Neuropharmacology Core
神经药理学核心
基本信息
- 批准号:10374825
- 负责人:
- 金额:$ 28.13万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2013
- 资助国家:美国
- 起止时间:2013-12-01 至 2024-03-31
- 项目状态:已结题
- 来源:
- 关键词:AcuteAddressAnalgesicsAnimalsAreaBehaviorBehavioralBehavioral AssayBiological AssayBrainBrain regionCancer Grant Supplements (P30)ChronicCollaborationsCollectionConsultationsCountryDataData AnalysesDevelopmentDrug abuseEffectivenessExperimental DesignsFamilyFundingFutureG-Protein-Coupled ReceptorsGoalsGrantHumanIndividualInstitutionInvestigational DrugsLaboratoriesLeadershipMeasuresMediatingMethodologyMethodsMicrodialysisMolecularMolecular TargetNeuroanatomyNeuropharmacologyNeurotransmittersNucleus AccumbensOpioidPainPathologicPharmaceutical PreparationsPharmacotherapyPhysiologicalPlayPostdoctoral FellowProceduresPsychological reinforcementReceptor SignalingRecording of previous eventsResearchResearch PersonnelResearch Project GrantsResourcesRewardsScientistSelf AdministrationSelf StimulationSerotoninSliceSubstance Use DisorderSupervisionSynthesis ChemistrySystemTechniquesTissuesTrainingUnited States National Institutes of HealthUniversitiesVentral Tegmental AreaVirginiaabuse liabilityawakebehavioral studyconditioned place preferencedrug actiondrug of abusedrug rewardexperiencegraduate studentin vivoinnovationmeetingsmonoamineneurochemistrynon-drugnovelpre-clinicalpre-clinical assessmentranpirnasereceptorreceptor bindingreceptor expressionreceptor functionreinforcerrelating to nervous systemsubstance use treatmenttool
项目摘要
Project Summary – Neuropharmacology Core
The Neuropharmacology Core is a new core that proposes to serve NIH-funded investigators affiliated with the
P30 grant by increasing their access to key neurochemical and behavioral methodologies that are fundamental
to advancement of preclinical drug abuse research. These methodologies will include techniques to assess
expression and function of receptors in both tissue homogenates and tissue slices, in vivo microdialysis
techniques to assess neurotransmitter levels in target brain areas in awake and behaving animals, and
behavioral techniques to assess rewarding/reinforcing effects of drugs under different physiological or
environmental conditions. Although this is a new core, the investigators have decades of expertise in their
respective areas and a history of collaboration both with each other and with other VCU investigators.
The rationale for this core is founded on the proposition that drugs of abuse act on molecular targets to
modulate activity in brain reward systems and alter behavior, and preclinical drug abuse research benefits from
coordinated investigation of drug effects along the entire continuum from molecular to behavioral levels of
analysis. However, individual grants typically focus on a portion of this continuum and often lack resources for
rapid and rational extension of important findings to other, related research domains. As one example, a
synthetic chemistry grant might identify a new molecular entity with promising analgesic effects but lack
resources for preclinical assessment of that compound's abuse liability or potential utility as a treatment for
substance use disorders. As another example, a grant focused on behavioral studies to treat drug abuse might
identify an effective medication strategy but lack resources to investigate candidate mechanisms that underlie
medication efficacy. The Neuropharmacology Core proposes to address these gaps and strengthen the
breadth and impact of drug abuse research at VCU. Studies of receptor expression and function (Aim 1), in
vivo microdialysis (Aim 2), and behavioral expression of reward/reinforcement (Aim 3) will enable investigators
to evaluate effects of pathological states or of acute/chronic drug treatments on neural systems and behavioral
endpoints known to be important in drug abuse.
项目摘要 - 神经药理学核心
神经药理学核心是一个新的核心,该核心提议为NIH资助的研究人员提供服务
P30赠款通过增加其对基本的关键神经化学和行为方法的访问
临床前药物滥用研究的进步。这些方法将包括评估的技术
受体在组织匀浆和组织切片中的表达和功能,体内微透析
评估醒着和行为动物的目标大脑区域中神经递质水平的技术,
在不同的生理学或
环境条件。尽管这是一个新的核心,但调查人员在其上拥有数十年的专业知识
彼此以及其他VCU调查人员的各个领域和合作历史。
该核心的理由是建立在以下主张的基础上,即滥用药物对分子靶标的作用
调节大脑奖励系统和改变行为的活动,临床前药物滥用研究受益于
对整个分子至行为水平的整个药物作用的协调研究
分析。但是,个人赠款通常专注于此连续体的一部分,并且通常缺乏资源
重要发现的快速,合理地扩展到其他相关的研究领域。作为一个例子,一个
合成化学补助金可能会确定一个具有承诺镇痛作用但缺乏承诺的新分子实体
用于临床前评估该化合物的滥用责任或潜在效用的资源作为治疗
物质使用障碍。作为另一个例子,专注于治疗药物滥用的行为研究的赠款可能
确定有效的药物策略,但缺乏资源来调查候选机制的基础
用药效率。神经药理学的核心核心提议解决这些差距并加强
VCU吸毒研究的广度和影响。研究受体表达和功能(目标1),
体内微透析(AIM 2)和奖励/强化的行为表达(AIM 3)将使研究人员能够
评估病理状态或急性/慢性药物治疗对神经元系统和行为的影响
终点在药物滥用中很重要。
项目成果
期刊论文数量(0)
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专利数量(0)
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{{ truncateString('Sidney S Negus', 18)}}的其他基金
A Novel Assay to Improve Translation in Analgesic Drug Development
改善镇痛药物开发转化的新方法
- 批准号:
10726834 - 财政年份:2023
- 资助金额:
$ 28.13万 - 项目类别:
Endocannabinoid modulation of pain-depressed behavior
内源性大麻素对疼痛抑制行为的调节
- 批准号:
8653551 - 财政年份:2011
- 资助金额:
$ 28.13万 - 项目类别:
Endocannabinoid modulation of pain-depressed behavior
内源性大麻素对疼痛抑制行为的调节
- 批准号:
8462583 - 财政年份:2011
- 资助金额:
$ 28.13万 - 项目类别:
Endocannabinoid modulation of pain-depressed behavior
内源性大麻素对疼痛抑制行为的调节
- 批准号:
8287528 - 财政年份:2011
- 资助金额:
$ 28.13万 - 项目类别:
Endocannabinoid modulation of pain-depressed behavior
内源性大麻素对疼痛抑制行为的调节
- 批准号:
8115635 - 财政年份:2011
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$ 28.13万 - 项目类别:
Endocannabinoid modulation of pain-depressed behavior
内源性大麻素对疼痛抑制行为的调节
- 批准号:
9403737 - 财政年份:2011
- 资助金额:
$ 28.13万 - 项目类别:
Endocannabinoid modulation of pain-depressed behavior
内源性大麻素对疼痛抑制行为的调节
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8851547 - 财政年份:2011
- 资助金额:
$ 28.13万 - 项目类别:
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