Sigma Receptor and cocaine sensitization
Sigma Receptor and cocaine sensitization
批准号:
8736779
负责人:
ANTONELLO BONCI
金额:
$69.09万
依托单位国家:
美国
项目类别:
财政年份:
--
资助国家:
美国
项目状态:
未结题
起止时间:
至
关键词:
BehaviorBehavioralBrainCell membraneCellular biologyCentral Nervous System DiseasesChronic DiseaseCocaineComplexDevelopmentDrug AddictionElectrophysiology (science)Endoplasmic ReticulumIn VitroIon ChannelKv1.2&apos channelLigandsLinkMembraneMitochondriaMolecular ChaperonesMotivationNeuronsNucleus AccumbensPharmaceutical PreparationsPlayPotassium ChannelPropertyProteinsResearchRewardsRoleShapesSignal TransductionSiteStructureSynapsesTestingUp-Regulationaddictioncocaine exposuredrug seeking behaviorexperienceinterdisciplinary approachneural circuitneuroadaptationneuronal excitabilityneurotransmissionreceptor bindingresponsesigma receptorssigma-1 receptorvoltage
中文摘要
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英文摘要
The sigma-1 receptor (Sig-1R), an endoplasmic reticulum (ER) chaperone protein, is an interorganelle signaling modulator that potentially plays a role in drug-seeking behaviors. However, the brain site of action and underlying cellular mechanisms remain unidentified. We found that cocaine exposure triggers a Sig-1R-dependent upregulation of D-type K+ current in the nucleus accumbens (NAc) that results in neuronal hypoactivity and thereby enhances behavioral cocaine response. Combining ex vivo and in vitro studies, we demonstrated that this neuroadaptation is caused by a persistent protein-protein association between Sig-1Rs and Kv1.2 channels, a phenomenon that is associated to a redistribution of both proteins from intracellular compartments to the plasma membrane. In conclusion, the dynamic Sig-1R-Kv1.2 complex represents a mechanism that shapes neuronal and behavioral response to cocaine. Functional consequences of Sig-1R binding to K+ channels may have implications for other chronic diseases where maladaptive intrinsic plasticity and Sig-1Rs are engaged.
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海外基金
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依托单位: