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首页> 外文期刊>British Journal of Pharmaceutical Research >Molecular Mechanisms of the Modulatory Effect of Vitamin E on Tacrolimus (FK506)-Induced Renal Injury in Rats
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Molecular Mechanisms of the Modulatory Effect of Vitamin E on Tacrolimus (FK506)-Induced Renal Injury in Rats

机译:维生素E调节他克莫司(FK506)致大鼠肾损伤的分子机制

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摘要

Aim: This study was designed to evaluate the possible modulatory effect of vitamine E on tacrolimus (FK506)-induced renal injury in rats. Methods: Twenty-four male Wistar rats (6 animals in each group) were used in this study. The first group (Control) received normal saline intraperitoneal (i.p.) daily for 21 days. The second group received FK506 (1 mg/kg/day i.p.) daily for 21 days. The third group was administered Vitamin E (250 mg/kg/day by oral gavage) 5 days before and concurrently during FK506 administration daily for 21 days. The fourth group received Vitamin E alone (as previously described in the third group). Results: Administration of FK506 significantly increased blood urea nitrogen and serum creatinine levels. In addition, FK506 has also reduced the renal content of reduced glutathione, as well as the enzymatic activities of superoxide dismutase and catalase. Furthermore, these effects were associated with an increase in lipid peroxidation, inducible NO-synthase (iNOS), and NF-kB expression. Moreover, histopathological examinations showed severe damage of the renal tissues in animals treated with FK506. Interestingly, it was found that concomitant administration of vitamin E along with FK506 ameliorated all these parameters and improved renal function. Furthermore, the immunosuppressive effect of FK506 was not affected by vitamin E. Conclusion: The findings of the present study suggest that concomitant use of vitamin E might be useful in reducing nephrotoxicity induced by FK506.
机译:目的:本研究旨在评估维生素E对他克莫司(FK506)诱导的大鼠肾损伤的可能调节作用。方法:24只雄性Wistar大鼠(每组6只)用于这项研究。第一组(对照组)每天接受腹膜内生理盐水(i.p.),持续21天。第二组每天接受FK506(1 mg / kg /天,腹腔注射),持续21天。第三组在每天FK506给药前5天以及在每天FK506给药期间连续21天服用维生素E(250 mg / kg /天,经口管饲)。第四组仅接受维生素E(如先前在第三组中所述)。结果:FK506的使用显着增加了血液尿素氮和血清肌酐水平。此外,FK506还降低了还原型谷胱甘肽的肾脏含量,以及超氧化物歧化酶和过氧化氢酶的酶促活性。此外,这些作用与脂质过氧化,诱导型一氧化氮合酶(iNOS)和NF-kB表达的增加有关。此外,组织病理学检查显示,用FK506处理的动物肾脏组织受到严重损害。有趣的是,发现维生素E与FK506的同时给药改善了所有这些参数并改善了肾功能。此外,FK506的免疫抑制作用不受维生素E的影响。结论:本研究的发现表明,同时使用维生素E可能有助于减少FK506引起的肾毒性。

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