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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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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. |
format | Online Article Text |
id | pubmed-9287025 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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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