Haustein K O
Basic Res Cardiol. 1984;79 Suppl:147-53. doi: 10.1007/978-3-642-72376-6_20.
The narrow therapeutic range of cardiac glycosides continually challenges chemists to synthetize new derivatives with improved therapeutic properties. One of the best investigated semi-synthetic glycosides is 16 alpha-gitoxin. Compared to ouabain and gitoxin, it produces positive inotropic effects on the isolated guinea-pig heart in a wider range of concentrations and causes less pronounced rhythmic disturbances. These results were confirmed by electrophysiological investigations in isolated fibres of the canine myocardium and of the Purkinje system, by investigations in the anaesthetized cat and dog and in healthy volunteers. The effects of various semi-synthetic compounds (e.g. actodigin, ASI-222) are described and possibilities to trigger these effects are discussed. Of some significance seem to be differences in the structure of the (Na+ + K+)-ATPase system of different tissues, e.g. the working muscle and the Purkinje system of the heart, as well as differences due to the formation and dissociation of the glycoside-enzyme complex. The significance of K+, Ca2+ and of several pharmacokinetic parameters (e.g. the volume of distribution) for these reactions are briefly discussed.
强心苷狭窄的治疗窗持续促使化学家合成具有改善治疗特性的新衍生物。研究得最充分的半合成糖苷之一是16α-吉托辛。与哇巴因和吉托辛相比,它在更宽的浓度范围内对离体豚鼠心脏产生正性肌力作用,且引起的节律紊乱不太明显。这些结果在犬心肌和浦肯野系统的离体纤维电生理研究、麻醉猫和犬以及健康志愿者的研究中得到了证实。描述了各种半合成化合物(如阿克多苷、ASI-222)的作用,并讨论了引发这些作用的可能性。不同组织(如工作肌肉和心脏浦肯野系统)的(Na+ + K+)-ATP酶系统结构差异,以及糖苷-酶复合物形成和解离导致的差异似乎具有一定意义。简要讨论了K+、Ca2+以及几个药代动力学参数(如分布容积)对这些反应的重要性。