Goto A, Yamada K, Yagi N, Hui C, Nagoshi H, Sasabe M, Yoshioka M
Second Department of Internal Medicine, Faculty of Medicine, University of Tokyo, Japan.
J Cardiovasc Pharmacol. 1993;22 Suppl 2:S58-9. doi: 10.1097/00005344-199322002-00019.
We isolated two candidates for endogenous digitalis-like factors from human urine based on the inhibition of [3H]ouabain binding to intact human erythrocytes. The more-polar ouabain-displacing compound-1 (ODC-1) closely resembled ouabain in biological, physicochemical, and chromatographic properties. Moreover, anti-ouabain IgG dose-dependently neutralized the action of ODC-1. The less-polar ODC-2 behaved identically to digoxin in three analytical high-performance liquid chromatography and thin layer chromatography systems. Fast atom bombardment mass spectrum and proton nuclear magnetic resonance spectrum supported the notion that ODC-2 may be indistinguishable from digoxin. The possibility that substances quite similar to cardenolides are synthesized in the mammalian body must be seriously considered.
基于[3H]哇巴因与完整人红细胞结合的抑制作用,我们从人尿中分离出两种内源性洋地黄样因子的候选物。极性较强的哇巴因置换化合物-1(ODC-1)在生物学、物理化学和色谱性质方面与哇巴因非常相似。此外,抗哇巴因IgG能剂量依赖性地中和ODC-1的作用。极性较弱的ODC-2在三种分析型高效液相色谱和薄层色谱系统中的行为与地高辛相同。快原子轰击质谱和质子核磁共振谱支持ODC-2可能与地高辛无法区分的观点。必须认真考虑哺乳动物体内合成与强心甾类非常相似的物质的可能性。