Satoh H, Azumi T, Yoshida T, Nakajima T
Arch Int Pharmacodyn Ther. 1979 Oct;241(2):307-15.
Effect of procaine on the SA node of the dog heart was studied in situ using a selective perfusion technique of the SA node artery. Procaine in doses from 100 mug to 1 mg produced a sinus depression followed by a prolonged phase of the increased heart rate. The depression became more prominent with increasing the dose. The threshold dose for inducing the tachycardiac response was lower, but the sinus acceleration was not proportional to the dose. The initial depression was not affected by atropine, whereas the occurrence of the stimulatory phase was inhibited by prior administration of propranolol or tetrodotoxin into the SA node artery or in the reserpine-treated dogs. The results indicate that the biphasic response is induced by a direct negative chronotropic action of procaine on the SA node and by an indirect effect mediated by an interaction with the postganglionic adrenergic nerves.
采用窦房结动脉选择性灌注技术,在体研究了普鲁卡因对犬心脏窦房结的作用。剂量为100微克至1毫克的普鲁卡因可引起窦性抑制,随后出现心率增加的延长阶段。随着剂量增加,抑制作用变得更加明显。诱发心动过速反应的阈剂量较低,但窦性加速与剂量不成比例。初始抑制不受阿托品影响,而在窦房结动脉内预先给予普萘洛尔或河豚毒素或在利血平处理的犬中,刺激阶段的出现受到抑制。结果表明,双相反应是由普鲁卡因对窦房结的直接负性变时作用以及与节后肾上腺素能神经相互作用介导的间接效应所诱发的。