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Effect of Sensory Deprivation of Nasal Respiratory on Behavior of C57BL/6J Mice
Nasal breathing is a dynamic cortical organizer involved in various behaviors and states, such as locomotion, exploration, memory, emotion, introspection. However, the effect of sensory deprivation of nasal respiratory breath (NRD) on behavior remain poorly understood. Herein, general locomotor acti...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8699203/ https://www.ncbi.nlm.nih.gov/pubmed/34942927 http://dx.doi.org/10.3390/brainsci11121626 |
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author | Zhu, Yongji Ye, Yujing Zhou, Chenyang Sun, Siqi Zhang, Jingjing Zhao, Zixuan Sun, Tingting Li, Jing Yang, Jing Li, Weiyun Li, Shanshan |
author_facet | Zhu, Yongji Ye, Yujing Zhou, Chenyang Sun, Siqi Zhang, Jingjing Zhao, Zixuan Sun, Tingting Li, Jing Yang, Jing Li, Weiyun Li, Shanshan |
author_sort | Zhu, Yongji |
collection | PubMed |
description | Nasal breathing is a dynamic cortical organizer involved in various behaviors and states, such as locomotion, exploration, memory, emotion, introspection. However, the effect of sensory deprivation of nasal respiratory breath (NRD) on behavior remain poorly understood. Herein, general locomotor activity, emotion, learning and memory, social interaction, and mechanical pain were evaluated using a zinc sulfate nasal irrigation induced nasal respiratory sensory deprivation animal model (ZnSO(4)-induced mouse model). In the open field test, the elevated O-maze test, and forced swim test, NRD mice exhibited depressive and anxiety-like behaviors. In memory-associated tests, NRD mice showed cognitive impairments in the hippocampal-dependent memory (Y maze, object recognition task, and contextual fear conditioning (CFC)) and amygdala-dependent memory (the tone-cued fear conditioning test (TFC)). Surprisingly, NRD mice did not display deficits in the acquisition of conditional fear in both CFC and TFC tests. Still, they showed significant memory retrieval impairment in TFC and enhanced memory retrieval in CFC. At the same time, in the social novelty test using a three-chamber setting, NRD mice showed impaired social and social novelty behavior. Lastly, in the von Frey filaments test, we found that the pain sensitivity of NRD mice was reduced. In conclusion, this NRD mouse model showed a variety of behavioral phenotypic changes, which could offer an important insight into the behavioral impacts of patients with anosmia or those with an impaired olfactory bulb (OB) (e.g., in COVID-19, Alzheimer’s disease, Parkinson’s disease, etc.). |
format | Online Article Text |
id | pubmed-8699203 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-86992032021-12-24 Effect of Sensory Deprivation of Nasal Respiratory on Behavior of C57BL/6J Mice Zhu, Yongji Ye, Yujing Zhou, Chenyang Sun, Siqi Zhang, Jingjing Zhao, Zixuan Sun, Tingting Li, Jing Yang, Jing Li, Weiyun Li, Shanshan Brain Sci Article Nasal breathing is a dynamic cortical organizer involved in various behaviors and states, such as locomotion, exploration, memory, emotion, introspection. However, the effect of sensory deprivation of nasal respiratory breath (NRD) on behavior remain poorly understood. Herein, general locomotor activity, emotion, learning and memory, social interaction, and mechanical pain were evaluated using a zinc sulfate nasal irrigation induced nasal respiratory sensory deprivation animal model (ZnSO(4)-induced mouse model). In the open field test, the elevated O-maze test, and forced swim test, NRD mice exhibited depressive and anxiety-like behaviors. In memory-associated tests, NRD mice showed cognitive impairments in the hippocampal-dependent memory (Y maze, object recognition task, and contextual fear conditioning (CFC)) and amygdala-dependent memory (the tone-cued fear conditioning test (TFC)). Surprisingly, NRD mice did not display deficits in the acquisition of conditional fear in both CFC and TFC tests. Still, they showed significant memory retrieval impairment in TFC and enhanced memory retrieval in CFC. At the same time, in the social novelty test using a three-chamber setting, NRD mice showed impaired social and social novelty behavior. Lastly, in the von Frey filaments test, we found that the pain sensitivity of NRD mice was reduced. In conclusion, this NRD mouse model showed a variety of behavioral phenotypic changes, which could offer an important insight into the behavioral impacts of patients with anosmia or those with an impaired olfactory bulb (OB) (e.g., in COVID-19, Alzheimer’s disease, Parkinson’s disease, etc.). MDPI 2021-12-09 /pmc/articles/PMC8699203/ /pubmed/34942927 http://dx.doi.org/10.3390/brainsci11121626 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Zhu, Yongji Ye, Yujing Zhou, Chenyang Sun, Siqi Zhang, Jingjing Zhao, Zixuan Sun, Tingting Li, Jing Yang, Jing Li, Weiyun Li, Shanshan Effect of Sensory Deprivation of Nasal Respiratory on Behavior of C57BL/6J Mice |
title | Effect of Sensory Deprivation of Nasal Respiratory on Behavior of C57BL/6J Mice |
title_full | Effect of Sensory Deprivation of Nasal Respiratory on Behavior of C57BL/6J Mice |
title_fullStr | Effect of Sensory Deprivation of Nasal Respiratory on Behavior of C57BL/6J Mice |
title_full_unstemmed | Effect of Sensory Deprivation of Nasal Respiratory on Behavior of C57BL/6J Mice |
title_short | Effect of Sensory Deprivation of Nasal Respiratory on Behavior of C57BL/6J Mice |
title_sort | effect of sensory deprivation of nasal respiratory on behavior of c57bl/6j mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8699203/ https://www.ncbi.nlm.nih.gov/pubmed/34942927 http://dx.doi.org/10.3390/brainsci11121626 |
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