Chiba S
Arch Int Pharmacodyn Ther. 1977 Jan;225(1):104-13.
In the isolated, blood-perfused canine atrium preparations, procaine given into the cannulated sinus node artery induced frequently significantly positive chronotropic and inotropic effects at a dose level of 30-1000 microng. Above a dose of 100 microng, initially brief negative chronotropic and inotropic effects were usually observed. Procaine-induced negative effects were not blocked by an adequate dose level of atropine. Procaine-induced positive effects were inhibited by treatment with propranolol but not modified by tetrodotoxin or desmethylimipramine. Procaine suppressed acetylcholine-induced negative chronotropic and inotropic effects. On the other hand, procaine did not block norepinephrine-induced positive inotropic and chronotropic effects. From these results, it is concluded that procaine may have sympathomimetic and atropine-like properties.
在离体、血液灌注的犬心房制备物中,将普鲁卡因注入插管的窦房结动脉,在剂量为30 - 1000微克时,常常会产生显著的正性变时和变力作用。剂量超过100微克时,最初通常会观察到短暂的负性变时和变力作用。普鲁卡因引起的负性作用不能被适当剂量的阿托品阻断。普鲁卡因引起的正性作用可被普萘洛尔抑制,但不受河豚毒素或去甲丙咪嗪影响。普鲁卡因可抑制乙酰胆碱引起的负性变时和变力作用。另一方面,普鲁卡因不能阻断去甲肾上腺素引起的正性变力和变时作用。从这些结果可以得出结论,普鲁卡因可能具有拟交感神经和类似阿托品的特性。