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Plasticity of spatial hearing: behavioural effects of cortical inactivation

The contribution of auditory cortex to spatial information processing was explored behaviourally in adult ferrets by reversibly deactivating different cortical areas by subdural placement of a polymer that released the GABA(A) agonist muscimol over a period of weeks. The spatial extent and time cour...

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Autores principales: Nodal, Fernando R, Bajo, Victoria M, King, Andrew J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Science Inc 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3464400/
https://www.ncbi.nlm.nih.gov/pubmed/22547635
http://dx.doi.org/10.1113/jphysiol.2011.222828
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author Nodal, Fernando R
Bajo, Victoria M
King, Andrew J
author_facet Nodal, Fernando R
Bajo, Victoria M
King, Andrew J
author_sort Nodal, Fernando R
collection PubMed
description The contribution of auditory cortex to spatial information processing was explored behaviourally in adult ferrets by reversibly deactivating different cortical areas by subdural placement of a polymer that released the GABA(A) agonist muscimol over a period of weeks. The spatial extent and time course of cortical inactivation were determined electrophysiologically. Muscimol-Elvax was placed bilaterally over the anterior (AEG), middle (MEG) or posterior ectosylvian gyrus (PEG), so that different regions of the auditory cortex could be deactivated in different cases. Sound localization accuracy in the horizontal plane was assessed by measuring both the initial head orienting and approach-to-target responses made by the animals. Head orienting behaviour was unaffected by silencing any region of the auditory cortex, whereas the accuracy of approach-to-target responses to brief sounds (40 ms noise bursts) was reduced by muscimol-Elvax but not by drug-free implants. Modest but significant localization impairments were observed after deactivating the MEG, AEG or PEG, although the largest deficits were produced in animals in which the MEG, where the primary auditory fields are located, was silenced. We also examined experience-induced spatial plasticity by reversibly plugging one ear. In control animals, localization accuracy for both approach-to-target and head orienting responses was initially impaired by monaural occlusion, but recovered with training over the next few days. Deactivating any part of the auditory cortex resulted in less complete recovery than in controls, with the largest deficits observed after silencing the higher-level cortical areas in the AEG and PEG. Although suggesting that each region of auditory cortex contributes to spatial learning, differences in the localization deficits and degree of adaptation between groups imply a regional specialization in the processing of spatial information across the auditory cortex.
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spelling pubmed-34644002012-10-05 Plasticity of spatial hearing: behavioural effects of cortical inactivation Nodal, Fernando R Bajo, Victoria M King, Andrew J J Physiol Neuroscience: Behavioural/Systems/Cognitive The contribution of auditory cortex to spatial information processing was explored behaviourally in adult ferrets by reversibly deactivating different cortical areas by subdural placement of a polymer that released the GABA(A) agonist muscimol over a period of weeks. The spatial extent and time course of cortical inactivation were determined electrophysiologically. Muscimol-Elvax was placed bilaterally over the anterior (AEG), middle (MEG) or posterior ectosylvian gyrus (PEG), so that different regions of the auditory cortex could be deactivated in different cases. Sound localization accuracy in the horizontal plane was assessed by measuring both the initial head orienting and approach-to-target responses made by the animals. Head orienting behaviour was unaffected by silencing any region of the auditory cortex, whereas the accuracy of approach-to-target responses to brief sounds (40 ms noise bursts) was reduced by muscimol-Elvax but not by drug-free implants. Modest but significant localization impairments were observed after deactivating the MEG, AEG or PEG, although the largest deficits were produced in animals in which the MEG, where the primary auditory fields are located, was silenced. We also examined experience-induced spatial plasticity by reversibly plugging one ear. In control animals, localization accuracy for both approach-to-target and head orienting responses was initially impaired by monaural occlusion, but recovered with training over the next few days. Deactivating any part of the auditory cortex resulted in less complete recovery than in controls, with the largest deficits observed after silencing the higher-level cortical areas in the AEG and PEG. Although suggesting that each region of auditory cortex contributes to spatial learning, differences in the localization deficits and degree of adaptation between groups imply a regional specialization in the processing of spatial information across the auditory cortex. Blackwell Science Inc 2012-08-15 2012-04-30 /pmc/articles/PMC3464400/ /pubmed/22547635 http://dx.doi.org/10.1113/jphysiol.2011.222828 Text en © 2012 The Authors. The Journal of Physiology © 2012 The Physiological Society
spellingShingle Neuroscience: Behavioural/Systems/Cognitive
Nodal, Fernando R
Bajo, Victoria M
King, Andrew J
Plasticity of spatial hearing: behavioural effects of cortical inactivation
title Plasticity of spatial hearing: behavioural effects of cortical inactivation
title_full Plasticity of spatial hearing: behavioural effects of cortical inactivation
title_fullStr Plasticity of spatial hearing: behavioural effects of cortical inactivation
title_full_unstemmed Plasticity of spatial hearing: behavioural effects of cortical inactivation
title_short Plasticity of spatial hearing: behavioural effects of cortical inactivation
title_sort plasticity of spatial hearing: behavioural effects of cortical inactivation
topic Neuroscience: Behavioural/Systems/Cognitive
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3464400/
https://www.ncbi.nlm.nih.gov/pubmed/22547635
http://dx.doi.org/10.1113/jphysiol.2011.222828
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