Regulation of ventral hippocampal system function
Regulation of ventral hippocampal system function
批准号:
9024375
负责人:
Daniel Lodge
金额:
$48.81万
依托单位国家:
美国
项目类别:
财政年份:
2010
资助国家:
美国
项目状态:
已结题
起止时间:
2010-07-01 至 2020-06-30
关键词:
AddressAffectAmphetaminesAntipsychotic AgentsAutopsyBehaviorBehavioralCognitiveCognitive deficitsDataDevelopmentDimensionsDiseaseDopamineErbB4 geneEstrusFemaleFunctional disorderFundingHippocampus (Brain)HumanHyperactive behaviorImageImmunohistochemistryInterneuron functionInterneuronsLeadLocomotionMalnutritionMeasuresMedialMidbrain structureMusNRG1 geneNeurobehavioral ManifestationsNeurobiologyNeuronsParvalbuminsPathogenesisPathologyPatientsPharmaceutical PreparationsPhysiologicalPoly I-CPopulationPsychotic DisordersRNA SequencesRattusRegulationRelative (related person)ReportingResearch Domain CriteriaReversal LearningRisk FactorsRodent ModelRoleSchizophreniaSocial InteractionSomatostatinStem cell transplantSymptomsSystemTherapeuticTherapeutic StudiesTransplantationbrain pathwaycognitive functiondopamine systemdopaminergic neuronembryonic stem cellfetalflexibilityinhibitory neuronmigrationneurophysiologynovel therapeutic interventionprenatalpublic health relevanceresponsesmall hairpin RNAtranscriptome sequencingtransmission process
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Schizophrenia is a devastating psychiatric condition that affects up to 1% of the US population. During the previous funding period, we reported that a loss of hippocampal interneuron function, recapitulates the hyperdopaminergic state thought to underlie psychosis in patients. In addition, we have recently provided one of the first reports describing the feasibility of interneuron transplants (derived from fetal medial ganglionic eminence) as a novel therapeutic approach for the treatment of schizophrenia. In these initial studies we focused primarily on the hyperdopaminergic state thought to underlie psychosis. In the present proposal, we will now address the issues of negative and cognitive deficits that are not only severely debilitating, but are not well treated by antipsychotic medications. Towards this
end, we plan to examine the role of two separate interneuron populations, namely parvalbumin and somatostatin, in discrete but interconnected neuronal systems (the vHipp and mPFC) that likely underlie these symptoms clusters in schizophrenia. More broadly, this concept is central to understanding dimensions of behavior and neurobiological measures as detailed in the Research Domain Criteria project (RDoC). Taken together, the studies proposed will provide an understanding into the role of discrete interneuron populations in the pathophysiology of schizophrenia and will examine the utility of stem cell transplants as a potential treatment for this disease.
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会议论文
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依托单位:
Regulation of ventral hippocampal system function
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资助金额:$33.08万
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Regulation of ventral hippocampal system function
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Regulation of ventral hippocampal system function
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依托单位:
海外基金