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Environmental enrichment ameliorates perinatal brain injury and promotes functional white matter recovery

Hypoxic damage to the developing brain due to preterm birth causes many anatomical changes, including damage to the periventricular white matter. This results in the loss of glial cells, significant disruptions in myelination, and thereby cognitive and behavioral disabilities seen throughout life. E...

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Autores principales: Forbes, Thomas A., Goldstein, Evan Z., Dupree, Jeffrey L., Jablonska, Beata, Scafidi, Joseph, Adams, Katrina L., Imamura, Yuka, Hashimoto-Torii, Kazue, Gallo, Vittorio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7031237/
https://www.ncbi.nlm.nih.gov/pubmed/32075970
http://dx.doi.org/10.1038/s41467-020-14762-7
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author Forbes, Thomas A.
Goldstein, Evan Z.
Dupree, Jeffrey L.
Jablonska, Beata
Scafidi, Joseph
Adams, Katrina L.
Imamura, Yuka
Hashimoto-Torii, Kazue
Gallo, Vittorio
author_facet Forbes, Thomas A.
Goldstein, Evan Z.
Dupree, Jeffrey L.
Jablonska, Beata
Scafidi, Joseph
Adams, Katrina L.
Imamura, Yuka
Hashimoto-Torii, Kazue
Gallo, Vittorio
author_sort Forbes, Thomas A.
collection PubMed
description Hypoxic damage to the developing brain due to preterm birth causes many anatomical changes, including damage to the periventricular white matter. This results in the loss of glial cells, significant disruptions in myelination, and thereby cognitive and behavioral disabilities seen throughout life. Encouragingly, these neurological morbidities can be improved by environmental factors; however, the underlying cellular mechanisms remain unknown. We found that early and continuous environmental enrichment selectively enhances endogenous repair of the developing white matter by promoting oligodendroglial maturation, myelination, and functional recovery after perinatal brain injury. These effects require increased exposure to socialization, physical activity, and cognitive enhancement of surroundings—a complete enriched environment. Using RNA-sequencing, we identified oligodendroglial-specific responses to hypoxic brain injury, and uncovered molecular mechanisms involved in enrichment-induced recovery. Together, these results indicate that myelin plasticity induced by modulation of the neonatal environment can be targeted as a therapeutic strategy for preterm birth.
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spelling pubmed-70312372020-03-04 Environmental enrichment ameliorates perinatal brain injury and promotes functional white matter recovery Forbes, Thomas A. Goldstein, Evan Z. Dupree, Jeffrey L. Jablonska, Beata Scafidi, Joseph Adams, Katrina L. Imamura, Yuka Hashimoto-Torii, Kazue Gallo, Vittorio Nat Commun Article Hypoxic damage to the developing brain due to preterm birth causes many anatomical changes, including damage to the periventricular white matter. This results in the loss of glial cells, significant disruptions in myelination, and thereby cognitive and behavioral disabilities seen throughout life. Encouragingly, these neurological morbidities can be improved by environmental factors; however, the underlying cellular mechanisms remain unknown. We found that early and continuous environmental enrichment selectively enhances endogenous repair of the developing white matter by promoting oligodendroglial maturation, myelination, and functional recovery after perinatal brain injury. These effects require increased exposure to socialization, physical activity, and cognitive enhancement of surroundings—a complete enriched environment. Using RNA-sequencing, we identified oligodendroglial-specific responses to hypoxic brain injury, and uncovered molecular mechanisms involved in enrichment-induced recovery. Together, these results indicate that myelin plasticity induced by modulation of the neonatal environment can be targeted as a therapeutic strategy for preterm birth. Nature Publishing Group UK 2020-02-19 /pmc/articles/PMC7031237/ /pubmed/32075970 http://dx.doi.org/10.1038/s41467-020-14762-7 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Forbes, Thomas A.
Goldstein, Evan Z.
Dupree, Jeffrey L.
Jablonska, Beata
Scafidi, Joseph
Adams, Katrina L.
Imamura, Yuka
Hashimoto-Torii, Kazue
Gallo, Vittorio
Environmental enrichment ameliorates perinatal brain injury and promotes functional white matter recovery
title Environmental enrichment ameliorates perinatal brain injury and promotes functional white matter recovery
title_full Environmental enrichment ameliorates perinatal brain injury and promotes functional white matter recovery
title_fullStr Environmental enrichment ameliorates perinatal brain injury and promotes functional white matter recovery
title_full_unstemmed Environmental enrichment ameliorates perinatal brain injury and promotes functional white matter recovery
title_short Environmental enrichment ameliorates perinatal brain injury and promotes functional white matter recovery
title_sort environmental enrichment ameliorates perinatal brain injury and promotes functional white matter recovery
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7031237/
https://www.ncbi.nlm.nih.gov/pubmed/32075970
http://dx.doi.org/10.1038/s41467-020-14762-7
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