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首页> 外文期刊>International Journal of Biochemistry Research & Review >Toxicological Evaluation of Some ArtemisininCombination Therapies (ACTs) on the Kidney andLiver of Albino Wistar Rats
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Toxicological Evaluation of Some ArtemisininCombination Therapies (ACTs) on the Kidney andLiver of Albino Wistar Rats

机译:青蒿素联合疗法对白化Wistar大鼠肾脏和肝脏的毒理学评价

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World Health Organisation (WHO) recommends the use of artemisinin-based combination therapies (ACTs) as drug of choice for the treatment of malaria in endemic regions of the world. This study was designed to evaluate the effects of therapeutic doses of ACTs: Artesunate (Artesunat®), Artesunate-Mefloquine (Artequin®), Artemether-Lumefantrin (Coartem®) and Dihydroartesiminin-Piperaquine (P-Alaxin®) on the integrity of the liver and kidneys of albino Wistar rats. Thirty (30) albino Wistar rats weighing between 200 g – 280 g were randomly divided into 5 groups with 6 animals per group. Group 1 served as control (CTR) while Group 2 received artesunate (AS) for 5 days. Groups 3, 4 and 5 received therapeutic doses of artequine (AQ), coartem (CT) and p-alaxin (PA) respectively for 3 days. The animals were sacrificed under chloroform anaesthesia and blood samples obtained through cardiac puncture for biochemical investigations. Serum ALT activity of Groups 2 and 3 were significantly elevated (p0.05) while Groups 4 and 5 experienced marginal increased. Group 4 also showed significant increase in total bilirubin though it was marginally increased in all other groups when compared to the control. Creatinine levels were marginally increased in all groups while the urea levels were relatively stable across all groups except in Group 3 where significant increase was observed. The results therefore indicate possible hepatic injury and renal toxicity in albino Wistar rats hence the need for caution and proper attention while undergoing malaria treatment with ACTs.
机译:世界卫生组织(WHO)建议使用基于青蒿素的联合疗法(ACTs)作为治疗世界流行地区疟疾的首选药物。这项研究旨在评估ACTs的治疗剂量:青蒿琥酯(Artesunat®),青蒿琥酯-甲氟喹(Artequin®),青蒿琥酯-卢美芬特(Coartem®)和二氢青蒿琥酯-哌拉喹(P-Alaxin®)的完整性。白化Wistar大鼠的肝脏和肾脏。将三十(30)只体重在200克至280克之间的白化Wistar大鼠随机分为5组,每组6只动物。第1组作为对照组(CTR),第2组接受青蒿琥酯(AS)5天。第3、4和5组分别接受3天的治疗剂量的Artequine(AQ),Coartem(CT)和p-alaxin(PA)。在氯仿麻醉下处死动物,并通过心脏穿刺获得血样用于生化研究。第2组和第3组的血清ALT活性显着升高(p <0.05),而第4组和第5组的边缘性升高。第4组也显示总胆红素显着增加,尽管与对照组相比在所有其他组中均略有增加。除第3组中观察到明显增加外,所有组中肌酐水平均略有增加,而所有组中尿素水平相对稳定。因此,结果表明在白化病Wistar大鼠中可能存在肝损伤和肾毒性,因此在进行ACTs疟疾治疗时需要谨慎和适当注意。

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