Yue Wei-dong, Zhang Yun-hong, Li Yu-rong, Zhang Shu-zhuo, Yang Lei
Department of Neurology, Harbin Medical University, Harbin 150086, China.
Zhongguo Ying Yong Sheng Li Xue Za Zhi. 2003 May;19(2):150-3.
To investigate the effects of morphine on synaptic transmission of neurons of central nervous system and reveal the mechanism underlying it.
New born wistar rats were used for primary culture of hippocampus neurons. Using whole-cell patch-clamp technique, we observed the excitatory and spontaneous inhibitory postsynaptic current (EPSC, sIPSC) and glutamate-induced current before and after morphine treatment.
(1) sEPSC of hippocampal neurons was markedly increased after morphine application. The effect of morphine was blocked by opioid antagonist naloxone (n=18, P < 0.01). (2) The frequency of mEPSC and the amplitude of glutamate-induced current of hippocampal neurons had no significant changes after morphine treatment (P > 0.05). (3) Morphine inhibited sIPSC of hippocampal neurons markedly and naloxone could block this effect (n=13, P < 0.01).
The results suggest that the exciting effect of morphine on hippocampal neurons are not due to direct influence of morphine on glutamate synapses transmission, but may result from the inhibition on interneurons, that is "disinhibition" way.
研究吗啡对中枢神经系统神经元突触传递的影响并揭示其潜在机制。
采用新生Wistar大鼠进行海马神经元原代培养。运用全细胞膜片钳技术,观察吗啡处理前后兴奋性和自发性抑制性突触后电流(EPSC、sIPSC)以及谷氨酸诱导电流。
(1)应用吗啡后海马神经元的sEPSC显著增加。吗啡的作用被阿片类拮抗剂纳洛酮阻断(n = 18,P < 0.01)。(2)吗啡处理后海马神经元的微小兴奋性突触后电流(mEPSC)频率和谷氨酸诱导电流幅度无显著变化(P > 0.05)。(3)吗啡显著抑制海马神经元的sIPSC,纳洛酮可阻断此效应(n = 13,P < 0.01)。
结果表明,吗啡对海马神经元的兴奋作用并非由于吗啡对谷氨酸突触传递的直接影响,而可能是由于对中间神经元的抑制,即“去抑制”方式。