Cargando…

Determination of steady-state transcriptome modifications associated with repeated homotypic stress in the rat rostral posterior hypothalamic region

Chronic stress is epidemiologically correlated with physical and psychiatric disorders. Whereas many animal models of chronic stress induce symptoms of psychopathology, repeated homotypic stressors to moderate intensity stimuli typically reduce stress-related responses with fewer, if any, pathologic...

Descripción completa

Detalles Bibliográficos
Autores principales: Campeau, Serge, McNulty, Connor, Stanley, Jacob T., Gerber, Anthony N., Sasse, Sarah K., Dowell, Robin D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10288150/
https://www.ncbi.nlm.nih.gov/pubmed/37360161
http://dx.doi.org/10.3389/fnins.2023.1173699
_version_ 1785062019295084544
author Campeau, Serge
McNulty, Connor
Stanley, Jacob T.
Gerber, Anthony N.
Sasse, Sarah K.
Dowell, Robin D.
author_facet Campeau, Serge
McNulty, Connor
Stanley, Jacob T.
Gerber, Anthony N.
Sasse, Sarah K.
Dowell, Robin D.
author_sort Campeau, Serge
collection PubMed
description Chronic stress is epidemiologically correlated with physical and psychiatric disorders. Whereas many animal models of chronic stress induce symptoms of psychopathology, repeated homotypic stressors to moderate intensity stimuli typically reduce stress-related responses with fewer, if any, pathological symptoms. Recent results indicate that the rostral posterior hypothalamic (rPH) region is a significant component of the brain circuitry underlying response reductions (habituation) associated with repeated homotypic stress. To test whether posterior hypothalamic transcriptional regulation associates with the neuroendocrine modifications induced by repeated homotypic stress, RNA-seq was performed in the rPH dissected from adult male rats that experienced either no stress, 1, 3, or 7 stressful loud noise exposures. Plasma samples displayed reliable increases of corticosterone in all stressed groups, with the smallest increase in the group exposed to 7 loud noises, indicating significant habituation compared to the other stressed groups. While few or no differentially expressed genes were detected 24-h after one or three loud noise exposures, relatively large numbers of transcripts were differentially expressed between the group exposed to 7 loud noises when compared to the control or 3-stress groups, respectively, which correlated with the corticosterone response habituation observed. Gene ontology analyses indicated multiple significant functional terms related to neuron differentiation, neural membrane potential, pre- and post-synaptic elements, chemical synaptic transmission, vesicles, axon guidance and projection, glutamatergic and GABAergic neurotransmission. Some of the differentially expressed genes (Myt1l, Zmat4, Dlx6, Csrnp3) encode transcription factors that were independently predicted by transcription factor enrichment analysis to target other differentially regulated genes in this study. A similar experiment employing in situ hybridization histochemical analysis in additional animals validated the direction of change of the 5 transcripts investigated (Camk4, Gabrb2, Gad1, Grin2a and Slc32a) with a high level of temporal and regional specificity for the rPH. In aggregate, the results suggest that distinct patterns of gene regulation are obtained in response to a repeated homotypic stress regimen; they also point to a significant reorganization of the rPH region that may critically contribute to the phenotypic modifications associated with repeated homotypic stress habituation.
format Online
Article
Text
id pubmed-10288150
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-102881502023-06-24 Determination of steady-state transcriptome modifications associated with repeated homotypic stress in the rat rostral posterior hypothalamic region Campeau, Serge McNulty, Connor Stanley, Jacob T. Gerber, Anthony N. Sasse, Sarah K. Dowell, Robin D. Front Neurosci Neuroscience Chronic stress is epidemiologically correlated with physical and psychiatric disorders. Whereas many animal models of chronic stress induce symptoms of psychopathology, repeated homotypic stressors to moderate intensity stimuli typically reduce stress-related responses with fewer, if any, pathological symptoms. Recent results indicate that the rostral posterior hypothalamic (rPH) region is a significant component of the brain circuitry underlying response reductions (habituation) associated with repeated homotypic