Cooper B R, Konkol R J, Breese G R
J Pharmacol Exp Ther. 1978 Mar;204(3):592-605.
6-Hydroxydopamine treatments which preferentially depleted either norepinephrine or dopamine were used to define the importance of these transmitter systems in the behavioral alterations produced by catecholamine synthesis inhibitors and d-amphetamine on self-stimulation of the locus coeruleus and substantia nigra. After chronic reduction of brain dopamine, an acute depression of self-stimulation of both the locus coeruleus and substantia nigra occurred. Preferential depletion of norepinephrine with 6-hydroxydopamine did not result in a significant decrease in self-stimulation of locus coeruleus or substantia nigra. However, a dose of alpha-methyltyrosine wihch had no effect in control rats or in rats with brain norepinephrine depleted caused a significant reduction in responding at both electrode placements in animals depleted of brain dopamine. Administration of U-14,624 affected neither substantia nigra nor locus coeruleus self-stimulation, even though it produced an additional 70% depletion of norepinephrine. When d-amphetamine sulfate was given to 6-hydroxydopamine-treated rats, the facilitation of self-stimulation produced by this compound was significantly attenuated in rats with prior depletion of brain dopamine. Depletion of brain norepinephrine did not affect the actions of d-amphetamine on self-stimulation. In other experiments, the actions of d-amphetamine to increase self-stimulation of animals pretreated with reserpine was found to be antagonized by alpha-methyltyrosine but not by U-14,624. Results suggest that drugs can alter self-stimulation of a site in brain anatomically associated with noradrenergic neural pathways and self-stimulation of a site primarily associated with dopaminergic pathways in a similar manner. These data also provided evidence for the involvement of dopamine fibers in the pharmacological actions of d-amphetamine, reserpine and alpha-methyltyrosine.
采用优先耗竭去甲肾上腺素或多巴胺的6-羟基多巴胺处理方法,来确定这些递质系统在儿茶酚胺合成抑制剂和右旋苯丙胺对蓝斑和黑质自我刺激所产生的行为改变中的重要性。在长期降低脑内多巴胺水平后,蓝斑和黑质的自我刺激出现急性抑制。用6-羟基多巴胺优先耗竭去甲肾上腺素,并未导致蓝斑或黑质自我刺激的显著减少。然而,在对照大鼠或脑内去甲肾上腺素已耗竭的大鼠中无作用的α-甲基酪氨酸剂量,却能使脑内多巴胺已耗竭的动物在两个电极位置的反应显著减少。给予U-14,624,即使它使去甲肾上腺素额外耗竭70%,也不影响黑质或蓝斑的自我刺激。当给6-羟基多巴胺处理的大鼠给予硫酸右旋苯丙胺时,该化合物所产生的自我刺激促进作用在预先脑内多巴胺已耗竭的大鼠中显著减弱。脑内去甲肾上腺素的耗竭并不影响右旋苯丙胺对自我刺激的作用。在其他实验中,发现右旋苯丙胺对利血平预处理动物自我刺激增加的作用,可被α-甲基酪氨酸拮抗,但不能被U-14,624拮抗。结果表明,药物可以以类似的方式改变与去甲肾上腺素能神经通路在解剖学上相关部位的自我刺激,以及主要与多巴胺能通路相关部位的自我刺激。这些数据也为多巴胺纤维参与右旋苯丙胺、利血平和α-甲基酪氨酸的药理作用提供了证据。