Grund E, Müller-Ruchholtz E R, Lapp E R, Lösch H M, Lochner W
Arzneimittelforschung. 1978;28(9):1624-8.
The effect of nitroglycerin, N-carboxy-3-morpholino-sydnonimine-ethylester (molsidomine, Corvaton), and its metabolite 3-morpholinosydnonimine upon the peripheral circulation was investigated in 38 dogs with cardio-pulmonary bypass. The three compounds increased the integrated systemic venous blood volume and decreased the mean arterial pressure. The time course of the action of nitroglycerin was different from that of molsidomine: The arterial and venous effects of nitroglycerin began immediately after the injection was started, reached a maximum, and had disappeared after 7 min. The effects of molsidomine started later and showed no tendency to decrease during the observation period of 30 min. When referred to the same decrease in arterial blood pressure, molsidomine acted more strongly upon the systemic venous bed than did nitroglycerin. The arterial and venous effects of the molsidomine metabolite could be antagonized by a dopamine infusion. It is concluded that the hypotensive effect of the three compounds observed in the intact circulation is due to the diminuation of peripheral resistance as well as to the dilatation of the systemic venous bed. The dilatation of the veins effects a decrease in the venous return and thereby in the cardiac output and the arterial pressure. It can be concluded that the antianginal effect of the three compounds is not only due to the diminution of the afterload of the heart; the diminution of the heart; the diminution of the preload also represents an important component of action.
在38只接受体外循环的犬身上研究了硝酸甘油、N-羧基-3-吗啉代西多胺乙酯(吗多明,可洛万)及其代谢产物3-吗啉代西多胺对外周循环的影响。这三种化合物均增加了体循环静脉血容量总和并降低了平均动脉压。硝酸甘油和吗多明的作用时程不同:硝酸甘油的动静脉效应在注射开始后立即出现,达到最大值,并在7分钟后消失。吗多明的效应出现较晚,且在30分钟的观察期内无下降趋势。当动脉血压下降幅度相同时,吗多明对体循环静脉床的作用比硝酸甘油更强。吗多明代谢产物的动静脉效应可被多巴胺输注拮抗。得出结论:在完整循环中观察到的这三种化合物的降压作用是由于外周阻力降低以及体循环静脉床扩张。静脉扩张导致静脉回流减少,进而使心输出量和动脉压降低。可以得出结论,这三种化合物的抗心绞痛作用不仅归因于心脏后负荷的降低;心脏前负荷的降低也是其作用的重要组成部分。