Neuromodulation in the auditory system
听觉系统的神经调节
基本信息
- 批准号:9086809
- 负责人:
- 金额:$ 2.87万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2014
- 资助国家:美国
- 起止时间:2014-01-14 至 2018-12-31
- 项目状态:已结题
- 来源:
- 关键词:AcousticsAffectAgonistAttentionAuditoryAuditory Perceptual DisordersAuditory systemBehavioralBrainBrain regionCodeCommunication impairmentComplexDataDiseaseDopamineDopamine AgonistsDopamine ReceptorEnvironmentFiberFutureGenetic studyGenetically Engineered MouseHealthHearingIndividualInferior ColliculusInjection of therapeutic agentLinkLocationMembraneMusNeurodegenerative DisordersNeuronsParkinson DiseasePatientsPhysiologicalProcessPropertyReceptor ActivationResearchRoleShapesSignal TransductionSiteSliceSocial EnvironmentSourceSpeechStaining methodStainsStimulusStructureSynapsesSynaptic TransmissionSystemTestingTimeTracerTyrosine 3-MonooxygenaseWhole-Cell Recordingsauditory pathwayawakecell typeimprovedin vivonerve supplynervous system disorderneural circuitneurophysiologyneuroregulationreceptorrelating to nervous systemresponsesoundspeech processingvocalization
项目摘要
DESCRIPTION (provided by applicant): Understanding speech depends on the capacity of the auditory system to accurately represent salient sounds. This representation may be altered by a variety of factors, including disorders involving neuromodulatory systems. For example, patients with Parkinson's disease have speech processing problems suggesting that dopamine alters normal representation of these salient signals. The proposed studies focus on the role of dopamine in altering representation of salient sounds in the inferior colliculus (IC). The IC is a prime location for modulating auditory processing of salient signals because it receives input from multiple auditory and non-auditory source, it contains dopamine receptors and fibers, and preliminary data from this proposal indicate that dopamine modulates IC auditory responses. The objective of this proposal is to determine the mechanisms by which dopamine alters the representation of vocalizations in IC. The first Aim will use in vivo single unit recordings with application of pharmacological agents in the IC of awake mice to determine the effects of dopamine receptor activation on responses to vocalizations. The second Aim will use whole-cell recordings in mouse IC brain slices to determine the effects of dopamine on intrinsic and synaptic properties of different neuron types. The third Aim will use in vivo whole-cell recordings
to identify how intrinsic properties of different neuron types shape selectivity to vocalizations. Aims 1-3 will thus provide an integrated understanding of the cellular and synaptic mechanisms underlying auditory responses to complex sounds. The fourth Aim will determine the sources of dopaminergic input to the IC, an important step towards understanding the behavioral contexts that elicit dopamine release into the IC. The significance of this proposal is that it is the first
integrated study of the effects of dopamine on the cellular, synaptic and circuit properties underlying IC responses to salient sounds. The results will increase our mechanistic understanding of auditory processing of meaningful sounds and how this encoding changes with different social contexts, physiological states and communication disorders. These studies using mice with normal hearing will facilitate future studies of genetically engineered mice to further probe the mechanisms underlying specific communication and neurological disorders.
描述(申请人提供):理解语音取决于听觉系统准确表示突出声音的能力。这种表现可能会被多种因素改变,包括涉及神经调节系统的紊乱。例如,帕金森氏症患者的语音处理问题表明,多巴胺改变了这些显著信号的正常表达。拟议的研究集中在多巴胺在改变下丘(IC)显著音的表征中的作用。IC是调节显著信号听觉处理的最佳位置,因为它接受来自多个听觉和非听觉来源的输入,它含有多巴胺受体和纤维,来自这一提议的初步数据表明,多巴胺调节IC听觉反应。这项建议的目的是确定多巴胺改变IC中发声表征的机制。第一个目标是使用体内单一单位记录,并在清醒小鼠的IC中应用药物,以确定多巴胺受体激活对发声反应的影响。第二个目标将使用小鼠IC脑片的全细胞记录来确定多巴胺对不同类型神经元的内在和突触特性的影响。第三个目标将使用活体全细胞记录
以确定不同神经元类型的内在属性如何形成对发声的选择性。因此,AIMS 1-3将提供对复杂声音的听觉反应潜在的细胞和突触机制的综合理解。第四个目标将确定多巴胺能输入到IC的来源,这是了解导致多巴胺释放到IC的行为背景的重要一步。这项提议的意义在于,它是第一个
综合研究多巴胺对突触反应的细胞、突触和电路特性的影响。结果将增加我们对有意义声音的听觉处理的机械性理解,以及这种编码如何随着不同的社会背景、生理状态和沟通障碍而变化。这些利用听力正常的小鼠进行的研究将有助于未来对基因工程小鼠的研究,以进一步探索特定沟通和神经障碍的潜在机制。
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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DAVID J PERKEL其他文献
DAVID J PERKEL的其他文献
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Mechanisms of adult forebrain neural circuit regeneration
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- 批准号:
10362563 - 财政年份:2018
- 资助金额:
$ 2.87万 - 项目类别:
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