Honerjäger P
Institut für Pharmakologie und Toxikologie Technischen Universität München, Federal Republic of Germany.
Am Heart J. 1991 Jun;121(6 Pt 2):1939-44. doi: 10.1016/0002-8703(91)90828-6.
The bipyridine phosphodiesterase III inhibitors amrinone and milrinone form a new class of positive inotropic vasodilator agents that are beneficial in the treatment of acute or decompensated heart failure. These agents inhibit the intracellular hydrolysis of cyclic adenosine monophosphate, thereby promoting cyclic adenosine monophosphate--catalyzed phosphorylation of sarcolemmal calcium channels and activating the calcium pump. They have a wider therapeutic index than do the cardiac glycosides. They also have vasodilator and lusitropic actions and are devoid of the central stimulant actions that narrow the therapeutic index of theophylline and other methylxanthines. Receptor down-regulation, which curtails the inotropic efficacy of beta-adrenoreceptor agonists, does not compromise the efficacy of phosphodiesterase inhibitors. The effectiveness of these new agents is, however, dependent on some degree of basal adenylate cyclase activity.
双吡啶磷酸二酯酶III抑制剂氨力农和米力农构成了一类新型的正性肌力血管扩张剂,对急性或失代偿性心力衰竭的治疗有益。这些药物抑制细胞内环磷酸腺苷的水解,从而促进环磷酸腺苷催化的肌膜钙通道磷酸化并激活钙泵。它们比强心苷具有更宽的治疗指数。它们还具有血管扩张和变时性作用,且没有像茶碱和其他甲基黄嘌呤那样会缩小治疗指数的中枢兴奋作用。受体下调会降低β肾上腺素能受体激动剂的正性肌力作用,但不会影响磷酸二酯酶抑制剂的疗效。然而,这些新药的有效性在一定程度上依赖于基础腺苷酸环化酶的活性。