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Gene expression changes in the brain of a Cushing's syndrome mouse model

Excess glucocorticoid exposure affects emotional and cognitive brain functions. The extreme form, Cushing's syndrome, is adequately modelled in the AdKO(2.0) mouse, consequential to adrenocortical hypertrophy and hypercorticosteronemia. We previously reported that the AdKO(2.0) mouse brain unde...

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Autores principales: Amaya, Jorge Miguel, Viho, Eva M. G., Sips, Hetty C. M., Lalai, Reshma A., Sahut‐Barnola, Isabelle, Dumontet, Typhanie, Montanier, Nathanaëlle, Pereira, Alberto M., Martinez, Antoine, Meijer, Onno C.
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/PMC9287025/
https://www.ncbi.nlm.nih.gov/pubmed/35365898
http://dx.doi.org/10.1111/jne.13125
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author Amaya, Jorge Miguel
Viho, Eva M. G.
Sips, Hetty C. M.
Lalai, Reshma A.
Sahut‐Barnola, Isabelle
Dumontet, Typhanie
Montanier, Nathanaëlle
Pereira, Alberto M.
Martinez, Antoine
Meijer, Onno C.
author_facet Amaya, Jorge Miguel
Viho, Eva M. G.
Sips, Hetty C. M.
Lalai, Reshma A.
Sahut‐Barnola, Isabelle
Dumontet, Typhanie
Montanier, Nathanaëlle
Pereira, Alberto M.
Martinez, Antoine
Meijer, Onno C.
author_sort Amaya, Jorge Miguel
collection PubMed
description Excess glucocorticoid exposure affects emotional and cognitive brain functions. The extreme form, Cushing's syndrome, is adequately modelled in the AdKO(2.0) mouse, consequential to adrenocortical hypertrophy and hypercorticosteronemia. We previously reported that the AdKO(2.0) mouse brain undergoes volumetric changes that resemble closely those of Cushing's syndrome human patients, as well as changes in expression of glial related marker proteins. In the present work, the expression of genes related to glial and neuronal cell populations and functions was assessed in regions of the anterior brain, hippocampus, amygdala and hypothalamus. Glucocorticoid target genes were consistently regulated, including CRH mRNA suppression in the hypothalamus and induction in amygdala and hippocampus, even if glucocorticoid receptor protein was downregulated. Expression of glial genes was also affected in the AdKO(2.0) mouse brain, indicating a different activation status in glial cells. Generic markers for neuronal cell populations, and cellular integrity were only slightly affected. Our findings highlight the vulnerability of glial cell populations to chronic high levels of circulating glucocorticoids.
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spelling pubmed-92870252022-07-19 Gene expression changes in the brain of a Cushing's syndrome mouse model Amaya, Jorge Miguel Viho, Eva M. G. Sips, Hetty C. M. Lalai, Reshma A. Sahut‐Barnola, Isabelle Dumontet, Typhanie Montanier, Nathanaëlle Pereira, Alberto M. Martinez, Antoine Meijer, Onno C. J Neuroendocrinol Fundamental and Mechanistic Neuroendocrinology Excess glucocorticoid exposure affects emotional and cognitive brain functions. The extreme form, Cushing's syndrome, is adequately modelled in the AdKO(2.0) mouse, consequential to adrenocortical hypertrophy and hypercorticosteronemia. We previously reported that the AdKO(2.0) mouse brain undergoes volumetric changes that resemble closely those of Cushing's syndrome human patients, as well as changes in expression of glial related marker proteins. In the present work, the expression of genes related to glial and neuronal cell populations and functions was assessed in regions of the anterior brain, hippocampus, amygdala and hypothalamus. Glucocorticoid target genes were consistently regulated, including CRH mRNA suppression in the hypothalamus and induction in amygdala and hippocampus, even if glucocorticoid receptor protein was downregulated. Expression of glial genes was also affected in the AdKO(2.0) mouse brain, indicating a different activation status in glial cells. Generic markers for neuronal cell populations, and cellular integrity were only slightly affected. Our findings highlight the vulnerability of glial cell populations to chronic high levels of circulating glucocorticoids. John Wiley and Sons Inc. 2022-04-01 2022-04 /pmc/articles/PMC9287025/ /pubmed/35365898 http://dx.doi.org/10.1111/jne.13125 Text en © 2022 The Authors. Journal of Neuroendocrinology published by John Wiley & Sons Ltd on behalf of British Society for Neuroendocrinology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Fundamental and Mechanistic Neuroendocrinology
Amaya, Jorge Miguel
Viho, Eva M. G.
Sips, Hetty C. M.
Lalai, Reshma A.
Sahut‐Barnola, Isabelle
Dumontet, Typhanie
Montanier, Nathanaëlle
Pereira, Alberto M.
Martinez, Antoine
Meijer, Onno C.
Gene expression changes in the brain of a Cushing's syndrome mouse model
title Gene expression changes in the brain of a Cushing's syndrome mouse model
title_full Gene expression changes in the brain of a Cushing's syndrome mouse model
title_fullStr Gene expression changes in the brain of a Cushing's syndrome mouse model
title_full_unstemmed Gene expression changes in the brain of a Cushing's syndrome mouse model
title_short Gene expression changes in the brain of a Cushing's syndrome mouse model
title_sort gene expression changes in the brain of a cushing's syndrome mouse model
topic Fundamental and Mechanistic Neuroendocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9287025/
https://www.ncbi.nlm.nih.gov/pubmed/35365898
http://dx.doi.org/10.1111/jne.13125
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