NEUROGENIC TARGETS OF ANTIDEPRESSANT THERAPIES
NEUROGENIC TARGETS OF ANTIDEPRESSANT THERAPIES
批准号:
7428804
负责人:
GRIGORI N ENIKOLOPOV
金额:
$18.9万
依托单位国家:
美国
项目类别:
财政年份:
2007
资助国家:
美国
项目状态:
已结题
起止时间:
2007-07-01 至 2010-06-30
关键词:
AddressAdolescentAdultAffectAnimal ModelAnimalsAntidepressive AgentsAreaBehavioralBiochemicalBrainCell NucleusCell divisionCellsCellular MorphologyClassClinicalClinical ResearchCytoplasmic GranulesDataDeep Brain StimulationDevelopmentDiseaseDrug Delivery SystemsElectroconvulsive ShockElectroconvulsive TherapyEnvironmentExploratory/Developmental GrantExposure toFamilyFluoxetineFunctional disorderGene ExpressionGene TargetingGenerationsGenesGlobal ChangeGoalsGrantHippocampus (Brain)ImipramineInvestigationLabelLasersLeadLinkMental DepressionMicroscopyMitotic ActivityModelingMolecularMusNervous system structureNeuronal DifferentiationNeuronsNorepinephrineNuclear Localization SignalParoxetinePatientsPatternPharmaceutical PreparationsProceduresProteinsRNARangeRateReporterResearch Project GrantsRodentSchemeSelective Serotonin Reuptake InhibitorSeriesStem cellsTarget PopulationsTimeTransgenic AnimalsTransgenic MiceTransgenic OrganismsWeekbasecellular targetingclinical effectdentate gyrusdesigninhibitor/antagonistinnovationinsightlaser capture microdissectionnerve stem cellnestin proteinneuroblastneurogenesisnovelnovel strategiesprecursor cellprogenitorreboxetinerelating to nervous systemresearch studyresponsereuptakeself-renewalstemvenlafaxine
中文摘要
描述(由申请人提供):最近的证据表明,抗抑郁药的作用与成人海马体中神经发生的增加之间存在联系;此外,它还表明,抗抑郁药的作用可能需要神经发生。然而,目前尚不清楚抗抑郁药物和治疗针对的是神经元分化级联中的哪一类细胞。我们开发了一种新的方法来识别和分类神经元前体,并获得由神经源性药物引起的变化的精确定量。我们用这种方法证明了抗抑郁剂氟西汀影响成年海马体中早期祖细胞类别的对称分裂。在这一探索性应用中,我们将使用这种方法来确定一系列抗抑郁药物和治疗的细胞和基因靶点。在第一系列实验中,我们将确定四个主要药物家族(SSRIs、SNRIs、NRIs和TCAs)、电惊厥和脑深部刺激的抗抑郁药物的神经源性细胞靶点。在第二系列实验中,我们将使用激光捕获显微镜和微阵列转录图谱来确定各种抗抑郁疗法在成年海马神经干细胞和前体细胞中的共同基因靶点。相关性:新的证据表明,成人神经发生与抑郁症的病理生理学和抗抑郁药的作用有关。我们在这里建议使用一种新的方法来确定一系列抗抑郁药物和治疗的细胞和基因靶点。我们的研究将导致对抗抑郁药物作用机制的新假说,并将有助于设计更具体和有效的抗抑郁药物治疗。新出现的证据表明,成人神经发生与抑郁症的病理生理学和抗抑郁药的作用有关。我们在这里建议使用一种新的方法来确定一系列抗抑郁药物和治疗的细胞和基因靶点。我们的研究将导致对抗抑郁药物作用机制的新假说,并将有助于设计更具体和有效的抗抑郁药物治疗。
英文摘要
DESCRIPTION (provided by applicant): Recent evidence demonstrates a link between the action of antidepressants and increased neurogenesis in the adult hippocampus; moreover, it suggests that neurogenesis may be required for the action of antidepressants. However, it is not known which class of cells within the neuronal differentiation cascade is targeted by the antidepressant drugs and treatments. We have developed a novel approach to identify and classify neuronal precursors and to obtain precise quantitation of changes induced by neurogenic agents. We used this approach to demonstrate that antidepressant fluoxetine affects symmetric division of an early progenitor cell class in the adult hippocampus. In this exploratory application we will use this approach to determine the cellular and gene targets of a range of antidepressant drugs and treatments. In the first series of experiments, we will determine the neurogenic cellular targets of antidepressants of four major families of the drugs (SSRIs, SNRIs, NRIs, and TCAs), of electroconvulsive shock, and of deep brain stimulation. In the second series of experiments we will use laser capture microscopy and transcriptional profiling with microarrays to determine the common gene targets of various antidepressant therapies in neural stem and progenitor cells in the adult hippocampus. Relevance: Emerging evidence implicates adult neurogenesis in the pathophysiology of depression and the action of antidepressants. We here propose to use a novel approach to identify cellular and gene targets for a range of antidepressant drugs and treatments. Our studies will lead to new hypotheses on the mechanisms of action of antidepressants and will help design more specific and effective antidepressant therapies. Emerging evidence implicates adult neurogenesis in the pathophysiology of depression and the action of antidepressants. We here propose to use a novel approach to identify cellular and gene targets for a range of antidepressant drugs and treatments. Our studies will lead to new hypotheses on the mechanisms of action of antidepressants and will help design more specific and effective antidepressant therapies.
