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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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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. |
format | Online Article Text |
id | pubmed-7031237 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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