Modeling Gene Networks in Neuronal Adaptation to Alcohol
Modeling Gene Networks in Neuronal Adaptation to Alcohol
批准号:
7154774
负责人:
JAMES SCHWABER
金额:
$34.08万
依托单位国家:
美国
项目类别:
财政年份:
2005
资助国家:
美国
项目状态:
已结题
起止时间:
2005-12-10 至 2009-11-30
关键词:
AcuteAdvanced DevelopmentAlcohol dependenceAlcohol withdrawal syndromeAlcoholsAmygdaloid structureAnimalsBioinformaticsBiologicalBrainCell NucleusCell physiologyCellsChronicComplexConsensusDataData SetDevelopmentDiseaseExperimental DesignsFutureGene ExpressionGenesGenomicsHealthHomeostasisHourLinkLiteratureMediatingMicroarray AnalysisModelingNervous system structureNeuraxisNeuronsNucleus solitariusNumbersPathway AnalysisPathway interactionsPatternPhenotypePhysiologicalPopulationProcessPropertyProteinsReadingRegulationRegulator GenesResearch PersonnelRiskRoleSeriesSignal PathwaySignal TransductionSolidStatistical ModelsStimulusStressStructureSymptomsTimeTissue-Specific Gene ExpressionTranscriptional RegulationUnited States Public Health ServiceUrsidae FamilyWithdrawalalcohol abuse therapyalcohol effectalcohol responsebasecell typecomputerized toolsdata modelingdrinkinginsightinterestnovelproblem drinkerprogramsresearch studyresponsetranscription factorvalidation studies
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The present proposal has public health service relevance by providing understanding of the neuronal processes underlying the dysregulation of homeostasis and anxiogenic effects of alcohol withdrawal. These effects keep alcoholics from quitting drinking, and in fact make sudden cessation of drinking not just unpleasant but a significant health risk itself. We will discover new processes involved in this that can be explored as potential new targets for amelioration of the negative consequences of alcohol withdrawal. This proposal seeks to perform animal studies to identify and characterize genes associated with alcohol withdrawal. Alcohol's effects on the central nervous system (CNS) are mediated by genes and gene products differentially expressed in a variety of regions and specific neuron types. These changes can be different or opposite in specific cell types, or may occur in only particular cell types, and may be relatively large or very subtle. Furthermore, it is clear that the response to alcohol withdrawal is not confined to one or a few genes, but rather is a complex, dynamical process involving the coordinate regulation of large numbers of genes over time. We propose to collect a time series of global gene expression datasets that will reveal the genomic processes and mechanisms of the alcohol withdrawal of neurons in order to discover and model the gene networks and cellular controls of alcohol withdrawal in the brain. The major strengths of the approach we propose are the novel and robust microarray technology and advanced bioinformatics/mathematical analyses we have developed and employed. We propose two specific aims: (1) develop statistical models of the patterns of transcriptional response during acute alcohol withdrawal across time as compared to the chronic alcohol state and the normal state and within two key neuronal populations (2)) Identify the evolving gene regulatory network activities and mechanisms, and derived signaling pathway activities by which a alcohol withdrawal develops using computational approaches to develop models of the process of alcohol withdrawal, and perform appropriate experimental validation studies leading to future studies.
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会议论文
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资助金额:$19.38万
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财政年份:2013
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Neuroimmune Cell Networks in Opioid Dependence and Withdrawal
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批准号:8600490
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资助金额:$19.38万
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财政年份:2013
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财政年份:2012
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负责人:JAMES SCHWABER
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Modeling Central Autonomic Regulatory Network Adaptation to Hypertension
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资助金额:$58.27万
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财政年份:2012
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负责人:JAMES SCHWABER
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依托单位:
Modeling Central Autonomic Regulatory Network Adaptation to Hypertension
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批准号:8843930
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项目类别:
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资助金额:$59.2万
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财政年份:2012
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负责人:JAMES SCHWABER
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依托单位:
Modeling Central Autonomic Regulatory Network Adaptation to Hypertension
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批准号:8657102
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项目类别:
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资助金额:$59.18万
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财政年份:2012
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负责人:JAMES SCHWABER
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依托单位:
Novel Low Cost, High Throughput DNA Sequencing Platform
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批准号:7989338
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资助金额:$1.8万
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依托单位:
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批准号:8054877
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财政年份:2009
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依托单位:
Integrated Signaling and Transcriptional Networks in Circadian Clock Neurons
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资助金额:$47.55万
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财政年份:2009
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依托单位:
Novel Low Cost, High Throughput DNA Sequencing Platform
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批准号:7671858
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资助金额:$15.69万
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财政年份:2009
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依托单位:
Integrated Modeling of Adaptive Neuronal Regulation
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批准号:8248271
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资助金额:$37.86万
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财政年份:2009
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负责人:JAMES SCHWABER
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依托单位:
Integrated Modeling of Adaptive Neuronal Regulation
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批准号:7826945
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财政年份:2009
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负责人:JAMES SCHWABER
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Integrated Signaling and Transcriptional Networks in Circadian Clock Neurons
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资助金额:$39.27万
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依托单位:
Integrated Signaling and Transcriptional Networks in Circadian Clock Neurons
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批准号:7670496
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资助金额:$40.43万
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财政年份:2007
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负责人:JAMES SCHWABER
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Integrated Signaling and Transcriptional Networks in Circadian Clock Neurons
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项目类别:
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资助金额:$40.66万
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财政年份:2007
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负责人:JAMES SCHWABER
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Integrated Signaling and Transcriptional Networks in Circadian Clock Neurons
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依托单位:
海外基金