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Critical Period Regulation by Thyroid Hormones: Potential Mechanisms and Sex-Specific Aspects
Adequate perinatal levels of thyroid hormones (THs) are required for normal brain function and development. Studies in non-mammalian species suggest that TH might be involved in the regulation of critical periods (CPs) of heightened plasticity. Yet, it is largely unknown what mechanisms controlling...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6461013/ https://www.ncbi.nlm.nih.gov/pubmed/31024251 http://dx.doi.org/10.3389/fnmol.2019.00077 |
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author | Batista, Gervasio Hensch, Takao K. |
author_facet | Batista, Gervasio Hensch, Takao K. |
author_sort | Batista, Gervasio |
collection | PubMed |
description | Adequate perinatal levels of thyroid hormones (THs) are required for normal brain function and development. Studies in non-mammalian species suggest that TH might be involved in the regulation of critical periods (CPs) of heightened plasticity. Yet, it is largely unknown what mechanisms controlling such CPs might be under TH regulation. Here, we briefly review the influence of TH in early life across evolution. We discuss possible links between TH and known circuit and/or molecular mechanisms determining the timing of CPs of heightened brain plasticity. We focus on the role of parvalbumin-positive (PV) interneurons since their maturation defines CP onset and closure. Specifically, abnormal PV circuits are associated with low perinatal levels of TH, possibly because thyroid hypofunction may increase oxidative stress and/or dysregulate Otx2-mediated maturation of neuroprotective perineuronal nets. In addition, the level of cholinergic transmission is important for CP plasticity. Potentially, TH levels could affect gain changes in cholinergic transmission that can alter brain development. We believe that understanding how TH impacts CPs of circuit refinement will shed light onto the principles underlying normal developmental trajectories. Given that the thyroid gland expresses estrogen and androgen receptors, its activity can potentially be regulated differently between the sexes, contributing to sexually dimorphic behaviors. |
format | Online Article Text |
id | pubmed-6461013 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-64610132019-04-25 Critical Period Regulation by Thyroid Hormones: Potential Mechanisms and Sex-Specific Aspects Batista, Gervasio Hensch, Takao K. Front Mol Neurosci Neuroscience Adequate perinatal levels of thyroid hormones (THs) are required for normal brain function and development. Studies in non-mammalian species suggest that TH might be involved in the regulation of critical periods (CPs) of heightened plasticity. Yet, it is largely unknown what mechanisms controlling such CPs might be under TH regulation. Here, we briefly review the influence of TH in early life across evolution. We discuss possible links between TH and known circuit and/or molecular mechanisms determining the timing of CPs of heightened brain plasticity. We focus on the role of parvalbumin-positive (PV) interneurons since their maturation defines CP onset and closure. Specifically, abnormal PV circuits are associated with low perinatal levels of TH, possibly because thyroid hypofunction may increase oxidative stress and/or dysregulate Otx2-mediated maturation of neuroprotective perineuronal nets. In addition, the level of cholinergic transmission is important for CP plasticity. Potentially, TH levels could affect gain changes in cholinergic transmission that can alter brain development. We believe that understanding how TH impacts CPs of circuit refinement will shed light onto the principles underlying normal developmental trajectories. Given that the thyroid gland expresses estrogen and androgen receptors, its activity can potentially be regulated differently between the sexes, contributing to sexually dimorphic behaviors. Frontiers Media S.A. 2019-04-05 /pmc/articles/PMC6461013/ /pubmed/31024251 http://dx.doi.org/10.3389/fnmol.2019.00077 Text en Copyright © 2019 Batista and Hensch. 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 or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) 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 Batista, Gervasio Hensch, Takao K. Critical Period Regulation by Thyroid Hormones: Potential Mechanisms and Sex-Specific Aspects |
title | Critical Period Regulation by Thyroid Hormones: Potential Mechanisms and Sex-Specific Aspects |
title_full | Critical Period Regulation by Thyroid Hormones: Potential Mechanisms and Sex-Specific Aspects |
title_fullStr | Critical Period Regulation by Thyroid Hormones: Potential Mechanisms and Sex-Specific Aspects |
title_full_unstemmed | Critical Period Regulation by Thyroid Hormones: Potential Mechanisms and Sex-Specific Aspects |
title_short | Critical Period Regulation by Thyroid Hormones: Potential Mechanisms and Sex-Specific Aspects |
title_sort | critical period regulation by thyroid hormones: potential mechanisms and sex-specific aspects |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6461013/ https://www.ncbi.nlm.nih.gov/pubmed/31024251 http://dx.doi.org/10.3389/fnmol.2019.00077 |
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