Neuropharmacology Core
神经药理学核心
基本信息
- 批准号:10604270
- 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 2025-03-31
- 项目状态:未结题
- 来源:
- 关键词:AcuteAddressAnalgesicsAnimalsAreaBehaviorBehavioralBehavioral AssayBiological AssayBrainBrain regionCenter Core GrantsChronicCollaborationsCollectionConsultationsCountryDataData AnalysesDevelopmentDrug abuseEffectivenessExperimental DesignsFamilyFundingFutureG-Protein-Coupled ReceptorsGoalsGrantHumanIndividualInstitutionInvestigationLaboratoriesLeadershipMeasuresMediatingMethodologyMethodsMicrodialysisMolecularMolecular TargetNeuroanatomyNeuropharmacologyNeurotransmittersNucleus AccumbensOpioidPainPathologicPharmaceutical PreparationsPharmacotherapyPhysiologicalPlayPostdoctoral FellowProceduresPsychological reinforcementReceptor SignalingRecording of previous eventsResearchResearch PersonnelResearch Project GrantsResourcesRewardsScientistSelf AdministrationSelf StimulationSerotoninSliceSubstance Use DisorderSynthesis ChemistrySystemTechniquesTissuesTrainingUnited States National Institutes of HealthUniversitiesVentral Tegmental AreaVirginiaabuse liabilityawakebehavioral studyconditioned place preferencedrug actiondrug of abusedrug rewardexperiencegraduate studentin vivoinnovationmeetingsmonoamineneuralneurochemistrynon-drugnovelpre-clinicalpre-clinical assessmentreceptorreceptor bindingreceptor expressionreceptor functionreinforcersubstance 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,旨在为隶属于 NIH 资助的研究人员提供服务
P30 通过增加他们获得关键神经化学和行为方法的机会来资助
这些方法将包括评估技术。
组织匀浆和组织切片中受体的表达和功能,体内微透析
评估清醒和行为动物目标大脑区域神经递质水平的技术,以及
行为技术来评估药物在不同生理或心理条件下的奖励/强化作用
尽管这是一个新的核心,但研究人员在其领域拥有数十年的专业知识。
各自的领域以及彼此之间以及与其他弗吉尼亚联邦大学研究人员的合作历史。
这一核心的基本原理是基于这样的主张:滥用药物作用于分子靶点,
调节大脑奖励系统的活动并改变行为,临床前药物滥用研究受益于
从分子水平到行为水平的整个连续体中药物效应的协调研究
然而,个人赠款通常侧重于这一连续体的一部分,并且往往缺乏资源。
快速、合理地将重要发现扩展到其他相关研究领域。
合成化学资助可能会发现一种具有良好镇痛作用的新分子实体,但是缺乏
用于临床前评估该化合物的滥用倾向或作为治疗的潜在效用的资源
另一个例子是,针对治疗药物滥用的行为研究的拨款可能会有所增加。
确定有效的药物治疗策略,但缺乏资源来研究潜在的候选机制
神经药理学核心建议弥补这些差距并加强药物疗效。
VCU 药物滥用研究的广度和影响。受体表达和功能的研究(目标 1),
体内微透析(目标 2)和奖励/强化的行为表达(目标 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系统和行为的影响
已知对药物滥用很重要的终点。
项目成果
期刊论文数量(0)
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会议论文数量(0)
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:
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:
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
- 批准号:
8851547 - 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
- 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:
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
- 批准号:
8653551 - 财政年份:2011
- 资助金额:
$ 28.13万 - 项目类别:
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