Bradley P B, Dray A
Br J Pharmacol. 1974 Jan;50(1):47-55. doi: 10.1111/j.1476-5381.1974.tb09591.x.
1 The effects of microiontophoretically applied morphine and its interactions with the effects of microiontophoretic applications of either acetylcholine, (-)-noradrenaline or 5-hydroxytryptamine have been studied on single neurones in the brain stem of rats anaesthetized with urethane.2 Morphine excited or inhibited most neurones tested and the effects, especially excitation, were often extremely powerful. However, the time course of the excitatory and inhibitory effects were somewhat different.3 Desensitization to the excitation produced by morphine was seen after repeated or prolonged applications and it is suggested that this phenomenon may be related to the tolerance which develops after chronic administration of morphine. No desensitization was observed to inhibition of neuronal activity by morphine.4 Morphine usually reduced the excitation of neurones by acetylcholine, noradrenaline or 5-hydroxytryptamine but sometimes potentiated the effect, although not always on the same neurones. Inhibition of neuronal activity by these compounds was never modified by morphine and neither were the effects of glutamate or D,L-homocysteic acid when used as control agonists.5 The in vitro release of morphine from six micropipettes was determined and the transport number was calculated to be 0.051 (s.d. 0.021).6 The implications of these observations in explaining the pharmacological actions of morphine are discussed.
研究了微电泳施加吗啡的作用及其与微电泳施加乙酰胆碱、(-)-去甲肾上腺素或5-羟色胺的作用之间的相互作用,实验对象为用乌拉坦麻醉的大鼠脑干中的单个神经元。
吗啡使大多数受试神经元兴奋或抑制,其作用,尤其是兴奋作用,往往极其强烈。然而,兴奋和抑制作用的时间进程有所不同。
重复或长时间施加吗啡后,可观察到对吗啡产生的兴奋作用出现脱敏现象,提示该现象可能与长期给予吗啡后产生的耐受性有关。未观察到对吗啡抑制神经元活动的脱敏现象。
吗啡通常会减弱乙酰胆碱、去甲肾上腺素或5-羟色胺对神经元的兴奋作用,但有时会增强这种作用,不过并非总是对同一神经元起作用。这些化合物对神经元活动的抑制作用从未被吗啡改变,用作对照激动剂的谷氨酸或D,L-高胱氨酸的作用也未被改变。
测定了六个微量移液器中吗啡的体外释放量,计算得出转运数为0.051(标准差0.021)。
讨论了这些观察结果在解释吗啡药理作用方面的意义。