Yamazaki M, Ito Y, Kuze S, Shibuya N, Momose Y
Department of Anesthesiology, Faculty of Medicine, Toyama Medical and Pharmaceutical University, Japan.
Pharmacology. 1992;45(3):162-9. doi: 10.1159/000138994.
The effects of ketamine on membrane potentials and long-lasting type (L-type) voltage-dependent Ca2+ currents were investigated in dispersed single smooth muscle cells from rabbit portal veins. The amplitude and duration of the action potentials evoked by intracellular stimulation were inhibited by ketamine and were completely blocked by 10(-3) mol/l ketamine. Ketamine, however, did not alter the resting membrane potential. Whole cell voltage clamp experiments revealed that ketamine at concentrations higher than 10(-4) mol/l reduced the peak L-type voltage-dependent Ca2+ currents. These effects of ketamine were concentration-dependent and reversible at concentrations from 10(-4) to 10(-3) mol/l. Moreover, the activation threshold of L-type Ca2+ current (approximately -30 mV) was slightly shifted to the positive potential side by ketamine. This effect can explain that the action potential was abolished by 10(-3) mol/l ketamine. It is concluded that relaxation of the vascular smooth muscle by ketamine may have to be attributed to the inhibition of L-type voltage-dependent Ca2+ current.
在兔门静脉分离的单个平滑肌细胞中,研究了氯胺酮对膜电位和持久型(L型)电压依赖性Ca2+电流的影响。细胞内刺激诱发的动作电位的幅度和持续时间受到氯胺酮的抑制,10(-3)mol/L氯胺酮可完全阻断动作电位。然而,氯胺酮并未改变静息膜电位。全细胞电压钳实验表明,浓度高于10(-4)mol/L的氯胺酮可降低L型电压依赖性Ca2+电流的峰值。氯胺酮的这些作用具有浓度依赖性,在10(-4)至10(-3)mol/L的浓度范围内是可逆的。此外,氯胺酮使L型Ca2+电流的激活阈值(约-30mV)轻微向正电位侧偏移。这种作用可以解释10(-3)mol/L氯胺酮为何能消除动作电位。得出的结论是,氯胺酮使血管平滑肌松弛可能归因于对L型电压依赖性Ca2+电流的抑制。