Ruiz F, Hernández J, Pérez D
Department of Pharmacology, University of Murcia Medical School, Spain.
Arch Int Pharmacodyn Ther. 1989 May-Jun;299:77-85.
The effect of diazepam on nomotopic cardiac automaticity was examined in the spontaneously beating isolated right atria of the rat. We also investigated whether "central"- or "peripheral"-type benzodiazepine receptors are involved and studied the role of calcium and adenosine in the possible effect of diazepam by the interaction of this drug with either GABA, picrotoxin, RO 15-1788, PK 11195, diltiazem or theophylline. Diazepam (400-500 microM) completely abolished atrial automaticity. This effect was not modified by the presence of either RO 15-1788 (30 microM), PK 11195 (0.1 microM), GABA (100 microM), picrotoxin (7 microM), theophylline (5 microM), diltiazem (0.6 microM) or hypercalcic media (3.6 mM). It is concluded that the diazepam-induced reduction of atrial frequency is mediated neither by "central"- nor "peripheral"- type benzodiazepine receptors, adenosine or calcium and could be due to a nonspecific interaction with the cell membrane.
在地鼠自发跳动的离体右心房中研究了地西泮对异位性心脏自律性的影响。我们还研究了“中枢”型或“外周”型苯二氮䓬受体是否参与其中,并通过该药物与γ-氨基丁酸、匹鲁卡品、RO 15-1788、PK 11195、地尔硫䓬或茶碱的相互作用,研究了钙和腺苷在地西泮可能作用中的作用。地西泮(400 - 500微摩尔)完全消除了心房自律性。RO 15-1788(30微摩尔)、PK 11195(0.1微摩尔)、γ-氨基丁酸(100微摩尔)、匹鲁卡品(7微摩尔)、茶碱(5微摩尔)、地尔硫䓬(0.6微摩尔)或高钙培养基(3.6毫摩尔)的存在均未改变这种作用。得出的结论是,地西泮诱导的心房频率降低既不是由“中枢”型也不是由“外周”型苯二氮䓬受体、腺苷或钙介导的,可能是由于与细胞膜的非特异性相互作用。