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在用选择性 D-1 和 D-2 拮抗剂反复治疗后对选择性 D-1 和 D-2 激动剂的反应。

Responses to selective D-1 and D-2 agonists after repeated treatment with selective D-1 and D-2 antagonists.

作者信息

Gandolfi O, Dall'olio R, Vaccheri A, Roncada P, Montanaro N

机构信息

Institute of Pharmacology, University of Bologna, Italy.

出版信息

Pharmacol Biochem Behav. 1988 Jun;30(2):463-9. doi: 10.1016/0091-3057(88)90481-9.

DOI:10.1016/0091-3057(88)90481-9
PMID:3262877
Abstract

This study was aimed at achieving a better understanding of the functional role of D-1 and D-2 receptors in some dopamine-mediated behaviors. Hypermotility, grooming behavior and stereotyped behavior were induced, respectively, by LY 171555 (D-2 agonist), SKF 38393 (D-1 agonist) and apomorphine (mixed agonist). Acute pretreatment either with the D-1 selective antagonist SCH 23390 (0.02 mg/kg) or with the D-2 receptor blocker YM 09151-2 (0.02 mg/kg, IP) blocked all these behaviors, suggesting the existence of functional interactions between D-1 and D-2 receptors. Striatal membranes prepared from rats receiving repeated administrations with SCH 23390 (0.05 mg/kg, twice daily for 21 days) showed an increase in the number of D-1 but not of D-2 receptors. On the contrary the repeated treatments with YM 09151-2 increased only the Bmax values of D-2 receptors. While the D-1 supersensitive rats showed only enhancement of apomorphine-induced stereotyped behavior, the D-2 supersensitive rats exhibited an increase of both apomorphine-elicited stereotypy and LY 171555-elicited hypermotility. SKF 38393-induced grooming was unaffected by any pretreatments. Moreover when D-2 supersensitive rats were acutely pretreated with SCH 23390, the enhancement of apomorphine-induced stereotyped behavior was abolished. It is concluded that the behavioral expression of D-1 receptor supersensitivity requires the simultaneous activation of D-1 and D-2 receptors.

摘要

本研究旨在更好地理解D-1和D-2受体在某些多巴胺介导行为中的功能作用。分别用LY 171555(D-2激动剂)、SKF 38393(D-1激动剂)和阿扑吗啡(混合激动剂)诱导大鼠出现运动亢进、理毛行为和刻板行为。用D-1选择性拮抗剂SCH 23390(0.02mg/kg)或D-2受体阻滞剂YM 09151-2(0.02mg/kg,腹腔注射)进行急性预处理可阻断所有这些行为,提示D-1和D-2受体之间存在功能相互作用。对接受重复给予SCH 23390(0.05mg/kg,每日两次,共21天)的大鼠制备的纹状体膜进行检测,结果显示D-1受体数量增加,而D-2受体数量未增加。相反,用YM 09151-2进行重复处理仅增加了D-2受体的Bmax值。D-1超敏大鼠仅表现出阿扑吗啡诱导的刻板行为增强,而D-2超敏大鼠则表现出阿扑吗啡诱导的刻板行为和LY 171555诱导的运动亢进均增加。SKF 38393诱导的理毛行为不受任何预处理的影响。此外,当对D-2超敏大鼠用SCH 23390进行急性预处理时,阿扑吗啡诱导的刻板行为增强被消除。得出结论:D-1受体超敏的行为表达需要D-1和D-2受体同时激活。

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