Cortical Inhibition and Corpus Callosum Integrity in Cocaine Users

可卡因使用者的皮质抑制和胼胝体完整性

基本信息

  • 批准号:
    8596808
  • 负责人:
  • 金额:
    $ 16.79万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    2010
  • 资助国家:
    美国
  • 起止时间:
    2010-01-15 至 2014-12-31
  • 项目状态:
    已结题

项目摘要

DESCRIPTION (provided by applicant): This is a request for 5 years of funding through the "Mentored Research Scientist Development Award" (K01) mechanism. The applicant, Dr. Colleen Hanlon, is a neurobiologist with experience using functional magnetic resonance imaging to examine neural networks affected in chronic cocaine users. To further characterize changes in cortical activity in cocaine users, this application proposes a program of training in diffusion tensor imaging (DTI) and transcranial magnetic stimulation (TMS). The long- term goal of the applicant is to become an independent investigator, skilled in the application of multiple imaging modalities that may be used to guide treatment strategies in substance abusing populations. The training plan includes structured training courses in TMS acquisition and analysis, DTI image analysis, and multivariate statistics, as well as ongoing training by a team of mentors. Career development is also a strong component of this application with time devoted to Training in the Responsible Conduct of Research, manuscript and grant writing, mentoring students, attendance at scientific meetings, and interactions with the institutional review board. The research component of this award extends prior NIH-funded research complete by Dr. Hanlon, and has been carefully designed to parallel the training plan. The overarching goal of this proposal is to determine the extent to which changes in corpus callosum integrity (Specific Aim #1) and cortical inhibitory tone (Specific Aim #2) are related to atypical BOLD signal changes in the cortex of chronic cocaine users. In addition to extending investigations on sensorimotor laterality, the impact of loss of cortical laterality on cognitive function in cocaine users will also be addressed (Specific Aim #3). These experiments will reveal the extent to which changes in cortical inhibitory tone and corpus callosal integrity may contribute to neurofunctional and behavioral deficiencies in chronic cocaine users. The results of these experiments will be used to further the investigation and development of therapeutic treatment strategies in stimulant dependent individuals. PUBLIC HEALTH RELEVANCE: This is a request for 5 years of funding through the "Mentored Research Scientist Development Award" (K01) mechanism. The applicant, Dr. Colleen Hanlon, is a neurobiologist with experience using functional magnetic resonance imaging to examine neural networks affected in chronic cocaine users. To further characterize changes in cortical activity in cocaine users, this application proposes a program of training in diffusion tensor imaging (DTI) and transcranial magnetic stimulation (TMS). The long- term goal of the applicant is to become an independent investigator, skilled in the application of multiple imaging modalities that may be used to guide treatment strategies in substance abusing populations. The training plan includes structured training courses in TMS acquisition and analysis, DTI image analysis, and multivariate statistics, as well as ongoing training by a team of mentors. Career development is also a strong component of this application with time devoted to Training in the Responsible Conduct of Research, manuscript and grant writing, mentoring students, attendance at scientific meetings, and interactions with the institutional review board. The research component of this award extends prior NIH-funded research complete by Dr. Hanlon, and has been carefully designed to parallel the training plan. The overarching goal of this proposal is to determine the extent to which changes in corpus callosum integrity (Specific Aim #1) and cortical inhibitory tone (Specific Aim #2) are related to atypical BOLD signal changes in the cortex of chronic cocaine users. In addition to extending investigations on sensorimotor laterality, the impact of loss of cortical laterality on cognitive function in cocaine users will also be addressed (Specific Aim #3). These experiments will reveal the extent to which changes in cortical inhibitory tone and corpus callosal integrity may contribute to neurofunctional and behavioral deficiencies in chronic cocaine users. The results of these experiments will be used to further the investigation and development of therapeutic treatment strategies in stimulant dependent individuals.
描述(由申请人提供):这是一个通过“指导研究科学家发展奖”(K01)机制获得5年资助的请求。申请人Colleen Hanlon博士是一名神经生物学家,具有使用功能性磁共振成像检查慢性可卡因使用者受影响的神经网络的经验。为了进一步表征可卡因使用者皮层活动的变化,本申请提出了弥散张量成像(DTI)和经颅磁刺激(TMS)的培训计划。申请人的长期目标是成为一名独立的研究者,熟练应用多种成像模式,可用于指导药物滥用人群的治疗策略。培训计划包括TMS采集和分析,DTI图像分析和多元统计的结构化培训课程,以及由导师团队进行的持续培训。职业发展也是这个应用程序的一个重要组成部分,时间用于研究,手稿和赠款写作,指导学生,参加科学会议,并与机构审查委员会的互动负责任的行为培训。该奖项的研究部分扩展了由Hanlon博士完成的先前NIH资助的研究,并经过精心设计以与培训计划并行。该提案的首要目标是确定胼胝体完整性(特定目标#1)和皮质抑制性音调(特定目标#2)的变化与慢性可卡因使用者皮质中的非典型BOLD信号变化相关的程度。除了扩大对感觉运动偏侧性的研究外,还将解决皮质偏侧性丧失对可卡因使用者认知功能的影响(具体目标#3)。这些实验将揭示在何种程度上皮质抑制音和胼胝体的完整性的变化可能有助于慢性可卡因用户的神经功能和行为缺陷。这些实验的结果将被用于进一步调查和开发兴奋剂依赖个体的治疗策略。 公共卫生相关性:这是一项通过“指导研究科学家发展奖”(K01)机制提供5年资金的申请。申请人Colleen Hanlon博士是一名神经生物学家,具有使用功能性磁共振成像检查慢性可卡因使用者受影响的神经网络的经验。为了进一步表征可卡因使用者皮层活动的变化,本申请提出了弥散张量成像(DTI)和经颅磁刺激(TMS)的培训计划。申请人的长期目标是成为一名独立的研究者,熟练应用多种成像模式,可用于指导药物滥用人群的治疗策略。培训计划包括TMS采集和分析,DTI图像分析和多元统计的结构化培训课程,以及由导师团队进行的持续培训。职业发展也是这个应用程序的一个重要组成部分,时间用于研究,手稿和赠款写作,指导学生,参加科学会议,并与机构审查委员会的互动负责任的行为培训。该奖项的研究部分扩展了由Hanlon博士完成的先前NIH资助的研究,并经过精心设计以与培训计划并行。该提案的首要目标是确定胼胝体完整性(特定目标#1)和皮质抑制性音调(特定目标#2)的变化与慢性可卡因使用者皮质中的非典型BOLD信号变化相关的程度。除了扩大对感觉运动偏侧性的研究外,还将解决皮质偏侧性丧失对可卡因使用者认知功能的影响(具体目标#3)。这些实验将揭示在何种程度上皮质抑制音和胼胝体的完整性的变化可能有助于慢性可卡因用户的神经功能和行为缺陷。这些实验的结果将被用于进一步调查和开发兴奋剂依赖个体的治疗策略。

