Protection from renal ischemia reperfusion injury by an endothelin-A receptor antagonist BQ-123 in relation to nitric oxide production

被引:21
作者
Erdogan, Hasan [1 ]
Fadillioglu, Ersin
Emre, Memet Hanifi
机构
[1] Gaziomanpasa Univ, Fac Med, Dept Physiol, TR-60100 Tokat, Turkey
[2] Hacettepe Univ, Fac Med, Dept Physiol, TR-06100 Ankara, Turkey
[3] Inonu Univ, Fac Med, Dept Physiol, Malatya, Turkey
关键词
endothelin-1; nitric oxide; renal ischemia reperfusion; endothelin-A receptor antagonist;
D O I
10.1016/j.tox.2006.08.039
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The aim of this study was to investigate whether the protective effect of endothelin-A (ETA) receptor antagonist BQ-123 against renal ischemia reperfusion (I/R) injury is related to nitric oxide (NO) production. Sprague-Dawley rats were divided into six,groups: control, I/R, N sup omega nitro-L-arginine methyl ester (L-NAME), BQ, BQ + L-NAME, BQ + L-NAME + L-Arg groups. After urethane anesthesia, 30 min renal ischemia and 2 h reperfusion were performed in all groups except control group. Mean arterial pressures (MAP) during reperfusion in all L-NAME-treated groups were higher than during pre-ischemia and ischemia, however, MAP at 60th and 120th minute of reperfusion in control and BQ groups were lower than during ischemia. MAP Of NAME-treated groups were significantly higher than the other groups during reperfusion period. The I/R caused lipid peroxidation and protein oxidation, however, BQ-123 treatment prevented oxidant injury. The inhibition of NO production prevented effect of BQ- 123 treatment. Also, BQ-123 treatment caused an increase in superoxide dismutase and catalase activities. Both BQ- 123 and L-NAME treatments prevented high xanthine oxidase activity. BQ-123 prevented risen myeloperoxidase activity and L-NAME reversed this effect of BQ-123 just like the addition Of L-arginine to the treatment altered the effect Of L-NAME. The plasma BUN was affected as increasing manner from L-NAME treatments; on the other hand, plasma Cr and Na. concentrations were affected as decreasing manner from BQ-123 treatments. ETA receptor antagonist BQ-123 may be revealed a protective agent against renal I/R injury with a possible secondary pathway via its antioxidant effects. We suggest that BQ-123 may mediate the protective effect via a NO-dependent mechanism. (c) 2006 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:219 / 228
页数:10
相关论文
共 50 条
[1]  
Aebi H., 1974, Methods in Enzymatic Analysis, V2, P674, DOI [DOI 10.1016/B978-0-12-091302-2.50032-3, 10.1016/B978-0-12-091302-2.50032-3]
[2]   CLONING AND EXPRESSION OF A CDNA-ENCODING AN ENDOTHELIN RECEPTOR [J].
ARAI, H ;
HORI, S ;
ARAMORI, I ;
OHKUBO, H ;
NAKANISHI, S .
NATURE, 1990, 348 (6303) :730-732
[3]   NITRIC-OXIDE IN THE KIDNEY - SYNTHESIS, LOCALIZATION, AND FUNCTION [J].
BACHMANN, S ;
MUNDEL, P .
AMERICAN JOURNAL OF KIDNEY DISEASES, 1994, 24 (01) :112-129
[4]   The many aspects of endothelins in ischemia-reperfusion injury: Emergence of a key mediator [J].
Battistini, B ;
Dussault, P .
JOURNAL OF INVESTIGATIVE SURGERY, 1998, 11 (05) :297-313
[5]  
BROOKS DP, 1994, J PHARMACOL EXP THER, V271, P769
[6]  
Buyukgebiz O, 1996, TRANSPL INT, V9, P201
[7]  
CORTAS NK, 1990, CLIN CHEM, V36, P1440
[8]   THE VALUE AND LIMITATIONS OF L-ARGININE INFUSION ON GLOMERULAR AND TUBULAR FUNCTION IN THE ISCHEMIC/REPERFUSED KIDNEY [J].
DAGHER, F ;
POLLINA, RM ;
ROGERS, DM ;
GENNARO, M ;
ASCER, E .
JOURNAL OF VASCULAR SURGERY, 1995, 21 (03) :453-458
[9]  
DENUCCI G, 1988, P NATL ACAD SCI USA, V85, P2334
[10]   Kidney ischemia-reperfusion: Modulation of antioxidant defenses [J].
Dobashi, K ;
Ghosh, B ;
Orak, JK ;
Singh, I ;
Singh, AK .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 2000, 205 (1-2) :1-11