天麻果浆甲醇提取物对四氯化碳致Wistar大鼠肝毒性的保护作用

M. Issa, A. Agbon, S. Balogun, Onesimus Mahdi, K. Bobbo, F. Ayegbusi
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引用次数: 6

摘要

背景:香蕉果肉在民间医学中被用于治疗各种疾病,如痢疾、腹泻、支气管炎、溃疡、发烧和出血,在全球不同地区,包括尼日利亚、西非。目的:采用组织学和生化方法评价天顶螺甲醇果肉提取物(MFMP)对四氯化碳(CCl4)致Wistar大鼠肝毒性的保护作用。材料与方法:24只Wistar大鼠分为6组(I-VI;n = 4)。I组(对照组)给予蒸馏水(2 ml/kg), II、III、IV组分别给予MFMP (500 mg/kg、1000 mg/kg、1500 mg/kg), V组给予水飞蓟素(100 mg/kg)作为对照药,疗程14 d。CCl4(1 ml, 1:1溶液:橄榄油)对大鼠产生肝毒性。第15天,II-VI组给予单剂量CCl4。所有的药物都是口服的。给药12 h后,取大鼠肝器官进行常规(h和E)组织学处理,采集血样进行血清肝酶(丙氨酸转氨酶、天冬氨酸转氨酶和碱性磷酸酶)生化分析。结果:mfmp对CCl4引起的肝损伤有明显的组织结构保护作用,降低了CCl4引起的血清肝酶水平(P < 0.05)。肝保护活性与对照药水飞蓟素相当。结论:MFMP对化学诱导的Wistar大鼠急性肝毒性具有保护肝的作用。由于其抗氧化特性,MFMP具有保护肝脏的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hepatoprotective effect of methanol fruit pulp extract of Musa paradisiaca on carbon tetrachloride-induced liver toxicity in Wistar rats
CONTEXT: Musa paradisiaca (Banana) fruit pulp has been used in folk medicine to treat various kinds of ailments, such as dysentery, diarrhea, bronchitis, ulcer, fevers, and hemorrhages in different parts of the globe, including Nigeria, Western Africa. AIM: This study was designed to histologically and biochemically assess the protective effect of methanol fruit pulp extract of M. paradisiaca (MFMP) on carbon tetrachloride (CCl4)-induced hepatotoxicity in Wistar rats. MATERIALS AND METHODS: Twenty-four Wistar rats were divided into six groups (I–VI; n = 4). Group I (control) was administered distilled H2O (2 ml/kg), whereas Groups II, III, and IV were administered MFMP (500 mg/kg, 1000 mg/kg, and 1500 mg/kg, respectively) and Group V administered Silymarin (100 mg/kg), as the reference drug, for a period of 14 days. Hepatotoxicity was induced in rats by the administration of CCl4(1 ml, 1:1 solution: olive oil). On the 15th day, Groups II–VI were administered single dose of CCl4. All administrations were through the oral route. After 12 h of CCl4administration, rats were euthanized and liver organs harvested for routine (H and E) histological tissue processing and blood samples collected for biochemical analysis of serum liver enzymes (alanine transaminase, aspartate transaminase, and alkaline phosphatase). RESULTS: MFMP-treatment revealed remarkable histoarchitectural preservation of the liver parenchyma against CCl4-induced liver damage and decreased (P < 0.05) serum liver enzyme levels elevated by CCl4. Hepatoprotective activity was comparable with that of the reference drug, Silymarin. CONCLUSION: Result suggests that MFMP possesses hepatoprotective potentials against chemically-induced acute hepatotoxicity in Wistar rats. Hepatoprotective potential of MFMP is possible as a result of its antioxidant properties.
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