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环孢素A介导的氧化和亚硝化应激所致肾细胞损伤:硫酸化多糖的作用

Oxidative and nitrosative stress mediated renal cellular damage induced by cyclosporine A: role of sulphated polysaccharides.

作者信息

Josephine Anthony, Amudha Ganapathy, Veena Coothan Kandaswamy, Preetha Sreenivasan P, Varalakshmi Palaninathan

机构信息

Department of Medical Biochemistry, Dr. ALM. Post Graduate Institute of Basic Medical Sciences, University of Madras, Taramani Campus, Chennai, India.

出版信息

Biol Pharm Bull. 2007 Jul;30(7):1254-9. doi: 10.1248/bpb.30.1254.

Abstract

Oxidative and nitrosative stress are known to exert various adverse effects on biological systems and this seems to be one of the major contributor of nephrotoxicity induced by cyclosporine A (CsA), which is a major clinical challenge, despite its potent immunosuppressive effect. Sulphated polysaccharides of marine origin are well known for its antioxidant properties, among its other biological applications. CsA administration (25 mg/kg body weight, orally, for 21 d) showed increased level of oxidants and xanthine oxidase activity. CsA induced nitrosative stress was evident from a marked elevation in the expression of inducible nitric oxide synthase mRNA in renal tissue and a concomitant increase in plasma nitric oxide level. Augmented levels of malondialdehyde, 8-hydroxy-2-deoxyguanosine and protein carbonyl coupled with diminished protein thiols; hallmarks of lipid peroxidation, DNA damage and protein oxidation were noted in CsA administered rats. Membrane damage was further confirmed by altered ATPase activities in the renal tissue. Simultaneous treatment with sulphated polysaccharides (5 mg/kg body weight, subcutaneously) remarkably prevented the above alterations mediated by oxidative and/or nitrosative stress during CsA induction. Hence, these findings conclude that the use of an antioxidant agent like sulphated polysaccharides could be a useful tool in reducing CsA-induced nephrotoxicity.

摘要

已知氧化应激和亚硝化应激会对生物系统产生各种不利影响,这似乎是环孢素A(CsA)诱导肾毒性的主要原因之一,尽管CsA具有强大的免疫抑制作用,但肾毒性仍是一个重大的临床挑战。海洋来源的硫酸化多糖以其抗氧化特性以及其他生物学应用而闻名。给予CsA(25 mg/kg体重,口服,持续21天)后,氧化剂水平和黄嘌呤氧化酶活性增加。CsA诱导的亚硝化应激从肾组织中诱导型一氧化氮合酶mRNA表达的显著升高以及血浆一氧化氮水平的相应增加中明显可见。在给予CsA的大鼠中,丙二醛、8-羟基-2-脱氧鸟苷和蛋白质羰基水平升高,同时蛋白质巯基减少;这些都是脂质过氧化、DNA损伤和蛋白质氧化的标志。肾组织中ATP酶活性的改变进一步证实了膜损伤。同时给予硫酸化多糖(5 mg/kg体重,皮下注射)可显著预防CsA诱导过程中由氧化和/或亚硝化应激介导的上述改变。因此,这些研究结果得出结论,使用硫酸化多糖等抗氧化剂可能是减少CsA诱导的肾毒性一种有用方法。

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