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MicroRNAs in Basolateral Amygdala Associated with Stress and Fear Memories Regulate Rapid Eye Movement Sleep in Rats

Stress-related sleep disturbances are distressing clinical symptoms in posttraumatic stress disorder patients. Intensely stressful events and their memories change rapid eye movement (REM) sleep in animal models. REM sleep varies with individual differences of stress resilience or vulnerability. The...

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Autores principales: Balakathiresan, Nagaraja S., Bhomia, Manish, Zhai, Min, Sweeten, Brook L. W., Wellman, Laurie L., Sanford, Larry D., Knollmann-Ritschel, Barbara
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8069888/
https://www.ncbi.nlm.nih.gov/pubmed/33921465
http://dx.doi.org/10.3390/brainsci11040489
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author Balakathiresan, Nagaraja S.
Bhomia, Manish
Zhai, Min
Sweeten, Brook L. W.
Wellman, Laurie L.
Sanford, Larry D.
Knollmann-Ritschel, Barbara
author_facet Balakathiresan, Nagaraja S.
Bhomia, Manish
Zhai, Min
Sweeten, Brook L. W.
Wellman, Laurie L.
Sanford, Larry D.
Knollmann-Ritschel, Barbara
author_sort Balakathiresan, Nagaraja S.
collection PubMed
description Stress-related sleep disturbances are distressing clinical symptoms in posttraumatic stress disorder patients. Intensely stressful events and their memories change rapid eye movement (REM) sleep in animal models. REM sleep varies with individual differences of stress resilience or vulnerability. The basolateral amygdala (BLA) is a primary mediator of the effects of stress and fear memories on sleep. However, the molecular mechanisms in BLA regulating the effects of fear conditioning, shock training (ST) and context re-exposure (CTX) on REM sleep are not well known. MicroRNAs (miRNAs) are small, non-coding RNAs and posttranscriptional gene regulators of diverse biological processes. The aim of this study is to investigate ST- and CTX-altered miRNAs in the BLA of resilience and vulnerable animals and on REM sleep regulation. MiRNAs expression profiles in BLA were generated following ST and CTX using the Taqman Low Density rodent microRNA array. The altered BLA miRNAs expression and REM sleep reduction observed in ST and CTX vulnerable animals. AntagomiR-221 microinjection into BLA for one of the upregulated miRNAs, miR-221 in BLA, attenuated the REM sleep reduction. This study suggests that miRNAs in the BLA may play a significant role in mediating the effects of stress and fear memories on REM sleep.
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spelling pubmed-80698882021-04-26 MicroRNAs in Basolateral Amygdala Associated with Stress and Fear Memories Regulate Rapid Eye Movement Sleep in Rats Balakathiresan, Nagaraja S. Bhomia, Manish Zhai, Min Sweeten, Brook L. W. Wellman, Laurie L. Sanford, Larry D. Knollmann-Ritschel, Barbara Brain Sci Article Stress-related sleep disturbances are distressing clinical symptoms in posttraumatic stress disorder patients. Intensely stressful events and their memories change rapid eye movement (REM) sleep in animal models. REM sleep varies with individual differences of stress resilience or vulnerability. The basolateral amygdala (BLA) is a primary mediator of the effects of stress and fear memories on sleep. However, the molecular mechanisms in BLA regulating the effects of fear conditioning, shock training (ST) and context re-exposure (CTX) on REM sleep are not well known. MicroRNAs (miRNAs) are small, non-coding RNAs and posttranscriptional gene regulators of diverse biological processes. The aim of this study is to investigate ST- and CTX-altered miRNAs in the BLA of resilience and vulnerable animals and on REM sleep regulation. MiRNAs expression profiles in BLA were generated following ST and CTX using the Taqman Low Density rodent microRNA array. The altered BLA miRNAs expression and REM sleep reduction observed in ST and CTX vulnerable animals. AntagomiR-221 microinjection into BLA for one of the upregulated miRNAs, miR-221 in BLA, attenuated the REM sleep reduction. This study suggests that miRNAs in the BLA may play a significant role in mediating the effects of stress and fear memories on REM sleep. MDPI 2021-04-12 /pmc/articles/PMC8069888/ /pubmed/33921465 http://dx.doi.org/10.3390/brainsci11040489 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Balakathiresan, Nagaraja S.
Bhomia, Manish
Zhai, Min
Sweeten, Brook L. W.
Wellman, Laurie L.
Sanford, Larry D.
Knollmann-Ritschel, Barbara
MicroRNAs in Basolateral Amygdala Associated with Stress and Fear Memories Regulate Rapid Eye Movement Sleep in Rats
title MicroRNAs in Basolateral Amygdala Associated with Stress and Fear Memories Regulate Rapid Eye Movement Sleep in Rats
title_full MicroRNAs in Basolateral Amygdala Associated with Stress and Fear Memories Regulate Rapid Eye Movement Sleep in Rats
title_fullStr MicroRNAs in Basolateral Amygdala Associated with Stress and Fear Memories Regulate Rapid Eye Movement Sleep in Rats
title_full_unstemmed MicroRNAs in Basolateral Amygdala Associated with Stress and Fear Memories Regulate Rapid Eye Movement Sleep in Rats
title_short MicroRNAs in Basolateral Amygdala Associated with Stress and Fear Memories Regulate Rapid Eye Movement Sleep in Rats
title_sort micrornas in basolateral amygdala associated with stress and fear memories regulate rapid eye movement sleep in rats
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8069888/
https://www.ncbi.nlm.nih.gov/pubmed/33921465
http://dx.doi.org/10.3390/brainsci11040489
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