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A Baldwin interpretation of adult hippocampal neurogenesis: from functional relevance to physiopathology

Hippocampal adult neurogenesis has been associated to many cognitive, emotional, and behavioral functions and dysfunctions, and its status as a selected effect or an “appendix of the brain” has been debated. In this review, we propose to understand hippocampal neurogenesis as the process underlying...

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Autores principales: Abrous, Djoher Nora, Koehl, Muriel, Lemoine, Maël
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8960398/
https://www.ncbi.nlm.nih.gov/pubmed/34103674
http://dx.doi.org/10.1038/s41380-021-01172-4
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author Abrous, Djoher Nora
Koehl, Muriel
Lemoine, Maël
author_facet Abrous, Djoher Nora
Koehl, Muriel
Lemoine, Maël
author_sort Abrous, Djoher Nora
collection PubMed
description Hippocampal adult neurogenesis has been associated to many cognitive, emotional, and behavioral functions and dysfunctions, and its status as a selected effect or an “appendix of the brain” has been debated. In this review, we propose to understand hippocampal neurogenesis as the process underlying the “Baldwin effect”, a particular situation in evolution where fitness does not rely on the natural selection of genetic traits, but on “ontogenetic adaptation” to a changing environment. This supports the view that a strong distinction between developmental and adult hippocampal neurogenesis is made. We propose that their functions are the constitution and the lifelong adaptation, respectively, of a basic repertoire of cognitive and emotional behaviors. This lifelong adaptation occurs through new forms of binding, i.e., association or dissociation of more basic elements. This distinction further suggests that a difference is made between developmental vulnerability (or resilience), stemming from dysfunctional (or highly functional) developmental hippocampal neurogenesis, and adult vulnerability (or resilience), stemming from dysfunctional (or highly functional) adult hippocampal neurogenesis. According to this hypothesis, developmental and adult vulnerability are distinct risk factors for various mental disorders in adults. This framework suggests new avenues for research on hippocampal neurogenesis and its implication in mental disorders.
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spelling pubmed-89603982022-04-07 A Baldwin interpretation of adult hippocampal neurogenesis: from functional relevance to physiopathology Abrous, Djoher Nora Koehl, Muriel Lemoine, Maël Mol Psychiatry Expert Review Hippocampal adult neurogenesis has been associated to many cognitive, emotional, and behavioral functions and dysfunctions, and its status as a selected effect or an “appendix of the brain” has been debated. In this review, we propose to understand hippocampal neurogenesis as the process underlying the “Baldwin effect”, a particular situation in evolution where fitness does not rely on the natural selection of genetic traits, but on “ontogenetic adaptation” to a changing environment. This supports the view that a strong distinction between developmental and adult hippocampal neurogenesis is made. We propose that their functions are the constitution and the lifelong adaptation, respectively, of a basic repertoire of cognitive and emotional behaviors. This lifelong adaptation occurs through new forms of binding, i.e., association or dissociation of more basic elements. This distinction further suggests that a difference is made between developmental vulnerability (or resilience), stemming from dysfunctional (or highly functional) developmental hippocampal neurogenesis, and adult vulnerability (or resilience), stemming from dysfunctional (or highly functional) adult hippocampal neurogenesis. According to this hypothesis, developmental and adult vulnerability are distinct risk factors for various mental disorders in adults. This framework suggests new avenues for research on hippocampal neurogenesis and its implication in mental disorders. Nature Publishing Group UK 2021-06-08 2022 /pmc/articles/PMC8960398/ /pubmed/34103674 http://dx.doi.org/10.1038/s41380-021-01172-4 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Expert Review
Abrous, Djoher Nora
Koehl, Muriel
Lemoine, Maël
A Baldwin interpretation of adult hippocampal neurogenesis: from functional relevance to physiopathology
title A Baldwin interpretation of adult hippocampal neurogenesis: from functional relevance to physiopathology
title_full A Baldwin interpretation of adult hippocampal neurogenesis: from functional relevance to physiopathology
title_fullStr A Baldwin interpretation of adult hippocampal neurogenesis: from functional relevance to physiopathology
title_full_unstemmed A Baldwin interpretation of adult hippocampal neurogenesis: from functional relevance to physiopathology
title_short A Baldwin interpretation of adult hippocampal neurogenesis: from functional relevance to physiopathology
title_sort baldwin interpretation of adult hippocampal neurogenesis: from functional relevance to physiopathology
topic Expert Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8960398/
https://www.ncbi.nlm.nih.gov/pubmed/34103674
http://dx.doi.org/10.1038/s41380-021-01172-4
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