无花果醇提物对二乙基亚硝胺致Wistar大鼠肝毒性的改善作用

O. Yakubu, E. Ojogbane, V. O. Nwaneri-Ch, P. N. Ibuzo, E. M. Ale, S. S. Awudu
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引用次数: 1

摘要

背景与目的:二乙基亚硝胺(DEN)是一种肝毒性化合物,存在于许多食品和药物中,可导致肝癌。本研究旨在探讨榕叶乙醇提取物对DEN所致肝损伤的保护作用。材料与方法:将20只白化Wistar大鼠分为4组,A组为正常对照组,给予水,B组给予200 mg kgG1 DEN 1次,C组给予200 mg kgG1无花果醇提物并给予DEN, D组给予200 mg kgG1水飞蓟素作为参比品并给予DEN。实验2周后处死动物,采血进行生化分析。结果:DEN使大鼠谷丙转氨酶、谷丙转氨酶活性显著(p<0.05)升高,总胆红素和直接胆红素浓度显著(p<0.05)升高,白蛋白和总蛋白水平显著(p<0.05)降低。然而,用无花果提取物治疗可以改善实验组中这些生物标志物的水平。与标准药物水飞蓟素比较,其效果无统计学差异(p<0.05)。结论:无花果醇提物对den诱导的Wistar大鼠肝毒性具有一定的保护作用,在现代保肝药物的开发中具有重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ameliorative Effects of Ethanol Extract of Ficus sur on Diethylnitrosamine-induced Hepatotoxicity in Wistar Rats
Background and Objective: Diethylnitrosamine (DEN) is a hepatotoxic compound found in many foods and drugs capable of causing liver cancer. This study was undertaken in order t o investigate the hepatoprotective efficacy of the ethanolic extract of the leaf of Ficus sur on liver damage induced by DEN. Materials and Methods: Twenty Albino Wistar rats were divided into 4 groups, group A served as the normal control group, received water, group B received 200 mg kgG1 DEN once, group C received 200 mg kgG1 ethanolic extract of Ficus sur along with DEN and group D received 200 mg kgG1 silymarin as reference standard along with DEN. The experiment lasted for 2 weeks after which the animals were sacrificed and the blood collected for biochemical analyses. Results: Administration of DEN caused a significant (p<0.05) increase in the activities of AST and ALT as well as the concentration of total and direct bilirubin, while the levels of albumin and total protein were markedly (p<0.05) reduced. However, treatment with Ficus sur extract ameliorated the levels of these biomarkers in the experimental group. The effect elicited by the extract was not statistically different (p<0.05) when compared to silymarin, a standard drug. Conclusion: The ethanolic extract of Ficus sur protects against DEN-induced hepatotoxicity on Wistar rats and can play a crucial role in the development of modern hepatoprotective drug.
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