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Elevated Anxiety and Impaired Attention in Super-Smeller, Kv1.3 Knockout Mice

It has long been recognized that olfaction and emotion are linked. While chemosensory research using both human and rodent models have indicated a change in emotion can contribute to olfactory dysfunction, there are few studies addressing the contribution of olfaction to a modulation in emotion. In...

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Autores principales: Huang, Zhenbo, Hoffman, Carlie A., Chelette, Brandon M., Thiebaud, Nicolas, Fadool, Debra A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5867313/
https://www.ncbi.nlm.nih.gov/pubmed/29615878
http://dx.doi.org/10.3389/fnbeh.2018.00049
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author Huang, Zhenbo
Hoffman, Carlie A.
Chelette, Brandon M.
Thiebaud, Nicolas
Fadool, Debra A.
author_facet Huang, Zhenbo
Hoffman, Carlie A.
Chelette, Brandon M.
Thiebaud, Nicolas
Fadool, Debra A.
author_sort Huang, Zhenbo
collection PubMed
description It has long been recognized that olfaction and emotion are linked. While chemosensory research using both human and rodent models have indicated a change in emotion can contribute to olfactory dysfunction, there are few studies addressing the contribution of olfaction to a modulation in emotion. In mice, olfactory deficits have been linked with heightened anxiety levels, suggesting that there could be an inverse relationship between olfaction and anxiety. Furthermore, increased anxiety is often co-morbid with psychiatric conditions such as attention disorders. Our study aimed to investigate the roles of olfaction in modulating anxiety. Voltage-gated potassium ion channel Kv1.3 knockout mice (Kv1.3−/−), which have heightened olfaction, and wild-type (WT) mice were examined for anxiety-like behaviors using marble burying (MB), light-dark box (LDB) and elevated-plus maze (EPM) tests. Because Kv1.3−/− mice have increased locomotor activity, inattentive and hyperactive behaviors were quantified for both genotypes. Kv1.3−/− mice showed increased anxiety levels compared to their WT counterparts and administration of methylphenidate (MPH) via oral gavage alleviated their increased anxiety. Object-based attention testing indicated young and older Kv1.3−/− mice had attention deficits and treatment with MPH also ameliorated this condition. Locomotor testing through use of a metabolic chamber indicated that Kv1.3−/− mice were not significantly hyperactive and MPH treatment failed to modify this activity. Our data suggest that heightened olfaction does not necessarily lead to decreased anxiety levels, and that Kv1.3−/− mice may have behaviors associated with inattentiveness.
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spelling pubmed-58673132018-04-03 Elevated Anxiety and Impaired Attention in Super-Smeller, Kv1.3 Knockout Mice Huang, Zhenbo Hoffman, Carlie A. Chelette, Brandon M. Thiebaud, Nicolas Fadool, Debra A. Front Behav Neurosci Neuroscience It has long been recognized that olfaction and emotion are linked. While chemosensory research using both human and rodent models have indicated a change in emotion can contribute to olfactory dysfunction, there are few studies addressing the contribution of olfaction to a modulation in emotion. In mice, olfactory deficits have been linked with heightened anxiety levels, suggesting that there could be an inverse relationship between olfaction and anxiety. Furthermore, increased anxiety is often co-morbid with psychiatric conditions such as attention disorders. Our study aimed to investigate the roles of olfaction in modulating anxiety. Voltage-gated potassium ion channel Kv1.3 knockout mice (Kv1.3−/−), which have heightened olfaction, and wild-type (WT) mice were examined for anxiety-like behaviors using marble burying (MB), light-dark box (LDB) and elevated-plus maze (EPM) tests. Because Kv1.3−/− mice have increased locomotor activity, inattentive and hyperactive behaviors were quantified for both genotypes. Kv1.3−/− mice showed increased anxiety levels compared to their WT counterparts and administration of methylphenidate (MPH) via oral gavage alleviated their increased anxiety. Object-based attention testing indicated young and older Kv1.3−/− mice had attention deficits and treatment with MPH also ameliorated this condition. Locomotor testing through use of a metabolic chamber indicated that Kv1.3−/− mice were not significantly hyperactive and MPH treatment failed to modify this activity. Our data suggest that heightened olfaction does not necessarily lead to decreased anxiety levels, and that Kv1.3−/− mice may have behaviors associated with inattentiveness. Frontiers Media S.A. 2018-03-19 /pmc/articles/PMC5867313/ /pubmed/29615878 http://dx.doi.org/10.3389/fnbeh.2018.00049 Text en Copyright © 2018 Huang, Hoffman, Chelette, Thiebaud and Fadool. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Huang, Zhenbo
Hoffman, Carlie A.
Chelette, Brandon M.
Thiebaud, Nicolas
Fadool, Debra A.
Elevated Anxiety and Impaired Attention in Super-Smeller, Kv1.3 Knockout Mice
title Elevated Anxiety and Impaired Attention in Super-Smeller, Kv1.3 Knockout Mice
title_full Elevated Anxiety and Impaired Attention in Super-Smeller, Kv1.3 Knockout Mice
title_fullStr Elevated Anxiety and Impaired Attention in Super-Smeller, Kv1.3 Knockout Mice
title_full_unstemmed Elevated Anxiety and Impaired Attention in Super-Smeller, Kv1.3 Knockout Mice
title_short Elevated Anxiety and Impaired Attention in Super-Smeller, Kv1.3 Knockout Mice
title_sort elevated anxiety and impaired attention in super-smeller, kv1.3 knockout mice
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5867313/
https://www.ncbi.nlm.nih.gov/pubmed/29615878
http://dx.doi.org/10.3389/fnbeh.2018.00049
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