Dose-Dependent Protective Effect of Ivabradine against Ischemia-Reperfusion-Induced Renal Injury in Rats

被引:10
|
作者
Beytur, Ali [1 ]
Binbay, Murat [2 ]
Sarihan, M. Ediz [3 ]
Parlakpinar, Hakan [4 ]
Polat, Alaadin [5 ]
Gunaydin, M. Orhun [1 ]
Acet, Ahmet [4 ]
机构
[1] Inonu Univ, Fac Med, Dept Urol, TR-44280 Malatya, Turkey
[2] Haseki Training Hosp, Dept Urol, Istanbul, Turkey
[3] Inonu Univ, Fac Med, Dept Emergency Med, TR-44280 Malatya, Turkey
[4] Inonu Univ, Fac Med, Dept Pharmacol, TR-44280 Malatya, Turkey
[5] Inonu Univ, Fac Med, Dept Physiol, TR-44280 Malatya, Turkey
来源
KIDNEY & BLOOD PRESSURE RESEARCH | 2012年 / 35卷 / 02期
关键词
Endothelial dysfunction; Ivabradine; Oxidative stress; Rat; Renal ischemia; HEART-RATE REDUCTION; PARTIAL NEPHRECTOMY; DYSFUNCTION; KIDNEY; FAILURE;
D O I
10.1159/000330501
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Background/Aims: This study was designed to investigate the dose-dependent protective effect of ivabradine, a specific inhibitor of the cardiac sinoatrial node, on renal ischemia-reperfusion (I/R) injury in rats. Methods: Rats were divided into six groups: group 1, control; group 2, I/R (60 min ischemia followed by 24 h reperfusion); groups 3 and 4, 0.6-6 mg/kg ivabradine; and groups 5 and 6, sham+0.6-6 mg/kg ivabradine. At the end of the study, malondialdehyde (MDA), superoxide dismutase (SOD), catalase (CAT) and glutathione peroxidase contents were assayed in the kidney tissues; serum blood levels of urea nitrogen (BUN), creatinine (Cr) and albumin also were determined. Results: Tissue MDA levels were found to be significantly higher in the I/R group, whereas SOD and CAT levels were lower when compared to the control group. Ivabradine (0.6 mg/kg) treatment reduced the MDA levels and elevated the SOD and CAT enzyme activity. Treatment with a dose of 6 mg/kg ivabradine further increased MDA levels and did not ameliorate SOD or CAT activities. Serum levels of BUN and Cr were significantly higher in the I/R group. I/R+0.6 mg ivabradine reduced the elevated BUN and Cr levels. Conclusion:This study indicates that ivabradine exerts a dose-dependent response beyond heart rate reduction against renal I/R injury. Copyright (C) 2011 S. Karger AG, Basel
引用
收藏
页码:114 / 119
页数:6
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