Ronca-Testoni S, Hrelia S, Hakim G, Ronca G, Rossi C A
Boll Soc Ital Biol Sper. 1984 Apr 30;60(4):713-9.
Some smooth muscle relaxant drugs devoid of anticholinergic action have been tested for their interaction with calmodulin, calmodulin-stimulated cyclic nucleotide phosphodiesterase activity, and uterine membrane binding sites for nitrendipine and adenosine. The myolytic activity of octylonium bromide and pinaverium bromide may be due to their interaction with calmodulin-dependent systems. Trimebutine maleate does not bind either to calmodulin or to nitrendipine and adenosine receptors. Tiropramide has no effect on calmodulin-dependent systems and on Ca2+ channels but it shows a competition for the A2-type adenosine receptors.
已对一些无抗胆碱能作用的平滑肌松弛药物进行了测试,以研究它们与钙调蛋白、钙调蛋白刺激的环核苷酸磷酸二酯酶活性以及尼群地平和腺苷的子宫膜结合位点之间的相互作用。溴化奥替溴铵和匹维溴铵的溶肌活性可能归因于它们与钙调蛋白依赖性系统的相互作用。马来酸曲美布汀既不与钙调蛋白结合,也不与尼群地平和腺苷受体结合。替罗普肽对钙调蛋白依赖性系统和Ca2+通道没有影响,但它对A2型腺苷受体表现出竞争作用。