Stephen P M, Marks B H, Hollander P B
Arch Int Pharmacodyn Ther. 1976 Nov;224(1):43-54.
The effects of 10(-7) and 10(-6) M digitoxin, and some of its metabolites, digitoxigenin-bis-digitoxoside, digitoxigenin-mono-digitoxoside and digitoxigenin on the transmembrane potential and contractile characteristics of guinea-pig right ventricle strips were studied to define the role of the sugar side-chain in these cleavage products of digitoxin. Digitoxin and digitoxigenin produced their maximum inotropic responses, without induction of arrhythmias, at about 30 min. However, the bis and mono compounds produced arrhythmias within 12 min, so the inotropy recorded may not be the maximum response. Digitoxin with 3 sugar residues and the bis compound with 2 sugar residues produced a prolongation in the action potenital duration. In contrast, the mono compound with one sugar residue and the digitoxigenin with no sugar residue produced a shortening of the action potential duration. There may be a relationship between the number of sugar moieties and the action potential duration; digitoxin and its bis derivative increased the action potential duration and mono- and digitoxigenin decreased the action potential duration. There also appeared to be an unusual relationship between the number of sugar moieties and induction of arrhythmias; arrhythmogenicity occurred at the doses employed with only the bis- and mono-digitoxoside. Finally, there appeared to be no simple relationship between chemical structure and inotropic potency.
研究了10⁻⁷和10⁻⁶ M洋地黄毒苷及其部分代谢产物洋地黄毒苷元双洋地黄毒糖苷、洋地黄毒苷元单洋地黄毒糖苷和洋地黄毒苷元对豚鼠右心室条带跨膜电位和收缩特性的影响,以确定糖侧链在这些洋地黄毒苷裂解产物中的作用。洋地黄毒苷和洋地黄毒苷元在约30分钟时产生最大正性肌力反应,且未诱发心律失常。然而,双糖苷和单糖苷化合物在12分钟内诱发了心律失常,因此记录到的正性肌力作用可能不是最大反应。具有3个糖残基的洋地黄毒苷和具有2个糖残基的双糖苷化合物使动作电位持续时间延长。相反,具有1个糖残基的单糖苷化合物和无糖残基的洋地黄毒苷元使动作电位持续时间缩短。糖部分的数量与动作电位持续时间之间可能存在关系;洋地黄毒苷及其双衍生物增加动作电位持续时间,而单糖苷和洋地黄毒苷元则缩短动作电位持续时间。糖部分的数量与心律失常的诱发之间似乎也存在异常关系;在所使用的剂量下,只有双洋地黄毒糖苷和单洋地黄毒糖苷会诱发心律失常。最后,化学结构与正性肌力效力之间似乎没有简单的关系。