Concurrent Short Term Administration of Artesunate and Methanol Extract of Ficus Platyphylla Has No HepatoRenal Consequences in Rats

M. Oraebosi, Waaka Thankgod Abalubu
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Abstract

Many believe that the use of orthodox drugs alongside herbal medications brings about enhanced efficacy. Thus, it is not uncommon to see these combinations in malaria treatment. However, this combination may lead to toxicity through drug-herb interaction. The liver and kidneys being important organs in metabolism and excretion of xenobiotics are potential target organs for the suspected adverse effects. This study hypothesized that the co-administration of artesunate and methanol stem bark extract of Ficus platyphylla may result in hepato-renal consequences. Twenty male wistar rats were divided into four groups of five rats each. Group one served as the normal control group and was treated with normal saline at a dose of 1 ml/kg. Rats in group two were treated with 300 mg/kg of Ficus platyphylla alone while rats in group three were treated with 2.9 mg/kg of artesunate alone. Furthermore, rats in group four were treated with Ficus platyphylla and artesunate at a dose of 300 mg/kg and 2.9 mg/kg respectively. All treatments were done orally for five continuous days within which body weight was determined. At the end of the treatment period, liver markers levels (alanine aminotransferase, aspartate aminotransferase and alkaline phosphatase) and kidney markers (urea, creatinine, uric acid, albumin and total protein) were determined. There were no statistically significant differences (p>0.05) in body weights, hepatic and renal biomarkers across all treated groups when compared to the control. These results may indicate the safety of this drug-herb combination when used in malaria therapy.
Artesunate和Ficus Platyphylla甲醇提取物同时短期给药对大鼠肝肾无影响
许多人认为,将传统药物与草药一起使用可以提高疗效。因此,在疟疾治疗中看到这些组合并不罕见。然而,这种组合可能通过药物-草药相互作用导致毒性。肝脏和肾脏是异种药物代谢和排泄的重要器官,是可疑不良反应的潜在靶器官。本研究假设白叶榕茎皮提取物与青蒿琥酯联合使用可能导致肝肾损害。将20只雄性wistar大鼠分为4组,每组5只。第一组为正常对照组,给予生理盐水1 ml/kg的剂量。2组大鼠单独给予300 mg/kg白叶榕,3组大鼠单独给予2.9 mg/kg青蒿琥酯。第4组大鼠分别给予300 mg/kg的白叶榕和2.9 mg/kg的青蒿琥酯。所有治疗均为连续5天口服,在此期间测定体重。在治疗期结束时,测定肝脏标志物(丙氨酸转氨酶、天冬氨酸转氨酶和碱性磷酸酶)和肾脏标志物(尿素、肌酐、尿酸、白蛋白和总蛋白)水平。与对照组相比,所有治疗组的体重、肝脏和肾脏生物标志物均无统计学差异(p>0.05)。这些结果可能表明这种药物-草药组合用于疟疾治疗时的安全性。
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