Ebunoluwa Asenuga, T O Ajibade, Abiola Adejumobi, Bukola Alaba, Williams Nabofa, Ademola Oyagbemi, Temidayo Omobowale, Joseph Badejo, Olajide Akinboye
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引用次数: 0
摘要
铅(Pb)等有毒金属会对人类和动物的肝脏造成严重损害,氧化应激是醋酸铅诱发肝损伤的主要发病机制。Azadirachta indica 因其抗氧化作用而具有保肝作用。本研究以 70 只成年雄性大鼠为研究对象,将其分为 A 组--对照组(蒸馏水);B 组--仅 0.1% LA;C 组和 D 组--0.1% LA + 100 mg/kg 和 0.1% LA + 200 mg/kg AI;E 组--0.2% LA;F 组和 G 组--0.2% LA + 100 mg/kg 和 0.2% LA + 200 mg/kg AI。对氧化应激指标(MDA 和 H2O2)、抗氧化指标(GSH、SOD、CAT、GPx、GST)、炎症指标(MPO 和 NO)、丙氨酸氨基转移酶(ALT)和肝脏组织病理学研究进行了评估。结果表明,服用 LA 会导致 GSH、GPx 和 GST 下降,而同时服用 AI 会提高抗氧化剂的活性。此外,服用 LA 会增加 MPO、NO、MDA 和 H2O2 的水平,而 AI 则会显著降低 MPO、NO、MDA 和 H2O2 的水平(P<0.05)。
Antioxidant and Chemopreventive Effects of Azadirachta indica on Lead Acetate-induced Hepatotoxicity in Male Wistar Rats.
Toxic metals such as lead (Pb) cause severe liver damage in humans and animals, with oxidative stress prominently implicated in the pathogenesis of lead acetate‑induced liver injury. Azadirachta indica is hepatoprotective due to its antioxidative effect. This study investigated the antioxidative role of A. indica (AI) and its chemopreventive effect on lead acetate (LA)-induced hepatocellular dysfunction with seventy adult male rats classified into group A- Control (distilled water), group B 0.1% LA only, group C and D- 0.1% LA + 100 mg/kg and 0.1% LA + 200 mg/kg AI respectively, group E- 0.2% LA, group F and G- 0.2% LA + 100 mg/kg and 0.2% LA + 200 mg/kg AI. Oxidative stress markers (MDA and H2O2), antioxidant parameters (GSH, SOD, CAT, GPx, GST), inflammatory markers (MPO and NO), alanine aminotransferase (ALT) and histopathological studies of the liver were evaluated. The results showed that LA administration caused a decrease in GSH, GPx, and GST while AI co-administration increased the activities of the antioxidants. Moreover, LA administration increased MPO, NO, MDA, and H2O2 levels whereas AI significantly reduced (P<0.05) these parameters. Histopathological examination revealed necrosis and mild infiltration by inflammatory cells in LA administered rats, whereas these lesions were absent in AI administered rats. In conclusion, A. indica demonstrates a protective role in lead acetate-induced hepatotoxicity, mainly via oxidative stress inhibition.