Nakajima T, Kaneshiro S, Yatabe Y, Azumi T, Iwasaki H
Arch Int Pharmacodyn Ther. 1979 Sep;241(1):153-64.
Effect of diazepam on the AV nodal conductivity was studied using a direct perfusion technique of the canine AV node artery in situ. As compared to acetylcholine which induced a rapid onset of third degree AV block with prompt recovery, diazepam injected into the AV node artery in doses from 300 micrograms to 3 mg elicited first to third degree AV blocks of longer duration following gradual prolongation of PR interval. The response was not affected by bilateral vagotomy and sympathectomy. Pretreatment of the AV node with hexamethonium or atropine also failed to modify the diazepam-induced AV blocks. Thus, diazepam seemed to suppress conductivity of the AV node by a direct action. The AV nodal tachycardia induced by infusion of norepinephrine was readily antagonized by a single injection of diazepam, but norepinephrine failed to reverse the AV block induced by diazepam infusion.
采用犬房室结动脉原位直接灌注技术,研究了地西泮对房室结传导性的影响。与乙酰胆碱相比,乙酰胆碱可迅速诱发三度房室传导阻滞并迅速恢复,向房室结动脉注射剂量为300微克至3毫克的地西泮后,随着PR间期逐渐延长,会引发持续时间更长的一度至三度房室传导阻滞。该反应不受双侧迷走神经切断术和交感神经切除术的影响。用六甲铵或阿托品对房室结进行预处理也未能改变地西泮诱导的房室传导阻滞。因此,地西泮似乎通过直接作用抑制房室结的传导性。单次注射地西泮可轻易拮抗由去甲肾上腺素输注诱发的房室结性心动过速,但去甲肾上腺素未能逆转由地西泮输注诱导的房室传导阻滞。