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Adolescent but not adult-born neurons are critical for susceptibility to chronic social defeat
Recent evidence implicates adult hippocampal neurogenesis in regulating behavioral and physiologic responses to stress. Hippocampal neurogenesis occurs across the lifespan, however the rate of cell birth is up to 300% higher in adolescent mice compared to adults. Adolescence is a sensitive period in...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4147831/ https://www.ncbi.nlm.nih.gov/pubmed/25221485 http://dx.doi.org/10.3389/fnbeh.2014.00289 |
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author | Kirshenbaum, Greer S. Lieberman, Sophie R. Briner, Tamara J. Leonardo, E. David Dranovsky, Alex |
author_facet | Kirshenbaum, Greer S. Lieberman, Sophie R. Briner, Tamara J. Leonardo, E. David Dranovsky, Alex |
author_sort | Kirshenbaum, Greer S. |
collection | PubMed |
description | Recent evidence implicates adult hippocampal neurogenesis in regulating behavioral and physiologic responses to stress. Hippocampal neurogenesis occurs across the lifespan, however the rate of cell birth is up to 300% higher in adolescent mice compared to adults. Adolescence is a sensitive period in development where emotional circuitry and stress reactivity undergo plasticity establishing life-long set points. Therefore neurogenesis occurring during adolescence may be particularly important for emotional behavior. However, little is known about the function of hippocampal neurons born during adolescence. In order to assess the contribution of neurons born in adolescence to the adult stress response and depression-related behavior, we transiently reduced cell proliferation either during adolescence, or during adulthood in GFAP-Tk mice. We found that the intervention in adolescence did not change adult baseline behavioral response in the forced swim test, sucrose preference test or social affiliation test, and did not change adult corticosterone responses to an acute stressor. However following chronic social defeat, adult mice with reduced adolescent neurogenesis showed a resilient phenotype. A similar transient reduction in adult neurogenesis did not affect depression-like behaviors or stress induced corticosterone. Our study demonstrates that hippocampal neurons born during adolescence, but not in adulthood are important to confer susceptibility to chronic social defeat. |
format | Online Article Text |
id | pubmed-4147831 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-41478312014-09-12 Adolescent but not adult-born neurons are critical for susceptibility to chronic social defeat Kirshenbaum, Greer S. Lieberman, Sophie R. Briner, Tamara J. Leonardo, E. David Dranovsky, Alex Front Behav Neurosci Neuroscience Recent evidence implicates adult hippocampal neurogenesis in regulating behavioral and physiologic responses to stress. Hippocampal neurogenesis occurs across the lifespan, however the rate of cell birth is up to 300% higher in adolescent mice compared to adults. Adolescence is a sensitive period in development where emotional circuitry and stress reactivity undergo plasticity establishing life-long set points. Therefore neurogenesis occurring during adolescence may be particularly important for emotional behavior. However, little is known about the function of hippocampal neurons born during adolescence. In order to assess the contribution of neurons born in adolescence to the adult stress response and depression-related behavior, we transiently reduced cell proliferation either during adolescence, or during adulthood in GFAP-Tk mice. We found that the intervention in adolescence did not change adult baseline behavioral response in the forced swim test, sucrose preference test or social affiliation test, and did not change adult corticosterone responses to an acute stressor. However following chronic social defeat, adult mice with reduced adolescent neurogenesis showed a resilient phenotype. A similar transient reduction in adult neurogenesis did not affect depression-like behaviors or stress induced corticosterone. Our study demonstrates that hippocampal neurons born during adolescence, but not in adulthood are important to confer susceptibility to chronic social defeat. Frontiers Media S.A. 2014-08-28 /pmc/articles/PMC4147831/ /pubmed/25221485 http://dx.doi.org/10.3389/fnbeh.2014.00289 Text en Copyright © 2014 Kirshenbaum, Lieberman, Briner, Leonardo and Dranovsky. http://creativecommons.org/licenses/by/3.0/ 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) or licensor 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 Kirshenbaum, Greer S. Lieberman, Sophie R. Briner, Tamara J. Leonardo, E. David Dranovsky, Alex Adolescent but not adult-born neurons are critical for susceptibility to chronic social defeat |
title | Adolescent but not adult-born neurons are critical for susceptibility to chronic social defeat |
title_full | Adolescent but not adult-born neurons are critical for susceptibility to chronic social defeat |
title_fullStr | Adolescent but not adult-born neurons are critical for susceptibility to chronic social defeat |
title_full_unstemmed | Adolescent but not adult-born neurons are critical for susceptibility to chronic social defeat |
title_short | Adolescent but not adult-born neurons are critical for susceptibility to chronic social defeat |
title_sort | adolescent but not adult-born neurons are critical for susceptibility to chronic social defeat |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4147831/ https://www.ncbi.nlm.nih.gov/pubmed/25221485 http://dx.doi.org/10.3389/fnbeh.2014.00289 |
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