Neural substrates of emotion: Impact of childhood trauma and cocaine dependence

情绪的神经基础：童年创伤和可卡因依赖的影响

• 批准号: 9237248
• 负责人: Jane E Joseph
• 金额: $ 31.77万
• 依托单位: MEDICAL UNIVERSITY OF SOUTH CAROLINA
• 依托单位国家: 美国
• 财政年份: 2015
• 资助国家: 美国
• 起止时间: 2015-05-01 至 2020-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/9237248
• 关键词: Abstinence; Acute; Address; Affect; Amygdaloid structure; Anterior; Anti-Anxiety Agents; Anxiety; Attenuated; Behavior; Behavior Disorders; Behavior Therapy; Biomedical Research; Brain; Brain region; Cocaine; Cocaine Dependence; Controlled Study; Coupled; Cues; Data; Development; Disease; Double-Blind Method; Drug usage; Emotional; Emotions; Exhibits; Exposure to; FDA approved; Face; Functional Magnetic Resonance Imaging; Image; Individual; Intervention; Lead; Literature; Measures; Medial; Mediating; Neurobiology; Neuropeptides; Oxytocin; Participant; Patients; Pharmaceutical Preparations; Placebos; Play; Population; Prefrontal Cortex; Prevention strategy; Psychophysiology; Relapse; Reporting; Rest; Risk Factors; Role; Running; Scanning; Seeds; Signal Transduction; Social Anxiety Disorder; Social Interaction; Stimulus; Stress; Time; Treatment Efficacy; Treatment outcome; Trust; United States; blood oxygen level dependent; cingulate cortex; cocaine use; craving; drug craving; drug relapse; effective therapy; human data; improved; insight; neurobiological mechanism; neuroimaging; pediatric trauma; prevent; public health relevance; relating to nervous system; research study; response; social; social stress; success; therapy development; treatment group; treatment strategy

 DESCRIPTION (provided by applicant): Social stress can lead to drug craving and relapse in cocaine-dependent (CD) individuals. In addition, CD individuals often favor drug use over social interactions. Moreover, social avoidance and lack of trust are significant obstacles to effective treatment. Currently, there are no FDA approved medications for the treatment of cocaine dependence and behavioral interventions have had limited success in sustaining abstinence. Data from human neuroimaging studies using blood oxygen level dependent (BOLD) functional magnetic resonance imaging (fMRI) suggest that "top-down" prefrontal cortical control of amygdala reactivity to social stimuli plays an important role in mediating emotion related behavior. Dysregulation in the functional connectivity between the prefrontal cortex and amygdala has been found in CD subjects at rest and attenuated corticolimbic functional connectivity was associated with a shorter time to relapse. Thus, dysregulation in corticolimbic network activity may underscore the vulnerability of CD individuals to social stress. In addition, interventions that restore functional connectivity between the prefrontal cortex and amygdala, and attenuate bottom-up amygdala drive may reduce anxiety and improve treatment outcomes for CD individuals. Oxytocin (OT) is an anxiolytic neuropeptide that reduces amygdala reactivity to aversive social cues. In addition, OT increases functional connectivity between the amygdala and prefrontal cortex in patients with generalized social anxiety disorder. The broad and long-term objectives of this proposal are to (1) to identify the neurobiologic mechanisms that control emotional responses to social stimuli in CD individuals and (2) use these data to facilitate the development of effective therapeutic treatments and preventative strategies for behavioral disorders and disease. To meet these objectives we propose two specific aims: Specific Aim 1: To determine the impact of cocaine dependence and oxytocin on functional connectivity between corticolimbic brain regions during acute social stress. Specific Aim 2: Use an implicit facial affect recognition paradigm to determine the impact of cocaine dependence and oxytocin on amygdala activity in response to fearful faces. The BOLD signal measured during neutral faces will be subtracted from the BOLD signal measured during fearful faces. To address the hypotheses associated with Specific Aims 1 and 2 we propose a we propose a double-blind placebo (PBO) controlled study using BOLD fMRI to measure (1) corticolimbic functional connectivity during the Montreal Imaging Stress Task (MIST) and (2) amygdala activity in response to an implicit facial affect recognition paradigm in groups of CD individuals (CD n=80) and healthy non-dependent controls (HC, n=80). Prior to the scanning session, participants will receive either intranasal OT (24 IU) or PBO spray (n=40 per treatment group). Psychophysiologic interaction (PPI) analysis using the amygdala as the seed region will be used to assess significant task (stress condition > control condition) x seed interactions. Subjective anxiety and craving data will be collected at baseline and after each run of the MIST. The order of the tasks will be counterbalanced.

 描述(由申请人提供)：社会压力可能导致可卡因依赖(CD)个人对药物的渴望和复发。此外，CD患者往往更喜欢吸毒而不是社交互动。此外，社交回避和缺乏信任是有效治疗的重大障碍。目前，还没有FDA批准的治疗可卡因依赖的药物，行为干预在维持戒断方面的成功也有限。使用血氧水平依赖(BOLD)功能磁共振成像(FMRI)的人类神经成像研究数据表明，杏仁核前额叶皮质对社会刺激的自上而下的反应性控制在调节情绪相关行为方面发挥着重要作用。在静息状态下，CD受试者前额叶皮质和杏仁核之间的功能连接失调，皮质边缘功能连接减弱与复发时间较短有关。因此，皮质边缘网络活动的失调可能突显了CD个体对社会压力的脆弱性。此外，恢复前额叶皮质和杏仁核之间的功能连接，并减弱自下而上的杏仁核驱动的干预措施，可能会减少焦虑，改善CD患者的治疗结果。催产素(OT)是一种抗焦虑的神经肽，可以降低杏仁核对厌恶的社交暗示的反应。此外，在广泛性社交焦虑障碍患者中，OT增加了杏仁核和前额叶皮质之间的功能连接。这项建议的广泛和长期目标是：(1)确定控制CD患者对社会刺激的情绪反应的神经生物学机制，以及(2)利用这些数据促进针对行为障碍和疾病的有效治疗方法和预防策略的发展。为了达到这些目标，我们提出了两个具体目标：具体目标1：确定在急性社会应激期间可卡因依赖和催产素对边缘皮质脑区之间功能连接的影响。具体目标2：使用内隐面部情绪识别范式来确定可卡因依赖和催产素对杏仁核活动的影响，以应对恐惧的面孔。中性脸部测量的粗体信号将从恐惧面孔测量的粗体信号中减去。为了解决与特定目标1和2相关的假设，我们提出了一项使用BOLD功能磁共振成像的双盲安慰剂(PBO)对照研究，以测量(1)蒙特利尔成像应激任务(MIST)过程中皮质边缘功能的连通性，以及(2)CD个体(CD n=80)和健康非依赖对照组(HC，n=80)对内隐面部情感识别范式反应的杏仁核活动。在扫描之前，参与者将接受鼻腔OT(24IU)或PBO喷雾(每个治疗组40例)。以杏仁核为种子区域的心理生理交互作用(PPI)分析将用于评估显著任务(应激条件和控制条件)×种子交互作用。主观焦虑和渴望的数据将在基线和每次雾化后收集。任务的顺序将被平衡。