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Sub-acute and protective effect of Cymbopogon citratus against carbon tetrachloride-induced liver damage

机译:Cymbobogon Citratus对四氯化碳诱导肝损伤的亚急性和保护作用

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The study evaluates the sub-acute toxicity and antioxidant potential of ethanolic leaf extract of Cymbopogon citratus against CCl4-induced toxicity in Sprague Dawley rats. The ethanolic leaf extract of C. citratus was prepared by solvent maceration method. The phytochemicals present in the extract were determined using standard methods. The potential sub-acute toxicities were evaluated using OECD procedure. The sub-acute toxicity of the extract at the doses of 125, 250 and 500 mg/kg, b.wt. was administered orally for 28 days. Another sets of rats were made hepatotoxic by orally administered with CCl4 (20% CCl4 in olive oil) twice per week for a period of five weeks. They were treated with C. citratus extract (300 and 600 mg/kg body weight) once a day for 35 days. Biochemical parameters were used to assess the hepatoprotective effects of the extract on liver tissues. Phytochemical screening of C citratus shows the presence of anthraquinones, alkaloids, flavonoids, etc. The administration of C. citratus is not hematotoxic and significantly reduced (P<0.05) elevated liver biomarker enzymes, urea, creatinine and the level of malondialdehyde. Treatment with the extract was found to significantly increase (P<0.05) TP level, the activities of superoxide dismutase and catalase. Liver histopathology shows that the extract reduced the incidence of liver lesions induced by CCl4. The administration of C. citratus did not produce any toxic effects in the sub-acute study. The plant exhibits potent protective effects in CCl4-induced liver damage due to decrease in liver biomarker enzymes activities, increase of antioxidant-defense system and inhibition of lipid peroxidation.
机译:该研究评估了CCL4诱导的CCL4诱导的CCL4诱导毒性乙醇叶提取物的亚急性毒性和抗氧化剂潜力在Sprague Dawley大鼠中。通过溶剂浸渍法制备C.Citratus的乙醇叶提取物。提取物中存在的植物化学物质使用标准方法测定。使用经合组织程序评估潜在的亚急性毒性。提取物的亚急性毒性为125,250和500mg / kg,B.Wt。口服给药28天。通过在每周两次用CCl4(20%CCL4)口服给予肝毒性,每周每周两次,为期五周。每天用C. citratus提取物(300和600mg / kg体重)治疗35天。生化参数用于评估提取物对肝组织的肝脏保护作用。 C citratus的植物化学筛查显示蒽醌,生物碱,黄酮类化合物等的存在。C.Citratus的给药不是血管毒性,显着降低(P <0.05)肝脏生物标志物酶,尿素,肌酐和丙二醛水平。发现用提取物治疗显着增加(P <0.05)TP水平,超氧化物歧化酶和过氧化氢酶的活性。肝脏组织病理学表明,提取物降低了CCL4诱导的肝脏病变的发生率。 C.Citratus的给药在亚急性研究中没有产生任何毒性作用。由于肝脏生物标志物酶活性降低,抗氧化剂 - 防御系统的增加和脂质过氧化的抑制,该植物在CCL4诱导的肝损伤中表现出有效的保护作用。

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