Cargando…

Early Maternal and Social Deprivation Expands Neural Stem Cell Population Size and Reduces Hippocampus/Amygdala-Dependent Fear Memory

Early life stress can exert detrimental or beneficial effects on neural development and postnatal behavior depending on the timing, duration, strength, and ability to control the stressors. In this study, we utilized a maternal and social deprivation (MSD) model to investigate the effects of early l...

Descripción completa

Detalles Bibliográficos
Autores principales: Daun, Kenny Anak, Fuchigami, Takahiro, Koyama, Natsu, Maruta, Noriko, Ikenaka, Kazuhiro, Hitoshi, Seiji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7000530/
https://www.ncbi.nlm.nih.gov/pubmed/32063832
http://dx.doi.org/10.3389/fnins.2020.00022
_version_ 1783494062387494912
author Daun, Kenny Anak
Fuchigami, Takahiro
Koyama, Natsu
Maruta, Noriko
Ikenaka, Kazuhiro
Hitoshi, Seiji
author_facet Daun, Kenny Anak
Fuchigami, Takahiro
Koyama, Natsu
Maruta, Noriko
Ikenaka, Kazuhiro
Hitoshi, Seiji
author_sort Daun, Kenny Anak
collection PubMed
description Early life stress can exert detrimental or beneficial effects on neural development and postnatal behavior depending on the timing, duration, strength, and ability to control the stressors. In this study, we utilized a maternal and social deprivation (MSD) model to investigate the effects of early life stress on neural stem cells (NSCs) and neurogenesis in the adult brain. We found that MSD during the stress-hyporesponsive period (SHRP) (early-MSD), when corticosterone secretion is suppressed, increased the size of the NSC population, whereas the same stress beyond the SHRP abrogated these effects. Early-MSD enhanced neurogenesis not only in the dentate gyrus of the hippocampus, one of the classic neurogenic regions, but also in the amygdala. In addition, mice exposed to early-MSD exhibited a reduction in amygdala/hippocampus-dependent fear memory. These results suggest that animals exposed to early life stress during the SHRP have reinforced stress resilience to cope with perceived stressors to maintain a normal homeostatic state.
format Online
Article
Text
id pubmed-7000530
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-70005302020-02-14 Early Maternal and Social Deprivation Expands Neural Stem Cell Population Size and Reduces Hippocampus/Amygdala-Dependent Fear Memory Daun, Kenny Anak Fuchigami, Takahiro Koyama, Natsu Maruta, Noriko Ikenaka, Kazuhiro Hitoshi, Seiji Front Neurosci Neuroscience Early life stress can exert detrimental or beneficial effects on neural development and postnatal behavior depending on the timing, duration, strength, and ability to control the stressors. In this study, we utilized a maternal and social deprivation (MSD) model to investigate the effects of early life stress on neural stem cells (NSCs) and neurogenesis in the adult brain. We found that MSD during the stress-hyporesponsive period (SHRP) (early-MSD), when corticosterone secretion is suppressed, increased the size of the NSC population, whereas the same stress beyond the SHRP abrogated these effects. Early-MSD enhanced neurogenesis not only in the dentate gyrus of the hippocampus, one of the classic neurogenic regions, but also in the amygdala. In addition, mice exposed to early-MSD exhibited a reduction in amygdala/hippocampus-dependent fear memory. These results suggest that animals exposed to early life stress during the SHRP have reinforced stress resilience to cope with perceived stressors to maintain a normal homeostatic state. Frontiers Media S.A. 2020-01-29 /pmc/articles/PMC7000530/ /pubmed/32063832 http://dx.doi.org/10.3389/fnins.2020.00022 Text en Copyright © 2020 Daun, Fuchigami, Koyama, Maruta, Ikenaka and Hitoshi. http://creativecommons.org/licenses/by/4.0/ 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) and the copyright owner(s) 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
Daun, Kenny Anak
Fuchigami, Takahiro
Koyama, Natsu
Maruta, Noriko
Ikenaka, Kazuhiro
Hitoshi, Seiji
Early Maternal and Social Deprivation Expands Neural Stem Cell Population Size and Reduces Hippocampus/Amygdala-Dependent Fear Memory
title Early Maternal and Social Deprivation Expands Neural Stem Cell Population Size and Reduces Hippocampus/Amygdala-Dependent Fear Memory
title_full Early Maternal and Social Deprivation Expands Neural Stem Cell Population Size and Reduces Hippocampus/Amygdala-Dependent Fear Memory
title_fullStr Early Maternal and Social Deprivation Expands Neural Stem Cell Population Size and Reduces Hippocampus/Amygdala-Dependent Fear Memory
title_full_unstemmed Early Maternal and Social Deprivation Expands Neural Stem Cell Population Size and Reduces Hippocampus/Amygdala-Dependent Fear Memory
title_short Early Maternal and Social Deprivation Expands Neural Stem Cell Population Size and Reduces Hippocampus/Amygdala-Dependent Fear Memory
title_sort early maternal and social deprivation expands neural stem cell population size and reduces hippocampus/amygdala-dependent fear memory
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7000530/
https://www.ncbi.nlm.nih.gov/pubmed/32063832
http://dx.doi.org/10.3389/fnins.2020.00022
work_keys_str_mv AT daunkennyanak earlymaternalandsocialdeprivationexpandsneuralstemcellpopulationsizeandreduceshippocampusamygdaladependentfearmemory
AT fuchigamitakahiro earlymaternalandsocialdeprivationexpandsneuralstemcellpopulationsizeandreduceshippocampusamygdaladependentfearmemory
AT koyamanatsu earlymaternalandsocialdeprivationexpandsneuralstemcellpopulationsizeandreduceshippocampusamygdaladependentfearmemory
AT marutanoriko earlymaternalandsocialdeprivationexpandsneuralstemcellpopulationsizeandreduceshippocampusamygdaladependentfearmemory
AT ikenakakazuhiro earlymaternalandsocialdeprivationexpandsneuralstemcellpopulationsizeandreduceshippocampusamygdaladependentfearmemory
AT hitoshiseiji earlymaternalandsocialdeprivationexpandsneuralstemcellpopulationsizeandreduceshippocampusamygdaladependentfearmemory