Suppr超能文献

选择性多巴胺D₃受体拮抗剂SB - 277011A可减弱雄性斯普拉格-道利大鼠中药物或食物剥夺对可卡因条件性位置偏爱表达的重新激活作用。

The selective dopamine D₃ receptor antagonist SB-277011A attenuates drug- or food-deprivation reactivation of expression of conditioned place preference for cocaine in male Sprague-Dawley rats.

作者信息

Ashby Charles R, Rice Onarae V, Heidbreder Christian A, Gardner Eliot L

机构信息

Department of Pharmaceutical Sciences, College of Pharmacy and Allied Health Professions, St. John's University, Jamaica, New York, 11439.

出版信息

Synapse. 2015 Jun;69(6):336-44. doi: 10.1002/syn.21820.

Abstract

We determined the effect of the selective dopamine D3 receptor antagonist SB-277011A on reactivation of conditioned place preference (CPP) to cocaine elicited by priming injections of cocaine or exposure to food deprivation stress (21 h) in male Sprague-Dawley rats. Animals paired with the cocaine-associated chamber displayed a robust and consistent CPP response. This CPP was extinguished after repeated pairings of the conditioned stimuli (cocaine-paired chamber contextual cues) in the absence of the unconditioned stimulus (cocaine). Twenty-four hours later, the administration of 5 mg kg(-1) i.p. of cocaine (immediately before the test) or exposure to 21 h of food deprivation reactivated the expression of the cocaine-induced CPP. In contrast, administration of 1 ml kg(-1) i.p. of vehicle did not reactivate the CPP response. Administration of the selective dopamine D3 receptor antagonist SB-277011A (3-24 mg kg(-1) i.p.) 30 min before cocaine administration on the test day produced a significant attenuation of CPP reactivation. Reactivation of the CPP response produced by food deprivation was also significantly attenuated by SB-277011A (6 or 12 mg kg(-1) i.p.) given 30 min before the test session. SB-277011A (12 or 24 mg kg(-1) i.p.) did not itself produce reactivation of the CPP response. Overall, these results suggest that the reactivation of the incentive value of drug-associated cues by cocaine or food deprivation is attenuated by selective antagonism of D3 receptors.

摘要

我们研究了选择性多巴胺D3受体拮抗剂SB - 277011A对雄性Sprague - Dawley大鼠中由可卡因引发的条件性位置偏爱(CPP)再激活的影响,该再激活是由可卡因的激发注射或暴露于食物剥夺应激(21小时)引起的。与可卡因相关的实验箱配对的动物表现出强烈且一致的CPP反应。在没有非条件刺激(可卡因)的情况下,经过条件刺激(可卡因配对实验箱的环境线索)的重复配对后,这种CPP反应被消除。24小时后,腹腔注射5 mg kg(-1)的可卡因(在测试前立即注射)或暴露于21小时的食物剥夺会使可卡因诱导的CPP表达重新激活。相比之下,腹腔注射1 ml kg(-1)的溶剂不会重新激活CPP反应。在测试当天,在注射可卡因前30分钟腹腔注射选择性多巴胺D3受体拮抗剂SB - 277011A(3 - 24 mg kg(-1))会显著减弱CPP的重新激活。在测试前30分钟给予SB - 277011A(6或12 mg kg(-1)腹腔注射)也会显著减弱由食物剥夺产生的CPP反应的重新激活。SB - 277011A(12或24 mg kg(-i)腹腔注射)本身不会引起CPP反应的重新激活。总体而言,这些结果表明,可卡因或食物剥夺对与药物相关线索的激励价值的重新激活会因D3受体的选择性拮抗作用而减弱。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验