项目成果

期刊论文数量(2)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Executive control circuitry differentiates degree of success in weight loss following gastric-bypass surgery.
执行控制电路可区分胃 - bypass手术后体重减轻的成功程度。
  • DOI:
    10.1002/oby.20575
  • 发表时间:
    2013-11
  • 期刊:
  • 影响因子:
    6.9
  • 作者:
    Goldman, Rachel L.;Canterberry, Melanie;Borckardt, Jeffrey J.;Madan, Alok;Byrne, T. Karl;George, Mark S.;O'Neil, Patrick M.;Hanlon, Colleen A.
  • 通讯作者:
    Hanlon, Colleen A.
{{ item.title }}
{{ item.translation_title }}
  • DOI:
    {{ item.doi }}
  • 发表时间:
    {{ item.publish_year }}
  • 期刊:
  • 影响因子:
    {{ item.factor }}
  • 作者:
    {{ item.authors }}
  • 通讯作者:
    {{ item.author }}

数据更新时间:{{ journalArticles.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ monograph.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ sciAawards.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ conferencePapers.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ patent.updateTime }}

Colleen A Hanlon其他文献

Colleen A Hanlon的其他文献

{{ item.title }}
{{ item.translation_title }}
  • DOI:
    {{ item.doi }}
  • 发表时间:
    {{ item.publish_year }}
  • 期刊:
  • 影响因子:
    {{ item.factor }}
  • 作者:
    {{ item.authors }}
  • 通讯作者:
    {{ item.author }}

