Sub-chronic Hepatotoxicity Assessment of Ghana Cleanser® in Exposed Wistar Rats

U. P. Ise, T. Famojuro, Ambi Ibrahim Maman, Ponman Nanpon Samuel, Patience Duppe, M. Builders
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Abstract

This study evaluated the toxicity of a polyherbal Formulation (Ghana Cleanser®) on liver function markers of exposed albino rats. Thirty (30) male and female rats of the Wistar strain were randomly allotted into six (6) groups with n=5. 10.0 mL/kg distilled water was given to control groups 1 and 4. Polyherbal formulation doses of 374.0 mg/kg and 187.0 mg/kg were administered to groups 2-3 and 5-6, respectively. A modified Lorke's approach was used to compute acute toxicity.  Animals were euthanized after 60 days under diethyl ether. Blood was collected for biochemical analyses through cardiac puncture. The liver was excised from each animal and was fixed in 10% buffered formaldehyde and prepared for histological assessment. LD50 of the polyherbal preparation was calculated as 3740 mg/kg (oral). The results indicated an appreciable increase (p<0.05) in ALT activity at 374.0 mg/kg in female rats; while there was no increase recorded at 187.0mg/kg in male rats. A significant increase in ALT activity was recorded at 374 mg/kg in male rats as well and increased AST activities were recorded at 187mg/kg in female rats. In the treated animals of both sexes, ALP activities were significantly elevated. Histopathology assessment of the hepatocytes showed no significant damage at 187 mg/kg in rats of both sexes when compared with their respective controls while some degrees of pathologies such as hepatocyte inflammation, hyperplasia, and congestion were recorded at 374 mg/kg in rats of both sexes. Results suggest caution on the long-term use of the polyherbal mixture due to its hepatotoxic potential.
对暴露于 Ghana Cleanser® 的 Wistar 大鼠进行亚慢性肝毒性评估
本研究评估了一种多草药配方(Ghana Cleanser®)对暴露白化大鼠肝功能指标的毒性。将 30 只 Wistar 品系的雌雄大鼠随机分为 6 组,每组 5 只。对照组 1 和 4 给药 10.0 毫升/千克蒸馏水。2-3 组和 5-6 组分别服用 374.0 毫克/千克和 187.0 毫克/千克的多草药配方。计算急性毒性时采用了改进的 Lorke 方法。 60 天后,动物在二乙醚中安乐死。通过心脏穿刺采集血液进行生化分析。从每只动物身上切除肝脏,用 10%缓冲甲醛固定,准备进行组织学评估。计算得出多草药制剂的半数致死剂量为 3740 毫克/千克(口服)。结果表明,雌性大鼠口服 374.0 毫克/千克时,ALT 活性明显增加(p<0.05);而雄性大鼠口服 187.0 毫克/千克时,ALT 活性没有增加。雄性大鼠的谷丙转氨酶(ALT)活性在 374 毫克/千克时也明显升高,而雌性大鼠的谷草转氨酶(AST)活性在 187 毫克/千克时升高。在接受治疗的雌雄动物中,ALP 活性都明显升高。肝细胞组织病理学评估显示,与各自的对照组相比,187 毫克/千克剂量下的雌雄大鼠肝细胞均未出现明显损伤,而 374 毫克/千克剂量下的雌雄大鼠肝细胞均出现了一定程度的病变,如肝细胞炎症、增生和充血。结果表明,由于多草药混合物具有潜在的肝毒性,因此应谨慎长期使用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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