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格列本脲对离体大鼠心脏缺血再灌注时室性心律失常和心脏功能的影响。

Effects of glibenclamide on ventricular arrhythmias and cardiac function in ischaemia and reperfusion in isolated rat heart.

作者信息

Bril A, Laville M P, Gout B

机构信息

SmithKline Beecham Laboratories Pharmaceutiques, Unité de Recherche, Saint Grégoire, France.

出版信息

Cardiovasc Res. 1992 Nov;26(11):1069-76. doi: 10.1093/cvr/26.11.1069.

Abstract

OBJECTIVE

The aim was to investigate the effects of glibenclamide, a specific blocker of the ATP sensitive potassium channel, on the incidence of ventricular arrhythmias and the functional changes occurring during myocardial ischaemia and reperfusion.

METHODS

Hearts (n = 10 per group) were obtained from male Wistar rats, weight 250-300 g. The study was performed in isolated Langendorff perfused rat hearts subjected to ligation of the left coronary artery and reperfusion. Because of the occurrence of arrhythmias, cardiac function was not evaluated during reperfusion. Glibenclamide (1 or 10 microM) was added to the perfusion solution before the coronary artery occlusion, during ischaemia or after reperfusion. In some experiments the incidence of various durations of ischaemia (5, 10, 15, and 30 min) was evaluated.

RESULTS

During the preischaemic period, glibenclamide induced a marked reduction in coronary flow, with a slight decrease in heart rate and left ventricular pressure. The ischaemia induced decrease in left ventricular pressure was markedly attenuated when glibenclamide was given before ischaemia. Thus the isovolumetric left ventricular pressure measured after 15 min ischaemia, which represents 59(SEM 6)% of the preischaemic value in the control group, was increased to 82(9) and 94(8)% in presence of glibenclamide (1 and 10 microM, p < 0.05 respectively). The effect was less pronounced when glibenclamide was added to the perfusion fluid during the ischaemic period. None of the hearts showed ventricular fibrillation during the ischaemic period. Glibenclamide (1 and 10 microM) did not reduce the incidence of reperfusion induced ventricular fibrillation. However, a defibrillatory action was observed since glibenclamide reduced the duration of ventricular fibrillation during reperfusion.

CONCLUSIONS

Glibenclamide may increase the probability of spontaneous termination of ventricular fibrillation and facilitate the restoration of the myocardial function during regional ischaemia.

摘要

目的

旨在研究ATP敏感性钾通道特异性阻滞剂格列本脲对室性心律失常发生率以及心肌缺血和再灌注期间发生的功能变化的影响。

方法

从体重250 - 300克的雄性Wistar大鼠获取心脏(每组10个)。该研究在离体Langendorff灌注的大鼠心脏上进行,使其经历左冠状动脉结扎和再灌注。由于心律失常的发生,在再灌注期间未评估心脏功能。在冠状动脉闭塞前、缺血期间或再灌注后,将格列本脲(1或10微摩尔)添加到灌注液中。在一些实验中评估了不同时长(5、10、15和30分钟)缺血的发生率。

结果

在缺血前期,格列本脲导致冠状动脉血流量显著减少,心率和左心室压力略有下降。当在缺血前给予格列本脲时,缺血诱导的左心室压力下降明显减弱。因此,缺血15分钟后测得的左心室等容压力,在对照组中占缺血前值的59(标准误6)%,在存在格列本脲(1和10微摩尔)时分别增加到82(9)%和94(8)%(p均<0.05)。当在缺血期间将格列本脲添加到灌注液中时,这种作用不太明显。在缺血期间,没有心脏出现心室颤动。格列本脲(1和10微摩尔)并未降低再灌注诱导的心室颤动发生率。然而,观察到一种除颤作用,因为格列本脲缩短了再灌注期间心室颤动的持续时间。

结论

格列本脲可能增加心室颤动自发终止的可能性,并有助于在局部缺血期间恢复心肌功能。

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