首页> 外文期刊>International Journal of Pharmacy and Pharmaceutical Sciences >HEPATOPROTECTIVE AND HEPATOTHERAPUTIC EFFECTS OF PROPOLIS AGAINST D-GALACTOSAMINE/LIPOPOLYSACCHARIDE-INDUCED LIVER DAMAGE IN RATS
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HEPATOPROTECTIVE AND HEPATOTHERAPUTIC EFFECTS OF PROPOLIS AGAINST D-GALACTOSAMINE/LIPOPOLYSACCHARIDE-INDUCED LIVER DAMAGE IN RATS

机译:蜂胶对D-半乳糖胺/脂多糖诱导的大鼠肝脏损伤的肝保护和肝治疗作用

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Objective: The aim of the present study was to investigate the potential hepatoprotective and hepatotherapeutic activities of propolis against D-galactosamine and lipopolysaccharide (D-GaIN/LPS)-induced hepatotoxicity in rats. Methods: Hepatotoxicity was induced in rats by intra peritoneal injection of GalN (300?mg/kg) and LPS (30?μg/kg). In the hepatoprotection experiment, propolis was administered orally for 10 days before induction of hepatoxicity. In another experiment (hepatotherapy), propolis was dosed immediately after GalN/LPS injection. Results: Injection of GalN/LPS to rats induced hepatic damage that was manifested by a significant increase in the activities of aminotransferases, alkaline phosphatase, lactate dehydrogenase and levels of tumor necrosis factor-alpha (TNF-α) and total bilirubin in serum. Liver homogenate of intoxicated animals had the lower content of reduced glutathione with increased levels of the hepatic malondialdehyde and caspase-3 enzyme. Histological data presented marked damage in liver sections of intoxicated rats. Oral dosing of propolis before or once immediately after intoxication reversed these altered parameters near to normal values. Conclusion: Liver apoptotic events such as DNA fragmentation and increased caspase-3 activity observed during intoxication were prevented by pre and post- propolis treatment. These results suggest that propolis could afford significant protection and therapy in alleviation of hepatotoxicity. Keywords: Propolis, Galactosamine, Lipopolysaccharide, Hepatotoxicity, Rats.
机译:目的:本研究的目的是研究蜂胶对D-半乳糖胺和脂多糖(D-GaIN / LPS)诱导的大鼠肝毒性的潜在肝保护和肝治疗活性。方法:腹腔注射GalN(300?mg / kg)和LPS(30?μg/ kg)可引起大鼠肝毒性。在保肝实验中,在诱导肝毒性之前口服蜂胶10天。在另一个实验(肝疗法)中,在注射GalN / LPS后立即服用蜂胶。结果:向大鼠注射GalN / LPS可引起肝损伤,其表现为氨基转移酶,碱性磷酸酶,乳酸脱氢酶的活性以及血清中肿瘤坏死因子-α(TNF-α)和总胆红素水平的显着增加。醉酒动物的肝匀浆中还原型谷胱甘肽含量较低,肝丙二醛和caspase-3酶水平较高。组织学数据显示中毒大鼠肝脏切片明显受损。在中毒之前或之后立即口服一次蜂胶,使这些改变的参数接近正常值。结论:蜂胶治疗前后,可以预防中毒期间观察到的肝细胞凋亡事件,例如DNA片段化和caspase-3活性增加。这些结果表明蜂胶可以在减轻肝毒性方面提供重要的保护和治疗。关键词:蜂胶,半乳糖胺,脂多糖,肝毒性,大鼠。

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