Neural circuitry mediating behavioral flexibility
调节行为灵活性的神经回路
基本信息
- 批准号:9385375
- 负责人:
- 金额:$ 12.02万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2017
- 资助国家:美国
- 起止时间:2017-09-01 至 2019-08-31
- 项目状态:已结题
- 来源:
- 关键词:AbstinenceAssociation LearningAutomobile DrivingBehaviorBehavioralBiological Neural NetworksCellsCocaineCognitiveCorpus striatum structureCuesDecision MakingDiseaseDorsalDrug AddictionDrug usageElectrophysiology (science)EnvironmentEquilibriumFoundationsGoalsHabitsImpairmentLateralLearningLinkMeasuresMedialMediatingMentorsNatureNeuronsNucleus AccumbensOutcomePathway interactionsPatientsPerformancePhasePrefrontal CortexRattusRecording of previous eventsResponse to stimulus physiologyRewardsSignal TransductionSubstance abuse problemSubstantia nigra structureTherapeutic InterventionTrainingaddictionbehavioral impairmentcareercocaine usecognitive functionflexibilityinsightneural circuitoptogeneticsreinforcerrelating to nervous systemresponsetargeted treatment
项目摘要
Project Summary/Abstract
Balancing habitual and flexible strategies for navigating the environment is necessary for behavior that is both
cognitively efficient and adaptive to change, and perturbations that disrupt this balance can result in significant
behavioral impairments. For example, patients with substance abuse disorders often have difficulty altering
their behavior to respond to changing outcomes, leading to poor decision-making. In the rat, a history of
cocaine impairs the ability to adjust behavior away from reward-predictive cues following reward devaluation, a
canonical measure of flexible behavior (i.e., cocaine leads to inflexible behavior). Interestingly, different striatal
substrates underlie flexible, goal-directed behaviors (nucleus accumbens, NAc) and inflexible, habitual
behaviors (dorsal lateral striatum, DLS), and proper balance between the NAc and DLS and their associated
networks is critical for adaptive (flexible) but efficient (habitual) behavior. Thus, the current application will
examine how a history of cocaine tips that balance and alters the neural network signaling that drives flexible
and inflexible strategies. Balancing these subcortical networks requires cortical input. Specifically, distinct
mPFC subregions (prelimbic cortex, PrL; and infralimbic cortex, IL) are differentially involved in flexible and
inflexible strategies, respectively. Thus, to more fully characterize how a history of cocaine results in lasting
behavioral impairments, I propose 4 specific aims to examine specific effects of a history of cocaine or effects
of specific manipulations to networks driving flexibility. In aim 1, I will determine how a history of cocaine alters
PrL and NAc cell firing and network dynamics (local field potentials) to reward predictive cues during learning
and flexible behavior. In aim 2, I will determine if prelimbic cortical (PrL) inputs to the NAc core are causally
linked to both flexible behavior and its neural encoding in the NAc. In aim 3, I will independently determine how
a history of cocaine alters IL and DLS cell firing and network dynamics to reward predictive cues during
learning and flexible behavior. Finally, in aim 4, I will determine if the IL to substania nigra (the primary input
into DLS) pathway is causally linked to flexible behavior and neural encoding in the DLS. Together, these
specific aims will characterize the balance between two parallel circuits (one involving PrL and NAc, and one
involving IL and DLS) in behavioral flexibility and determine how a history of cocaine shifts this balance
towards inflexible (habitual) circuitry and behavior. Understanding the neural circuitry underlying flexible vs
habitual behavior and how neural encoding in these regions is altered by drug use will provide critical insight
into new and more selective targets for therapeutic intervention for patients with substance abuse disorders.
项目总结/文摘
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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{{ truncateString('Elizabeth A West', 18)}}的其他基金
Prefrontal neural modulation to restore cognitive deficits in an Alzheimer's Disease rat model
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10373174 - 财政年份:2022
- 资助金额:
$ 12.02万 - 项目类别:
NEURAL CIRCUITRY MEDIATING BEHAVIORAL FLEXIBILITY
神经回路调节行为灵活性
- 批准号:
10055804 - 财政年份:2020
- 资助金额:
$ 12.02万 - 项目类别:
B1 noradrenergic blockade in early withdrawal to reduce cocaine induced behavioral flexibility deficit
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- 批准号:
10550086 - 财政年份:2020
- 资助金额:
$ 12.02万 - 项目类别:
NEURAL CIRCUITRY MEDIATING BEHAVIORAL FLEXIBILITY
神经回路调节行为灵活性
- 批准号:
10363725 - 财政年份:2020
- 资助金额:
$ 12.02万 - 项目类别:
Neural circuitry mediating behavioral flexibility
调节行为灵活性的神经回路
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9548189 - 财政年份:2017
- 资助金额:
$ 12.02万 - 项目类别:
NEURAL CIRCUITRY MEDIATING BEHAVIORAL FLEXIBILITY
神经回路调节行为灵活性
- 批准号:
10121211 - 财政年份:2017
- 资助金额:
$ 12.02万 - 项目类别:
The role of accumbens neural activity and dopamine release in flexible behavior
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