Blockers of sulfonylureas receptor 1 subunits may lead to cardiac protection against isoprenaline-induced injury in obese rats

被引:2
作者
Bao, Yige
Sun, Xiaodong [1 ]
Yu, Yerong [1 ]
Lu, Shuyuan
Wu, Yang
机构
[1] W China Hosp, Dept Endocrinol & Metab, Chengdu, Peoples R China
关键词
Obesity; Ischemic injury; SUR1; Nonselective cation channel; K-ATP channel; MYOCARDIAL ISCHEMIA/REPERFUSION INJURY; SENSITIVE POTASSIUM CHANNELS; NONSELECTIVE CATION CHANNEL; DIABETIC-PATIENTS; ATP-CHANNELS; INFARCTION; MORTALITY; ISOPROTERENOL; REPERFUSION; ARRHYTHMIAS;
D O I
10.1016/j.ejphar.2012.06.039
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Recent studies have found that blockers of sulfonylureas receptor 1(SUR1) might have cardiac ischemic protective effects. We evaluated the effects of a selective SUR1 blocker gliclazide on cardiac function and arrhythmia after isoprenaline-induced myocardial injury in obese rats. Diet-induced obese rats received isoprenaline or saline shots subcutaneously. Gliclazide or saline was given q12h for 48 h to rats received isoprenaline. We measured ECG and hemodynamic parameters and collected blood samples for CK-MB, glucose and lipid profile determination, and then harvested hearts for water content, histological and immunohistochemical analysis and infarct size measurements. The obese rats' hearts receiving isoprenaline-induced myocardial injury showed up-regulated SUR-1 expression in the peri-microvascular area. Obese rats receiving gliclazide lavage had less severe arrhythmia (ASI: 4.00 +/- 0.61 vs. 2.14 +/- 0.39, P<0.05) and myocardial edema (water percentage: 85.16 +/- 0.46% vs. 81.56 +/- 0.57%, P<0.05). Less infarct size (47.6 +/- 12.8% vs. 32.7 +/- 9.1%, P<0.05) and improved diastolic function (LVEDP: 6.86 +/- 0.85% vs. 2.51 +/- 1.09%, P<0.05; -(dp/dt)(max): -1663.6 +/- 387.91 mmHg/s vs. -2834.8 +/- 290.76 mmHg/s, P<0.05) were also observed in rats receiving gliclazide lavage. Blocking of the SUR1 thus exerts a protective effect on the isoprenaline-induced myocardial injury in obese rats. That SUR1 blocker leads to ischemic protection suggesting a critical biological role of SUR1 in regulating the function of the cardiovascular system than previously recognized under pathophysiological conditions. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:142 / 148
页数:7
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