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N-乙酰半胱氨酸可减轻二甲基亚硝胺诱导的大鼠氧化应激。

N-acetylcysteine attenuates dimethylnitrosamine induced oxidative stress in rats.

机构信息

Department of Pharmacology and Environmental Toxicology, Dr. A.L.M. Postgraduate Institute of Basic Medical Sciences, University of Madras, Taramani, Chennai - 600 113, India.

出版信息

Eur J Pharmacol. 2011 Mar 5;654(2):181-6. doi: 10.1016/j.ejphar.2010.10.080. Epub 2010 Nov 27.

Abstract

Oxidative stress has been implicated in the pathogenesis and progression of various hepatic disorders and hence screening for a good hepatoprotective and antioxidant agent is the need of the hour. The present study was aimed to investigate the hepatoprotective and antioxidant property of N-acetylcysteine (NAC) against dimethylnitrosamine (DMN) induced oxidative stress and hepatocellular damage in male Wistar albino rats. Administration of single dose of DMN (5mg/kg b.w.; i.p.) resulted in significant elevation in the levels of serum aspartate transaminase and alanine transaminase, indicating hepatocellular damage. Oxidative stress induced by DMN treatment was confirmed by an elevation in the status of lipid peroxidation (LPO) and reduction in the activities of enzymic antioxidants such as superoxide dismutase, catalase, glutathione peroxidase, glutathione reductase and glutathione-S-transferase and in the levels of non-enzymic antioxidants, reduced glutathione, vitamin-C and vitamin-E in the liver tissue. DMN induced oxidative stress and hepatocellular membrane instability was further substantiated by a decline in the status of the membrane bound ATPases in the liver tissue. Post-treatment with NAC (50mg/kg b.w.; p.o.) for 7days effectively protected against the DMN induced insult to liver by preventing the elevation in the status of the serum marker enzymes and LPO, and restoring the activities of both the enzymic and non-enzymic antioxidants and membrane bound ATPases towards normalcy. These results demonstrate that NAC acts as a good hepatoprotective and antioxidant agent in attenuating DMN induced oxidative stress and hepatocellular damage.

摘要

氧化应激与各种肝疾病的发病机制和进展有关,因此筛选出一种良好的肝保护和抗氧化剂是当前的需要。本研究旨在探讨 N-乙酰半胱氨酸(NAC)对二甲基亚硝胺(DMN)诱导的雄性 Wistar 白化大鼠氧化应激和肝细胞损伤的肝保护和抗氧化作用。单次腹腔注射 DMN(5mg/kg b.w.)导致血清天冬氨酸转氨酶和丙氨酸转氨酶水平显著升高,表明肝细胞损伤。DMN 处理诱导的氧化应激通过升高脂质过氧化(LPO)水平和降低超氧化物歧化酶、过氧化氢酶、谷胱甘肽过氧化物酶、谷胱甘肽还原酶和谷胱甘肽-S-转移酶等酶抗氧化剂的活性以及非酶抗氧化剂还原型谷胱甘肽、维生素-C 和维生素-E 的水平来证实。DMN 诱导的氧化应激和肝细胞膜不稳定性进一步通过肝脏组织中膜结合 ATP 酶的状态下降得到证实。NAC(50mg/kg b.w.;p.o.)连续 7 天治疗可有效防止 DMN 对肝脏的损伤,防止血清标志物酶和 LPO 升高,恢复酶和非酶抗氧化剂以及膜结合 ATP 酶的活性至正常水平。这些结果表明,NAC 作为一种良好的肝保护和抗氧化剂,可减轻 DMN 诱导的氧化应激和肝细胞损伤。

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