{{ truncateString('Colleen A Hanlon', 18)}}的其他基金

Longitudinal investigation of TMS as a tool to improve alcohol treatment outcomes
TMS 作为改善酒精治疗结果工具的纵向调查
  • 批准号:
    10019314
  • 财政年份:
    2019
  • 资助金额:
    $ 16.79万
  • 项目类别:
COCA: Project 4. Neurocircuit Strategy to Decrease Cocaine Cue Reactivity
COCA:项目 4。降低可卡因提示反应性的神经回路策略
  • 批准号:
    10630236
  • 财政年份:
    2019
  • 资助金额:
    $ 16.79万
  • 项目类别:
COCA: Project 4. Neurocircuit Strategy to Decrease Cocaine Cue Reactivity
COCA:项目 4。降低可卡因提示反应性的神经回路策略
  • 批准号:
    10916599
  • 财政年份:
    2019
  • 资助金额:
    $ 16.79万
  • 项目类别:
Longitudinal investigation of TMS as a tool to improve alcohol treatment outcomes
TMS 作为改善酒精治疗结果工具的纵向调查
  • 批准号:
    10245130
  • 财政年份:
    2019
  • 资助金额:
    $ 16.79万
  • 项目类别:
Longitudinal investigation of TMS as a tool to improve alcohol treatment outcomes
TMS 作为改善酒精治疗结果工具的纵向调查
  • 批准号:
    10052962
  • 财政年份:
    2019
  • 资助金额:
    $ 16.79万
  • 项目类别:
COCA: Project 4. Neurocircuit Strategy to Decrease Cocaine Cue Reactivity
COCA:项目 4。降低可卡因提示反应性的神经回路策略
  • 批准号:
    10404587
  • 财政年份:
    2019
  • 资助金额:
    $ 16.79万
  • 项目类别:
Pilot Projects Core
试点项目核心
  • 批准号:
    10526642
  • 财政年份:
    2017
  • 资助金额:
    $ 16.79万
  • 项目类别:
Impact of vMPFC Brain Stimulation on Outcomes in Treatment-Engaged Cocaine Users
vMPFC 大脑刺激对接受治疗的可卡因使用者的结果的影响
  • 批准号:
    9092998
  • 财政年份:
    2016
  • 资助金额:
    $ 16.79万
  • 项目类别:
Longitudinal study of functional connectivity among cocaine users in treatment
可卡因使用者在治疗中功能连接的纵向研究
  • 批准号:
    9067266
  • 财政年份:
    2014
  • 资助金额:
    $ 16.79万
  • 项目类别:
Investigating the Neurobiologic Basis for Loss of Cortical Laterality in Chronic
研究慢性病患者皮质偏侧性丧失的神经生物学基础
  • 批准号:
    8663383
  • 财政年份:
    2014
  • 资助金额:
    $ 16.79万
  • 项目类别:

相似海外基金

Hormone therapy, age of menopause, previous parity, and APOE genotype affect cognition in aging humans.
激素治疗、绝经年龄、既往产次和 APOE 基因型会影响老年人的认知。
  • 批准号:
    495182
  • 财政年份:
    2023
  • 资助金额:
    $ 16.79万
  • 项目类别:
Parkinson's disease and aging affect neural activation during continuous gait alterations to the split-belt treadmill: An [18F] FDG PET Study.
帕金森病和衰老会影响分体带跑步机连续步态改变期间的神经激活:[18F] FDG PET 研究。
  • 批准号:
    400097
  • 财政年份:
    2019
  • 资助金额:
    $ 16.79万
  • 项目类别:
The elucidation of the mechanism by which intestinal epithelial cells affect impaired glucose tolerance during aging
阐明衰老过程中肠上皮细胞影响糖耐量受损的机制
  • 批准号:
    19K09017
  • 财政年份:
    2019
  • 资助金额:
    $ 16.79万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Does aging of osteocytes adversely affect bone metabolism?
骨细胞老化会对骨代谢产生不利影响吗?
  • 批准号:
    18K09531
  • 财政年份:
    2018
  • 资助金额:
    $ 16.79万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Links between affect, executive function, and prefrontal structure in aging: A longitudinal analysis
衰老过程中情感、执行功能和前额叶结构之间的联系:纵向分析
  • 批准号:
    9766994
  • 财政年份:
    2018
  • 资助金额:
    $ 16.79万
  • 项目类别:
Affect regulation and Beta Amyloid: Maturational Factors in Aging and Age-Related Pathology
影响调节和 β 淀粉样蛋白:衰老和年龄相关病理学中的成熟因素
  • 批准号:
    9320090
  • 财政年份:
    2017
  • 资助金额:
    $ 16.79万
  • 项目类别:
Affect regulation and Beta Amyloid: Maturational Factors in Aging and Age-Related Pathology
影响调节和 β 淀粉样蛋白:衰老和年龄相关病理学中的成熟因素
  • 批准号:
    10166936
  • 财政年份:
    2017
  • 资助金额:
    $ 16.79万
  • 项目类别:
Affect regulation and Beta Amyloid: Maturational Factors in Aging and Age-Related Pathology
影响调节和 β 淀粉样蛋白:衰老和年龄相关病理学中的成熟因素
  • 批准号:
    9761593
  • 财政年份:
    2017
  • 资助金额:
    $ 16.79万
  • 项目类别:
Experimental Model of Depression in Aging: Insomnia, Inflammation, and Affect Mechanisms
衰老过程中抑郁症的实验模型:失眠、炎症和影响机制
  • 批准号:
    9925164
  • 财政年份:
    2016
  • 资助金额:
    $ 16.79万
  • 项目类别:
Experimental Model of Depression in Aging: Insomnia, Inflammation, and Affect Mechanisms
衰老过程中抑郁症的实验模型:失眠、炎症和影响机制
  • 批准号:
    9345997
  • 财政年份:
    2016
  • 资助金额:
    $ 16.79万
  • 项目类别:
{{ showInfoDetail.title }}

作者:{{ showInfoDetail.author }}

知道了