Hyperacusis and Central Gain
听觉过敏和中央增益
基本信息
- 批准号:9897505
- 负责人:
- 金额:$ 45.37万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2016
- 资助国家:美国
- 起止时间:2016-04-01 至 2022-03-31
- 项目状态:已结题
- 来源:
- 关键词:Acoustic StimulationAcousticsAffectAmygdaloid structureAuditory ThresholdBasic ScienceBehavioralBehavioral AssayClinical SciencesCochleaCochlear Hearing LossDoseEarElectrophysiology (science)EmotionalEnvironmentFrequenciesGABA AgonistsGoalsGrowthHair CellsHyperactive behaviorHyperacusisIndividualInferior ColliculusLateralLightLoudnessMeasuresMethodsModelingNeurotransmittersNoiseOutputPainPharmaceutical PreparationsPharmacologyPrevalencePropertyRattusReportingSelective Serotonin Reuptake InhibitorSeriesSerotonin AgonistsStructureSystemTemporary Threshold ShiftTestingTimeanxiousauditory deprivationauditory pathwaybehavior measurementbehavior testclinically relevantdeprivationefficacy testingexperienceexperimental studygamma-Aminobutyric Acidhearing impairmenthidden hearing lossinsightneuromechanismototoxicitypublic health relevancerelating to nervous systemsound
项目摘要
DESCRIPTION (provided by applicant): Hearing loss from intense noise exposure and ototoxic drugs greatly reduces the neural output of the cochlea. Despite a reduced cochlear output, neural activity in the central auditory pathway often becomes hyperactive at suprathreshold intensities indicative of Enhanced Central Gain. Enhanced Central Gain is believed to be responsible for hyperacusis, a condition in which listeners experience everyday sounds as unbearably loud or even painful. The goals of this project are: (1) Determine if Enhanced Central Gain is responsible for the temporal and spectral features of hyperacusis, (2) Determine how the acoustic environment (sound enrichment/deprivation) modulates hyperacusis/loudness growth and Central Gain and (3) Determine how serotonin and GABA agonists/antagonists affect hyperacusis and Central Gain. The proposed studies will increase our understanding of the neural mechanisms of hyperacusis and test the efficacy of pharmacological agents to treat hyperacusis.
描述(由申请人提供):由于强噪声暴露和耳毒性药物导致的听力损失大大降低了耳蜗的神经输出。尽管耳蜗输出减少,但中枢听觉通路中的神经活动在指示增强的中枢增益的阈上强度下常常变得过度活跃。增强的中央增益被认为是听觉过敏的原因,听觉过敏是一种情况,在这种情况下,听众每天都会听到难以忍受的声音,甚至是痛苦的声音。本项目的目标是:(1)确定增强的中央增益是否负责听觉过敏的时间和频谱特征,(2)确定声学环境(声音丰富/剥夺)如何调节听觉过敏/响度增长和中央增益,以及(3)确定5-羟色胺和GABA激动剂/拮抗剂如何影响听觉过敏和中央增益。这些研究将增加我们对听觉过敏的神经机制的理解,并测试药物治疗听觉过敏的疗效。
项目成果
期刊论文数量(10)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Roles of Bak and Sirt3 in Paraquat-Induced Cochlear Hair Cell Damage.
- DOI:10.1007/s12640-021-00366-6
- 发表时间:2021-08
- 期刊:
- 影响因子:3.7
- 作者:Ding D;Prolla T;Someya S;Manohar S;Salvi R
- 通讯作者:Salvi R
Inner Hair Cell Loss Disrupts Hearing and Cochlear Function Leading to Sensory Deprivation and Enhanced Central Auditory Gain.
- DOI:10.3389/fnins.2016.00621
- 发表时间:2016
- 期刊:
- 影响因子:4.3
- 作者:Salvi R;Sun W;Ding D;Chen GD;Lobarinas E;Wang J;Radziwon K;Auerbach BD
- 通讯作者:Auerbach BD
Tone-in-noise detection deficits in elderly patients with clinically normal hearing.
- DOI:10.1016/j.amjoto.2018.09.012
- 发表时间:2019-01
- 期刊:
- 影响因子:2.5
- 作者:Ralli M;Greco A;De Vincentiis M;Sheppard A;Cappelli G;Neri I;Salvi R
- 通讯作者:Salvi R
Auditory central gain compensates for changes in cochlear output after prolonged low-level noise exposure.
- DOI:10.1016/j.neulet.2018.09.054
- 发表时间:2018-11-20
- 期刊:
- 影响因子:2.5
- 作者:Sheppard A;Liu X;Ding D;Salvi R
- 通讯作者:Salvi R
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RICHARD J SALVI其他文献
RICHARD J SALVI的其他文献
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{{ truncateString('RICHARD J SALVI', 18)}}的其他基金
Mechanisms of Loudness Intolerance in a Rat Model of Fragile X
脆性 X 大鼠模型的响度不耐受机制
- 批准号:
9978352 - 财政年份:2020
- 资助金额:
$ 45.37万 - 项目类别:
Animal Models of Tinnitus, Brain Imaging & Therapy
耳鸣动物模型、脑成像
- 批准号:
7850334 - 财政年份:2009
- 资助金额:
$ 45.37万 - 项目类别:
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