Byrnes E M, Abrams D, Bruno J P
Department of Psychology, Ohio State University, Columbus 43210.
Behav Brain Res. 1994 Apr 18;61(2):205-14. doi: 10.1016/0166-4328(94)90161-9.
The motoric effects of the D1-like agonist SKF 38393 (5.0 or 20.0 mg/kg) and the D2-like agonist quinpirole (0.2, 1.0, or 3.0 mg/kg) were determined in adult rats treated with 6-OHDA (100 micrograms) or its vehicle on postnatal Day 3. Quinpirole, but not SKF 38393, produced stereotypy and modest motor activity in vehicle-treated rats. These effects of quinpirole were blocked by either the D1-like antagonist SCH 23390 (0.2 or 0.4 mg/kg) or the D2-like antagonist clebopride (10.0 mg/kg). In contrast, administration of either D1- or D2-like agonists enhanced stereotypy and motor behavior in animals depleted of dopamine with 6-OHDA. However, in these animals, only the D1-like antagonist was able to block D1-induced behaviors and only the D2-like antagonist was able to block D2-induced behaviors. A separate group of adult rats, treated with 6-OHDA (200 micrograms) on postnatal Day 20, was studied to determine whether these effects depended upon age at the time of DA depletion. Animals depleted on Day 20 resembled animals depleted on Day 3 in that D2-, but not D1-like antagonists, blocked D2 agonist-induced responses. These results demonstrate that in animals depleted of DA during development, qualitative changes in D1/D2 receptor interactions result in the ability of each receptor subtype to independently activate stereotypy and motor behavior.
在出生后第3天用6-羟基多巴胺(100微克)或其溶剂处理的成年大鼠中,测定了D1类激动剂SKF 38393(5.0或20.0毫克/千克)和D2类激动剂喹吡罗(0.2、1.0或3.0毫克/千克)的运动效应。喹吡罗而非SKF 38393在溶剂处理的大鼠中产生刻板行为和适度的运动活动。喹吡罗的这些效应被D1类拮抗剂SCH 23390(0.2或0.4毫克/千克)或D2类拮抗剂氯波必利(10.0毫克/千克)阻断。相反,给予D1或D2类激动剂会增强用6-羟基多巴胺使多巴胺耗竭的动物的刻板行为和运动行为。然而,在这些动物中,只有D1类拮抗剂能够阻断D1诱导的行为,只有D2类拮抗剂能够阻断D2诱导的行为。研究了另一组在出生后第20天用6-羟基多巴胺(200微克)处理的成年大鼠,以确定这些效应是否取决于多巴胺耗竭时的年龄。在第20天耗竭多巴胺的动物与在第3天耗竭多巴胺的动物相似,即D2类而非D1类拮抗剂阻断D2激动剂诱导的反应。这些结果表明,在发育过程中多巴胺耗竭的动物中,D1/D2受体相互作用的质的变化导致每个受体亚型能够独立激活刻板行为和运动行为。