Knudsen T, Ferjan I, Johansen T
Department of Pharmacology, Odense University, Denmark.
FEBS Lett. 1993 Apr 26;321(2-3):127-31. doi: 10.1016/0014-5793(93)80092-9.
Rat peritoneal mast cells were used to study the effects of digitalis glycosides on potassium uptake and histamine release induced by compound 48/80, substance P and egg-albumin (immunological release). In the absence of calcium all glycosides inhibited potassium uptake. Ouabain and digoxin enhanced the histamine release while digitoxigenin either had no effect or was slightly inhibitory. In the presence of calcium, the glycosides only affected potassium uptake and histamine release slightly. In the presence of lithium or lanthanum the enhancement of the histamine release was counteracted. Hydrophilic digitalis glycosides seem to enhance histamine release secondary to an increase in intracellular sodium. Lipophilic glycosides have no effect on the release.
采用大鼠腹膜肥大细胞研究洋地黄苷对由化合物48/80、P物质和卵清蛋白诱导的钾摄取及组胺释放(免疫释放)的影响。在无钙情况下,所有苷类均抑制钾摄取。哇巴因和地高辛增强组胺释放,而洋地黄毒苷要么无作用,要么有轻微抑制作用。在有钙情况下,苷类仅对钾摄取和组胺释放有轻微影响。在有锂或镧存在时,则可抵消组胺释放的增强作用。亲水性洋地黄苷似乎继发于细胞内钠增加而增强组胺释放。亲脂性苷类对释放无作用。