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Decreasing auditory input induces neurogenesis impairment in the hippocampus
Hearing loss is associated with cognitive decline and dementia risk. Sensorineural hearing loss suppresses hippocampal neurogenesis, resulting in cognitive decline. However, the underlying mechanism of impaired neurogenesis and the role of microglial activation and stress responses related to hearin...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7801596/ https://www.ncbi.nlm.nih.gov/pubmed/33432038 http://dx.doi.org/10.1038/s41598-020-80218-z |
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author | Kurioka, Takaomi Mogi, Sachiyo Yamashita, Taku |
author_facet | Kurioka, Takaomi Mogi, Sachiyo Yamashita, Taku |
author_sort | Kurioka, Takaomi |
collection | PubMed |
description | Hearing loss is associated with cognitive decline and dementia risk. Sensorineural hearing loss suppresses hippocampal neurogenesis, resulting in cognitive decline. However, the underlying mechanism of impaired neurogenesis and the role of microglial activation and stress responses related to hearing loss in the hippocampus remains unknown. Using a conductive hearing loss (CHL) model, we investigated whether a decrease in sound level could induce impairment of hippocampal neurogenesis and examined the differences between unilateral CHL (uCHL) and bilateral CHL (bCHL). To establish the CHL mouse model, ears were unilaterally or bilaterally occluded for five weeks by auditory canal ligation. Although hearing thresholds were significantly increased following CHL, CHL mice exhibited no significant loss of spiral ganglion or hippocampal neurons. Hippocampal neurogenesis was significantly and equally decreased in both sides following uCHL. More severe decreases in hippocampal neurogenesis were observed in both sides in bCHL mice compared with that in uCHL mice. Furthermore, microglial invasion significantly increased following CHL. Serum cortisol levels, which indicate stress response, significantly increased following bCHL. Therefore, auditory deprivation could lead to increased microglial invasion and stress responses and might be a risk factor for hippocampal neurogenesis impairment. |
format | Online Article Text |
id | pubmed-7801596 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-78015962021-01-12 Decreasing auditory input induces neurogenesis impairment in the hippocampus Kurioka, Takaomi Mogi, Sachiyo Yamashita, Taku Sci Rep Article Hearing loss is associated with cognitive decline and dementia risk. Sensorineural hearing loss suppresses hippocampal neurogenesis, resulting in cognitive decline. However, the underlying mechanism of impaired neurogenesis and the role of microglial activation and stress responses related to hearing loss in the hippocampus remains unknown. Using a conductive hearing loss (CHL) model, we investigated whether a decrease in sound level could induce impairment of hippocampal neurogenesis and examined the differences between unilateral CHL (uCHL) and bilateral CHL (bCHL). To establish the CHL mouse model, ears were unilaterally or bilaterally occluded for five weeks by auditory canal ligation. Although hearing thresholds were significantly increased following CHL, CHL mice exhibited no significant loss of spiral ganglion or hippocampal neurons. Hippocampal neurogenesis was significantly and equally decreased in both sides following uCHL. More severe decreases in hippocampal neurogenesis were observed in both sides in bCHL mice compared with that in uCHL mice. Furthermore, microglial invasion significantly increased following CHL. Serum cortisol levels, which indicate stress response, significantly increased following bCHL. Therefore, auditory deprivation could lead to increased microglial invasion and stress responses and might be a risk factor for hippocampal neurogenesis impairment. Nature Publishing Group UK 2021-01-11 /pmc/articles/PMC7801596/ /pubmed/33432038 http://dx.doi.org/10.1038/s41598-020-80218-z Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Kurioka, Takaomi Mogi, Sachiyo Yamashita, Taku Decreasing auditory input induces neurogenesis impairment in the hippocampus |
title | Decreasing auditory input induces neurogenesis impairment in the hippocampus |
title_full | Decreasing auditory input induces neurogenesis impairment in the hippocampus |
title_fullStr | Decreasing auditory input induces neurogenesis impairment in the hippocampus |
title_full_unstemmed | Decreasing auditory input induces neurogenesis impairment in the hippocampus |
title_short | Decreasing auditory input induces neurogenesis impairment in the hippocampus |
title_sort | decreasing auditory input induces neurogenesis impairment in the hippocampus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7801596/ https://www.ncbi.nlm.nih.gov/pubmed/33432038 http://dx.doi.org/10.1038/s41598-020-80218-z |
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