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Alcohol and the Developing Brain: Why Neurons Die and How Survivors Change
The consequences of alcohol drinking during pregnancy are dramatic and usually referred to as fetal alcohol spectrum disorders (FASD). This condition is one of the main causes of intellectual disability in Western countries. The immature fetal brain exposed to ethanol undergoes massive neuron death....
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6213645/ https://www.ncbi.nlm.nih.gov/pubmed/30274375 http://dx.doi.org/10.3390/ijms19102992 |
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author | Granato, Alberto Dering, Benjamin |
author_facet | Granato, Alberto Dering, Benjamin |
author_sort | Granato, Alberto |
collection | PubMed |
description | The consequences of alcohol drinking during pregnancy are dramatic and usually referred to as fetal alcohol spectrum disorders (FASD). This condition is one of the main causes of intellectual disability in Western countries. The immature fetal brain exposed to ethanol undergoes massive neuron death. However, the same mechanisms leading to cell death can also be responsible for changes of developmental plasticity. As a consequence of such a maladaptive plasticity, the functional damage to central nervous system structures is amplified and leads to permanent sequelae. Here we review the literature dealing with experimental FASD, focusing on the alterations of the cerebral cortex. We propose that the reciprocal interaction between cell death and maladaptive plasticity represents the main pathogenetic mechanism of the alcohol-induced damage to the developing brain. |
format | Online Article Text |
id | pubmed-6213645 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62136452018-11-14 Alcohol and the Developing Brain: Why Neurons Die and How Survivors Change Granato, Alberto Dering, Benjamin Int J Mol Sci Review The consequences of alcohol drinking during pregnancy are dramatic and usually referred to as fetal alcohol spectrum disorders (FASD). This condition is one of the main causes of intellectual disability in Western countries. The immature fetal brain exposed to ethanol undergoes massive neuron death. However, the same mechanisms leading to cell death can also be responsible for changes of developmental plasticity. As a consequence of such a maladaptive plasticity, the functional damage to central nervous system structures is amplified and leads to permanent sequelae. Here we review the literature dealing with experimental FASD, focusing on the alterations of the cerebral cortex. We propose that the reciprocal interaction between cell death and maladaptive plasticity represents the main pathogenetic mechanism of the alcohol-induced damage to the developing brain. MDPI 2018-09-30 /pmc/articles/PMC6213645/ /pubmed/30274375 http://dx.doi.org/10.3390/ijms19102992 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Granato, Alberto Dering, Benjamin Alcohol and the Developing Brain: Why Neurons Die and How Survivors Change |
title | Alcohol and the Developing Brain: Why Neurons Die and How Survivors Change |
title_full | Alcohol and the Developing Brain: Why Neurons Die and How Survivors Change |
title_fullStr | Alcohol and the Developing Brain: Why Neurons Die and How Survivors Change |
title_full_unstemmed | Alcohol and the Developing Brain: Why Neurons Die and How Survivors Change |
title_short | Alcohol and the Developing Brain: Why Neurons Die and How Survivors Change |
title_sort | alcohol and the developing brain: why neurons die and how survivors change |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6213645/ https://www.ncbi.nlm.nih.gov/pubmed/30274375 http://dx.doi.org/10.3390/ijms19102992 |
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