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首页> 外文期刊>Comparative clinical pathology >Ameliorative property of Kigelia africana crude and flavonoid leaf extracts on aluminum-induced hepatotoxicity in albino rats
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Ameliorative property of Kigelia africana crude and flavonoid leaf extracts on aluminum-induced hepatotoxicity in albino rats

机译:Kigelia Africana原油和黄酮类叶片提取物在白化大鼠铝诱导的肝毒性中的修复性质

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摘要

Liver diseases could be life threatening. The liver, being an organ of biotransformation of xenobiotics, makes it a target for oxidative stress since most toxins are pro-oxidants. This study investigated the protective property of Kigelia africana crude leaf extract (KAE) and its flavonoid-rich fraction (FKAE) on AlCl3-induced hepatotoxicity in rats. Forty-two adult male Sprague Dawley rats were divided into seven groups (n = 6). Animals in the negative control group received tap water orally. The hepatotoxic group received 17 mg/kg AlCl3 daily, for four consecutive weeks. Positive control group received rivastigmine (0.3 mg/kg/day), while groups 4 and 5 received 50 and 100 mg/kg KAE, respectively, daily for 2 weeks followed by combination of KAE treatment with AlCl3 administration for a further 4 weeks. Groups 6 and 7 were treated in a similar way to groups 4 and 5 but with 50 and 100 mg/kg FKAE, respectively. Markers of oxidative stress, electrolyte levels, and histopathological changes were evaluated in the liver of animals after the period of treatment. Results obtained revealed that 100 mg/kg KAE and both doses of FKAE significantly mitigated AlCl3-induced oxidative stress, electrolyte disturbance, and histological alterations in rats. It is suggested that Kigelia africana could be a potential source of effective hepatoprotectants.
机译:肝病可能是危及生命的。作为异丙酸的生物转化器官的肝脏使其成为氧化胁迫的靶标,因为大多数毒素是促氧化剂。本研究调查了Kigelia Africana原油叶提取物(KAE)及其黄酮类化合物(FKAE)对大鼠肝毒性的保护性质。将四十二个成年雄性Sprague Dawley大鼠分为七组(n = 6)。阴性对照组中的动物口服接受自来水。肝毒性组每天接受17mg / kg Alcl3,连续四周。阳性对照组接受菌活性(0.3mg / kg /天),而组4和5分别接受50和100mg / kg Kae,每天2周,然后用AlCl3给药的Kae治疗组合4周。将组6和7以与组4和5类似的方式处理,但分别具有50和100mg / kg FKAE。在治疗期后,在动物的肝脏中评估氧化应激,电解质水平和组织病理学变化的标记。得到的结果显示,100mg / kg Kae和两种剂量的FKAE显着减轻了all3诱导的氧化应激,电解质干扰和大鼠的组织学改变。有人建议,基丽亚非洲人可能是有效肝脏保护剂的潜在来源。

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