Isoprostanes and the kidney

被引:35
作者
Badr, KF
Abi-Antoun, TE
机构
[1] Amer Univ Beirut, Dept Physiol, Beirut 72020, Lebanon
[2] Amer Univ Beirut, Dept Med, Beirut 72020, Lebanon
关键词
D O I
10.1089/ars.2005.7.236
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
Isoprostanes are not mere bystanders of oxidative injury, but possess potent biological activity and may thus contribute to the pathophysiology of various disorders associated with an increase in free radical formation. 15-F-2t IsoP (8-iso-prostaglandin F-2alpha) and 15-E-2t-IsoP (8-iso-prostaglandin E-2), two of the most abundant isoprostanes, are potent vasoconstrictors in various vascular beds, including the kidney. Since their discovery, numerous studies have aimed to define the receptors through which isoprostanes exert their effects. Whether the thromboxane receptor and/or other prostaglandin receptors mediate the actions of isoprostanes, or whether these compounds interact with their own unique receptors, remains to be clarified. Regardless of their exact mode of action, isoprostanes are being implicated in the pathophysiology of a variety of diseases, and their discovery might give rise to novel therapies for these diseases. Here we describe early studies that defined the vasoactive properties of isoprostanes in the kidney, and subsequent discoveries relating to their renal actions and pathophysiologic significance.
引用
收藏
页码:236 / 243
页数:8
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