Szekeres L, Udvary E, Végh A
Br J Pharmacol. 1987 May;91(1):127-37. doi: 10.1111/j.1476-5381.1987.tb08991.x.
The effects of nifedipine were studied in a model of local myocardial ischaemia, comprising anaesthetized thoracotomized dogs in which a critical constriction of the left circumflex coronary artery (LCX) was combined with sudden occlusion of the left anterior descending coronary artery (LAD). Since more than one coronary artery is involved in ischaemic heart disease, the model seems to reflect the clinical situation very closely. In this model, infusion of 1 microgram kg-1 min-1 nifedipine increased myocardial blood flow within the stenosed area served by the LCX as well as in the myocardial region supplied by the LAD, mainly in the subepicardium. Accordingly, the drug reduced ischaemic ST-segment elevation only in the epicardium. It is suggested that nifedipine directed flow to the sub-epicardium of the ischaemic area by improving the collateral circulation. This redistribution of flow resulted in a decrease in the endo/epicardial flow ratio. Nifedipine did not change the inhomogeneity of electrical activation indicating that it has no effect on the ischaemia-induced conduction delay. At the same time nifedipine was not able to reduce either the number of extrasystoles appearing in the early postocclusion and reperfusion phase or the incidence of ventricular fibrillation occurring mainly during reperfusion.
在局部心肌缺血模型中研究了硝苯地平的作用,该模型包括麻醉开胸犬,其中左旋冠状动脉(LCX)的临界狭窄与左前降支冠状动脉(LAD)的突然闭塞相结合。由于缺血性心脏病涉及不止一条冠状动脉,该模型似乎非常接近地反映了临床情况。在该模型中,以1微克·千克⁻¹·分钟⁻¹的速度输注硝苯地平可增加LCX供血的狭窄区域以及LAD供血的心肌区域(主要是心外膜下)的心肌血流量。因此,该药物仅减少了心外膜的缺血性ST段抬高。提示硝苯地平通过改善侧支循环将血流导向缺血区域的心外膜下。这种血流重新分布导致心内膜/心外膜血流比值降低。硝苯地平未改变电激活的不均匀性,表明它对缺血诱导的传导延迟没有影响。同时,硝苯地平既不能减少闭塞后早期和再灌注阶段出现的早搏数量,也不能降低主要在再灌注期间发生的心室颤动的发生率。