Results: In male rats, aqueous extract showed significant decreases in relative weight of liver with extreme significance P<0.001 at a dose of 200mg/kg (vs. control group), P<0.001 of lung at all the doses, P<0.05 (200 and 500mg/kg) and P<0.01 (1000mg/kg) in heart weight. In relative kidney weight, only the dose of 1000mg/kg showed a significant increase vs. normal control male rats. Unlike male rats, only relative kidney weight in female rats was significantly different from the control group in a dose-dependent manner. The aqueous extract treated male groups showed significant increases P<0.001 (1000mg/kg) of total WBC count and MCHC, significant decreases of %HTC (dose response manner), P<0.05 total RBC count (at doses of 500 and 1000mg/kg) and Hb P<0.01 (500mg/kg) vs. normal male rats. In female rats, the haematological study showed significant increase P<0.01 of total WBC count (at the doses of 500 and 1000mg/kg), significant decreases P<0.05 and P<0.01 of total RBC respectively at the doses of 200 and 1000mg/kg, significant decrease of Hb with extreme significance P<0.001 at the dose 1000mg/kg, %HTC also decrease dose response manner vs. control female rats. Biochemical study showed in male rats significant decreases in level of TG P<0.001 (at the doses of 200 and 500mg/kg) and urea, although it showed any dose-dependent effect vs. control male rats. AST also decreases (P<0.05) in male rats at the dose of 200mg/kg but significantly increase P<0.001 at the dose of 500mg/kg. In the female rats, biochemical study revealed significant increases in level of TG P<0.001 and urea P<0.01 at the dose of 200mg/kg and significant decreases in level of TG P<0.01, AST P<0.05 and urea P<0.05 at the dose of 500mg/kg (vs. control female rats). Microscopically, there were mild hepatic and renal tissue injuries supporting the hematological analysis.Conclusion: The results indicated that aqueous extract of Alstonia boonei De Wild is toxic in high doses.

Key concepts: Apocynaceae, Kidney, Internal medicine, Toxicity, Body weight, Endocrinology, Medicine, Traditional medicine

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