Integrated Program in Neuroscience, McGill University, Montreal, Quebec, Canada.
Sunnybrook Research Institute, University of Toronto, Toronto, Ontario, Canada.
Addict Biol. 2024 Jan;29(1):e13358. doi: 10.1111/adb.13358.
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 [ C]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. [ C]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 [ C]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.
成瘾被认为是由药物相关线索引起的调节不良的中脑边缘奖赏反应的出现所促成的。这些反应的发展和持续可能是由谷氨酸传递的改变所促进的,包括对 5 型代谢型谷氨酸受体 (mGluR5s) 的改变。然而,尚不清楚这些变化何时发生,以及 mGluR5 和中脑边缘改变是否相关。为了研究这一点,非依赖可卡因多药使用者和可卡因-naive 健康对照者接受了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) 与 [C]ABP688,并进行了功能磁共振成像扫描 (15/组),同时观看了描述有无可卡因使用的活动的视频。对于一些毒品视频,参与者被指示使用认知策略来降低渴望。两组都表现出药物线索诱导的中脑边缘奖赏反应,在会议的后半段,可卡因多药使用者的反应比健康对照组更大。在认知调节试验中,可卡因使用者的皮质纹状体反应减少。与健康对照组相比,可卡因使用者的 [C]ABP688 结合无改变,但事后分析发现,那些有 75 次或更多可卡因使用疗程的人的结合减少了。最后,在可卡因使用者中(n=12),前额叶 [C]ABP688 结合的个体差异与调节试验期间中脑和边缘区域的激活有关。总之,这些初步发现提出了以下可能性:(i)娱乐性多药可卡因使用者对可卡因相关线索表现出偏向的大脑过程;(ii)反复可卡因使用可以降低皮质 mGluR5 水平,从而降低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,并确定早期干预的目标。