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Anti-arrhythmic effects of kappa-opioid receptor and its changes in ischemia and reperfusion.

机译:κ阿片受体的抗心律失常作用及其在缺血和再灌注中的变化。

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BACKGROUND: It remains unclear whether the kappa-opioid receptor (kappa-OR) is altered during ischemia and reperfusion. Therefore, the present study was designed to investigate changes in the kappa-OR. Additionally, the anti-arrhythmic effect induced by kappa-OR stimulation was also determined during ischemia and reperfusion (I/R). METHODS: Rats were randomly divided into different groups according to two experimental protocols. The anti-arrhythmic effects of U50,488H, a selective kappa-OR agonist, in an I/R model of 15-min ischemia were studied followed by 15 min of reperfusion. The content of kappa-OR mRNA and protein were measured by RT-PCR and Western blotting techniques in an I/R model of 30-min ischemia followed by 360 min of reperfusion. RESULTS: Limited numbers of premature ventricular contractions (PVCs) were revealed in the control group. Administration of U50,488H in the control group had no effect on occurrence of PVCs. Incidence of arrhythmia in the I/R group was significantly increased. Treated with U50,488H in the I/R group, the incidence of arrhythmia was significantly reduced. With prior use of nor-BNI, a selective kappa-OR antagonist, the anti-arrhythmic effect of U50,488H was completely blocked. Compared with the control group, the content of kappa-OR mRNA and the density of kappa-OR protein increased significantly at 0 min, 60 min, and 180 min during reperfusion. CONCLUSIONS: The present study provides evidence for the first time that the expressions of kappa-OR mRNA and protein are upregulated in the heart of I/R rats. This alteration may produce a strengthened anti-arrhythmic effect upon kappa-OR stimulation during I/R.
机译:背景:尚不清楚缺血和再灌注过程中κ阿片受体(kappa-OR)是否发生改变。因此,本研究旨在调查kappa-OR的变化。此外,在缺血和再灌注(I / R)期间还确定了由κ-OR刺激引起的抗心律不齐作用。方法:根据两种实验方案将大鼠随机分为不同的组。研究了U50,488H(一种选择性κ-OR激动剂)在缺血15分钟的I / R模型中的抗心律不齐作用,然后进行了15分钟的再灌注。通过RT-PCR和Western blotting技术,在缺血30分钟,再灌注360分钟的I / R模型中测量κ-ORmRNA和蛋白质的含量。结果:在对照组中发现了数量有限的室性早搏(PVC)。对照组服用U50,488H对PVC的发生没有影响。 I / R组心律失常的发生率显着增加。 I / R组用U50,488H治疗,心律不齐的发生率显着降低。在事先使用选择性kappa-OR拮抗剂nor-BNI的情况下,U50,488H的抗心律失常作用被完全阻断。与对照组相比,再灌注0、60、180min时κ-ORmRNA的含量和κ-OR蛋白的密度显着增加。结论:本研究首次为I / R大鼠心脏中kappa-OR mRNA和蛋白的表达上调提供了证据。在I / R期间,这种改变可能会对κ-OR刺激产生增强的抗心律不齐作用。

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