Akera T, Hirai M, Oka T
Eur J Pharmacol. 1979 Dec 7;60(2-3):189-98. doi: 10.1016/0014-2999(79)90218-8.
Factors that determine the interaction of ouabain with the positive inotropic receptor were examined in isolated perfused guinea-pig hearts. The hearts were exposed to ouabain during a perfusion with a modified Krebs-Henseleit solution. The interaction of ouabain with the inotropic receptors under those conditions was estimated by subsequently perfusing the heart with a regular Krebs-Henseleit solution and monitoring the resting and developed tension. Ouabain failed to cause an increase in the force of contraction when the cardiac tissue was exposed to this agent in the absence of Na+ and Ca2+ either in the presence of a low or high concentration of K+. The absence of Ca2+ or the lack of contraction was not responsible for the failure of ouabain to interact with the inotropic receptor, since the exposure of cardiac tissue to ouabain in a Ca,+-free medium containing Na+ resulted in a development of the positive inotropic effect. Thus, ouabain does not interact with its inotropic receptor in the absence of Na+. The properties of the ouabain-receptor interaction resemble those of ouabain binding to Na+, K+-ATPase. In addition, ouabain increases the mobility of superficially bound Ca2+.
在离体灌注豚鼠心脏中研究了决定哇巴因与正性肌力受体相互作用的因素。在用改良的克雷布斯 - 亨泽莱特溶液灌注期间,使心脏暴露于哇巴因。通过随后用常规克雷布斯 - 亨泽莱特溶液灌注心脏并监测静息张力和收缩张力来评估在这些条件下哇巴因与正性肌力受体的相互作用。当心脏组织在低浓度或高浓度钾存在的情况下,在无钠和钙的情况下暴露于该试剂时,哇巴因未能引起收缩力增加。缺乏钙或缺乏收缩并非哇巴因未能与正性肌力受体相互作用的原因,因为在含有钠的无钙培养基中将心脏组织暴露于哇巴因会导致正性肌力作用的产生。因此,在没有钠的情况下,哇巴因不会与其正性肌力受体相互作用。哇巴因 - 受体相互作用的特性类似于哇巴因与钠钾 - ATP酶结合的特性。此外,哇巴因增加了表面结合钙的流动性。