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谷氨酸代谢型受体5(mGlu5)和腺苷A2A受体的联合拮抗作用相互作用,以调节大鼠的觅酒行为。

Combined antagonism of glutamate mGlu5 and adenosine A2A receptors interact to regulate alcohol-seeking in rats.

作者信息

Adams Cameron L, Cowen Michael S, Short Jennifer L, Lawrence Andrew J

机构信息

Department of Pharmaceutical Biology, Victorian College of Pharmacy, Monash University, Australia.

出版信息

Int J Neuropsychopharmacol. 2008 Mar;11(2):229-41. doi: 10.1017/S1461145707007845. Epub 2007 May 22.

Abstract

Adenosine and glutamate have been implicated as mediators involved in the self-administration of alcohol. In the present study we sought to determine whether adenosine receptors could interact with metabotropic glutamate receptors to regulate operant responding for alcohol and also the integration of the salience of alcohol-paired cues. Alcohol-preferring (iP) rats were trained to self-administer alcohol under operant conditions. The availability of alcohol was paired with an olfactory cue plus a stimulus light. Rats were examined under fixed ratio responding and also following extinction under a cue-induced reinstatement paradigm. Administration of the selective adenosine A2A receptor antagonist, SCH 58261, reduced fixed ratio responding for alcohol in iP rats in a dose-related manner. Furthermore, the combination of a subthreshold dose of SCH 58261 with a subthreshold dose of the mGlu5 receptor antagonist MTEP also reduced alcohol self-administration and increased the latency to the first reinforced response, suggesting a pre-ingestive effect. Moreover, this combination of SCH 58261 and MTEP also prevented the conditioned reinstatement of alcohol-seeking elicited by the re-presentation of cues previously paired with alcohol availability. In contrast, combinations of the selective adenosine A1 receptor antagonist, DPCPX, with either SCH 58261 or MTEP had no effect on alcohol responding. Collectively, these data suggest a functional interaction between adenosine A2A and mGlu5 receptors in relation to alcohol-seeking and the integration of the drug-related cues.

摘要

腺苷和谷氨酸被认为是参与酒精自我给药的介质。在本研究中,我们试图确定腺苷受体是否能与代谢型谷氨酸受体相互作用,以调节对酒精的操作性反应,以及酒精配对线索的显著性整合。训练嗜酒(iP)大鼠在操作性条件下自我给药酒精。酒精的可得性与嗅觉线索加刺激光配对。在固定比率反应下对大鼠进行检查,并在线索诱导的恢复范式下进行消退后检查。给予选择性腺苷A2A受体拮抗剂SCH 58261,以剂量相关的方式降低了iP大鼠对酒精的固定比率反应。此外,亚阈值剂量的SCH 58261与亚阈值剂量的mGlu5受体拮抗剂MTEP联合使用也降低了酒精自我给药,并增加了首次强化反应的潜伏期,表明有摄食前效应。此外,SCH 58261和MTEP的这种联合使用还阻止了由先前与酒精可得性配对的线索重新呈现所引发的觅酒条件性恢复。相比之下,选择性腺苷A1受体拮抗剂DPCPX与SCH 58261或MTEP联合使用对酒精反应没有影响。总体而言,这些数据表明腺苷A2A和mGlu5受体在觅酒和药物相关线索整合方面存在功能相互作用。

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