L-arginine infusion after ischaemia-reperfusion of rat kidney enhances lipid peroxidation

被引:21
作者
Cristol, JP
Thiemermann, C
Guerin, MC
Torreilles, J
dePaulet, AC
机构
[1] INSERM U58,F-34090 MONTPELLIER,FRANCE
[2] ST BARTHOLOMEWS HOSP MED COLL,WILLIAM HARVEY RES INST,LONDON,ENGLAND
来源
JOURNAL OF LIPID MEDIATORS AND CELL SIGNALLING | 1996年 / 13卷 / 01期
关键词
renal ischaemia-reperfusion; lipid peroxidation; nitric oxide;
D O I
10.1016/0929-7855(95)00010-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
To assess the role of superoxide (O-2(.-)) and nitric oxide (NO) in ischaemic-reperfusion-induced acute renal failure, we investigated whether an activation of the L-arginine-NO pathway contributes to ischaemia-reperfusion-induced kidney membrane peroxidation by measurement of 4-hydroxynonenal (HNE) content in anaesthetized rats submitted to acute renal ischaemia. Following ischaemia-reperfusion injury, renal blood flow (RBF) was significantly reduced, while renal vascular resistance was significantly increased. Infusion of neither L-arginine nor D-arginine led to a recovery of RBF. L-Arginine, but not D-arginine, caused a significant increase in HNE accumulation in the ischaemic kidney. L-Arginine infusion enhanced the degree of lipid peroxidation afforded by ischaemia-reperfusion injury in the kidney suggesting that products of the endogenous L-arginine-NO pathway may react with O-2(.-) to initiate lipid peroxidation.
引用
收藏
页码:9 / 17
页数:9
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