Manabe M, Motomura S, Kumazawa T, Ookawa I, Oguchi T
Department of Anesthesiology, Yamanashi Medical College, Yamanashi, Japan.
J Anesth. 1988 Sep 1;2(2):202-6. doi: 10.1007/s0054080020202.
The positive inotropic and chronotropic potencies of pancuronium (Pc) and vecuronium (Vc) were compared with developed tension of the isolated papillary muscle (DT) and sinoatrial rate of the sinoatrial node preparation (SAR). Both Pc and Vc caused dose-dependent positive inotropic and chronotropic effects. Pc showed much more potent effect than Vc on DT (0.1, 0.3 mg; P << 0.05) or SAR (0.03, 0.1, 0.3 mg; P << 0.05). DT and SAR were increased by Pc and Vc, and the increase in DT was inhibited by propranolol or tetrodotoxin. These results suggest that the cardiac effects of Pc or Vc may be mediated by release of norepinephrine from the synpathetic nerve endings.
将泮库溴铵(Pc)和维库溴铵(Vc)的正性肌力和变时性效力与离体乳头肌的舒张张力(DT)和窦房结标本的窦房率(SAR)进行了比较。Pc和Vc均产生剂量依赖性的正性肌力和变时性作用。在DT方面(0.1、0.3mg;P << 0.05)或SAR方面(0.03、0.1、0.3mg;P << 0.05),Pc比Vc显示出更强的作用。Pc和Vc使DT和SAR增加,且DT的增加被普萘洛尔或河豚毒素抑制。这些结果表明,Pc或Vc的心脏效应可能是由交感神经末梢去甲肾上腺素的释放介导的。