The Orexin System as a Target for PTSD and Comorbid Psychosis
The Orexin System as a Target for PTSD and Comorbid Psychosis
批准号:
9891460
负责人:
Daniel Lodge
金额:
$0.0万
依托单位国家:
美国
项目类别:
财政年份:
2020
资助国家:
美国
项目状态:
已结题
起止时间:
2020-04-01 至 2024-03-31
关键词:
Adverse effectsAnatomyAutoradiographyBehaviorBehavioralCognitiveDataDelusionsDevelopmentDiseaseDopamineDopamine D2 ReceptorDoseElectrophysiology (science)Enterobacteria phage P1 Cre recombinaseFDA approvedFunctional disorderHallucinationsHerpesviridaeHigh PrevalenceHumanHypothalamic structureIndividualInterventionLigandsLocomotionLoxP-flanked alleleMajor Depressive DisorderMeasuresMediatingMedicineMood DisordersMotorNamesNeuronsNucleus AccumbensPathway interactionsPatientsPeptidesPharmaceutical PreparationsPharmacologyPhysiologicalPopulationPositioning AttributePositron-Emission TomographyPost-Traumatic Stress DisordersPsychotic DisordersRattusReportingResearchRodentRodent ModelRoleSensoryShockSleeplessnessStressStructure of paraventricular nucleus of thalamusSymptomsSystemTestingThalamic structureTherapeuticVentral Tegmental AreaVirusWorkbasebrain pathwaycomorbiditydesigner receptors exclusively activated by designer drugsdopamine systemdopaminergic neuroneffective therapyexperienceflexibilityhypocretininformation processingnerve supplyneurochemistryneurophysiologynew therapeutic targetnovelprepulse inhibitionpresynapticpsychotic symptomsreceptortherapeutic targettransmission processtraumatic event
中文摘要
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英文摘要
Project Summary/Abstract:
Psychotic symptoms are highly prevalent in PTSD patients and are typically treated with dopamine D2 receptor
antagonists; however, these drugs are associated with significant adverse effects. We have novel preliminary
data demonstrating that the paraventricular nucleus of the thalamus (PVT) regulates dopamine neuron activity.
We posit that the PVT therefore represents a potential therapeutic target for the treatment of PTSD as well as
comorbid psychosis. The PVT receives a particularly dense innervation from orexin containing neurons in the
hypothalamus. Thus, the orexin system is well positioned to regulate PVT activity and may be a novel target for
pharmacological intervention. One such drug, Suvorexant, an orexin receptor antagonist, is currently FDA-
approved for the treatment of insomnia. We will test the hypothesis that Suvorexant can reverse deficits in
rodents displaying circuit level alterations and corresponding behavioral deficits relevant to comorbid psychosis
in PTSD. Specifically, we will examine whether orexin receptor antagonists can reverse stress-induced
behavioral (Aim 1) or neurophysiological/neurochemical (Aim 2) deficits associated with PTSD. We will then
determine the role of discrete PVT projections to the nucleus accumbens in comorbid psychosis (Aim 3). This
proposal with therefore identify a potential novel therapeutic target and inform the development of more effective
treatment approaches for PTSD and comorbid psychosis.
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海外基金