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纳法多曲给药可增强 D1 及 D1/D2 多巴胺受体介导的行为。

Nafadotride administration increases D1 and D1/D2 dopamine receptor mediated behaviors.

作者信息

Dall'Olio R, Gaggi R, Voltattorni M, Tanda O, Gandolfi O

机构信息

Department of Pharmacology, University of Bologna, Via Irnerio 48, I 40126, Bologna, Italy.

出版信息

Behav Pharmacol. 2002 Dec;13(8):633-8. doi: 10.1097/00008877-200212000-00004.

Abstract

The administration of nafadotride, given at doses known to block the D3 dopamine receptors (0.75, 1.5, 3 mg/kg i.p.) increased locomotor activity both in naive and habituated rats and counteracted the hypothermia but not the hypomotility induced by a low dose of the putative D3 dopamine agonist (+/-)-7-hydroxy-2-(di-N-propylamino)-tetralin (7-OH-DPAT; 0.04 mg/kg). Nafadotride did not antagonize either the motor effects induced by different doses of the D2 agonist quinpirole (0.05 and 0.3 mg/kg) or the hypermotility induced by 7-OH-DPAT given at a dose (0.32 mg/kg) stimulating D2 dopamine receptors. The same nafadotride doses potentiated the grooming behavior induced by the D1 dopamine agonist SKF 38393 (10 mg/kg i.p.) as well as the stereotyped response to the D1/D2 agonist apomorphine (0.5 mg/kg s.c.). Stereotyped behavior was also observed in rats concomitantly treated with nafadotride and the D2 agonist quinpirole. As the activation of D1 dopamine receptors plays an important role in the occurrence of stereotypies, the results suggest that the blockade of D3 receptors by nafadotride could have favored D1/D2 dopamine receptor-mediated behaviors by potentiating D1 receptor function.

摘要

给予已知能阻断D3多巴胺受体的剂量(0.75、1.5、3毫克/千克腹腔注射)的萘法朵曲,可增加未接触过药物和习惯化大鼠的运动活性,并抵消低剂量假定的D3多巴胺激动剂(±)-7-羟基-2-(二-N-丙基氨基)-四氢萘(7-OH-DPAT;0.04毫克/千克)诱导的体温过低,但不能抵消其运动迟缓。萘法朵曲既不拮抗不同剂量的D2激动剂喹吡罗(0.05和0.3毫克/千克)诱导的运动效应,也不拮抗以刺激D2多巴胺受体的剂量(0.32毫克/千克)给予7-OH-DPAT诱导的运动亢进。相同剂量的萘法朵曲可增强D1多巴胺激动剂SKF 38393(10毫克/千克腹腔注射)诱导的梳理行为以及对D1/D2激动剂阿扑吗啡(0.5毫克/千克皮下注射)的刻板反应。在同时用萘法朵曲和D2激动剂喹吡罗治疗的大鼠中也观察到刻板行为。由于D1多巴胺受体的激活在刻板行为的发生中起重要作用,结果表明萘法朵曲对D3受体的阻断可能通过增强D1受体功能而有利于D1/D2多巴胺受体介导的行为。

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