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
相关论文
共 51 条
[41]   HYPERGLYCEMIA AND DIABETIC KIDNEY-DISEASE - THE CASE FOR TRANSFORMING GROWTH-FACTOR-BETA AS A KEY MEDIATOR [J].
SHARMA, K ;
ZIYADEH, FN .
DIABETES, 1995, 44 (10) :1139-1146
[42]   ESSENTIAL FATTY-ACID DEFICIENCY NORMALIZES FUNCTION AND HISTOLOGY IN RAT NEPHROTOXIC NEPHRITIS [J].
TAKAHASHI, K ;
KATO, T ;
SCHREINER, GF ;
EBERT, J ;
BADR, KF .
KIDNEY INTERNATIONAL, 1992, 41 (05) :1245-1253
[43]   GLOMERULAR ACTIONS OF A FREE RADICAL-GENERATED NOVEL PROSTAGLANDIN, 8-EPI-PROSTAGLANDIN-F2-ALPHA, IN THE RAT - EVIDENCE FOR INTERACTION WITH THROMBOXANE-A2 RECEPTORS [J].
TAKAHASHI, K ;
NAMMOUR, TM ;
FUKUNAGA, M ;
EBERT, J ;
MORROW, JD ;
ROBERTS, LJ ;
HOOVER, RL ;
BADR, KF .
JOURNAL OF CLINICAL INVESTIGATION, 1992, 90 (01) :136-141
[44]   PREDOMINANT FUNCTIONAL ROLES FOR THROMBOXANE-A2 AND PROSTAGLANDIN-E2 DURING LATE NEPHROTOXIC SERUM GLOMERULONEPHRITIS IN THE RAT [J].
TAKAHASHI, K ;
SCHREINER, GF ;
YAMASHITA, K ;
CHRISTMAN, BW ;
BLAIR, I ;
BADR, KF .
JOURNAL OF CLINICAL INVESTIGATION, 1990, 85 (06) :1974-1982
[45]   8-Isoprostaglandin E2 enhances receptor-activated NFκB ligand (RANKL)-dependent osteoclastic potential of marrow hematopoietic precursors via the cAMP pathway [J].
Tintut, Y ;
Parhami, F ;
Tsingotjidou, A ;
Tetradis, S ;
Territo, M ;
Demer, LL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (16) :14221-14226
[46]   Characterization of signal transduction events stimulated by 8-epi-prostaglandin(PG)F-2 alpha in rat aortic rings [J].
Wagner, RS ;
Weare, C ;
Jin, N ;
Mohler, ER ;
Rhoades, RA .
PROSTAGLANDINS, 1997, 54 (02) :581-599
[47]   Regulation of activator protein-1 by 8-iso-prostaglandin E2 in a thromboxane A2 receptor-dependent and -independent manner [J].
Weber, TJ ;
Markillie, LM .
MOLECULAR PHARMACOLOGY, 2003, 63 (05) :1075-1081
[48]   DDM-PGE2-mediated cytoprotection in renal epithelial cells by a thromboxane A2 receptor coupled to NF-κB [J].
Weber, TJ ;
Monks, TJ ;
Lau, SS .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2000, 278 (02) :F270-F278
[49]  
YIN K, 1994, J PHARMACOL EXP THER, V270, P1192
[50]  
YOSHIDA K, 1995, DIABETOLOGIA, V38, P201, DOI 10.1007/s001250050271