Brown L, Erdmann E
Arzneimittelforschung. 1984;34(2):204-8.
The effects of ouabain, dihydroouabain and 3 alpha-methyldigitoxigenin glucoside on force of contraction and 86Rb+-uptake were measured in contracting guinea pig left atria. Dihydroouabain and 3 alpha-methyldigitoxigenin glucoside were both about 40 times less potent than ouabain. All compounds gave approximately the same maximal increase in force of contraction. The results gave no evidence that either dihydroouabain or 3 alpha-methyldigitoxigenin glucoside has a greater therapeutic index than ouabain. All compounds showed similar effect on 86Rb+-uptake (no significant change at positive inotropic concentrations, significantly decreased 86Rb+-uptake only at toxic concentrations). These results imply that these three compounds have a similar mechanism of action.
在豚鼠离体左心房收缩实验中,测定了哇巴因、双氢哇巴因和3α-甲基洋地黄毒苷对收缩力和86Rb+摄取的影响。双氢哇巴因和3α-甲基洋地黄毒苷的效力均约为哇巴因的1/40。所有化合物使收缩力增加的最大值大致相同。结果表明,双氢哇巴因和3α-甲基洋地黄毒苷的治疗指数并不比哇巴因更高。所有化合物对86Rb+摄取的影响相似(正性肌力浓度下无显著变化,仅在中毒浓度下86Rb+摄取显著降低)。这些结果提示,这三种化合物具有相似的作用机制。