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Temporary conductive hearing loss in early life impairs spatial memory of rats in adulthood

INTRODUCTION: It is known that an interruption of acoustic input in early life will result in abnormal development of the auditory system. Here, we further show that this negative impact actually spans beyond the auditory system to the hippocampus, a system critical for spatial memory. METHODS: We i...

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Autores principales: Zhao, Han, Wang, Li, Chen, Liang, Zhang, Jinsheng, Sun, Wei, Salvi, Richard J., Huang, Yi‐Na, Wang, Ming, Chen, Lin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6043706/
https://www.ncbi.nlm.nih.gov/pubmed/29855161
http://dx.doi.org/10.1002/brb3.1004
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author Zhao, Han
Wang, Li
Chen, Liang
Zhang, Jinsheng
Sun, Wei
Salvi, Richard J.
Huang, Yi‐Na
Wang, Ming
Chen, Lin
author_facet Zhao, Han
Wang, Li
Chen, Liang
Zhang, Jinsheng
Sun, Wei
Salvi, Richard J.
Huang, Yi‐Na
Wang, Ming
Chen, Lin
author_sort Zhao, Han
collection PubMed
description INTRODUCTION: It is known that an interruption of acoustic input in early life will result in abnormal development of the auditory system. Here, we further show that this negative impact actually spans beyond the auditory system to the hippocampus, a system critical for spatial memory. METHODS: We induced a temporary conductive hearing loss (TCHL) in P14 rats by perforating the eardrum and allowing it to heal. The Morris water maze and Y‐maze tests were deployed to evaluate spatial memory of the rats. Electrophysiological recordings and anatomical analysis were made to evaluate functional and structural changes in the hippocampus following TCHL. RESULTS: The rats with the TCHL had nearly normal hearing at P42, but had a decreased performance with the Morris water maze and Y‐maze tests compared with the control group. A functional deficit in the hippocampus of the rats with the TCHL was found as revealed by the depressed long‐term potentiation and the reduced NMDA receptor‐mediated postsynaptic current. A structural deficit in the hippocampus of those animals was also found as revealed the abnormal expression of the NMDA receptors, the decreased number of dendritic spines, the reduced postsynaptic density and the reduced level of neurogenesis. CONCLUSIONS: Our study demonstrates that even temporary auditory sensory deprivation in early life of rats results in abnormal development of the hippocampus and consequently impairs spatial memory in adulthood.
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spelling pubmed-60437062018-07-15 Temporary conductive hearing loss in early life impairs spatial memory of rats in adulthood Zhao, Han Wang, Li Chen, Liang Zhang, Jinsheng Sun, Wei Salvi, Richard J. Huang, Yi‐Na Wang, Ming Chen, Lin Brain Behav Original Research INTRODUCTION: It is known that an interruption of acoustic input in early life will result in abnormal development of the auditory system. Here, we further show that this negative impact actually spans beyond the auditory system to the hippocampus, a system critical for spatial memory. METHODS: We induced a temporary conductive hearing loss (TCHL) in P14 rats by perforating the eardrum and allowing it to heal. The Morris water maze and Y‐maze tests were deployed to evaluate spatial memory of the rats. Electrophysiological recordings and anatomical analysis were made to evaluate functional and structural changes in the hippocampus following TCHL. RESULTS: The rats with the TCHL had nearly normal hearing at P42, but had a decreased performance with the Morris water maze and Y‐maze tests compared with the control group. A functional deficit in the hippocampus of the rats with the TCHL was found as revealed by the depressed long‐term potentiation and the reduced NMDA receptor‐mediated postsynaptic current. A structural deficit in the hippocampus of those animals was also found as revealed the abnormal expression of the NMDA receptors, the decreased number of dendritic spines, the reduced postsynaptic density and the reduced level of neurogenesis. CONCLUSIONS: Our study demonstrates that even temporary auditory sensory deprivation in early life of rats results in abnormal development of the hippocampus and consequently impairs spatial memory in adulthood. John Wiley and Sons Inc. 2018-05-31 /pmc/articles/PMC6043706/ /pubmed/29855161 http://dx.doi.org/10.1002/brb3.1004 Text en © 2018 The Authors. Brain and Behavior published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Zhao, Han
Wang, Li
Chen, Liang
Zhang, Jinsheng
Sun, Wei
Salvi, Richard J.
Huang, Yi‐Na
Wang, Ming
Chen, Lin
Temporary conductive hearing loss in early life impairs spatial memory of rats in adulthood
title Temporary conductive hearing loss in early life impairs spatial memory of rats in adulthood
title_full Temporary conductive hearing loss in early life impairs spatial memory of rats in adulthood
title_fullStr Temporary conductive hearing loss in early life impairs spatial memory of rats in adulthood
title_full_unstemmed Temporary conductive hearing loss in early life impairs spatial memory of rats in adulthood
title_short Temporary conductive hearing loss in early life impairs spatial memory of rats in adulthood
title_sort temporary conductive hearing loss in early life impairs spatial memory of rats in adulthood
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6043706/
https://www.ncbi.nlm.nih.gov/pubmed/29855161
http://dx.doi.org/10.1002/brb3.1004
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