Pollock J, Kornetsky C
Laboratory of Behavioral Pharmacology, Boston University School of Medicine, MA 02118.
Neurosci Lett. 1989 Jul 31;102(2-3):291-6. doi: 10.1016/0304-3940(89)90094-3.
In the course of studying the effects of morphine on the escape from electrical stimulation to the rat medial forebrain bundle, we observed that a combination of low doses of morphine and stimulation, neither of which caused stereotypy in the rat, resulted in marked stereotypic behavior that was similar to that seen with high doses of morphine alone. This behavior could be blocked by either naloxone or by the D1 antagonist SCH 23390, but not by the D2 antagonist raclopride. Furthermore, the stereotypy caused by chronically administered high doses of morphine was blocked by naloxone and the D1 antagonist. These results strongly implicate the role of dopamine D1 activation in morphine-induced stereotypies.
在研究吗啡对大鼠从电刺激中逃脱至内侧前脑束的影响过程中,我们观察到低剂量吗啡与刺激的组合,单独使用这两者均不会使大鼠产生刻板行为,但却导致了明显的刻板行为,这种行为类似于单独使用高剂量吗啡时所观察到的行为。这种行为可被纳洛酮或D1拮抗剂SCH 23390阻断,但不能被D2拮抗剂雷氯必利阻断。此外,长期给予高剂量吗啡所引起的刻板行为可被纳洛酮和D1拮抗剂阻断。这些结果有力地表明多巴胺D1激活在吗啡诱导的刻板行为中起作用。