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底丘脑核在5-羟色胺2C诱导的口部运动障碍中的作用。

A role for the subthalamic nucleus in 5-HT2C-induced oral dyskinesia.

作者信息

Eberle-Wang K, Lucki I, Chesselet M F

机构信息

Department of Pharmacology, University of Pennsylvania, Philadelphia 19104, USA.

出版信息

Neuroscience. 1996 May;72(1):117-28. doi: 10.1016/0306-4522(95)00548-x.

Abstract

The 5-hydroxytryptamine2C serotonin receptor is broadly distributed in brain, however, its functional role is unknown. Peripheral administration of drugs acting at the 5-hydroxytryptamine2C receptor induces abnormal oral dyskinesias, hyperkinetic motor disorders that often result from dysfunction of the basal ganglia. The subthalamic nucleus, a brain region anatomically and functionally related to the basal ganglia, has been implicated in oral dyskinesia. The subthalamic nucleus contains messenger RNA encoding 5-hydroxytryptamine2C receptors, suggesting its potential role in 5-hydroxytryptamine2C-mediated oral dyskinesia. Both systemic administration and local unilateral infusion of the 5-hydroxytryptamine2C/1B agonist, 1-(m-chlorophenyl)piperazine into the subthalamic nucleus increased orofacial movements. Oral movements following subthalamic infusion of 1-(m-chlorophenyl)piperazine were blocked by systemic administration of the 5-hydroxytryptamine2C/2A antagonists mianserin, ketanserin and mesulergine but were not altered by systemic pretreatment with either the 5-hydroxytryptamine1A/2A and dopamine antagonist spiperone or the 5-hydroxytryptamine1A/1B antagonist pindolol. Co-infusion of mesulergine with 1-(m-chlorophenyl)piperazine into the subthalamic nucleus blocked 1-(m-chlorophenyl)piperazine-stimulated oral movements. Oral bouts following systemically administered 1-(m-chlorophenyl)piperazine were markedly reduced following bilateral subthalamic infusion of either mesulergine or the selective 5-hydroxytryptamine2C antagonist SDZ SER 082. The findings indicate that stimulating 5-hydroxytryptamine2C receptors in the subthalamic nucleus elicits orofacial dyskinesia in the rat. These data are novel in providing a behavioral model for central 5-hydroxytryptamine2C receptor stimulation attributed to a specific anatomical location, and suggest that antagonists at the 5-hydroxytryptamine2C receptor could be useful in treating hyperkinetic motor disorders.

摘要

5-羟色胺2C血清素受体广泛分布于大脑中,然而,其功能作用尚不清楚。外周给予作用于5-羟色胺2C受体的药物会诱发异常的口腔运动障碍,这是一种通常由基底神经节功能障碍导致的运动亢进性运动障碍。底丘脑核是一个在解剖学和功能上与基底神经节相关的脑区,已被认为与口腔运动障碍有关。底丘脑核含有编码5-羟色胺2C受体的信使核糖核酸,表明其在5-羟色胺2C介导的口腔运动障碍中可能发挥的作用。全身给药以及将5-羟色胺2C/1B激动剂1-(间氯苯基)哌嗪局部单侧注入底丘脑核均会增加口面部运动。在底丘脑核注入1-(间氯苯基)哌嗪后出现的口腔运动,可被全身给予5-羟色胺2C/2A拮抗剂米安色林、酮色林和美舒麦角阻断,但用5-羟色胺1A/2A和多巴胺拮抗剂螺哌隆或5-羟色胺1A/1B拮抗剂吲哚洛尔进行全身预处理对此并无改变。将美舒麦角与1-(间氯苯基)哌嗪共同注入底丘脑核可阻断1-(间氯苯基)哌嗪刺激的口腔运动。在全身给予1-(间氯苯基)哌嗪后出现的口腔发作,在双侧底丘脑核注入美舒麦角或选择性5-羟色胺2C拮抗剂SDZ SER 082后明显减少。这些发现表明,刺激底丘脑核中的5-羟色胺2C受体会引发大鼠的口面部运动障碍。这些数据为归因于特定解剖位置的中枢5-羟色胺2C受体刺激提供了一种行为模型,具有创新性,并表明5-羟色胺2C受体拮抗剂可能对治疗运动亢进性运动障碍有用。

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