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氧化应激在梗阻性尿路病病理生理学中的意义

Implications of oxidative stress in the pathophysiology of obstructive uropathy.

作者信息

Zecher Martin, Guichard Cristián, Velásquez María José, Figueroa Gabriel, Rodrigo Ramón

机构信息

Faculty of Medicine, Institute of Biomedical Sciences, University of Chile, Santiago, Chile.

出版信息

Urol Res. 2009 Feb;37(1):19-26. doi: 10.1007/s00240-008-0163-3. Epub 2008 Dec 12.

Abstract

Although the functional and clinical alterations occurring in patients with obstructive uropathy are not well understood, it has been suggested that oxidative stress could contribute in the mechanism responsible for the impairment of sodium and water balance. This study aimed to test the hypothesis that red wine administration causes an amelioration of both the renal damage and impairment of renal Na(+), K(+)-ATPase activity occurring after ureteral obstruction in the rat. Twenty-four male Wistar adult rats weighting 200-250 g were used. Half of them received a 10-week treatment with wine as the sole fluid source, while the other group received water. Both groups were subjected to 24-h unilateral ureteral obstruction (UUO). Kidney tissue was collected following the relief of the ligature to perform the biochemical assessments. Urine and blood samples were taken at baseline and after the relief. Results show that the treatment with red wine significantly enhances the activity of antioxidant enzymes, and thus reduces renal lipid peroxidation secondary to UUO, which correlated negatively with Na(+), K(+)-ATPase activity. Based on this and other previous data, it could be suggested that red wine administration may prevent renal damage secondary to UUO by inducing enhanced antioxidant potential.

摘要

尽管目前对于梗阻性尿路病患者所发生的功能和临床改变尚未完全了解,但有研究表明氧化应激可能参与了导致钠和水平衡受损的机制。本研究旨在验证以下假设:给予大鼠红酒可改善输尿管梗阻后出现的肾损伤及肾钠钾ATP酶活性受损情况。选用24只体重200 - 250克的成年雄性Wistar大鼠。其中一半大鼠接受为期10周的以红酒作为唯一液体来源的处理,而另一组则给予水。两组大鼠均接受24小时单侧输尿管梗阻(UUO)。解除结扎后采集肾脏组织以进行生化评估。在基线期及解除结扎后采集尿液和血液样本。结果显示,红酒处理显著增强了抗氧化酶的活性,从而减少了UUO继发的肾脂质过氧化,而脂质过氧化与钠钾ATP酶活性呈负相关。基于此及其他先前数据,提示给予红酒可能通过诱导增强抗氧化潜能来预防UUO继发的肾损伤。

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