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Hippocampal Memory Recovery After Acute Stress: A Behavioral, Morphological and Molecular Study

Several studies have shown that a single exposure to stress may improve or impair learning and memory processes, depending on the timing in which the stress event occurs with relation to the acquisition phase. However, to date there is no information about the molecular changes that occur at the syn...

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Autores principales: Aguayo, Felipe Ignacio, Tejos-Bravo, Macarena, Díaz-Véliz, Gabriela, Pacheco, Aníbal, García-Rojo, Gonzalo, Corrales, Wladimir, Olave, Felipe Antonio, Aliaga, Esteban, Ulloa, José L., Avalos, Ana M., Román-Albasini, Luciano, Rojas, Paulina S., Fiedler, Jenny Lucy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6107681/
https://www.ncbi.nlm.nih.gov/pubmed/30174589
http://dx.doi.org/10.3389/fnmol.2018.00283
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author Aguayo, Felipe Ignacio
Tejos-Bravo, Macarena
Díaz-Véliz, Gabriela
Pacheco, Aníbal
García-Rojo, Gonzalo
Corrales, Wladimir
Olave, Felipe Antonio
Aliaga, Esteban
Ulloa, José L.
Avalos, Ana M.
Román-Albasini, Luciano
Rojas, Paulina S.
Fiedler, Jenny Lucy
author_facet Aguayo, Felipe Ignacio
Tejos-Bravo, Macarena
Díaz-Véliz, Gabriela
Pacheco, Aníbal
García-Rojo, Gonzalo
Corrales, Wladimir
Olave, Felipe Antonio
Aliaga, Esteban
Ulloa, José L.
Avalos, Ana M.
Román-Albasini, Luciano
Rojas, Paulina S.
Fiedler, Jenny Lucy
author_sort Aguayo, Felipe Ignacio
collection PubMed
description Several studies have shown that a single exposure to stress may improve or impair learning and memory processes, depending on the timing in which the stress event occurs with relation to the acquisition phase. However, to date there is no information about the molecular changes that occur at the synapse during the stress-induced memory modification and after a recovery period. In particular, there are no studies that have evaluated—at the same time—the temporality of stress and stress recovery period in hippocampal short-term memory and the effects on dendritic spine morphology, along with variations in N-methyl-D-aspartate (NMDA) and α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor subunits. The aim of our study was to take a multidimensional approach to investigate concomitant behavioral, morphological and molecular changes induced by a single restraint stress exposure (2.5 h) and a recovery period of 6 and 24 h in rats. We found that acute stress elicited a reduced preference to explore an object placed in a novel position (a hippocampal-dependent task). These changes were accompanied by increased activity of LIM kinase I (LIMK; an actin-remodeling protein) and increased levels of NR2A subunits of NMDA receptors. After 6 h of recovery from stress, rats showed similar preference to explore an object placed in a novel or familiar position, but density of immature spines increased in secondary CA1 apical dendrites, along with a transient rise in GluA2 AMPA receptor subunits. After 24 h of recovery from stress, the animals showed a preference to explore an object placed in a novel position, which was accompanied by a normalization of NMDA and AMPA receptor subunits to control values. Our data suggest that acute stress produces reversible molecular and behavioral changes 24 h after stress, allowing a full reestablishment of hippocampal-related memory. Further studies need to be conducted to deepen our understanding of these changes and their reciprocal interactions.Adaptive stress responses are a promising avenue to develop interventions aiming at restoring hippocampal function impaired by repetitive stress exposure.
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spelling pubmed-61076812018-08-31 Hippocampal Memory Recovery After Acute Stress: A Behavioral, Morphological and Molecular Study Aguayo, Felipe Ignacio Tejos-Bravo, Macarena Díaz-Véliz, Gabriela Pacheco, Aníbal García-Rojo, Gonzalo Corrales, Wladimir Olave, Felipe Antonio Aliaga, Esteban Ulloa, José L. Avalos, Ana M. Román-Albasini, Luciano Rojas, Paulina S. Fiedler, Jenny Lucy Front Mol Neurosci Neuroscience Several studies have shown that a single exposure to stress may improve or impair learning and memory processes, depending on the timing in which the stress event occurs with relation to the acquisition phase. However, to date there is no information about the molecular changes that occur at the synapse during the stress-induced memory modification and after a recovery period. In particular, there are no studies that have evaluated—at the same time—the temporality of stress and stress recovery period in hippocampal short-term memory and the effects on dendritic spine morphology, along with variations in N-methyl-D-aspartate (NMDA) and α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor subunits. The aim of our study was to take a multidimensional approach to investigate concomitant behavioral, morphological and molecular changes induced by a single restraint stress exposure (2.5 h) and a recovery period of 6 and 24 h in rats. We found that acute stress elicited a reduced preference to explore an object placed in a novel position (a hippocampal-dependent task). These changes were accompanied by increased activity of LIM kinase I (LIMK; an actin-remodeling protein) and increased levels of NR2A subunits of NMDA receptors. After 6 h of recovery from stress, rats showed similar preference to explore an object placed in a novel or familiar position, but density of immature spines increased in secondary CA1 apical dendrites, along with a transient rise in GluA2 AMPA receptor subunits. After 24 h of recovery from stress, the animals showed a preference to explore an object placed in a novel position, which was accompanied by a normalization of NMDA and AMPA receptor subunits to control values. Our data suggest that acute stress produces reversible molecular and behavioral changes 24 h after stress, allowing a full reestablishment of hippocampal-related memory. Further studies need to be conducted to deepen our understanding of these changes and their reciprocal interactions.Adaptive stress responses are a promising avenue to develop interventions aiming at restoring hippocampal function impaired by repetitive stress exposure. Frontiers Media S.A. 2018-08-17 /pmc/articles/PMC6107681/ /pubmed/30174589 http://dx.doi.org/10.3389/fnmol.2018.00283 Text en Copyright © 2018 Aguayo, Tejos-Bravo, Díaz-Véliz, Pacheco, García-Rojo, Corrales, Olave, Aliaga, Ulloa, Avalos, Román-Albasini, Rojas and Fiedler. 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
Aguayo, Felipe Ignacio
Tejos-Bravo, Macarena
Díaz-Véliz, Gabriela
Pacheco, Aníbal
García-Rojo, Gonzalo
Corrales, Wladimir
Olave, Felipe Antonio
Aliaga, Esteban
Ulloa, José L.
Avalos, Ana M.
Román-Albasini, Luciano
Rojas, Paulina S.
Fiedler, Jenny Lucy
Hippocampal Memory Recovery After Acute Stress: A Behavioral, Morphological and Molecular Study
title Hippocampal Memory Recovery After Acute Stress: A Behavioral, Morphological and Molecular Study
title_full Hippocampal Memory Recovery After Acute Stress: A Behavioral, Morphological and Molecular Study
title_fullStr Hippocampal Memory Recovery After Acute Stress: A Behavioral, Morphological and Molecular Study
title_full_unstemmed Hippocampal Memory Recovery After Acute Stress: A Behavioral, Morphological and Molecular Study
title_short Hippocampal Memory Recovery After Acute Stress: A Behavioral, Morphological and Molecular Study
title_sort hippocampal memory recovery after acute stress: a behavioral, morphological and molecular study
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6107681/
https://www.ncbi.nlm.nih.gov/pubmed/30174589
http://dx.doi.org/10.3389/fnmol.2018.00283
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