stress. To test whether posterior hypothalamic transcriptional regulation associates with the neuroendocrine modifications induced by repeated homotypic stress, RNA-seq was performed in the rPH dissected from adult male rats that experienced either no stress, 1, 3, or 7 stressful loud noise exposures. Plasma samples displayed reliable increases of corticosterone in all stressed groups, with the smallest increase in the group exposed to 7 loud noises, indicating significant habituation compared to the other stressed groups. While few or no differentially expressed genes were detected 24-h after one or three loud noise exposures, relatively large numbers of transcripts were differentially expressed between the group exposed to 7 loud noises when compared to the control or 3-stress groups, respectively, which correlated with the corticosterone response habituation observed. Gene ontology analyses indicated multiple significant functional terms related to neuron differentiation, neural membrane potential, pre- and post-synaptic elements, chemical synaptic transmission, vesicles, axon guidance and projection, glutamatergic and GABAergic neurotransmission. Some of the differentially expressed genes (Myt1l, Zmat4, Dlx6, Csrnp3) encode transcription factors that were independently predicted by transcription factor enrichment analysis to target other differentially regulated genes in this study. A similar experiment employing in situ hybridization histochemical analysis in additional animals validated the direction of change of the 5 transcripts investigated (Camk4, Gabrb2, Gad1, Grin2a and Slc32a) with a high level of temporal and regional specificity for the rPH. In aggregate, the results suggest that distinct patterns of gene regulation are obtained in response to a repeated homotypic stress regimen; they also point to a significant reorganization of the rPH region that may critically contribute to the phenotypic modifications associated with repeated homotypic stress habituation. Frontiers Media S.A. 2023-06-09 /pmc/articles/PMC10288150/ /pubmed/37360161 http://dx.doi.org/10.3389/fnins.2023.1173699 Text en Copyright © 2023 Campeau, McNulty, Stanley, Gerber, Sasse and Dowell. https://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
Campeau, Serge
McNulty, Connor
Stanley, Jacob T.
Gerber, Anthony N.
Sasse, Sarah K.
Dowell, Robin D.
Determination of steady-state transcriptome modifications associated with repeated homotypic stress in the rat rostral posterior hypothalamic region
title Determination of steady-state transcriptome modifications associated with repeated homotypic stress in the rat rostral posterior hypothalamic region
title_full Determination of steady-state transcriptome modifications associated with repeated homotypic stress in the rat rostral posterior hypothalamic region
title_fullStr Determination of steady-state transcriptome modifications associated with repeated homotypic stress in the rat rostral posterior hypothalamic region
title_full_unstemmed Determination of steady-state transcriptome modifications associated with repeated homotypic stress in the rat rostral posterior hypothalamic region
title_short Determination of steady-state transcriptome modifications associated with repeated homotypic stress in the rat rostral posterior hypothalamic region
title_sort determination of steady-state transcriptome modifications associated with repeated homotypic stress in the rat rostral posterior hypothalamic region
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10288150/
https://www.ncbi.nlm.nih.gov/pubmed/37360161
http://dx.doi.org/10.3389/fnins.2023.1173699
work_keys_str_mv AT campeauserge determinationofsteadystatetranscriptomemodificationsassociatedwithrepeatedhomotypicstressintheratrostralposteriorhypothalamicregion
AT mcnultyconnor determinationofsteadystatetranscriptomemodificationsassociatedwithrepeatedhomotypicstressintheratrostralposteriorhypothalamicregion
AT stanleyjacobt determinationofsteadystatetranscriptomemodificationsassociatedwithrepeatedhomotypicstressintheratrostralposteriorhypothalamicregion
AT gerberanthonyn determinationofsteadystatetranscriptomemodificationsassociatedwithrepeatedhomotypicstressintheratrostralposteriorhypothalamicregion
AT sassesarahk determinationofsteadystatetranscriptomemodificationsassociatedwithrepeatedhomotypicstressintheratrostralposteriorhypothalamicregion
AT dowellrobind determinationofsteadystatetranscriptomemodificationsassociatedwithrepeatedhomotypicstressintheratrostralposteriorhypothalamicregion