REV-ERB ligands for treatment of anxiety disorders
REV-ERB ligands for treatment of anxiety disorders
批准号:
8915743
负责人:
Thomas P Burris
金额:
$62.31万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2012
资助国家:
美国
项目状态:
已结题
起止时间:
2012-04-01 至 2017-05-31
关键词:
AddressAdultAdverse effectsAffectAgonistAnimal Disease ModelsAnimalsAnti-Anxiety AgentsAnxiety DisordersBehaviorBehavior DisordersBehavior assessmentBehavioralBehavioral AssayBindingCentral Nervous System DiseasesCircadian DysregulationCircadian RhythmsDevelopmentDiseaseDoseDrug KineticsDrug TargetingEvaluationExposure toFeedbackFundingGene ExpressionGoalsGrantHealthHemeHourLeadLigandsMedicalMental DepressionMolecularMusNuclear ReceptorsOrphanPathway interactionsPatternPharmaceutical PreparationsPharmacodynamicsPharmacologyPhysiologicalPhysiologyPlayPorphyrinsPropertyPublishingRecurrenceRegulationRelative (related person)ResearchRewardsRoleSedation procedureSeriesSourceSystemTestingTherapeuticUnited StatesWakefulnessWorkbasedesignhuman diseaseimprovedin vivoinnovationnervous system disordernovelreceptorsedativetreatment of anxiety disorders
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Dysregulation of the circadian rhythm is associated with several disorders of the nervous system including anxiety disorders. Anxiety disorders are a serious medical illness affecting approximately 40 million adults in the United States. Benzodiazepenes are the most commonly utilized anxiolytic drugs, but their use is associated with significant side effects including sedation, tolerance and potential for abuse. There are a number of anxiolytic drugs that are now available, but these also are less than optimal. Thus, there is a clear unmet medical need for additional classes of therapeutics to treat these disorders. This proposed research is based on our recent discovery that we can modulate the circadian rhythm in vivo with synthetic ligands for a particular nuclear receptor (NR), REV-ERB. REV-ERBalpha is an NR that has a well-characterized role in the regulation of the circadian rhythm. We have found that REV-ERB agonists that we have designed that has the ability to modulate the circadian rhythm in vivo also display anxiolytic activity in mice. Interestingly, thes compounds display no sedative activity at anxiolytic doses. The REV-ERB agonists we have developed are the first with sufficient in vivo exposure to allow evaluation of its effects in animals; however, their pharmacodynamic and pharmcokinetic properties are far from optimal. We hypothesize that optimized synthetic REV-ERB ligands will have utility in treatment of anxiety disorders. We will address this hypothesis by focusing on the following specific aims: 1) Optimize the pharmacodynamic and pharmacokinetic properties of synthetic REV-ERB ligands for use as anxiolytic agents, 2) Evaluate the ability of synthetic REV- ERB ligands for their abiliy to modulate circadian behavior/physiology in vivo, 3) Optimize the anxiolytic activity of REV-ERB agonists in vivo and characterize their sedative activity and potential for abuse. We have now developed a series of very potent and efficacious REV-ERB agonists that have properties that will allow for evaluation of these compounds in animal models of disease. Thus, our proposed research is highly innovative and has the potential to have high impact since this work may lead to novel drugs for the treatment of anxiety disorders as well as other behavioral disorders.
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海外基金