Myelination Deficits Underlying Auditory Issues in Fragile X Syndrome
Myelination Deficits Underlying Auditory Issues in Fragile X Syndrome
批准号:
10201325
负责人:
Elizabeth Anne McCullagh
金额:
$44.21万
依托单位国家:
美国
项目类别:
财政年份:
2021
资助国家:
美国
项目状态:
已结题
起止时间:
2021-09-09 至 2024-08-31
关键词:
AcousticsAddressAnatomyAreaAuditoryAuditory Brainstem ResponsesAxonBasic ScienceBehaviorBehavioralBinauralBiomedical ResearchBrainBrain StemCaliberCochleaCodeComplexDataDependenceDependovirusDevelopmentEarElectrophysiology (science)EnvironmentFMR1Financial SupportFragile X SyndromeFundingGoalsHearingHearing problemHypersensitivityImmunohistochemistryImpairmentIndividualKnowledgeLeadLengthLipidsLocationMeasurementMeasuresMorphologyMusMyelinNeural ConductionNoiseOklahomaPainPathway interactionsPatternPhenotypePhysiologicalPopulation HeterogeneityProcessProteinsRecordsResearchResearch PersonnelResponse LatenciesRoleScientistSensorySound LocalizationSourceStartle ReactionStimulusStreamStudent recruitmentStudentsSymptomsSynapsesTechniquesThickTreatment EfficacyUnited States National Institutes of HealthUniversitiesViralWorkadeno-associated viral vectorauditory pathwayauditory reflexautism spectrum disorderbasebehavior measurementbinaural hearingexperienceexperimental studyhearing impairmentindividuals with autism spectrum disordermyelinationneurotransmissionnovelprepulse inhibitionprogramssoundstudent participationteacherundergraduate student
中文摘要
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英文摘要
Project Summary
Autism spectrum disorder is characterized by an inability to function in environments with multiple competing
sound sources, such as noisy classroom. These auditory issues likely originate early in sound location processing
that occurs in the brainstem. The projections that make up the auditory brainstem circuit that processes binaural
(information from both ears), temporal, and intensity differences are dependent on heavily myelinated axons
that convey this very precise information accurately from the cochlea to the brain. Our preliminary data shows
that auditory brainstem axons are smaller in diameter and thinner in Fragile X Syndrome mice, a monogenetic
form of autism. Additionally, we see a decrease in the latency of binaural waves in the auditory brainstem
response (ABR), a non-invasive electrophysiological recording of this circuit, in FXS mice compared to controls.
Lastly, we see increased latencies to respond to reflexive auditory behavioral stimuli in FXS mice compared to
controls. These data suggest that myelination deficits may underly binaural hearing difficulties in FXS, and
perhaps ASD. We propose to further characterize myelination deficits in FXS mice using anatomical,
physiological, and behavioral measures of myelination (immunohistochemistry/lipid measurements, ABRs, and
prepulse inhibition of the acoustic startle response) to determine the mechanisms underlying myelination issues
in FXS across developmental timepoints. Additionally, we aim to determine the dependence of myelination
deficits on the presence of Fragile X Mental Retardation Protein (FMRP), the protein lacking in FXS, by
reintroducing FMRP through adeno-associated viruses (AAVs) expressing FMRP during development. Results
from this study will determine how myelination contributes to binaural hearing processing issues in FXS and
whether these deficits are rescued by re-expression of FMRP. All of the above mentioned experiments are
approachable for undergraduate researchers thus funding from NIH will further broaden participation of
students in biomedical research and increasing student's knowledge and ability to conduct basic research.
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Myelination Deficits Underlying Auditory Issues in Fragile X Syndrome
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批准号:10622759
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项目类别:
-
资助金额:$12.52万
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财政年份:2022
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负责人:Elizabeth Anne McCullagh
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依托单位:
DEIA supplement - Myelination Deficits Underlying Auditory Issues in Fragile X Syndrome
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批准号:10605699
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项目类别:
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资助金额:$43.77万
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财政年份:2021
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负责人:Elizabeth Anne McCullagh
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依托单位:
海外基金