摘要
目的 研究依托咪酯 (etomidate ,ET)在急性分离的大鼠骶髓后连合核 (sacraldorsalcommissuralnucleus,SDCN)神经元的药理学特性。方法 采用制霉菌素穿孔膜片钳全细胞记录。结果 在大鼠SDCN神经元 ,ET(10~ 30 0 0 μmol/L)在钳制电位为 - 40mV时 ,可引起内向电流 (IET) ,EC50 为 (33.35± 3.0 7) μmol/L ,该电流可被GABAA受体拮抗剂荷包牡丹碱 (bicuculline)及氯通道阻滞剂印防己毒素 (picrotoxin)以浓度依赖方式所阻断。结论 ET在大鼠SDCN神经元可通过作用于GABAA受体而诱发氯通道电流 。
ObjectiveTo investigate the pharmacological properties of etomidate (ET) in the dissociated rat sacral dorsal commissural nucleus (SDCN) neurons. MethodsNystatin perforated patch recording technique under voltage-clamp conditions was used. ResultsAt the holding potential of -40 mV, ET evoked inward current (I_(ET)) over the concentration range of 10 μmol/L to 3 mmol/L with the EC_(50) value of (33.35 ± 3.07) μmol/L. The I_(ET) was suppressed by bicuculline, the selective GABA_(A) receptor antagonist, and picrotoxin a selective blocker of Cl^(-) channel, in a concentration-dependent manner. ConclusionThe results indicate that ET acts on GABA_(A) receptors to result in the opening of the Cl^(-) channels in the SDCN neurons, which may contribute to its general anesthesia at spinal level.
基金
国家自然科学基金资助项目(30300077)
第四军医大学"后备人才"基金资助