可卡因多药使用者的中皮质边缘功能:对毒品线索反应性和认知调节的多模式研究

IF 3.1 3区 医学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Stephanie G. Scala, Min Su Kang, Sylvia M. L. Cox, Pedro Rosa-Neto, Gassan Massarweh, Marco Leyton
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引用次数: 0

摘要

人们认为,药物成瘾是由于大脑皮层中叶对与毒品有关的线索产生了调节不良的反应。谷氨酸传递的改变,包括 5 型代谢谷氨酸受体(mGluR5s)的改变,可能会促进这些反应的发展和持续。然而,这些变化是何时产生的,mGluR5 和皮质中层的改变是否相关,这些都是未知数。为了进行研究,非可卡因多药依赖者和未使用可卡因的健康对照者在观看描述使用和未使用可卡因的活动的视频时,接受了[11C]ABP688正电子发射断层扫描(15名可卡因使用者和14名健康对照者)和功能磁共振成像扫描(15人/组)。在观看某些药物视频时,研究人员会指导参与者使用认知策略来降低渴求度。两组受试者都表现出了由药物线索诱发的皮质中脑边缘激活,而且在后半部分,可卡因多种药物使用者的激活程度大于健康对照组。在认知调节试验中,可卡因使用者的皮质反应有所减弱。与健康对照组相比,可卡因使用者的[11C]ABP688结合率没有变化,但事后分析发现,那些一生中使用可卡因次数达到或超过 75 次的可卡因使用者的结合率有所降低。最后,在可卡因使用者(n = 12)中,前额叶[11C]ABP688结合的个体差异与调节试验期间中脑和边缘区的激活有关。综上所述,这些初步研究结果表明:(i) 休闲型多药可卡因使用者的大脑过程偏向于可卡因相关线索;(ii) 重复使用可卡因会降低大脑皮层 mGluR5 的水平,从而削弱调节药物线索反应的能力。这些改变可能会增加成瘾的易感性,并确定早期干预目标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Mesocorticolimbic function in cocaine polydrug users: A multimodal study of drug cue reactivity and cognitive regulation

Mesocorticolimbic function in cocaine polydrug users: A multimodal study of drug cue reactivity and cognitive regulation

Mesocorticolimbic function in cocaine polydrug users: A multimodal study of drug cue reactivity and cognitive regulation

Addictions are thought to be fostered by the emergence of poorly regulated mesocorticolimbic responses to drug-related cues. The development and persistence of these responses might be promoted by altered glutamate transmission, including changes to type 5 metabotropic glutamate receptors (mGluR5s). Unknown, however, is when these changes arise and whether the mGluR5 and mesocorticolimbic alterations are related. To investigate, non-dependent cocaine polydrug users and cocaine-naïve healthy controls underwent a positron emission tomography scan (15 cocaine users and 14 healthy controls) with [11C]ABP688, and a functional magnetic resonance imaging scan (15/group) while watching videos depicting activities with and without cocaine use. For some drug videos, participants were instructed to use a cognitive strategy to lower craving. Both groups exhibited drug cue-induced mesocorticolimbic activations and these were larger in the cocaine polydrug users than healthy controls during the session's second half. During the cognitive regulation trials, the cocaine users' corticostriatal responses were reduced. [11C]ABP688 binding was unaltered in cocaine users, relative to healthy controls, but post hoc analyses found reductions in those with 75 or more lifetime cocaine use sessions. Finally, among cocaine users (n = 12), individual differences in prefrontal [11C]ABP688 binding were associated with midbrain and limbic region activations during the regulation trials. Together, these preliminary findings raise the possibility that (i) recreational polydrug cocaine users show biased brain processes towards cocaine-related cues and (ii) repeated cocaine use can lower cortical mGluR5 levels, diminishing the ability to regulate drug cue responses. These alterations might promote susceptibility to addiction and identify early intervention targets.

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来源期刊
Addiction Biology
Addiction Biology 生物-生化与分子生物学
CiteScore
8.10
自引率
2.90%
发文量
118
审稿时长
6-12 weeks
期刊介绍: Addiction Biology is focused on neuroscience contributions and it aims to advance our understanding of the action of drugs of abuse and addictive processes. Papers are accepted in both animal experimentation or clinical research. The content is geared towards behavioral, molecular, genetic, biochemical, neuro-biological and pharmacology aspects of these fields. Addiction Biology includes peer-reviewed original research reports and reviews. Addiction Biology is published on behalf of the Society for the Study of Addiction to Alcohol and other Drugs (SSA). Members of the Society for the Study of Addiction receive the Journal as part of their annual membership subscription.
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