Compartment-Specific Signaling Of Striatal Opioid Peptides in Reward-Guided Behav
Compartment-Specific Signaling Of Striatal Opioid Peptides in Reward-Guided Behav
批准号:
8600669
负责人:
Matthew R. Banghart
金额:
$12.15万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2013
资助国家:
美国
项目状态:
已结题
起止时间:
2013-01-01 至 2016-06-30
关键词:
AcuteAgonistAreaAttention deficit hyperactivity disorderBasal GangliaBehaviorBehavioralBehavioral AssayBiological AssayBrainCalciumCellsChemicalsCorpus striatum structureDecision MakingDefectDiseaseDorsalDrug TargetingDrug abuseEndorphinsGene TransferGeneticGilles de la Tourette syndromeGoalsHuntington DiseaseImageLeadLearningLimbic SystemLinkMediatingMental disordersMentorsMethodsMonitorMotorMusNervous system structureNeuromodulatorNeuronsNeuropeptidesNeurotransmittersObsessive-Compulsive DisorderOperative Surgical ProceduresOpiatesOpioidOpioid PeptideOpioid ReceptorParkinson DiseasePathway interactionsPatternPharmaceutical PreparationsPharmacologyPrefrontal CortexProcessPropertyPsychological reinforcementPsychopathologyReagentReporterReportingResolutionRewardsRodent ModelRoleShapesSignal TransductionSignaling MoleculeSliceSocial InteractionSubstance abuse problemSubstance of AbuseSucroseSynapsesSynaptic TransmissionSystemTechniquesTrainingTranslatingViralWorkaddictioncellular targetingchemical geneticsdriving behaviorendogenous opioidsfeedinggoal oriented behaviorin vivointerestmotivational processesmotor learningneural circuitneurochemistrynoveloptical sensoroptogeneticspublic health relevancereceptorreceptor expressionrepairedresearch studyresponsespatiotemporalstriosometooltransmission processtwo-photon
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The striatum integrates limbic and sensorimotor information to drive goal-directed behaviors. Opioid peptides and their receptors are abundant in the striatum, but a clear role for endogenous opioid signaling in action selection has not been established. This proposal aims to define key components of the striatal circuitry that process limbic information in mice and to understand how opioid peptides alter these circuits in the context of reward-guided behavior. A systematic anatomical and functional analysis of limbic projections to opioid-rich striatal microcircuits will be conducted using genetic tracing methods and ontogenetic tools in brain slices. New photochemical reagents will be employed in combination with ontogenetic to identify opioid-sensitive circuit components and determine how intercompartmental volume transmission shapes the spatiotemporal dynamics of opioid signaling. Genetically-targeted calcium imaging experiments will reveal how these actions translate into changes in network function. To provide evidence for endogenous opioid release in the context of goal-directed behaviors, activity patterns observed during reward-guided tasks will be driven in brain slices ontogenetically while electrophysiological monitoring opioid signaling in brain slices. To identify a functional role, opioid receptors will be blocked during reward-guided behavioral assays using a new photoactivatable antagonist that enables transient inhibition within discrete striatal sub-regions in vivo. To detect the release and spread
of endogenous opioids with high sensitivity good spatiotemporal resolution, optical sensors will be developed by chemically modifying receptors so that they report the presence of endogenous agonists. A chemical- genetic strategy for cell-specific pharmacology will be developed to reveal which cellular targets of opioid signaling underlie behavioral responses to opioid peptides and opiate drugs. By targeting native receptors in genetically-identified cells, ths tool provides a powerful means to study opioidergic pathways in the brain. Collectively, these studies will uncover mechanisms by which opioids modulate a neural circuit involved in goal-oriented behavior. By quantifying signaling dynamics in new ways, the role of volume transmission will emerge. Although these novel techniques focus on opioids, the underlying principles are general, and should be applicable to signaling molecules beyond the nervous system. The anticipated findings should facilitate our understanding of disorders in which goal-directed actions are compromised such as Parkinson's and Huntington's diseases as well as attention deficit hyperactivity disorder (ADHD), obsessive-compulsive disorder (OCD), and addiction to substances of abuse.
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科研奖励(0)
会议论文
Development of opioid and ketamine probes for in vivo photopharmacology
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批准号:10401573
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项目类别:
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资助金额:$190.58万
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财政年份:2022
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负责人:Matthew R. Banghart
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依托单位:
Next generation all-optical toolkits for functional analysis of neuropeptide dynamics in neural circuits
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批准号:10394081
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资助金额:$8.62万
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财政年份:2021
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负责人:Matthew R. Banghart
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依托单位:
Next generation all-optical toolkits for functional analysis of neuropeptide dynamics in neural circuits
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批准号:10201785
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项目类别:
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资助金额:$87.67万
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财政年份:2019
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负责人:Matthew R. Banghart
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依托单位:
Next generation all-optical toolkits for functional analysis of neuropeptide dynamics in neural circuits
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批准号:10426199
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项目类别:
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资助金额:$82.52万
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财政年份:2019
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负责人:Matthew R. Banghart
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依托单位:
Next generation all-optical toolkits for functional analysis of neuropeptide dynamics in neural circuits
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批准号:10093949
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项目类别:
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资助金额:$2.46万
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财政年份:2019
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负责人:Matthew R. Banghart
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依托单位:
Molecular mechanisms of dense-core vesicle release
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批准号:10659044
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项目类别:
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资助金额:$37.39万
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财政年份:2019
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负责人:Matthew R. Banghart
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依托单位:
Molecular mechanisms of dense-core vesicle release
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批准号:10807380
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项目类别:
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资助金额:$1.34万
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财政年份:2019
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负责人:Matthew R. Banghart
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依托单位:
Molecular mechanisms of dense-core vesicle release
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批准号:10189663
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项目类别:
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资助金额:$37.39万
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财政年份:2019
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负责人:Matthew R. Banghart
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依托单位:
Molecular mechanisms of dense-core vesicle release
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批准号:10426137
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项目类别:
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资助金额:$37.39万
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财政年份:2019
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负责人:Matthew R. Banghart
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依托单位:
Compartment-specific signaling of striatal opioid peptides in reward-guided behavior
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批准号:9378801
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项目类别:
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资助金额:$24.9万
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财政年份:2017
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负责人:Matthew R. Banghart
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依托单位:
Compartment-Specific Signaling Of Striatal Opioid Peptides in Reward-Guided Behav
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批准号:8423569
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项目类别:
-
资助金额:$12.15万
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财政年份:2013
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负责人:Matthew R. Banghart
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依托单位:
国内基金
海外基金
Agonist-GPR119-Gs复合物的结构生物学研究
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批准号:32000851
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项目类别:青年科学基金项目
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资助金额:24.0万元
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批准年份:2020
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负责人:乔安娜
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依托单位: