首页> 外文期刊>British Journal of Pharmacology >Differential effects of OPC-18790, amrinone and dobutamine on cardiac function and energy metabolism in the guinea-pig isolated ischaemic heart
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Differential effects of OPC-18790, amrinone and dobutamine on cardiac function and energy metabolism in the guinea-pig isolated ischaemic heart

机译:OPC-18790,氨力农和多巴酚丁胺对豚鼠离体缺血心脏心脏功能和能量代谢的差异作用

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摘要

1. The effects of OPC-18790, a novel positive inotropic agent, on cardiac function and myocardial energy metabolism in the guinea-pig isolated heart with ischaemia were studied by ~(31)P-magnetic resonance spectroscopy (MRS) and compared with those of amrinone and dobutamine. 2. Cardiac ischaemia was induced by intracoronary infusion of 15 μm microspheres to reduce coronary perfusion flow (CPF) by 50%. Microsphere embolisation caused a 40% decrease in left ventricular systolic pressure (LVSP), cardiac contractility measured by peak of ventricular pressure development (LVdP/dt) and slightly reduced heart rate. There was also a decrease in ATP and creatine phosphate (PCr) by 20%, an increase in inorganic phosphate (P_i) by 25% and an acidic shift of intracellular pH in the ischaemic heart. 3. In the ischaemic heart, OPC-18790, amrinone and dobutamine were applied at concentrations which increased LVdP/dt by about 60%. These compounds increased LVP by 15% to 30% and increased CPF by about 10%. Amrinone and dobutamine but not OPC-18790 increased heart rate. When these drugs produced the haemodynamic changes described above, amrinone and dobutamine reduced ATP and PCr, increased P_i and produced further intracellular acidosis, whereas, OPC-18790 did not change these parameters. 4. Cardiac pacing at 285 beats min~(-1) produced decreases in LVP, LVdP/dt and CPF by about 30%, 20%, 5%, respectively and an increase in P_i, decreases in PCr and ATP, and intracellular acidosis. 5. These results suggest that degradation of high energy phosphate compounds closely relates to increase in heart rate in the ischaemic heart. Positive inotropic agents without chronotropic action seem to be beneficial in support of the ischaemic heart.
机译:1.通过〜(31)P-磁共振波谱(MRS)研究了新型正性肌力药物OPC-18790对豚鼠离体缺血性心肌心脏功能和心肌能量代谢的影响,并与之进行了比较。氨力农和多巴酚丁胺。 2.冠状动脉内灌注15μm微球可诱发心脏缺血,可将冠状动脉灌注流量(CPF)降低50%。微球栓塞导致左心室收缩压(LVSP)降低40%,通过心室压力发展高峰(LVdP / dt)测得的心脏收缩力和心律轻微降低。在缺血心脏中,ATP和磷酸肌酸(PCr)降低了20%,无机磷酸(P_i)升高了25%,并且细胞内pH发生了酸性变化。 3.在缺血性心脏中,以增加LVdP / dt约60%的浓度使用OPC-18790,氨力农和多巴酚丁胺。这些化合物使LVP增加15%至30%,并使CPF增加约10%。氨力农和多巴酚丁胺可提高心律,但OPC-18790不会。当这些药物产生上述血液动力学变化时,氨力农和多巴酚丁胺会降低ATP和PCr,增加P_i并进一步导致细胞内酸中毒,而OPC-18790不会改变这些参数。 4.心脏起搏频率在285次/分左右(-1)可使LVP,LVdP / dt和CPF分别降低约30%,20%,5%,P_i升高,PCr和ATP降低以及细胞内酸中毒。 5.这些结果表明,高能磷酸盐化合物的降解与缺血心脏的心率增加密切相关。没有变时性作用的正性变力剂似乎有利于支持缺血性心脏。

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