Evidence map›Paper›PMID 40591708›Full record

ArticlePLoS biology2025

Altered auditory feature discrimination in a rat model of Fragile X Syndrome.

D Walker Gauthier, Noelle James, Benjamin D Auerbach

Abstract read
In one paragraph

Article in PLoS biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors.

D Walker GauthierDepartment of Molecular & Integrative Physiology, School of Molecular & Cellular Biology, University of Illinois Urbana-Champaign, Urbana, Illinois, United States of America.
Noelle JamesDepartment of Molecular & Integrative Physiology, School of Molecular & Cellular Biology, University of Illinois Urbana-Champaign, Urbana, Illinois, United States of America.
Benjamin D AuerbachDepartment of Molecular & Integrative Physiology, School of Molecular & Cellular Biology, University of Illinois Urbana-Champaign, Urbana, Illinois, United States of America.ORCID 0000-0001-6253-2246

Funding

Identifying Convergent Circuit Disruptions Across Genetically-Distinct Models of AutismR01HD111753 · NICHD · UNIVERSITY OF ILLINOIS AT URBANA-CHAMPAIGN · PI Benjamin D Auerbach · 2023 to 2026
$1.7M
Mechanisms of sound hypersensitivity in a rat model of autismK01DC018310 · NIDCD · UNIVERSITY OF ILLINOIS AT URBANA-CHAMPAIGN · PI AUERBACH, BENJAMIN D · 2020 to 2024
$715k
NICHD NIH HHS R01 HD111753NIDCD NIH HHS K01 DC018310
6 · The paper itself

Abstract

Atypical sensory processing, particularly in the auditory domain, is one of the most common and quality-of-life affecting symptoms seen in autism spectrum disorders (ASD). Fragile X Syndrome (FXS) is a leading inherited cause of ASD and a majority of FXS individuals present with auditory processing alterations. While auditory hypersensitivity is a common phenotype observed in FXS and Fmr1 knockout (KO) rodent models, it is important to consider other auditory coding impairments that could contribute to sound processing difficulties and disrupted language comprehension in FXS. We have shown previously that a Fmr1 KO rat model of FXS exhibits heightened sound sensitivity that coincided with abnormal perceptual integration of stimulus bandwidth, indicative of altered spectral processing. Frequency discrimination is a fundamental aspect of sound encoding that is important for a range of auditory processes, such as source segregation and speech comprehension, and disrupted frequency coding could thus contribute to a range of auditory issues in FXS and ASD. Here we explicitly characterized spectral processing deficits in male Fmr1 KO rats using an operant conditioning tone discrimination assay and in vivo electrophysiological recordings from the auditory cortex and inferior colliculus. We found that Fmr1 KO rats exhibited poorer frequency resolution, which corresponded with neuronal hyperactivity and broader frequency tuning in auditory cortical but not collicular neurons. Using an experimentally informed population model, we show that these cortical physiological differences can recapitulate the observed behavior discrimination deficits, with decoder performance being tightly linked to differences in cortical tuning width and signal-to-noise ratios. Together, these findings indicate that cortical hyperexcitability in Fmr1 KO rats may act to preserve signal-to-noise ratios and signal detection threshold at the expense of sound sensitivity and fine feature discrimination, highlighting a potential mechanistic locus for a range of auditory behavioral phenotypes in FXS.

Indexed as

Auditory PerceptionFragile X SyndromeAcoustic StimulationAnimalsAuditory CortexDisease Models, AnimalFragile X Messenger Ribonucleoprotein 1MaleRatsFmr1 protein, ratFragile X Messenger Ribonucleoprotein 1

Identifiers

PMID40591708
PMCPMC12237272

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.