Pöpping S, Mruck S, Fischer Y, Kulsch D, Ionescu I, Kammermeier H, Rose H
Institute of Physiology, Medical Faculty, Rheinisch-Westfälische Technische Hochschule Aachen, Germany.
Am J Physiol. 1996 Jul;271(1 Pt 2):H357-64. doi: 10.1152/ajpheart.1996.271.1.H357.
In the present study the effects of the novel cardiotonic agent EMD-57033 on contraction and energetic demand of isolated, electrically stimulated cardiomyocytes were investigated and compared with the effects of enhancement of extracellular calcium and of the beta-mimetic isoproterenol. In a specially designed setup [H. Rose, K.H. Strotmann, S. Pöpping, Y. Fischer, D. Kulsch, and H. Kammermeier. Am. J. Physiol. 261 (Heart Circ. Physiol. 30): H1329-H1334, 1991] parameters of contractile behavior and metabolic demand (O2 consumption) of isolated cardiac myocytes were measured. For a given enhancement of contractile performance (cell shortening) the increase in energetic demand (VO2) after application of EMD-57033 were markedly lower than on treatment with elevated extracellular Ca2+ concentration or with isoproterenol. This economization of positive inotropic effects was proposed to be due to two factors. First, stimulation-related ion cycling was only slightly enhanced with marked increase in contraction amplitude after application of EMD-57033. Second, calcium sensitization reflected in a leftward shift of the calcium concentration needed for half-maximum force development could be interpreted to be mediated by modulation of the cross-bridge dynamics of the myofilaments, where reduction of the switch-off rate of the cross bridges and prolongation of their force-generating states were presumed to be involved. Lowered pH (7.0) decreased economy of contraction. EMD-57033 restored contraction amplitude and economy of contraction at lowered pH.
在本研究中,研究了新型强心剂EMD-57033对分离的、电刺激的心肌细胞收缩和能量需求的影响,并与细胞外钙增强和β-拟似剂异丙肾上腺素的作用进行了比较。在一个专门设计的装置中[H. Rose, K.H. Strotmann, S. Pöpping, Y. Fischer, D. Kulsch, and H. Kammermeier. Am. J. Physiol. 261 (Heart Circ. Physiol. 30): H1329-H1334, 1991],测量了分离心肌细胞的收缩行为和代谢需求(氧气消耗)参数。对于给定的收缩性能增强(细胞缩短),应用EMD-57033后能量需求(VO2)的增加明显低于细胞外Ca2+浓度升高或使用异丙肾上腺素治疗时。正性肌力作用的这种节约被认为是由于两个因素。首先,应用EMD-5703后,刺激相关的离子循环仅略有增强,而收缩幅度显著增加。其次,反映在产生最大力量一半所需钙浓度向左移动的钙致敏作用,可以解释为是由肌丝横桥动力学的调节介导的,其中推测涉及横桥关闭速率的降低和其产生力量状态的延长。降低pH(7.0)会降低收缩的经济性。EMD-57033在降低pH时恢复了收缩幅度和收缩的经济性。