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多巴胺介导的行为表达是否需要同时刺激 D1 和 D2 受体?

Is stimulation of both D1 and D2 receptors necessary for the expression of dopamine-mediated behaviors?

作者信息

White F J, Bednarz L M, Wachtel S R, Hjorth S, Brooderson R J

机构信息

University of Illinois, Department of Psychology, Champaign 61820.

出版信息

Pharmacol Biochem Behav. 1988 May;30(1):189-93. doi: 10.1016/0091-3057(88)90442-x.

Abstract

Recent electrophysiological findings have indicated that D1 dopamine (DA) receptor stimulation by SKF 38393 enables the inhibitory effects of the D2 receptor agonist quinpirole on nucleus accumbens neurons. In the present study, a similar interaction was shown for quinpirole-induced stereotyped behaviors. In control rats, SKF 38393 enhanced the stereotyped responses induced by quinpirole, converting lower-level stereotypies (sniffing and rearing) to more intense oral behaviors (licking and gnawing). In rats depleted of DA (79% reduction) by the tyrosine hydroxylase inhibitor alpha-methyl-p-tyrosine (AMPT), the behavioral effects of quinpirole were abolished. However, quinpirole-induced stereotyped responses were reinstated by SKF 38393 suggesting that D1 receptor stimulation by endogenous DA is necessary for D2 receptor-mediated stereotyped responses (sniffing, rearing). In support of this suggestion, stereotyped behaviors produced by the non-selective D1/D2 agonist apomorphine were not affected by AMPT pretreatment. In contrast to the effects of quinpirole, the ability of SKF 38393 to induce grooming responses was not abolished by AMPT pretreatment or by combined pretreatment with AMPT and reserpine (greater than 99% DA depletion). These results indicate that D1 receptor stimulation enables D2 receptor-mediated stereotyped responses, but that this relationship is not reciprocal since D2 receptor stimulation is not necessary for the grooming response elicited by SKF 38393.

摘要

最近的电生理研究结果表明,SKF 38393对D1多巴胺(DA)受体的刺激可使D2受体激动剂喹吡罗对伏隔核神经元产生抑制作用。在本研究中,喹吡罗诱导的刻板行为也表现出类似的相互作用。在对照大鼠中,SKF 38393增强了喹吡罗诱导的刻板反应,将较低水平的刻板行为(嗅探和竖毛)转变为更强烈的口腔行为(舔舐和啃咬)。在用酪氨酸羟化酶抑制剂α-甲基-p-酪氨酸(AMPT)使DA耗竭(减少79%)的大鼠中,喹吡罗的行为效应被消除。然而,SKF 38393恢复了喹吡罗诱导的刻板反应,这表明内源性DA对D1受体的刺激对于D2受体介导的刻板反应(嗅探、竖毛)是必要的。支持这一观点的是,非选择性D1/D2激动剂阿扑吗啡产生的刻板行为不受AMPT预处理的影响。与喹吡罗的作用相反,SKF 38393诱导梳理反应的能力并未因AMPT预处理或AMPT与利血平联合预处理(DA耗竭大于99%)而被消除。这些结果表明,D1受体刺激可使D2受体介导的刻板反应发生,但这种关系并非相互的,因为D2受体刺激对于SKF 38393引发的梳理反应并非必要。

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