Rusy B F, Amuzu J K, Bosscher H A, Redon D, Komai H
Department of Anesthesiology, University of Wisconsin, Madison 53792.
Anesth Analg. 1990 Sep;71(3):275-8. doi: 10.1213/00000539-199009000-00010.
The effect of ketamine on myocardial contractile force was examined in rabbit papillary muscles in order to determine the underlying mechanism of action of the anesthetic. Ketamine HCl (20 and 40 mg/L) inhibited rested-state contractions that are dependent on the transsarcolemmal influx of Ca2+ for activation and reduced the upstroke velocity of the slow action potential, which reflects Ca2+ influx through the slow Ca2+ channel. On the other hand, ketamine had a relatively small effect on potentiated-state contractions and no effect on rapid cooling induced contractures, both of which are activated by the release of Ca2+ stored in the sarcoplasmic reticulum. These results suggest that ketamine inhibition of transsarcolemmal Ca2+ influx plays a major role in the negative inotropic action of the anesthetic.
为确定氯胺酮麻醉作用的潜在机制,研究了氯胺酮对兔乳头肌心肌收缩力的影响。盐酸氯胺酮(20和40mg/L)抑制依赖跨肌膜Ca2+内流激活的静息状态收缩,并降低慢动作电位的上升速度,这反映了Ca2+通过慢Ca2+通道的内流。另一方面,氯胺酮对增强状态收缩的影响相对较小,对快速冷却诱导的挛缩无影响,这两种情况均由肌浆网中储存的Ca2+释放激活。这些结果表明,氯胺酮对跨肌膜Ca2+内流的抑制在该麻醉剂的负性肌力作用中起主要作用。