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

机译:伊伐布雷定对大鼠缺血再灌注所致肾脏损伤的剂量依赖性保护作用

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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.
机译:背景/目的:本研究旨在研究伊伐布雷定(一种心脏窦房结的特异性抑制剂)对大鼠肾脏缺血再灌注(I / R)损伤的剂量依赖性保护作用。方法:将大鼠分为六组:第一组,对照组;第二组。第2组,I / R(缺血60分钟,再灌注24小时);第3和第4组,0.6–6 mg / kg的伊伐布雷定;以及第5和第6组,假+ 0.6–6 mg / kg伊伐布雷定。在研究结束时,对肾脏组织中的丙二醛(MDA),超氧化物歧化酶(SOD),过氧化氢酶(CAT)和谷胱甘肽过氧化物酶含量进行了测定。还测定了血清尿素氮(BUN),肌酐(Cr)和白蛋白的水平。结果:与对照组相比,I / R组中的组织MDA水平明显升高,而SOD和CAT水平则较低。伊伐布雷定(0.6 mg / kg)治疗降低了MDA水平,并提高了SOD和CAT酶的活性。用6 mg / kg的伊伐布雷定治疗可进一步提高MDA水平,且未改善SOD或CAT活性。 I / R组的血清BUN和Cr水平显着升高。 I / R + 0.6 mg伊伐布雷定降低了升高的BUN和Cr水平。结论:这项研究表明,伊伐布雷定在降低心率方面对肾I / R损伤具有剂量依赖性反应。

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