Literature DB >> 27387138

Crossmodal plasticity in auditory, visual and multisensory cortical areas following noise-induced hearing loss in adulthood.

Ashley L Schormans1, Marei Typlt1, Brian L Allman2.   

Abstract

Complete or partial hearing loss results in an increased responsiveness of neurons in the core auditory cortex of numerous species to visual and/or tactile stimuli (i.e., crossmodal plasticity). At present, however, it remains uncertain how adult-onset partial hearing loss affects higher-order cortical areas that normally integrate audiovisual information. To that end, extracellular electrophysiological recordings were performed under anesthesia in noise-exposed rats two weeks post-exposure (0.8-20 kHz at 120 dB SPL for 2 h) and age-matched controls to characterize the nature and extent of crossmodal plasticity in the dorsal auditory cortex (AuD), an area outside of the auditory core, as well as in the neighboring lateral extrastriate visual cortex (V2L), an area known to contribute to audiovisual processing. Computer-generated auditory (noise burst), visual (light flash) and combined audiovisual stimuli were delivered, and the associated spiking activity was used to determine the response profile of each neuron sampled (i.e., unisensory, subthreshold multisensory or bimodal). In both the AuD cortex and the multisensory zone of the V2L cortex, the maximum firing rates were unchanged following noise exposure, and there was a relative increase in the proportion of neurons responsive to visual stimuli, with a concomitant decrease in the number of neurons that were solely responsive to auditory stimuli despite adjusting the sound intensity to account for each rat's hearing threshold. These neighboring cortical areas differed, however, in how noise-induced hearing loss affected audiovisual processing; the total proportion of multisensory neurons significantly decreased in the V2L cortex (control 38.8 ± 3.3% vs. noise-exposed 27.1 ± 3.4%), and dramatically increased in the AuD cortex (control 23.9 ± 3.3% vs. noise-exposed 49.8 ± 6.1%). Thus, following noise exposure, the cortical area showing the greatest relative degree of multisensory convergence transitioned ventrally, away from the audiovisual area, V2L, toward the predominantly auditory area, AuD. Overall, the collective findings of the present study support the suggestion that crossmodal plasticity induced by adult-onset hearing impairment manifests in higher-order cortical areas as a transition in the functional border of the audiovisual cortex.
Copyright © 2016 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Crossmodal plasticity; Extracellular electrophysiology; Extrastriate visual cortex; Multisensory integration; Rat; Sensory reorganization

Mesh:

Year:  2016        PMID: 27387138     DOI: 10.1016/j.heares.2016.06.017

Source DB:  PubMed          Journal:  Hear Res        ISSN: 0378-5955            Impact factor:   3.208


  16 in total

Review 1.  Do the Different Sensory Areas Within the Cat Anterior Ectosylvian Sulcal Cortex Collectively Represent a Network Multisensory Hub?

Authors:  M Alex Meredith; Mark T Wallace; H Ruth Clemo
Journal:  Multisens Res       Date:  2018-06-26       Impact factor: 2.286

2.  Adult-Onset Hearing Impairment Induces Layer-Specific Cortical Reorganization: Evidence of Crossmodal Plasticity and Central Gain Enhancement.

Authors:  Ashley L Schormans; Marei Typlt; Brian L Allman
Journal:  Cereb Cortex       Date:  2019-05-01       Impact factor: 5.357

3.  Afferent loss, GABA, and Central Gain in older adults: Associations with speech recognition in noise.

Authors:  Kelly C Harris; James W Dias; Carolyn M McClaskey; Jeffrey Rumschlag; James Prisciandaro; Judy R Dubno
Journal:  J Neurosci       Date:  2022-08-19       Impact factor: 6.709

Review 4.  Approaches to Understanding Multisensory Dysfunction in Autism Spectrum Disorder.

Authors:  Justin K Siemann; Jeremy Veenstra-VanderWeele; Mark T Wallace
Journal:  Autism Res       Date:  2020-09-01       Impact factor: 5.216

5.  What is a multisensory cortex? A laminar, connectional, and functional study of a ferret temporal cortical multisensory area.

Authors:  M Alex Meredith; Leslie P Keniston; Elizabeth H Prickett; Moazzum Bajwa; Alexandru Cojanu; H Ruth Clemo; Brian L Allman
Journal:  J Comp Neurol       Date:  2020-01-29       Impact factor: 3.215

6.  High-frequency Noise-induced Hearing Loss Disrupts Functional Connectivity in Non-auditory Areas with Cognitive Disturbances.

Authors:  Ying Luan; Richard Salvi; Lijie Liu; Chunqiang Lu; Yun Jiao; Tianyu Tang; Haiqing Liu; Gao-Jun Teng
Journal:  Neurosci Bull       Date:  2021-03-27       Impact factor: 5.203

7.  Audiovisual Temporal Processing and Synchrony Perception in the Rat.

Authors:  Ashley L Schormans; Kaela E Scott; Albert M Q Vo; Anna Tyker; Marei Typlt; Daniel Stolzberg; Brian L Allman
Journal:  Front Behav Neurosci       Date:  2017-01-10       Impact factor: 3.558

Review 8.  The Impact of Ecological Niche on Adaptive Flexibility of Sensory Circuitry.

Authors:  Sarah L Pallas
Journal:  Front Neurosci       Date:  2017-06-28       Impact factor: 4.677

9.  Changes of the Brain Causal Connectivity Networks in Patients With Long-Term Bilateral Hearing Loss.

Authors:  Gang Zhang; Long-Chun Xu; Min-Feng Zhang; Yue Zou; Le-Min He; Yun-Fu Cheng; Dong-Sheng Zhang; Wen-Bo Zhao; Xiao-Yan Wang; Peng-Cheng Wang; Guang-Yu Zhang
Journal:  Front Neurosci       Date:  2021-07-01       Impact factor: 4.677

10.  Somatosensory Cross-Modal Reorganization in Adults With Age-Related, Early-Stage Hearing Loss.

Authors:  Garrett Cardon; Anu Sharma
Journal:  Front Hum Neurosci       Date:  2018-05-03       Impact factor: 3.169

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.