Network Analysis and Computational Modeling Core
Network Analysis and Computational Modeling Core
批准号:
10526832
负责人:
CHRISTOPHER COURT LAPISH
金额:
$15.88万
依托单位国家:
美国
项目类别:
财政年份:
1989
资助国家:
美国
项目状态:
未结题
起止时间:
1989-12-01 至 2027-11-30
关键词:
ARHGEF5 geneAlcohol consumptionAlcoholsAreaArticulationArtificial IntelligenceBehavioralBiophysicsBrainComplementComputer ModelsDataData AnalysesData SetElectrophysiology (science)Functional Magnetic Resonance ImagingGenetic DeterminismGoalsHeritabilityHumanImpairmentIndianaLeadLinkMeasuresModelingNCAM1 geneNetwork-basedNeurobiologyNeurophysiology - biologic functionPathologyPathway AnalysisPopulationPopulation AnalysisPredispositionProsencephalonResearchRiskRodentServicesSignal TransductionSourceStatistical Data InterpretationSystemTechniquesTestingTranslationsWorkaddictionalcohol researchalcohol responsealcohol use disorderdynamic systemexperiencehigh intensity drinkinginsightmultidimensional dataneuralneural circuitnovelnovel strategiessynergismtranslational potentialvirtual
中文摘要
项目摘要
P60印第安纳州酒精研究中心(IARC)的这次更新将确定大脑活动的变化
使人容易酗酒和高强度饮酒(BHID)。为了实现这一目标,IARC将收集
来自人类和啮齿动物的大量、密集的数据集,使用一系列技术获取多个、
同时测量神经功能。
在网络分析和计算建模方面的专业知识,为中心的研究组件提供支持。的目标是
NACM将以翻译的方式询问BHID背后的大脑网络和神经电路。
因此,NCAM的目标是增加跨物种和组件的协同作用和翻译,
并将该中心的数据整合到能够阐明神经病理的计算模型中
BHID背后的电路。NACM将与研究部门密切合作,实施和
开发捕获网络和系统级交互的分析和计算建模技术。
实现这一点将增加IARC产生的更严格和更综合的、协同的结论
组件。因此,NCAM将提供先进的、有针对性的分析和计算模型
提高各组成部分之间的协同效应。这将传播目前IARC在统计分析方面的专业知识
以及更广泛的计算建模到中心。
这使得
每个组成部分更有效地评估他们的假设,长期目标是提供更多
BHID作用机理的综合模型。这将通过三个具体目标来实现:
具体目标1:确定BHID在人类和啮齿动物中的改变,潜在的翻译,网络功能。
BHID中对人类和啮齿动物数据的计算。
具体目标3:建立BHID改变的皮质边缘系统的计算模型。
NACM的积极影响将是提供对大脑网络如何执行计算的洞察
在BHID和AUD的风险人群中发生改变。了解这一点将启发治疗的新方法
这更紧密地将神经回路功能的可遗传变化与BHID联系在一起。
英文摘要
Project Summary
This renewal of the P60 Indiana Alcohol Research Center (IARC) will identify the changes in brain activity that
predispose one to Binge and High Intensity Drinking (BHID). Towards this goal, the IARC will be collecting
large, dense data sets from humans and rodents with a range of techniques that acquire multiple,
simultaneous measures of neural function. This creates a critical need for an IARC service core that provide
expertise in network analysis and computational modeling to the center’s research components. The goal of
the NACM is to interrogate the brain networks and neural circuits that underlie BHID in a translational manner.
The objective of the NCAM is to therefore increase synergy and translation across species and components,
and to integrate the center’s data into computational models capable of articulating the pathology in neural
circuits that underlie BHID. The NACM will work closely with the research components to implement and
develop analyses and computational modeling techniques that capture network and systems-level interactions.
Accomplishing this will provide added rigor and more integrated, synergistic conclusions generated by IARC
components. Thus, the NCAM will provide advanced, targeted analyses and computational models that
increase synergy among the components. This will disseminate current IARC expertise in statistical analyses
and computational modeling to the center more broadly. As a core, the NACM does not set out to test specific
hypotheses, but rather, to work closely with the research components to add rigor and synergy. This allows
each component to assess their hypotheses more effectively, with the long-term goal of providing more
integrated model of the mechanisms of BHID. This will be accomplished in three Specific Aims:
Specific Aim 1: Identify altered, potentially translational, network functions in BHID in humans and rodents.
Specific Aim 2: Apply population analysis and artificial intelligence-based approaches to identify altered
computations in BHID to human and rodent data.
Specific Aim 3: Build computational models of corticolimbic systems altered in BHID.
The positive impact of the NACM will be to provide insight into how computations performed by brain networks
are altered in those at risk for BHID and AUD. Understanding this will inspire novel approaches to treatment
that more tightly link heritable changes in neural circuit function to BHID.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
CORE 1/2: INIA Stress and Chronic Alcohol Interactions: Computational and Statistical Analysis Core (CSAC)
-
批准号:10411629
-
项目类别:
-
资助金额:$51.73万
-
财政年份:2022
-
负责人:CHRISTOPHER COURT LAPISH
-
依托单位:
CORE 1/2: INIA Stress and Chronic Alcohol Interactions: Computational and Statistical Analysis Core (CSAC)
-
批准号:10574618
-
项目类别:
-
资助金额:$49.39万
-
财政年份:2022
-
负责人:CHRISTOPHER COURT LAPISH
-
依托单位:
Determining the acute pharmacological effects of alcohol in rodent medial prefrontal cortex
-
批准号:10194666
-
项目类别:
-
资助金额:$21.39万
-
财政年份:2021
-
负责人:CHRISTOPHER COURT LAPISH
-
依托单位:
Determining the acute pharmacological effects of alcohol in rodent medial prefrontal cortex
-
批准号:10397093
-
项目类别:
-
资助金额:$17.37万
-
财政年份:2021
-
负责人:CHRISTOPHER COURT LAPISH
-
依托单位:
Prefrontal cortex regulation of ethanol-reinforced behavior
-
批准号:9240555
-
项目类别:
-
资助金额:$34.17万
-
财政年份:2015
-
负责人:CHRISTOPHER COURT LAPISH
-
依托单位:
Corticostriatal processing of alcohol-paired cues in aversion-resistant drinking
-
批准号:10310679
-
项目类别:
-
资助金额:$17.95万
-
财政年份:1989
-
负责人:CHRISTOPHER COURT LAPISH
-
依托单位:
海外基金