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A 28- Day Oral Toxicity Study ofPseudocedrela kotschyi Methanol Extract inSprague-Dawley Rats

机译:拟南芥假单胞菌甲醇提取物对大鼠的28天口服毒性研究

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Aims: To evaluate the safety profile of Pseudocedela kotschyi which is used in traditional medicine for the treatment of epilepsy, malaria, diarrhoea and pains, a 28 day sub chronic toxicity study was conducted was evaluated using the 28 day subchronic toxicity study.Place and Duration of Study: This study was conducted in the Departments of Pharmacology, Faculty of Pharmacy, University Sains Malaysia, during the period between January 2013 and February 2014.Methodology: The methanolic extract of P. kotschyi stem bark was evaluated for acute and sub chronic toxicity in female and male rats. In the acute oral toxicity study, a limit dose of 2000 mg/kg was administered to five non-pregnant female rats by oral gavage. They were observed for signs of toxicity/mortality for 14 days. In the sub chronic toxicity study 48 rats of both sexes were grouped into 4 groups of 12 animals (6 males, 6 females) and treated with P. kotschyi extract at a dose of 40, 200 and 1000 mg/kg respectively, the fourth group was considered as a control.Results: The 28 days acute oral toxicity study of P. kotschyi demonstrated a lack of toxicity of the methanol extract. Parameters such as general behavioural changes were observed to be normal; moreover no death was recorded at the end of the study period. Assessment for signs of chronic toxicity indicated no abnormalities in the test groups as compared to the controls. Haematological and biochemical values in treated groups were normal in comparison with the control group. Insignificant changes in body weight, internal organ weight and general behaviour were considered to be incidental.Conclusion: The stem bark methanol extract of P. kotschyi administered orally to female and male rats was relatively safe at the doses administered. We therefore conclude that toxic effects, if any occurred at doses higher than those used in our country.
机译:目的:为了评估在传统药物中用于治疗癫痫,疟疾,腹泻和疼痛的Pseudocedela kotschyi的安全性,使用28天的亚慢性毒性研究对28天的亚慢性毒性研究进行了评估。研究:该研究是在2013年1月至2014年2月期间在马来西亚塞恩大学药理学系药理学系进行的。方法:对P.kotschyi茎皮的甲醇提取物进行了急性和亚慢性毒性评估在雌性和雄性大鼠中。在急性口服毒性研究中,通过强饲法向五只未怀孕的雌性大鼠施用了2000 mg / kg的极限剂量。他们被观察了14天的毒性/死亡率的迹象。在亚慢性毒性研究中,将48只雄性和雄性大鼠分为4组,每组12只动物(雄性6只,雌性6只),并分别以40、200和1000 mg / kg的剂量对科奇奇提取物进行处理,第四组结果:对科氏假单胞菌进行的28天急性口服毒性研究表明,甲醇提取物没有毒性。诸如一般行为改变之类的参数被认为是正常的。而且在研究期末没有死亡记录。评估慢性毒性的迹象表明,与对照组相比,测试组没有异常。与对照组相比,治疗组的血液和生化指标正常。结论体重,内脏器官重量和一般行为的微不足道的变化是偶然的。结论:在雌性和雄性大鼠中口服给予科氏假单胞菌的茎皮甲醇提取物相对安全。因此,我们得出的结论是,毒性作用(如果有的话)的剂量要高于我国所使用的剂量。

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