小檗水提物对四氯化碳肝毒性及脂多糖/扑热息痛所致大鼠肝炎的预防作用

M. Moustafa, D. Ghareeb, Maha A El-Demellawy, M. M. Elsayed
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引用次数: 0

摘要

本研究的目的是在实验动物模型中评估小檗水提取物(BWE)对CCl4诱导的肝毒性和LPS/PCM诱导的肝炎症的影响。CCl4(100微克/公斤,口服)给药28天以及LPS(250微克/公斤体重)和PCM(2微克/公斤重量)联合给药28天后,导致血清和肝脏促氧化剂和炎症参数(硫代巴比妥酸反应物质(TBARS)、组织肿瘤坏死因子-α,白细胞介素6(IL-6)和IL-12以及一氧化氮(NO)与抗氧化剂系统(超氧化物歧化酶(SOD)和谷胱甘肽过氧化物酶(GPx))的耗竭。这些改变与血清肝功能测试(丙氨酸转氨酶(ALT)、天冬氨酸转氨酶(AST)和碱性磷酸酶水平和(ALP)的升高相结合。口服BWE(100 mg/kg)15天显示出对CCl4和LPS/PCM的护肝和抗炎作用,因为它增加了抗氧化酶的活性,降低了促氧化剂和炎症标志物的水平,并改善了血清肝功能测试水平。因此,所获得的结果表明,B.vulgaris水提取物由于其抗氧化和抗炎特性而对肝毒性和肝炎症具有保护作用。关键词:四氯化碳,对乙酰氨基酚,脂多糖,谷胱甘肽过氧化物酶,丙氨酸转移酶。
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Berberis vulgaris aqueous extract prevention of carbon tetrachloride induced hepatotoxicity and lipopolysaccharides/paracetamol induced hepatitis in rats
The aim of this study was to evaluate the effect of Berberis vulgaris water extract (BWE) against CCl4-induced hepatotoxicity and LPS/PCM induced- hepatic inflammation in the experimental animal models. CCl4 (100 ug/kg, oral) administration for 28 days as well as the co-administration of LPS (250 ug/kg bw) and PCM (2 g/kg bw) for 28 days resulted in massive elevation in serum and hepatic prooxidants and inflammatory parameters (thiobarbituric acid reactive substances (TBARS), tissue tumor necrosis factor–alpha (TNF-α), interleukin 6 (IL-6) and IL-12 and nitric oxide (NO) with depletion in antioxidants system (superoxide dismutase (SOD) and glutathione peroxidase (GPx). These alterations were combined with elevation of serum liver function tests (alanine transaminase (ALT), aspartate transaminase (AST) and alkaline phosphatase level and (ALP). Oral administration of the BWE (100 mg/kg) for 15 days showed hepatoprotective and anti-inflammatory effects against both CCl4 and LPS/PCM as it increased the activities of antioxidants enzymes, decreased the prooxidants and inflammatory markers levels and improved the serum liver function tests levels. The obtained findings thus suggest that B. vulgaris aqueous extract has protective roles against hepatic toxicity and hepatic inflammation due to its antioxidant and anti-inflammatory properties. Key words: Carbon tetrachloride, paracetamol, lipopolysaccharide, glutathione peroxidase, alanine transferase.
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