Iwasaki M
Department of Second Oral Surgery, Faculty of Dentistry, Kyushu University, Japan.
Br J Anaesth. 1989 Sep;63(3):306-14. doi: 10.1093/bja/63.3.306.
The effects of pentobarbitone, ketamine and lignocaine on synaptic transmission in the rat olfactory cortex were studied. All agents depressed the presynaptic spike, the excitatory postsynaptic potential (EPSP) and the population spike evoked by stimulation of the lateral olfactory tract in a concentration-dependent manner. However, each anaesthetic had different effects on the processes of excitatory synaptic transmission. Pentobarbitone depressed primarily the EPSP, ketamine primarily the excitability of the presynaptic fibres and lignocaine the excitability of the presynaptic fibres; lignocaine also reduced the release of excitatory transmitters. None of the three agents influenced the passive membrane properties or the excitability of olfactory pyramidal cells. These data indicate that these agents block synaptic transmission in the olfactory cortex by different mechanisms.
研究了戊巴比妥、氯胺酮和利多卡因对大鼠嗅觉皮层突触传递的影响。所有药物均以浓度依赖性方式抑制突触前峰电位、兴奋性突触后电位(EPSP)以及刺激外侧嗅束诱发的群体峰电位。然而,每种麻醉药对兴奋性突触传递过程具有不同影响。戊巴比妥主要抑制EPSP,氯胺酮主要抑制突触前纤维的兴奋性,利多卡因也抑制突触前纤维的兴奋性;利多卡因还减少兴奋性递质的释放。这三种药物均未影响嗅觉锥体细胞的被动膜特性或兴奋性。这些数据表明,这些药物通过不同机制阻断嗅觉皮层中的突触传递。