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Structural brain abnormalities in endothelial nitric oxide synthase‐deficient mice revealed by high‐resolution magnetic resonance imaging

INTRODUCTION: Endothelial nitric oxide synthase (eNOS) produces nitric oxide, which is essential for a variety of physiological functions in the brain. Previous work has demonstrated the detrimental effects of eNOS deficiency on brain function in male eNOS knockout (eNOS KO) mice. However, the effec...

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Autores principales: George, Hannah, Mercer, Grace V., Stapleton, Darcie, Dawson, Laura, MacCallum, Phillip E., Spring, Shoshana, Sled, John G., Blundell, Jacqueline, Cahill, Lindsay S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9660425/
https://www.ncbi.nlm.nih.gov/pubmed/36259950
http://dx.doi.org/10.1002/brb3.2801
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author George, Hannah
Mercer, Grace V.
Stapleton, Darcie
Dawson, Laura
MacCallum, Phillip E.
Spring, Shoshana
Sled, John G.
Blundell, Jacqueline
Cahill, Lindsay S.
author_facet George, Hannah
Mercer, Grace V.
Stapleton, Darcie
Dawson, Laura
MacCallum, Phillip E.
Spring, Shoshana
Sled, John G.
Blundell, Jacqueline
Cahill, Lindsay S.
author_sort George, Hannah
collection PubMed
description INTRODUCTION: Endothelial nitric oxide synthase (eNOS) produces nitric oxide, which is essential for a variety of physiological functions in the brain. Previous work has demonstrated the detrimental effects of eNOS deficiency on brain function in male eNOS knockout (eNOS KO) mice. However, the effect of eNOS deficiency on brain structure and any association between these effects and sex is unknown. METHODS: This study used three‐dimensional high‐resolution ex vivo magnetic resonance imaging and behavioral tests of anxiety and cognitive performance to investigate structure–function relationships in the brain of female and male eNOS KO mice in young adulthood. RESULTS: While there were no differences in anxiety‐like behavior or locomotion, there was a sex‐specific deficit in contextual fear memory retention in male, but not in female, eNOS mice compared to wild‐type controls. Moreover, we found that eNOS deficiency induced changes in multiple brain regions that are involved in learning and fear memory including the hippocampus, amygdala, hypothalamus, and areas of the cortex. Several of these MRI‐detectable neuroanatomical changes were dependent on sex. CONCLUSION: The observation that eNOS deficiency impacts brain structure at an early age demonstrates the importance of eNOS for healthy brain development.
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spelling pubmed-96604252022-11-14 Structural brain abnormalities in endothelial nitric oxide synthase‐deficient mice revealed by high‐resolution magnetic resonance imaging George, Hannah Mercer, Grace V. Stapleton, Darcie Dawson, Laura MacCallum, Phillip E. Spring, Shoshana Sled, John G. Blundell, Jacqueline Cahill, Lindsay S. Brain Behav Original Articles INTRODUCTION: Endothelial nitric oxide synthase (eNOS) produces nitric oxide, which is essential for a variety of physiological functions in the brain. Previous work has demonstrated the detrimental effects of eNOS deficiency on brain function in male eNOS knockout (eNOS KO) mice. However, the effect of eNOS deficiency on brain structure and any association between these effects and sex is unknown. METHODS: This study used three‐dimensional high‐resolution ex vivo magnetic resonance imaging and behavioral tests of anxiety and cognitive performance to investigate structure–function relationships in the brain of female and male eNOS KO mice in young adulthood. RESULTS: While there were no differences in anxiety‐like behavior or locomotion, there was a sex‐specific deficit in contextual fear memory retention in male, but not in female, eNOS mice compared to wild‐type controls. Moreover, we found that eNOS deficiency induced changes in multiple brain regions that are involved in learning and fear memory including the hippocampus, amygdala, hypothalamus, and areas of the cortex. Several of these MRI‐detectable neuroanatomical changes were dependent on sex. CONCLUSION: The observation that eNOS deficiency impacts brain structure at an early age demonstrates the importance of eNOS for healthy brain development. John Wiley and Sons Inc. 2022-10-19 /pmc/articles/PMC9660425/ /pubmed/36259950 http://dx.doi.org/10.1002/brb3.2801 Text en © 2022 The Authors. Brain and Behavior published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://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 Articles
George, Hannah
Mercer, Grace V.
Stapleton, Darcie
Dawson, Laura
MacCallum, Phillip E.
Spring, Shoshana
Sled, John G.
Blundell, Jacqueline
Cahill, Lindsay S.
Structural brain abnormalities in endothelial nitric oxide synthase‐deficient mice revealed by high‐resolution magnetic resonance imaging
title Structural brain abnormalities in endothelial nitric oxide synthase‐deficient mice revealed by high‐resolution magnetic resonance imaging
title_full Structural brain abnormalities in endothelial nitric oxide synthase‐deficient mice revealed by high‐resolution magnetic resonance imaging
title_fullStr Structural brain abnormalities in endothelial nitric oxide synthase‐deficient mice revealed by high‐resolution magnetic resonance imaging
title_full_unstemmed Structural brain abnormalities in endothelial nitric oxide synthase‐deficient mice revealed by high‐resolution magnetic resonance imaging
title_short Structural brain abnormalities in endothelial nitric oxide synthase‐deficient mice revealed by high‐resolution magnetic resonance imaging
title_sort structural brain abnormalities in endothelial nitric oxide synthase‐deficient mice revealed by high‐resolution magnetic resonance imaging
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9660425/
https://www.ncbi.nlm.nih.gov/pubmed/36259950
http://dx.doi.org/10.1002/brb3.2801
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