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Astrocytic estrogen receptors and impaired neurotrophic responses in a rat model of perimenopause

In a perimenopausal model of middle-aged rats, the astrocyte estrogen receptor-alpha (ERa): ER-beta (ERb) ratio increased with the onset of acyclicity (constant estrus, CE) in association with impaired neurotrophic responses to estradiol (E2). We report additional data on irregular cycling (IR) from...

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Autores principales: Morgan, Todd E., Finch, Caleb E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4586279/
https://www.ncbi.nlm.nih.gov/pubmed/26483679
http://dx.doi.org/10.3389/fnagi.2015.00179
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author Morgan, Todd E.
Finch, Caleb E.
author_facet Morgan, Todd E.
Finch, Caleb E.
author_sort Morgan, Todd E.
collection PubMed
description In a perimenopausal model of middle-aged rats, the astrocyte estrogen receptor-alpha (ERa): ER-beta (ERb) ratio increased with the onset of acyclicity (constant estrus, CE) in association with impaired neurotrophic responses to estradiol (E2). We report additional data on irregular cycling (IR) from this study of 9 month old perimenopausal subgroups. In particular, irregular cyclers (IR) also show increased ERa:ERb ratio in cerebral cortex astrocytes comparable to acyclic individuals in CE. In mixed glial cultures from these same cycling subgroups, the E2-dependent neurotrophic activity and glial fibrillary acidic protein (GFAP) repression by E2 were impaired in IR to the same degree as in CE-derived glia. The greater importance of cycling status than age during the perimenopause to astrocyte ERs are attributable to individual variations of the residual ovarian follicle pool, which determine the onset of acyclicity. The corresponding loss of E2-dependent GFAP repression and E2-dependent neurotrophic activity add further to the inverse relationship of GFAP expression and astrocyte neurotrophic activity across aging in both sexes. These findings are relevant to impairments of spatial learning and of hippocampal long-term potentiation during the onset of IR in middle-aged rats, and to perimenopausal factors mediating the higher risk of women for Alzheimer disease.
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spelling pubmed-45862792015-10-19 Astrocytic estrogen receptors and impaired neurotrophic responses in a rat model of perimenopause Morgan, Todd E. Finch, Caleb E. Front Aging Neurosci Neuroscience In a perimenopausal model of middle-aged rats, the astrocyte estrogen receptor-alpha (ERa): ER-beta (ERb) ratio increased with the onset of acyclicity (constant estrus, CE) in association with impaired neurotrophic responses to estradiol (E2). We report additional data on irregular cycling (IR) from this study of 9 month old perimenopausal subgroups. In particular, irregular cyclers (IR) also show increased ERa:ERb ratio in cerebral cortex astrocytes comparable to acyclic individuals in CE. In mixed glial cultures from these same cycling subgroups, the E2-dependent neurotrophic activity and glial fibrillary acidic protein (GFAP) repression by E2 were impaired in IR to the same degree as in CE-derived glia. The greater importance of cycling status than age during the perimenopause to astrocyte ERs are attributable to individual variations of the residual ovarian follicle pool, which determine the onset of acyclicity. The corresponding loss of E2-dependent GFAP repression and E2-dependent neurotrophic activity add further to the inverse relationship of GFAP expression and astrocyte neurotrophic activity across aging in both sexes. These findings are relevant to impairments of spatial learning and of hippocampal long-term potentiation during the onset of IR in middle-aged rats, and to perimenopausal factors mediating the higher risk of women for Alzheimer disease. Frontiers Media S.A. 2015-09-29 /pmc/articles/PMC4586279/ /pubmed/26483679 http://dx.doi.org/10.3389/fnagi.2015.00179 Text en Copyright © 2015 Morgan and Finch. 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 and reproduction in other forums is permitted, provided the original author(s) or licensor 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
Morgan, Todd E.
Finch, Caleb E.
Astrocytic estrogen receptors and impaired neurotrophic responses in a rat model of perimenopause
title Astrocytic estrogen receptors and impaired neurotrophic responses in a rat model of perimenopause
title_full Astrocytic estrogen receptors and impaired neurotrophic responses in a rat model of perimenopause
title_fullStr Astrocytic estrogen receptors and impaired neurotrophic responses in a rat model of perimenopause
title_full_unstemmed Astrocytic estrogen receptors and impaired neurotrophic responses in a rat model of perimenopause
title_short Astrocytic estrogen receptors and impaired neurotrophic responses in a rat model of perimenopause
title_sort astrocytic estrogen receptors and impaired neurotrophic responses in a rat model of perimenopause
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4586279/
https://www.ncbi.nlm.nih.gov/pubmed/26483679
http://dx.doi.org/10.3389/fnagi.2015.00179
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