Hu S, Rubly N
Eur J Pharmacol. 1983 Nov 25;95(3-4):185-92. doi: 10.1016/0014-2999(83)90633-7.
The effects of externally or internally applied morphine hydrochloride on the node of Ranvier of the frog were studied under current and voltage clamp conditions. Externally applied morphine in a concentration of 0.5-1 mM prolonged the action potential and the absolute refractory period. It inhibited the repetitive response of sensory fibres to long-lasting depolarizing pulses. Externally applied morphine was more effective in depressing the steady state K current than the peak Na current. When added to the internal medium (by diffusion from the cut ends of the fibre) morphine had a stronger effect on the peak Na current. Morphine did not alter the kinetics of Na activation but increased the time constants of development or removal of Na inactivation by a factor of about 1.2. Morphine reduced both the fast and slow phase of the inward K tail currents recorded in Ringer with 30 mM K. Of the two components (gKf1 and gKf2) of fast K conductance described by J.M. Dubois (1981, J. Physiol. 318, 297) only gKf2 was affected. The morphine antagonist naloxone in a concentration of 0.1 mM completely and reversibly abolished the component gKf2 of the fast K conductance. Naloxone did not antagonize the effect of morphine. These findings show that there are no specific opiate receptors in the membrane of peripheral nerves.
在电流钳和电压钳条件下,研究了外用或内用盐酸吗啡对青蛙郎飞结的影响。外用浓度为0.5 - 1 mM的吗啡可延长动作电位和绝对不应期。它抑制了感觉纤维对持续去极化脉冲的重复反应。外用吗啡抑制稳态钾电流比抑制峰值钠电流更有效。当添加到内部介质中(通过从纤维切断端扩散)时,吗啡对峰值钠电流有更强的作用。吗啡不改变钠激活的动力学,但使钠失活的发展或消除的时间常数增加约1.2倍。吗啡降低了在含30 mM钾的林格液中记录的内向钾尾电流的快速和慢速相。J.M. 杜波依斯(1981年,《生理学杂志》318卷,297页)描述的快速钾电导的两个成分(gKf1和gKf2)中,只有gKf2受到影响。浓度为0.1 mM的吗啡拮抗剂纳洛酮完全且可逆地消除了快速钾电导的gKf2成分。纳洛酮不拮抗吗啡的作用。这些发现表明,外周神经膜中不存在特异性阿片受体。