Hertz F, Cloarec A
Int J Immunopharmacol. 1986;8(7):747-54. doi: 10.1016/0192-0561(86)90011-1.
The effects of four calcium entry blockers (diltiazem, nifedipine, mesudipine and verapamil) were studied on antigen-induced bronchoconstriction in sensitized rats and histamine release from rat mast cells, in comparison with compounds frequently used in atopic patients (theophylline, isoproterenol, disodium cromoglycate, ketotifen and clemastine). The four Ca2+ entry blockers produced a dose-related inhibition of the IgE-dependent bronchoconstriction in rat whereas the other drugs exhibited a weak effect or even were inactive. 48/80-induced histamine release was antagonized by nifedipine, verapamil and ketotifen. On the contrary, diltiazem, mesudipine, theophylline, isoproterenol, disodium cromoglycate and clemastine were not able to interfere with this release process. These data may suggest an important role of both extra- and intracellular calcium in such phenomena.
研究了四种钙通道阻滞剂(地尔硫䓬、硝苯地平、美舒地尔平和维拉帕米)对致敏大鼠抗原诱导的支气管收缩以及大鼠肥大细胞组胺释放的影响,并与特应性患者常用的化合物(茶碱、异丙肾上腺素、色甘酸钠、酮替芬和氯马斯汀)进行了比较。四种Ca2+通道阻滞剂对大鼠IgE依赖性支气管收缩产生剂量相关的抑制作用,而其他药物作用较弱甚至无活性。硝苯地平、维拉帕米和酮替芬可拮抗48/80诱导的组胺释放。相反,地尔硫䓬、美舒地尔平、茶碱、异丙肾上腺素、色甘酸钠和氯马斯汀不能干扰这一释放过程。这些数据可能表明细胞外和细胞内钙在这些现象中都起着重要作用。