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多巴胺能刺激大鼠丘脑底核会引发口部运动障碍。

Dopaminergic stimulation of subthalamic nucleus elicits oral dyskinesia in rats.

作者信息

Parry T J, Eberle-Wang K, Lucki I, Chesselet M F

机构信息

Department of Pharmacology, University of Pennsylvania, Philadelphia 19104.

出版信息

Exp Neurol. 1994 Aug;128(2):181-90. doi: 10.1006/exnr.1994.1126.

Abstract

The effects of dopaminergic stimulation of the subthalamic nucleus (STh) on motor behavior were examined in conscious rats. Unilateral infusion of apomorphine (0.1 to 3.2 micrograms) into the STh induced a dose-dependent increase in abnormal, nondirected orofacial movements without altering turning, sniffing, grooming, or rearing behaviors. Orofacial movements elicited by local infusion of apomorphine (1.0 microgram) into the STh were blocked by peripheral administration of the D1 antagonist, SCH 23390 (0.1 mg/kg, sc), but not by the D2 antagonists haloperidol (1.0 mg/kg, sc) or sulpiride (50 mg/kg, sc). Furthermore, coinfusion of SCH 23390 (1.0 microgram), but not sulpiride (5.0 micrograms), with apomorphine (1.0 microgram) into the STh blocked oral dyskinesia. Oral movements could not be reelicited by an infusion of apomorphine into the STh after a kainic acid lesion of the STh. In addition, infusion of apomorphine (1.0 microgram) into sites proximal to but deliberately outside of the STh failed to elicit nondirected oral movements above baseline levels. The results indicate that stimulation of D1 dopaminergic receptors within the STh induces abnormal orofacial movements. This highlights the importance of the dopaminergic input to the STh in the regulation of motor function and suggests that D1 receptor antagonists could prove useful in the treatment of orofacial dyskinesia in humans.

摘要

在清醒大鼠中研究了多巴胺能刺激丘脑底核(STh)对运动行为的影响。向STh单侧注入阿扑吗啡(0.1至3.2微克)可引起异常的、无定向的口面部运动呈剂量依赖性增加,而不会改变转身、嗅探、梳理或直立行为。向STh局部注入阿扑吗啡(1.0微克)所引发的口面部运动,可被外周给予D1拮抗剂SCH 23390(0.1毫克/千克,皮下注射)阻断,但不能被D2拮抗剂氟哌啶醇(1.0毫克/千克,皮下注射)或舒必利(50毫克/千克,皮下注射)阻断。此外,将SCH 23390(1.0微克)而非舒必利(5.0微克)与阿扑吗啡(1.0微克)共同注入STh可阻断口部运动障碍。在STh经 kainic 酸损伤后,向STh注入阿扑吗啡无法再次引发口部运动。此外,向紧邻STh但特意在其外部的部位注入阿扑吗啡(1.0微克),未能引发高于基线水平的无定向口部运动。结果表明,刺激STh内的D1多巴胺能受体会诱发异常的口面部运动。这突出了多巴胺能输入至STh在运动功能调节中的重要性,并表明D1受体拮抗剂可能对治疗人类口面部运动障碍有用。

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