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Sex-Specific Brain Transcriptional Signatures in Human MDD and Their Correlates in Mouse Models of Depression

Major depressive disorder (MDD) is amongst the most devastating psychiatric conditions affecting several millions of people worldwide every year. Despite the importance of this disease and its impact on modern societies, still very little is known about the etiological mechanisms. Treatment strategi...

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Autores principales: Touchant, Maureen, Labonté, Benoit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9110970/
https://www.ncbi.nlm.nih.gov/pubmed/35592639
http://dx.doi.org/10.3389/fnbeh.2022.845491
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author Touchant, Maureen
Labonté, Benoit
author_facet Touchant, Maureen
Labonté, Benoit
author_sort Touchant, Maureen
collection PubMed
description Major depressive disorder (MDD) is amongst the most devastating psychiatric conditions affecting several millions of people worldwide every year. Despite the importance of this disease and its impact on modern societies, still very little is known about the etiological mechanisms. Treatment strategies have stagnated over the last decades and very little progress has been made to improve the efficiency of current therapeutic approaches. In order to better understand the disease, it is necessary for researchers to use appropriate animal models that reproduce specific aspects of the complex clinical manifestations at the behavioral and molecular levels. Here, we review the current literature describing the use of mouse models to reproduce specific aspects of MDD and anxiety in males and females. We first describe some of the most commonly used mouse models and their capacity to display unique but also shared features relevant to MDD. We then transition toward an integral description, combined with genome-wide transcriptional strategies. The use of these models reveals crucial insights into the molecular programs underlying the expression of stress susceptibility and resilience in a sex-specific fashion. These studies performed on human and mouse tissues establish correlates into the mechanisms mediating the impact of stress and the extent to which different mouse models of chronic stress recapitulate the molecular changes observed in depressed humans. The focus of this review is specifically to highlight the sex differences revealed from different stress paradigms and transcriptional analyses both in human and animal models.
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spelling pubmed-91109702022-05-18 Sex-Specific Brain Transcriptional Signatures in Human MDD and Their Correlates in Mouse Models of Depression Touchant, Maureen Labonté, Benoit Front Behav Neurosci Behavioral Neuroscience Major depressive disorder (MDD) is amongst the most devastating psychiatric conditions affecting several millions of people worldwide every year. Despite the importance of this disease and its impact on modern societies, still very little is known about the etiological mechanisms. Treatment strategies have stagnated over the last decades and very little progress has been made to improve the efficiency of current therapeutic approaches. In order to better understand the disease, it is necessary for researchers to use appropriate animal models that reproduce specific aspects of the complex clinical manifestations at the behavioral and molecular levels. Here, we review the current literature describing the use of mouse models to reproduce specific aspects of MDD and anxiety in males and females. We first describe some of the most commonly used mouse models and their capacity to display unique but also shared features relevant to MDD. We then transition toward an integral description, combined with genome-wide transcriptional strategies. The use of these models reveals crucial insights into the molecular programs underlying the expression of stress susceptibility and resilience in a sex-specific fashion. These studies performed on human and mouse tissues establish correlates into the mechanisms mediating the impact of stress and the extent to which different mouse models of chronic stress recapitulate the molecular changes observed in depressed humans. The focus of this review is specifically to highlight the sex differences revealed from different stress paradigms and transcriptional analyses both in human and animal models. Frontiers Media S.A. 2022-05-03 /pmc/articles/PMC9110970/ /pubmed/35592639 http://dx.doi.org/10.3389/fnbeh.2022.845491 Text en Copyright © 2022 Touchant and Labonté. 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 Behavioral Neuroscience
Touchant, Maureen
Labonté, Benoit
Sex-Specific Brain Transcriptional Signatures in Human MDD and Their Correlates in Mouse Models of Depression
title Sex-Specific Brain Transcriptional Signatures in Human MDD and Their Correlates in Mouse Models of Depression
title_full Sex-Specific Brain Transcriptional Signatures in Human MDD and Their Correlates in Mouse Models of Depression
title_fullStr Sex-Specific Brain Transcriptional Signatures in Human MDD and Their Correlates in Mouse Models of Depression
title_full_unstemmed Sex-Specific Brain Transcriptional Signatures in Human MDD and Their Correlates in Mouse Models of Depression
title_short Sex-Specific Brain Transcriptional Signatures in Human MDD and Their Correlates in Mouse Models of Depression
title_sort sex-specific brain transcriptional signatures in human mdd and their correlates in mouse models of depression
topic Behavioral Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9110970/
https://www.ncbi.nlm.nih.gov/pubmed/35592639
http://dx.doi.org/10.3389/fnbeh.2022.845491
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