Role of Extinction in Circuit-Specific Modulation of Motivation and Mood in Cocaine Addiction
消退在可卡因成瘾的动机和情绪的电路特异性调节中的作用
基本信息
- 批准号:9551580
- 负责人:
- 金额:$ 36.45万
- 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 2022-06-30
- 项目状态:已结题
- 来源:
- 关键词:AMPA ReceptorsAbstinenceAmygdaloid structureAnhedoniaAttenuatedBehaviorBehavioralBiochemicalBiologicalBrainChronicCocaineCocaine DependenceDataData SetDiseaseDrug AddictionDrug userElectrophysiology (science)EnvironmentExtinction (Psychology)FrequenciesGlutamate ReceptorGoalsHippocampus (Brain)Homosynaptic DepressionIndividualLateral Hypothalamic NucleusLeadLearned HelplessnessMeasuresMedialMediatingMental disordersMethodsModelingModificationMoodsMotivationNeurobiologyNeuronal PlasticityNeuronsNucleus AccumbensOutputPharmaceutical PreparationsPlayPrefrontal CortexRattusRelapseResearchRoleSelf AdministrationSocietiesSourceSucroseSwimmingSynapsesTestingTherapeuticTherapeutic InterventionTrainingUp-RegulationWithdrawalWorkaddictionattenuationcocaine usedepressive symptomsdisturbance in affectdrug cravingdrug relapsedysphoriaeconomic costexperimental studynegative moodneural circuitneurophysiologyoptogeneticspreferencereceptorresearch studyresponsesevere mental illnesssocialtrafficking
项目摘要
PROJECT SUMMARY
Drug addiction is a serious and prolific mental illness involving persistent relapse despite sincere efforts to
abstain. Extinction training has been used as a therapeutic method to reduce drug craving and relapse,
although with limited efficacy due to an inability to fully capture contextual aspects unique to individual drug
users. The identification of extinction-induced modifications in distinct brain circuits could lead to better
neurostimulation approaches to treat drug addiction. This research studies modification of specific neural
circuits by the extinction of self-administration behavior in a rat model of cocaine addiction. Our previous data
indicate that extinction training enhances excitatory synaptic input to nucleus accumbens (NAc) shell neurons,
and this effect attenuates psychomotor sensitization and relapse to cocaine-seeking behavior. The primary
excitatory inputs to the NAc shell originate in the medial prefrontal cortex (PfC), basolateral amygdala (BlA)
and ventral hippocampus (VH). Using an optogenetic low frequency stimulation approach to selectively
depotentiate excitatory synaptic input emanating from these regions, this research will identify the specific
source(s) of extinction-induced neuroplasticity in the NAc shell (Aim I), and study the role of this circuit-specific
neuroplasticity in extinction-induced attenuation of sensitization and relapse behaviors (Aim II). Previous data
also suggest that extinction of cocaine self-administration may reverse negative mood effects produced by
chronic cocaine use. Thus, studies will determine the role of circuit-specific neuroplasticity in extinction-
induced antidepressive efficacy (Aim III).
Studies in Aim 1 will employ optogenetics to study the extinction circuits responsible for 1) extinction-
induced synaptic trafficking of AMPA GluA receptor subunits, 2) extinction-induced enhancement in excitatory
synaptic currents and 3) determine the direct and/or indirect NAc output neurons modified by extinction.
Experiments in Aim II will determine the role of extinction-potentiated circuits in 4) extinction-induced reversal
of locomotor sensitization and 5) extinction-induced attenuation of context- and cocaine-primed reinstatement
of cocaine-seeking behavior. Experiments in Aim III will investigate the role of extinction-specific
neuroplasticity in reversing negative mood effects in tests of 6) dysphoria in cocaine-conditioned place
aversion, 7) learned helplessness/behavioral despair in forced swim tests and 8) anhedonia in sucrose
preference tests. The integration of these neurobiological and behavioral datasets will determine the
significant role that circuit-specific neuroplasticity plays in the beneficial effects of extinction on motivational
and mood disturbances that contribute to cocaine addiction. A clear delineation of limbic circuits that mediate
such beneficial effects could lead to better behavioral and targeted neurostimulation approaches in the
treatment of cocaine and other addictions.
项目总结
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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David W Self其他文献
Monogamy: dopamine ties the knot
一夫一妻制:多巴胺系上了婚结。
- DOI:
10.1038/nn0106-7 - 发表时间:
2006-01-01 - 期刊:
- 影响因子:20.000
- 作者:
Scott Edwards;David W Self - 通讯作者:
David W Self
David W Self的其他文献
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{{ truncateString('David W Self', 18)}}的其他基金
Role of Extinction in Circuit-Specific Modulation of Motivation and Mood in Cocaine Addiction
消退在可卡因成瘾的动机和情绪的电路特异性调节中的作用
- 批准号:
10198877 - 财政年份:2017
- 资助金额:
$ 36.45万 - 项目类别:
Role of Extinction in Circuit-Specific Modulation of Motivation and Mood in Cocaine Addiction
消退在可卡因成瘾的动机和情绪的电路特异性调节中的作用
- 批准号:
9238093 - 财政年份:2017
- 资助金额:
$ 36.45万 - 项目类别:
Role of Extinction in Circuit-Specific Modulation of Motivation and Mood in Cocaine Addiction
消退在可卡因成瘾的动机和情绪的电路特异性调节中的作用
- 批准号:
9974501 - 财政年份:2017
- 资助金额:
$ 36.45万 - 项目类别:
Role of Endogenous Opiate Systems in Cocaine Relapse after Long-Term Abstinence
内源性阿片系统在长期戒断后可卡因复发中的作用
- 批准号:
8044146 - 财政年份:2010
- 资助金额:
$ 36.45万 - 项目类别:
Role of Endogenous Opiate Systems in Cocaine Relapse after Long-Term Abstinence
内源性阿片系统在长期戒断后可卡因复发中的作用
- 批准号:
8605866 - 财政年份:2010
- 资助金额:
$ 36.45万 - 项目类别:
Role of Endogenous Opiate Systems in Cocaine Relapse after Long-Term Abstinence
内源性阿片系统在长期戒断后可卡因复发中的作用
- 批准号:
8423318 - 财政年份:2010
- 资助金额:
$ 36.45万 - 项目类别:
Role of Endogenous Opiate Systems in Cocaine Relapse after Long-Term Abstinence
内源性阿片系统在长期戒断后可卡因复发中的作用
- 批准号:
8215776 - 财政年份:2010
- 资助金额:
$ 36.45万 - 项目类别:
Neuroadaptions in Drug Self-Administration and Relapse
药物自我给药和复发的神经适应
- 批准号:
7513609 - 财政年份:2007
- 资助金额:
$ 36.45万 - 项目类别:
VTA Ionotropic Glutamate Receptors in Cocaine Addiction
可卡因成瘾中的 VTA 离子型谷氨酸受体
- 批准号:
7169921 - 财政年份:2005
- 资助金额:
$ 36.45万 - 项目类别:
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