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Genetic alteration of anxiety and stress-like behavior in mice lacking CaMKIV

Calcium-calmodulin-dependent protein kinase IV (CaMKIV) phosphorylates the major transcription factor cyclic AMP-response element binding protein (CREB), which plays a role in emotional behavior. Here, CaMKIV knockout mice (CaMKIV(-/-)) were tested in a battery of stress and anxiety-related behavior...

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Autores principales: Shum, Fanny WF, Ko, Shanelle W, Lee, Yong-Seok, Kaang, Bong-Kiun, Zhuo, Min
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1208947/
https://www.ncbi.nlm.nih.gov/pubmed/16102169
http://dx.doi.org/10.1186/1744-8069-1-22
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author Shum, Fanny WF
Ko, Shanelle W
Lee, Yong-Seok
Kaang, Bong-Kiun
Zhuo, Min
author_facet Shum, Fanny WF
Ko, Shanelle W
Lee, Yong-Seok
Kaang, Bong-Kiun
Zhuo, Min
author_sort Shum, Fanny WF
collection PubMed
description Calcium-calmodulin-dependent protein kinase IV (CaMKIV) phosphorylates the major transcription factor cyclic AMP-response element binding protein (CREB), which plays a role in emotional behavior. Here, CaMKIV knockout mice (CaMKIV(-/-)) were tested in a battery of stress and anxiety-related behavioral tests, to determine if CaMKIV plays a role in emotional behavior. CaMKIV(-/-)exhibited a decrease in anxiety-like behavior in both the elevated plus maze and dark-light emergence tests when compared to wild-type mice. Both the acoustic startle response and prepulse inhibition of startle were decreased with the deletion of CaMKIV. In addition, CaMKIV(-/- )mice displayed a lack of stress-induced analgesia following restraint or cold swim stress. Our results demonstrate a key role for CaMKIV in anxiety and stress-related behavior.
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spelling pubmed-12089472005-09-16 Genetic alteration of anxiety and stress-like behavior in mice lacking CaMKIV Shum, Fanny WF Ko, Shanelle W Lee, Yong-Seok Kaang, Bong-Kiun Zhuo, Min Mol Pain Research Calcium-calmodulin-dependent protein kinase IV (CaMKIV) phosphorylates the major transcription factor cyclic AMP-response element binding protein (CREB), which plays a role in emotional behavior. Here, CaMKIV knockout mice (CaMKIV(-/-)) were tested in a battery of stress and anxiety-related behavioral tests, to determine if CaMKIV plays a role in emotional behavior. CaMKIV(-/-)exhibited a decrease in anxiety-like behavior in both the elevated plus maze and dark-light emergence tests when compared to wild-type mice. Both the acoustic startle response and prepulse inhibition of startle were decreased with the deletion of CaMKIV. In addition, CaMKIV(-/- )mice displayed a lack of stress-induced analgesia following restraint or cold swim stress. Our results demonstrate a key role for CaMKIV in anxiety and stress-related behavior. BioMed Central 2005-08-15 /pmc/articles/PMC1208947/ /pubmed/16102169 http://dx.doi.org/10.1186/1744-8069-1-22 Text en Copyright © 2005 Shum et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Shum, Fanny WF
Ko, Shanelle W
Lee, Yong-Seok
Kaang, Bong-Kiun
Zhuo, Min
Genetic alteration of anxiety and stress-like behavior in mice lacking CaMKIV
title Genetic alteration of anxiety and stress-like behavior in mice lacking CaMKIV
title_full Genetic alteration of anxiety and stress-like behavior in mice lacking CaMKIV
title_fullStr Genetic alteration of anxiety and stress-like behavior in mice lacking CaMKIV
title_full_unstemmed Genetic alteration of anxiety and stress-like behavior in mice lacking CaMKIV
title_short Genetic alteration of anxiety and stress-like behavior in mice lacking CaMKIV
title_sort genetic alteration of anxiety and stress-like behavior in mice lacking camkiv
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1208947/
https://www.ncbi.nlm.nih.gov/pubmed/16102169
http://dx.doi.org/10.1186/1744-8069-1-22
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