Slater P, Blundell C
Eur J Pharmacol. 1978 Apr 1;48(3):237-47. doi: 10.1016/0014-2999(78)90082-1.
The role of brain catecholamines in the antinociceptive action of morphine was investigated. Intraventricular 6-hydroxydopamine which depleted brain noradrenaline in the rat had no effect on morphine's antinociceptive action but combined treatment with pargyline and 6-hydroxydopamine to further deplete brain dopamine potentiated morphine's action. It was also shown that when dopamine receptors were blocked, the antinociceptive action of morphine was potentiated whereas alpha- and beta-adrenoceptor antagonists had no effect. 6-Hydroxydopamine had two effects in mice tested on the hot-plate. It produced a hyperalgesia and antagonized the antinociceptive action of morphine. This antagonism of morphine appeared to be the result of the depletion of noradrenaline rather than dopamine. Intraventricular injection of both catecholamines restored the antinociceptive action of morphine in 6-hydroxydopamine-treated mice but dopamine was ineffective in the presence of a dopamine beta-hydroxylase inhibitor. It is suggested that the antinociceptive action of morphine is expressed by noradrenergic neurones in the mouse and by both noradrenergic and dopaminergic neurones in the rat.
研究了脑内儿茶酚胺在吗啡抗伤害感受作用中的角色。脑室注射6-羟基多巴胺可耗尽大鼠脑内去甲肾上腺素,但对吗啡的抗伤害感受作用无影响,然而用帕吉林和6-羟基多巴胺联合处理以进一步耗尽脑内多巴胺可增强吗啡的作用。还表明,当多巴胺受体被阻断时,吗啡的抗伤害感受作用增强,而α和β肾上腺素能受体拮抗剂则无作用。在热板试验中,6-羟基多巴胺对小鼠有两种作用。它产生痛觉过敏并拮抗吗啡的抗伤害感受作用。吗啡的这种拮抗作用似乎是去甲肾上腺素而非多巴胺耗竭的结果。脑室注射两种儿茶酚胺可恢复6-羟基多巴胺处理小鼠中吗啡的抗伤害感受作用,但在多巴胺β-羟化酶抑制剂存在的情况下多巴胺无效。提示吗啡的抗伤害感受作用在小鼠中由去甲肾上腺素能神经元介导,在大鼠中由去甲肾上腺素能和多巴胺能神经元共同介导。