Sprgel W, Mitznegg P, Heim F
Arzneimittelforschung. 1977 Jul;27(7):1405-7.
The 10 mm muscle-strips from the guinea pig terminal ileum digitalis glycosides (0.4 microgram/ml beta-acetyl-digoxin or 0.5 microgram/ml k-strophanthin) induce contractions which are dose-dependently and reversibly prevented by the calcium antagonist N-(2-benzyl-ethyl)-N-(1-phenyl-ethyl)-amine hydrochloride (fendiline, Sensit) (0.01--1 microgram/ml). Therapeutic use of calcium antagonists for manifest symptoms of digitalis intoxication (diarrhoea, intestinal infarctions) is discussed as these symptoms may be caused by digitalis-induced increase of intracellular calcium ions.
取豚鼠回肠末端的10毫米肌条,洋地黄糖苷(0.4微克/毫升β-乙酰地高辛或0.5微克/毫升毒毛花苷K)可诱导其收缩,而钙拮抗剂N-(2-苄基乙基)-N-(1-苯乙基)胺盐酸盐(芬地林,Sensit)(0.01 - 1微克/毫升)可剂量依赖性且可逆地抑制这种收缩。文中讨论了使用钙拮抗剂治疗洋地黄中毒的明显症状(腹泻、肠梗死),因为这些症状可能是由洋地黄诱导的细胞内钙离子增加所引起的。