Department of Psychiatry, University of Pittsburgh, Pittsburgh, Pennsylvania; Intramural Research Program, National Institute on Drug Abuse, Baltimore, Maryland.
Intramural Research Program, National Institute on Drug Abuse, Baltimore, Maryland.
Biol Psychiatry. 2021 Feb 15;89(4):376-385. doi: 10.1016/j.biopsych.2020.08.008. Epub 2020 Aug 18.
An enduring question from cross-sectional clinical studies is whether the structural and functional differences often observed between cocaine users and healthy control subjects result from a history of drug use or instead reflect preexisting differences. To assess causality from drug exposure, true predrug baseline imaging and neurocognitive assessments are needed.
We addressed this fundamental question of causality using longitudinal anatomical magnetic resonance imaging and neurocognitive assessments in rhesus macaques. Cognitive tasks employed were stimulus reversal learning as a measure of cognitive flexibility/inhibitory control and delayed match to sample as a measure of visual working memory. Time points examined were before and following 12 months of chronic cocaine (n = 8) or water (n = 6) self-administration. A magnetic resonance imaging-only time point was also obtained following 2 years of forced abstinence.
We identified localized patterns of gray matter density (GMD) changes that were largely concordant with cross-sectional clinical studies. These included decreases in orbitofrontal cortex, insula, amygdala, and temporal cortex. There was also a prominent increase in GMD in the caudate putamen. GMD decreases were significantly correlated with cognitive impairments across individuals only in select cortical regions. Following abstinence, changes in GMD in some regions, including the orbitofrontal cortex, insula, and amygdala, were persistent and thus may play an important role in risk of relapse following extended abstinence.
Cocaine use is causal in producing regional changes in GMD, and those changes appear to drive cognitive impairments.
横断面临床研究中一个持久存在的问题是,可卡因使用者和健康对照者之间经常观察到的结构和功能差异是源于药物使用史,还是反映了预先存在的差异。为了评估药物暴露的因果关系,需要进行真正的药物使用前的基线影像学和神经认知评估。
我们使用恒河猴的纵向解剖磁共振成像和神经认知评估来解决这个因果关系的基本问题。使用的认知任务是刺激反转学习,作为认知灵活性/抑制控制的衡量标准,以及延迟匹配样本,作为视觉工作记忆的衡量标准。检查的时间点是在 12 个月的慢性可卡因(n=8)或水(n=6)自我给药之前和之后。在强制禁欲 2 年后,还获得了一个仅磁共振成像的时间点。
我们确定了与横断面临床研究大致一致的局部灰质密度(GMD)变化模式。这些变化包括眶额皮质、岛叶、杏仁核和颞叶皮质的减少。尾状核壳核的 GMD 也显著增加。只有在特定的皮质区域,GMD 的减少才与个体的认知障碍显著相关。禁欲后,一些区域的 GMD 变化,包括眶额皮质、岛叶和杏仁核,仍然存在,因此可能在延长禁欲后复发的风险中起重要作用。
可卡因使用是导致 GMD 区域变化的原因,这些变化似乎导致了认知障碍。