Role of novel VTA neurons in addiction-related behaviors
Role of novel VTA neurons in addiction-related behaviors
批准号:
10398902
负责人:
Thomas Hnasko
金额:
$42.53万
依托单位国家:
美国
项目类别:
财政年份:
2014
资助国家:
美国
项目状态:
已结题
起止时间:
2014-04-01 至 2024-04-30
关键词:
AdultAmino Acid NeurotransmittersAnabolismAnatomyAnimalsBasal GangliaBehaviorBehavior ControlBehavioralBiological AssayCRISPR/Cas technologyCell NucleusCellsClustered Regularly Interspaced Short Palindromic RepeatsComplexDevelopmentDiseaseDistalDopamineDrug AddictionDrug TargetingElectron MicroscopyElectrophysiology (science)FutureGeneticGlobus PallidusGlutamatesGoalsHabenulaHeterogeneityImageInterneuronsInterventionLabelLateralLearned HelplessnessLimbic SystemLinkMapsMediatingMembrane PotentialsMusNegative ReinforcementsNeuromodulatorNeuronsPathway interactionsPharmaceutical PreparationsPopulationPositioning AttributePositive ReinforcementsProcessPsychological reinforcementRecyclingResearchRewardsRoleSelective Serotonin Reuptake InhibitorShapesSignal TransductionSiteSynapsesTestingVentral StriatumVentral Tegmental Areaaddictionbasecell typedopaminergic neurondrug of abusefrontal lobegamma-Aminobutyric Acidgenetic approachlight microscopymotivated behaviorneural circuitneuropsychiatric disordernoveloptogeneticspostsynaptic neuronspreventprogramstargeted treatment
中文摘要
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英文摘要
PROJECT SUMMARY
The ventral tegmental area (VTA) is a core component of the neural circuitry that drives goal-directed behavior,
and a primary target through which drugs of abuse modulate behavior. Although generally regarded as a
dopaminergic nucleus, about half of VTA neurons signal through release of the amino acid neurotransmitters
GABA and glutamate. These neurons are also targets of drugs of abuse but much less studied. Recent evidence
from our lab and others has begun to show that, like VTA DA neurons, activity in VTA GABA and glutamate
neurons can profoundly shape motivated behaviors. Furthermore, sub-populations of VTA neurons release more
than one of these three recycling transmitters, including neurons that co-release dopamine and glutamate, or
glutamate and GABA. The goals of this proposal are to identify how transmitter co-release from VTA contributes
to the processes underlying behavioral reinforcement, and how co-releasing neurons functionally integrate into
the mesolimbic neural circuits that regulate motivated behavior. We will use an array of genetic approaches in
combination with behavioral, anatomical, and electrophysiological assays in mice to selectively probe the
connectivity and function of discrete VTA circuits. Together this continuing research program comprises a
thorough plan to define the form and function of novel classes of VTA neurons and enhance our understanding
of how intrinsic VTA heterogeneity shapes behaviors relevant to neuropsychiatric disease.
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海外基金