Synaptic regulation of single substantia nigra pars reticulata neurons
Synaptic regulation of single substantia nigra pars reticulata neurons
批准号:
7624257
负责人:
STEVEN WILLIAM JOHNSON
金额:
$27.56万
依托单位国家:
美国
项目类别:
财政年份:
2008
资助国家:
美国
项目状态:
已结题
起止时间:
2008-07-01 至 2013-06-30
关键词:
Action PotentialsAffectAgonistApplications GrantsAxonBasal GangliaBradykinesiaBrainBrain regionCell NucleusCellsChronicComplexDataDeep Brain StimulationDenervationDiseaseDopamineDopamine ReceptorElectric StimulationElectron MicroscopyExcitatory Postsynaptic PotentialsFrequenciesFunctional disorderGait abnormalityGlobus PallidusGlutamatesGoalsHumanIncidenceLaboratoriesLigandsMediatingMetabotropic Glutamate ReceptorsModelingMotorMovementMuscle RigidityNeuronsNeurotransmittersOperative Surgical ProceduresOutputParkinson DiseaseParkinsonian DisordersPathway interactionsPatternPharmaceutical PreparationsPharmacologyPhysiologicalPhysiologyPlayRattusRecurrenceRegulationReportingRoleSTN stimulationSeizuresSeriesSiteSliceSolutionsStructureStructure of subthalamic nucleusSubstantia nigra structureSymptomsSynapsesSynaptic PotentialsSystemTechniquesTestingTremorWorkbrain pathwaydepressiondopaminergic neurongamma-Aminobutyric Acidimprovedinterestnerve supplyneurophysiologynovelpars compactapublic health relevancereceptorresearch studysynaptic depressiontransmission process
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The subthalamic nucleus (STN) plays an important role in movement control by exerting its excitatory influence on the substantia nigra pars reticulata (SNR), a major output structure of the basal ganglia. In Parkinson's disease, increased bursting activity in the
subthalamonigral pathway is thought to contribute to motor symptoms such as rigidity, bradykinesia and tremor. Preliminary data from our lab show that focal electrical stimulation of the STN evokes an initial monosynaptic EPSC followed by a series of late EPSCs superimposed on a slow inward shift in holding current that lasts 200 - 500 ms. Results thus far support the hypothesis that this complex EPSC is generated by activation of recurrent axon collaterals within the STN. Because STN stimulation evokes
a burst of action potentials when recording under current-clamp, the complex EPSC may represent a novel mechanism for promoting burst firing in SNR neurons. In contrast, STN stimulation only evokes monophasic EPSCs in substantia nigra pars compacta (SNC) dopamine neurons, which suggests that the STN output to SNR may differ from the STN output to SNC dopamine neurons. The major goals of our proposed studies are to characterize the neurophysiology of complex EPSCs and their regulation by neurotransmitter systems. Experiments will use standard whole-cell patch pipette recording techniques to record from neurons in the rat brain slice. Complex EPSCs will be evoked in SNR neurons by focal electrical stimulation of the STN, and drug solutions will be delivered to specific regions of the brain slice using a fast-flow microapplicator. Planned experiments will use antidromic stimulation techniques of the SNR and SNC to characterize recurrent, polysynaptic connections within the STN. Other experiments will investigate sites of action and characterize receptor pharmacology for the regulation of complex EPSCs by GABA and dopamine receptor ligands. In conjunction with
neurophysiological experiments, brain slices will also be used to document recurrent axonal collateral innervation of STN neurons using electron microscopy. Due to the importance of the subthalamonigral pathway in regulating firing pattern of SNR neurons, results of these studies may have important implications for the pathophysiology and possible treatment of Parkinson's disease. PUBLIC HEALTH RELEVANCE: Many studies suggest that excessive bursting activity in the brain pathway from
subthalamic nucleus to substantia nigra pars reticulata contributes to symptoms of Parkinson's disease as well as the propagation of some types of seizures. Our studies show that activation of the subthalamonigral pathway causes long-lasting depolarization and bursts of action potentials in reticulata neurons recorded in the rat brain slice. By characterizing how synaptic connections and modulatory transmitter systems regulate this pathway, our studies may provide useful information to improve the therapy of these human disorders.
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资助金额:$27.01万
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资助金额:$27.29万
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批准号:8111305
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项目类别:
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资助金额:$27.01万
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负责人:STEVEN WILLIAM JOHNSON
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依托单位:
SYNAPTIC PHARMACOLOGY OF SINGLE SUBTHALAMIC NEURONS
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批准号:6338574
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资助金额:$0.21万
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Synaptic pharmacology of single subthalamic neurons
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依托单位:
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依托单位:
海外基金