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Functional consequences of cocaine expectation: findings in a non-human primate model of cocaine self-administration

机译:可卡因期望的功能后果:可卡因自我管理的非人类灵长类动物模型中的发现

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Exposure to stimuli and environments associated with drug use is considered one of the most important contributors to relapse among substance abusers. Neuroimaging studies have identified neural circuits underlying these responses in cocaine-dependent subjects. But these studies are often difficult to interpret because of the heterogeneity of the participants, substances abused, and differences in drug histories and social variables. Therefore, the goal of this study was to assess the functional effects of exposure to cocaine-associated stimuli in a non-human primate model of cocaine self-administration, providing precise control over these variables, with the 2-[C-14]deoxyglucose method. Rhesus monkeys self-administered 0.3mg/kg/injection cocaine (n=4) under a fixed-interval 3-minute (FI 3-min) schedule of reinforcement (30 injections/session) for 100 sessions. Control animals (n=4) underwent identical schedules of food reinforcement. Sessions were then discontinued for 30 days, after which time, monkeys were exposed to cocaine- or food-paired cues, and the 2-[C-14]deoxyglucose experiment was conducted. The presentation of the cocaine-paired cues resulted in significant increases in functional activity within highly restricted circuits that included portions of the pre-commissural striatum, medial prefrontal cortex, rostral temporal cortex and limbic thalamus when compared with control animals presented with the food-paired cues. The presentation of cocaine-associated cues increased brain functional activity in contrast to the decreases observed after cocaine consumption. Furthermore, the topography of brain circuits engaged by the expectation of cocaine is similar to the distribution of effects during the earliest phases of cocaine self-administration, prior to the onset of neuroadaptations that accompany chronic cocaine exposure.
机译:暴露于与毒品使用相关的刺激和环境被认为是滥用药物者复发的最重要因素之一。神经影像学研究已经确定了可卡因依赖性受试者中这些反应背后的神经回路。但是由于参与者的异质性,滥用的药物以及毒品史和社会变量的差异,这些研究通常难以解释。因此,本研究的目的是在可卡因自我给药的非人类灵长类动物模型中评估暴露于可卡因相关刺激的功能效应,并利用2- [C-14]脱氧葡萄糖提供对这些变量的精确控制。方法。恒河猴以固定间隔的3分钟(FI 3分钟)强化方案(每节30次注射)自我给药0.3mg / kg /注射可卡因(n = 4),共100次。对照动物(n = 4)接受相同的食物强化计划。然后中断会议30天,此后,将猴子暴露于可卡因或食物配对的提示下,然后进行2- [C-14]脱氧葡萄糖实验。可卡因配对提示的出现导致与限制食物配对的对照动物相比,高度受限的回路(包括连合前纹状体,内侧前额叶皮层,颞侧皮层和边缘丘脑)的部分功能功能显着增加。提示。与可卡因相关的提示的表现增加了脑功能活动,与食用可卡因后观察到的下降相反。此外,可卡因的期望所参与的大脑回路的拓扑结构类似于可卡因自我给药的最早阶段,即在伴随慢性可卡因暴露的神经适应发作之前,效应的分布。

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