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DSP4或6-羟基多巴胺预处理后,在放射状臂迷宫中安非他明诱导的持续性行为。

Amphetamine-induced perseverative behavior in a radial arm maze following DSP4 or 6-OHDA pretreatment.

作者信息

Bruto V, Beauchamp C, Zacharko R M, Anisman H

出版信息

Psychopharmacology (Berl). 1984;83(1):62-9. doi: 10.1007/BF00427424.

Abstract

Mice permitted to explore an 8-arm radial maze tended to visit those arms least recently entered. Treatment with D-amphetamine engendered a perseverative tendency, wherein mice repeatedly visited two arms of the maze. Administration of the norepinephrine (NE) neurotoxin, N-2-chloroethyl-N-ethyl-2-bromo-benzylamine (DSP4), appreciably reduced NE in the hippocampus and cortex, moderately reduced NE in the locus coeruleus, and had only a small effect on hypothalamic NE. The DSP4 treatment resulted in a decrease of locomotor activity among amphetamine-treated mice, coupled with an increase of stereotyped response patterns. Although the NE depletion did not affect the pattern of exploration that mice ordinarily displayed, DSP4 appreciably increased the perseverative tendency provoked by amphetamine. Reduction of dopamine (DA) and NE by intraventricular administration of the catecholamine neurotoxin, 6-hydroxydopamine (6-OHDA), antagonized the effects of amphetamine, such that the frequency of alternation responses was increased and the proportion of perseverative responses was reduced. The effectiveness of the 6-OHDA treatment in antagonizing the amphetamine-induced perseveration was not reduced among mice that were pretreated with desmethylimipramine, which resulted in partial prevention of the NE reduction by 6-OHDA administration. It is suggested that DA neuronal activity contributes to the amphetamine -provoked perseveration , whereas NE stimulation modifies the perseverative tendency by influencing exploration or habituation.

摘要

被允许探索八臂放射状迷宫的小鼠倾向于访问那些最近最少进入的臂。用右旋苯丙胺治疗会产生一种持续性倾向,即小鼠会反复访问迷宫的两个臂。给予去甲肾上腺素(NE)神经毒素N-2-氯乙基-N-乙基-2-溴苄胺(DSP4),可显著降低海马和皮质中的NE含量,适度降低蓝斑中的NE含量,而对下丘脑NE的影响较小。DSP4治疗导致苯丙胺处理的小鼠运动活动减少,同时刻板反应模式增加。虽然NE耗竭并不影响小鼠通常表现出的探索模式,但DSP4显著增加了苯丙胺引发的持续性倾向。通过脑室内注射儿茶酚胺神经毒素6-羟基多巴胺(6-OHDA)来降低多巴胺(DA)和NE,可拮抗苯丙胺的作用,从而增加交替反应的频率并降低持续性反应的比例。在用去甲丙咪嗪预处理的小鼠中,6-OHDA治疗拮抗苯丙胺诱导的持续性的有效性并未降低,去甲丙咪嗪可部分预防6-OHDA给药导致的NE减少。有人认为,DA神经元活动促成了苯丙胺引发的持续性,而NE刺激通过影响探索或习惯化来改变持续性倾向。

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