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D-1受体刺激对D-2介导的行为反应表达的允许作用:大鼠的定量现象学研究

Permissive role of D-1 receptor stimulation for the expression of D-2 mediated behavioral responses: a quantitative phenomenological study in rats.

作者信息

Longoni R, Spina L, Di Chiara G

机构信息

Institute of Experimental Pharmacology & Toxicology, University of Cagliari, Italy.

出版信息

Life Sci. 1987 Nov 2;41(18):2135-45. doi: 10.1016/0024-3205(87)90532-7.

Abstract

The syndrome of behavioral stimulation induced in male Sprague-Dawley rats by two dopaminergic agents was studied by distinguishing specific behavioral items and quantifying them in terms of their incidence. The specific D-2 agonist LY 171555 elicited yawning, genital grooming, exploratory behavior, downward sniffing and licking but failed to induce gnawing even at high doses. On the other hand, the D-1/D-2 agonist apomorphine elicited the full stereotyped syndrome including gnawing. Depletion of endogenous dopamine (DA) by alpha-methyltyrosine (alpha-MT) prevented the ability of LY 171555 to elicit all the items of behavioral stimulation including the stereotyped ones (sniffing and licking). In contrast, the ability of apomorphine to induce stereotypies was not reduced by depletion of endogenous DA by alpha-MT pretreatment. Blockade of D-1 receptors with SCH 23390 abolished the capacity of both LY 171555 and apomorphine to elicit all the items of behavioral stimulation. In alpha-MT pretreated rats, administration of low doses of the D-1 agonist SKF 38393 (2.5 mg/kg s.c.) reinstated the ability of LY 171555 to elicit behavioral stimulation and eventually conferred the ability of inducing gnawing. The results support the hypothesis that stimulation of D-1 receptors exerts a permissive role for the expression of behavioral stimulation following D-2 receptor stimulation. Endogenous DA appears to provide sufficient D-1 input to permit full expression of yawning, genital grooming, exploratory behavior, downward sniffing and licking following D-2 stimulation; pharmacological stimulation of D-1 in addition to D-2 receptors seems however necessary for full expression of the highest rank stereotypy item, gnawing.

摘要

通过区分特定行为项目并根据其发生率进行量化,研究了两种多巴胺能药物在雄性Sprague-Dawley大鼠中诱导的行为刺激综合征。特异性D-2激动剂LY 171555引发打哈欠、生殖器梳理、探索行为、向下嗅闻和舔舐,但即使在高剂量下也未能诱导啃咬行为。另一方面,D-1/D-2激动剂阿扑吗啡引发了包括啃咬在内的完整刻板综合征。α-甲基酪氨酸(α-MT)耗尽内源性多巴胺(DA)可阻止LY 171555引发所有行为刺激项目,包括刻板行为(嗅闻和舔舐)的能力。相比之下,α-MT预处理耗尽内源性DA并没有降低阿扑吗啡诱导刻板行为的能力。用SCH 23390阻断D-1受体消除了LY 171555和阿扑吗啡引发所有行为刺激项目的能力。在α-MT预处理的大鼠中,给予低剂量的D-1激动剂SKF 38393(2.5mg/kg皮下注射)恢复了LY 171555引发行为刺激的能力,并最终赋予了诱导啃咬的能力。结果支持以下假设:D-1受体的刺激对D-2受体刺激后行为刺激的表达起允许作用。内源性DA似乎提供了足够的D-1输入,以允许在D-2刺激后充分表达打哈欠、生殖器梳理、探索行为、向下嗅闻和舔舐;然而,除了D-2受体外,D-1的药理学刺激似乎是最高等级刻板行为项目啃咬充分表达所必需的。

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