期刊论文(1)
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科研奖励(0)
会议论文
DOI:
10.1016/j.expneurol.2010.01.004
发表时间:
2010-04
期刊:
EXPERIMENTAL NEUROLOGY
影响因子:
5.3
作者:
[Park, June-Hee, Enikolopov, Grigori]
通讯作者:
Enikolopov, Grigori
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批准号:10651861
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项目类别:
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资助金额:$77.8万
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财政年份:2022
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依托单位:
Endogenous barcoding to determine complex dynamics of adult neurogenesis in aging and Alzheimer's disease
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Neural stem cells in the aging brain
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Neural stem cells in the aging brain
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Neural stem cells in the aging brain
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财政年份:2011
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依托单位:
Neural stem cells in the aging brain
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项目类别:
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资助金额:$43.87万
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财政年份:2011
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依托单位:
Neural stem cells in the aging brain
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批准号:8327695
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项目类别:
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资助金额:$41.05万
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财政年份:2011
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依托单位:
Neural stem cells in the aging brain
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资助金额:$9.6万
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财政年份:2011
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依托单位:
CRCNS: Computational Model for Neural Stem Cell Divisions in the Adult Brain
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批准号:8111273
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项目类别:
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资助金额:$33.45万
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财政年份:2010
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负责人:GRIGORI N ENIKOLOPOV
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依托单位:
CRCNS: Computational Model for Neural Stem Cell Divisions in the Adult Brain
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批准号:8259207
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项目类别:
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资助金额:$35.66万
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财政年份:2010
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负责人:GRIGORI N ENIKOLOPOV
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依托单位:
CRCNS: Computational Model for Neural Stem Cell Divisions in the Adult Brain
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批准号:8440364
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项目类别:
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资助金额:$34.2万
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财政年份:2010
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负责人:GRIGORI N ENIKOLOPOV
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依托单位:
NEUROGENIC TARGETS OF ANTIDEPRESSANT THERAPIES
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批准号:7297375
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资助金额:$22.65万
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财政年份:2007
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依托单位:
Antagonizing NOS Activity to Induce Neurogenesis in the*
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依托单位:
Antagonizing NOS Activity to Induce Neurogenesis in the*
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资助金额:$20.75万
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负责人:GRIGORI N ENIKOLOPOV
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依托单位:
NITRIC OXIDE AND DROSOPHILA DEVELOPMENT
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依托单位:
NITRIC OXIDE AND DROSOPHILA DEVELOPMENT
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批准号:2900956
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项目类别:
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资助金额:$31.6万
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财政年份:1999
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负责人:GRIGORI N ENIKOLOPOV
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依托单位:
NITRIC OXIDE AND DROSOPHILA DEVELOPMENT
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批准号:6636939
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项目类别:
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资助金额:$35.05万
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财政年份:1999
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负责人:GRIGORI N ENIKOLOPOV
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依托单位:
NITRIC OXIDE AND DROSOPHILA DEVELOPMENT
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项目类别:
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资助金额:$33.49万
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负责人:GRIGORI N ENIKOLOPOV
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依托单位:
海外基金