Neural Connectivity and the Transition to Alcohol Dependence

神经连接和酒精依赖的转变

基本信息

  • 批准号:
    8509928
  • 负责人:
  • 金额:
    $ 11.23万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    2013
  • 资助国家:
    美国
  • 起止时间:
    2013-09-15 至 2015-08-31
  • 项目状态:
    已结题

项目摘要

DESCRIPTION (provided by applicant): The advent of functional magnetic resonance imaging (fMRI) has profoundly advanced understanding of the human brain. One of the most exciting cutting-edge applications of fMRI is connectivity analysis, which reveals not only the separate brain regions involved in a given neural process, but also the manner in which these regions interact with each other. Dysfunction in such interactions is arguably the crux of human psychopathology. Connectivity analysis may particularly advance understanding of the neurobiology of alcohol dependence (alcoholism), a progressive, chronically relapsing disease that affects eight million Americans annually. The disease often begins with reward-driven heavy drinking and ultimately develops into a pattern of habitual, compulsive use. Animal models of addiction suggest that one key factor in this transition is a pervasive shift in the connectivity of the brain's behavioral control system. Initially, drinking may co-opt a brain network that underlies goal-directed (reward-motivated) behavior. After dependence onsets, drinking may shift to a network that mediates habit learning, or compulsivity. Human fMRI studies suggest that these networks are active when individuals are exposed to alcohol cues and also when they are at rest. Further, their integrity may be related to neurocognitive deficits in executive functioning. However, these networks have not been studied systematically in human alcoholics. This proposal will use fMRI connectivity analysis to test connectivity of the goal-directed and habit learning networks among non-dependent heavy drinkers and alcohol-dependent individuals. There are three specific aims: 1) to identify the connectivity differences between these groups during alcohol cue reactivity; 2) to identify such differences between groups while at rest; and 3) to determine whether connectivity differences are related to individual differences in neurocognitive impairment. Understanding shifts in the dominance of brain networks subserving reward and habit will ultimately contribute to the development of more efficacious treatments for alcohol dependence.
描述(由申请人提供):功能磁共振成像(fMRI)的出现深刻地推进了对人类大脑的理解。功能磁共振成像最令人兴奋的前沿应用之一是连通性分析,它不仅揭示了参与给定神经过程的独立大脑区域,还揭示了这些区域相互作用的方式。这种相互作用中的功能障碍可以说是人类精神病理学的关键。连通性分析可以特别促进对酒精依赖(酒精中毒)的神经生物学的理解,酒精依赖是一种进行性慢性复发的疾病,每年影响800万美国人。这种疾病通常始于奖励驱动的大量饮酒,最终发展成习惯性的、强迫性的饮酒模式。成瘾的动物模型表明,这种转变的一个关键因素是大脑行为控制系统连接的普遍转变。最初,饮酒可能会影响大脑中目标导向(奖励激励)行为的网络。在依赖开始后,饮酒可能会转移到一个调节习惯学习或强迫性的网络。人类功能磁共振成像研究表明,当个体接触酒精时,这些网络是活跃的,当他们休息时也是如此。此外,它们的完整性可能与执行功能中的神经认知缺陷有关。然而,这些网络尚未在人类酗酒者中进行系统研究。本提案将使用功能磁共振连通性分析来测试非依赖性重度饮酒者和酒精依赖性个体之间目标导向和习惯学习网络的连通性。有三个具体目的:1)确定这些组在酒精线索反应过程中的连通性差异;2)在休息时识别群体之间的差异;3)确定连通性差异是否与神经认知障碍的个体差异有关。理解大脑网络控制奖励和习惯的转变,最终将有助于开发更有效的治疗酒精依赖的方法。

项目成果

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JOSEPH P. SCHACHT其他文献

JOSEPH P. SCHACHT的其他文献

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{{ truncateString('JOSEPH P. SCHACHT', 18)}}的其他基金

An exploratory randomized controlled trial of the effects of oral semaglutide on alcohol craving and consumption
口服索马鲁肽对酒精渴望和消费影响的探索性随机对照试验
  • 批准号:
    10747743
  • 财政年份:
    2023
  • 资助金额:
    $ 11.23万
  • 项目类别:
COMT inhibition as a potential therapeutic target among individuals with comorbid Alcohol Use Disorder and Attention-Deficit/Hyperactivity Disorder
COMT 抑制作为共病酒精使用障碍和注意力缺陷/多动障碍患者的潜在治疗靶点
  • 批准号:
    9918216
  • 财政年份:
    2019
  • 资助金额:
    $ 11.23万
  • 项目类别:
A pharmacogenetic human laboratory investigation of brexpiprazole in Alcohol Use Disorder
布瑞哌唑治疗酒精使用障碍的药物遗传学人类实验室研究
  • 批准号:
    10022084
  • 财政年份:
    2019
  • 资助金额:
    $ 11.23万
  • 项目类别:
A pharmacogenetic human laboratory investigation of brexpiprazole in Alcohol Use Disorder
布瑞哌唑治疗酒精使用障碍的药物遗传学人类实验室研究
  • 批准号:
    10678836
  • 财政年份:
    2019
  • 资助金额:
    $ 11.23万
  • 项目类别:
COMT inhibition as a potential therapeutic target among individuals with comorbid Alcohol Use Disorder and Attention-Deficit/Hyperactivity Disorder
COMT 抑制作为共病酒精使用障碍和注意力缺陷/多动障碍患者的潜在治疗靶点
  • 批准号:
    10369711
  • 财政年份:
    2019
  • 资助金额:
    $ 11.23万
  • 项目类别:
COMT inhibition as a potential therapeutic target among individuals with comorbid Alcohol Use Disorder and Attention-Deficit/Hyperactivity Disorder
COMT 抑制作为共病酒精使用障碍和注意力缺陷/多动障碍患者的潜在治疗靶点
  • 批准号:
    10597530
  • 财政年份:
    2019
  • 资助金额:
    $ 11.23万
  • 项目类别:
A pharmacogenetic human laboratory investigation of brexpiprazole in Alcohol Use Disorder
布瑞哌唑治疗酒精使用障碍的药物遗传学人类实验室研究
  • 批准号:
    10231165
  • 财政年份:
    2019
  • 资助金额:
    $ 11.23万
  • 项目类别:
A pharmacogenetic human laboratory investigation of brexpiprazole in Alcohol Use Disorder
布瑞哌唑治疗酒精使用障碍的药物遗传学人类实验室研究
  • 批准号:
    10473693
  • 财政年份:
    2019
  • 资助金额:
    $ 11.23万
  • 项目类别:
Neural Connectivity and the Transition to Alcohol Dependence
神经连接和酒精依赖的转变
  • 批准号:
    8733486
  • 财政年份:
    2013
  • 资助金额:
    $ 11.23万
  • 项目类别:
A Transdisciplinary Approach to Cannabis Addiction
大麻成瘾的跨学科方法
  • 批准号:
    7223240
  • 财政年份:
    2006
  • 资助金额:
    $ 11.23万
  • 项目类别:

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