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腺苷A1和A2A受体对大鼠短期社会记忆的调节作用

Modulation of short-term social memory in rats by adenosine A1 and A(2A) receptors.

作者信息

Prediger Rui D S, Takahashi Reinaldo N

机构信息

Departamento de Farmacologia, Centro de Ciências Biológicas, Universidade Federal de Santa Catarina, UFSC, Florianópolis, SC 88049-900, Brazil.

出版信息

Neurosci Lett. 2005 Mar 16;376(3):160-5. doi: 10.1016/j.neulet.2004.11.049. Epub 2004 Dec 9.

Abstract

The recognition of an unfamiliar juvenile rat by an adult rat has been shown to imply short-term memory processes. The present study was designed to examine the role of adenosine receptors in the short-term social memory of rats using the social recognition paradigm. Adenosine (5.0-10.0 mg/kg), the selective adenosine A1 receptor agonist 2-chloro-N6-cyclopentyladenosine (CCPA, 0.025-0.05 mg/kg) and the selective adenosine A(2A) receptor agonist N6-[2-(3,5-dimethoxyphenyl)-2-(2-methylphenyl)ethyl]adenosine (DPMA, 1.0-5.0 mg/kg), given by i.p. route 30 min before the test, disrupted the juvenile recognition ability of adult rats. This negative effect of adenosine (5.0 mg/kg, i.p.) on social memory was prevented by pretreatment with the non-selective adenosine receptor antagonist caffeine (10.0 mg/kg, i.p.), the adenosine A1 antagonist 8-cyclopentyl-1,3-dipropylxanthine (DPCPX, 1.0 mg/kg, i.p.) and the adenosine A(2A) antagonist 4-(2-[7-amino-2-{2-furyl}{1,2,4}triazolo-{2,3-a}{1,3,5}triazin-5-yl-amino]ethyl)phenol (ZM241385, 1.0 mg/kg, i.p.). Furthermore, acute administration of caffeine (10.0-30.0 mg/kg, i.p.), DPCPX (1.0-3.0 mg/kg, i.p.) or ZM241385 (0.5-1.0 mg/kg, i.p.) improved the short-term social memory in a specific manner. These results indicate that adenosine modulates the short-term social memory in rats by acting on both A1 and A(2A) receptors, with adenosine receptor agonists and antagonists, respectively, disrupting and enhancing the social memory.

摘要

成年大鼠对陌生幼鼠的识别已被证明涉及短期记忆过程。本研究旨在使用社会识别范式来研究腺苷受体在大鼠短期社会记忆中的作用。在测试前30分钟腹腔注射腺苷(5.0 - 10.0毫克/千克)、选择性腺苷A1受体激动剂2 - 氯 - N6 - 环戊基腺苷(CCPA,0.025 - 0.05毫克/千克)和选择性腺苷A(2A)受体激动剂N6 - [2 - (3,5 - 二甲氧基苯基)-2 - (2 - 甲基苯基)乙基]腺苷(DPMA,1.0 - 5.0毫克/千克),会破坏成年大鼠对幼鼠的识别能力。腹腔注射5.0毫克/千克腺苷对社会记忆的这种负面影响可被非选择性腺苷受体拮抗剂咖啡因(10.0毫克/千克,腹腔注射)、腺苷A1拮抗剂8 - 环戊基 - 1,3 - 二丙基黄嘌呤(DPCPX,1.0毫克/千克,腹腔注射)和腺苷A(2A)拮抗剂4 - (2 - [7 - 氨基 - 2 - {2 - 呋喃基}{1,2,4}三唑并 - {2,3 - a}{1,3,5}三嗪 - 5 - 基 - 氨基]乙基)苯酚(ZM241385,1.0毫克/千克,腹腔注射)预处理所预防。此外,急性腹腔注射咖啡因(10.0 - 30.0毫克/千克)、DPCPX(1.0 - 3.0毫克/千克)或ZM241385(0.5 - 1.0毫克/千克)能以特定方式改善短期社会记忆。这些结果表明,腺苷通过作用于A1和A(2A)受体来调节大鼠的短期社会记忆,腺苷受体激动剂和拮抗剂分别破坏和增强社会记忆。

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