Cognitive dysfunction and impaired inhibitory control in cocaine dependence

可卡因依赖的认知功能障碍和抑制控制受损

• 批准号: 8294808
• 负责人: CHARLES W BRADBERRY
• 金额: $ 38.67万
• 依托单位: UNIVERSITY OF PITTSBURGH AT PITTSBURGH
• 依托单位国家: 美国
• 财政年份: 2009
• 资助国家: 美国
• 起止时间: 2009-09-15 至 2014-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8294808
• 关键词: Address; Animal Model; Area; Atlases; Behavioral; Brain imaging; Cell physiology; Cellular Structures; Chronic; Clinical; Clinical Research; Cocaine; Cocaine Dependence; Cocaine Users; Cognitive; Cognitive deficits; Control Animal; Deltastab; Discrimination; Drug Addiction; Drug Exposure; Drug abuse; Drug usage; Electrophysiology (science); Etiology; Event; Human; Image; Imaging Techniques; Impaired cognition; Impairment; Impulsivity; Individual; Link; Macaca mulatta; Magnetic Resonance Imaging; Measures; Mediating; Methodology; Modeling; Monitor; Monkeys; Motor; Neurons; Performance; Predisposition; Prefrontal Cortex; Primates; Principal Investigator; Psychostimulant dependence; Reporting; Research Design; Role; Self Administration; Self-Administered; Signal Transduction; Societies; Source; Stimulus; Structure; System; Task Performances; Temporal Lobe; Therapeutic; Treatment Protocols; Treatment outcome; addiction; base; clinically relevant; cocaine use; cognitive control; gray matter; in vivo; morphometry; nonhuman primate; preclinical study; programs; response; white matter

DESCRIPTION (provided by applicant): Cognitive dysfunction and impaired inhibitory control are hallmarks of addiction. The prefrontal and temporal cortices are essential to effective cognitive performance, and drug abuse is associated with significant structural deficits therein. A crucial unresolved question in clinical studies is whether structural and functional differences in cortex predate, or are consequent to drug use. This application proposes longitudinal structural MR imaging in a monkey model of addiction-related cognitive and inhibitory control deficits to address the role of drug use per se in structural and functional cortical differences seen in cocaine addiction. It also will examine single unit activity to determine what cellular changes could mediate an association of altered structure and function. Animal models are key to addressing questions about the etiology and cellular basis of addiction-related cognitive dysfunction. This is especially so for primate models that share structural and cognitive similarities to humans at the cortical level and that can exploit common methodologies such as brain imaging techniques used clinically. This application will employ a clinically relevant rhesus monkey self- administration model that shows impaired performance virtually identical to that seen clinically on the Stop Task, which is used to measure impaired inhibitory control, and which is supported by a well- defined circuitry identified in clinical and pre-clinical studies. Deficits in stimulus discrimination consistent with clinical reports have also been established. We will employ the monkey model to address these fundamental questions: 1) Do structural alterations in prefrontal and temporal cortex observed in cocaine users result from drug exposure per se, rather than a preexisting condition? 2) Within individuals, does the degree of cognitive impairment correlate with extent of structural change? 3) What are cellular correlates of cognitive dysfunction associated with cocaine use? The integration of a longitudinal application of clinically employed structural and cognitive assessments, along with single unit studies, will help establish the relationship between cocaine use, altered structure, and cellular mechanisms associated with cognitive dysfunction observed clinically. Drug addiction causes extensive human suffering and financial loss to society. Understanding the source and mechanisms of cognitive dysfunction that predicts treatment outcome may help develop therapeutic approaches that lessen harm from addiction.

描述(由申请人提供)：认知功能障碍和抑制控制受损是成瘾的特征。前额叶和颞叶皮质对有效的认知表现是必不可少的，药物滥用与其中显著的结构缺陷有关。临床研究中一个关键的悬而未决的问题是，皮质结构和功能的差异是先天的，还是药物使用的结果。这项应用提出了在与成瘾相关的认知和抑制控制缺陷的猴子模型中进行纵向结构磁共振成像，以解决毒品使用本身在可卡因成瘾的结构和功能差异中所起的作用。它还将检查单个单位的活动，以确定哪些细胞变化可以调节结构和功能改变的关联。动物模型是解决成瘾相关认知功能障碍的病因和细胞基础问题的关键。对于灵长类动物模型来说尤其如此，这些模型在结构和认知上与人类在皮质水平上有相似之处，并且可以利用临床上使用的脑成像技术等常见方法。该应用程序将采用临床相关的恒河猴自我给药模型，该模型显示的性能受损与临床上在停止任务上看到的几乎相同，该任务用于测量抑制控制受损，并由临床和临床前研究中确定的明确电路支持。与临床报告一致的刺激辨别缺陷也已确定。我们将使用猴子模型来解决这些基本问题：1)在可卡因使用者中观察到的前额叶和颞叶皮质的结构变化是由药物暴露本身导致的，而不是预先存在的疾病？2)在个人内部，认知障碍的程度是否与结构变化的程度相关？3)与可卡因使用相关的认知功能障碍的细胞相关性是什么？整合临床使用的结构和认知评估的纵向应用，以及单一单元研究，将有助于建立可卡因使用、结构改变和与临床观察到的认知功能障碍相关的细胞机制之间的关系。毒品成瘾给社会造成广泛的人类痛苦和经济损失。了解认知功能障碍的来源和机制，预测治疗结果，可能有助于开发减少成瘾危害的治疗方法。