木犀草素对白化大鼠肝脏和造血系统影响的评价

Chima E. Orji, C. Okpoko, C. Agbata, J. Okoyeh, A. Okeke, C. Ihekwereme
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引用次数: 4

摘要

背景:木犀草素是一种黄酮类化合物,具有一些有用的药理特性,但其安全性尚未完全描述。本研究的目的是研究木犀草素对血液和肝脏功能的影响,并对木犀草素的治疗使用提出必要的建议。方法:选用体重平均的成年白化病大鼠33只。采用改良Lorke法对13只大鼠进行木犀草素口服LD50测定。其余20只大鼠分为4组,每组5只(n=5 /组),进行生化、血液学和组织病理学研究,共28 d。第一组为对照,口服蒸馏水10 ml/kg。II组、III组和IV组分别口服木犀草素50 mg/kg、100 mg/kg和200 mg/kg。各组大鼠分别于给药前、第14天和第28天及每日重复给药后采血。取大鼠肝脏,观察组织学变化。结果:各剂量木犀草素对大鼠部分血液指标(红细胞、PCV、Hb)均有显著(p<0.05)升高,而白细胞无明显升高。肝酶(ALT、AST、ALP)水平显著(p<0.05)升高。结论:高剂量(≥200mg /kg)和长期使用木犀草素可提高肝酶活性,低剂量(≤50mg /kg)可保护肝脏。组织病理学结果未见明显肝损伤。
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Evaluation of the Effect of Luteolin on the Hepatic and Hematopoietic Systems in Albino Rats
Background: Luteolin is a flavonoid with some useful pharmacological properties yet its safety profile has not been fully delineated .Objectives of the study were to investigate the effects of luteolin on blood and liver functions, and make necessary recommendations regarding therapeutic use of luteolin. Methods: A total of 33 adult albino rats (average weight) were used in this study. Oral LD50 of luteolin was carried out with 13 rats using modified Lorke’s method. The other 20 rats were divided into 4 groups comprising of 5 rats per group (n=5 per group) for biochemical, haematological and histopathological studies which were carried out for 28 days. Group I was used as control and received orally 10 ml/kg of distilled water. Groups II,III and IV also orally received 50 mg/kg,100 mg/kg and 200 mg/kg of luteolin respectively. Blood samples were collected from each rat in the different groups before treatment, on 14th and 28th days respectively and after repeated daily dosing. The liver of the rats were extracted and examined for histological changes. Results: Results show that all doses of luteolin had significant (p<0.05) elevation of some blood indices (RBCs, PCV, Hb) while WBCs was not elevated. There was significant (p<0.05) increase in liver enzymes such as ALT, AST and ALP. Conclusion: The study indicates that high doses ( ≥ 200 mg/kg) and prolonged use of luteolin may increase hepatic enzyme activity while low doses ( ≤ 50 mg/kg) and are hepatoprotective. No significant liver damage was observed based on histopathological results.
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