Vaugeois J M, Pouhé D, Zuccaro F, Costentin J
Unité de Neuropsychopharmacologie Expérimentale, URA CNRS 1969, Institut Fédératif de Recherches Multidisciplinaires sur les Peptides, Faculté de Médecine et Pharmacie de Rouen, Saint-Etienne du Rouvray, France.
Pharmacol Biochem Behav. 1996 May;54(1):235-9. doi: 10.1016/0091-3057(95)02131-0.
Both dexamphetamine and the pure dopamine reuptake inhibitor GBR 12783 elicit a stimulation of locomotion and increase swimming activity in the behavioral despair test in mice. The dopamine D1 dopamine receptor antagonist SCH 23390 dose dependently (7.5-30 micrograms/kg s.c.) antagonized the stimulant locomotor effect on both drugs but did not prevent their antiimmobility effect on the behavioral despair test. The D2 dopamine receptor antagonist haloperidol dose dependently (12.5-50 micrograms/kg i.p.) antagonized the effects of dexamphetamine on both locomotor activity and behavioral despair test. By contrast, haloperidol inhibited the effects of GBR 12783 in the forced swimming test but not on locomotion. It is concluded that indirect dopamine agonists are effective on the behavioral despair test independently of a stimulation of locomotor activity. Their effects on the despair test depend on the stimulation of D2 but not D1 dopamine receptors.
在小鼠行为绝望试验中,右旋苯丙胺和纯多巴胺再摄取抑制剂GBR 12783均可引起运动兴奋并增加游泳活动。多巴胺D1受体拮抗剂SCH 23390剂量依赖性地(皮下注射7.5 - 30微克/千克)拮抗这两种药物的兴奋运动效应,但并未阻止它们在行为绝望试验中的抗不动效应。多巴胺D2受体拮抗剂氟哌啶醇剂量依赖性地(腹腔注射12.5 - 50微克/千克)拮抗右旋苯丙胺对运动活性和行为绝望试验的影响。相比之下,氟哌啶醇在强迫游泳试验中抑制GBR 12783的作用,但对运动无抑制作用。得出的结论是,间接多巴胺激动剂在行为绝望试验中有效,且与运动活性的刺激无关。它们对绝望试验的作用取决于D2而非D1多巴胺受体的刺激。