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Molecular links between endocrine, nervous and immune system during chronic stress

INTRODUCTION: The stress response is different in various individuals, however, the mechanisms that could explain these distinct effects are not well known and the molecular correlates have been considered one at the time. Particular harmful conditions occur if the subject, instead to cope the stres...

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Autores principales: Zefferino, Roberto, Di Gioia, Sante, Conese, Massimo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7882157/
https://www.ncbi.nlm.nih.gov/pubmed/33295155
http://dx.doi.org/10.1002/brb3.1960
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author Zefferino, Roberto
Di Gioia, Sante
Conese, Massimo
author_facet Zefferino, Roberto
Di Gioia, Sante
Conese, Massimo
author_sort Zefferino, Roberto
collection PubMed
description INTRODUCTION: The stress response is different in various individuals, however, the mechanisms that could explain these distinct effects are not well known and the molecular correlates have been considered one at the time. Particular harmful conditions occur if the subject, instead to cope the stressful events, succumb to them, in this case, a cascade reaction happens that through different signaling causes a specific reaction named “sickness behaviour.” The aim of this article is to review the complex relations among important molecules belonging to Central nervous system (CNS), immune system (IS), and endocrine system (ES) during the chronic stress response. METHODS: After having verified the state of art concerning the function of cortisol, norepinephrine (NE), interleukin (IL)‐1β and melatonin, we describe as they work together. RESULTS: We propose a speculative hypothesis concerning the complex interplay of these signaling molecules during chronic stress, highlighting the role of IL‐1β as main biomarker of this effects, indeed, during chronic stress its increment transforms this inflammatory signal into a nervous signal (NE), in turn, this uses the ES (melatonin and cortisol) to counterbalance again IL‐1β. During cortisol resistance, a vicious loop occurs that increments all mediators, unbalancing IS, ES, and CNS networks. This IL‐1β increase would occur above all when the individual succumbs to stressful events, showing the Sickness Behaviour Symptoms. IL‐1β might, through melatonin and vice versa, determine sleep disorders too. CONCLUSION: The molecular links here outlined could explain how stress plays a role in etiopathogenesis of several diseases through this complex interplay.
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spelling pubmed-78821572021-02-19 Molecular links between endocrine, nervous and immune system during chronic stress Zefferino, Roberto Di Gioia, Sante Conese, Massimo Brain Behav Review INTRODUCTION: The stress response is different in various individuals, however, the mechanisms that could explain these distinct effects are not well known and the molecular correlates have been considered one at the time. Particular harmful conditions occur if the subject, instead to cope the stressful events, succumb to them, in this case, a cascade reaction happens that through different signaling causes a specific reaction named “sickness behaviour.” The aim of this article is to review the complex relations among important molecules belonging to Central nervous system (CNS), immune system (IS), and endocrine system (ES) during the chronic stress response. METHODS: After having verified the state of art concerning the function of cortisol, norepinephrine (NE), interleukin (IL)‐1β and melatonin, we describe as they work together. RESULTS: We propose a speculative hypothesis concerning the complex interplay of these signaling molecules during chronic stress, highlighting the role of IL‐1β as main biomarker of this effects, indeed, during chronic stress its increment transforms this inflammatory signal into a nervous signal (NE), in turn, this uses the ES (melatonin and cortisol) to counterbalance again IL‐1β. During cortisol resistance, a vicious loop occurs that increments all mediators, unbalancing IS, ES, and CNS networks. This IL‐1β increase would occur above all when the individual succumbs to stressful events, showing the Sickness Behaviour Symptoms. IL‐1β might, through melatonin and vice versa, determine sleep disorders too. CONCLUSION: The molecular links here outlined could explain how stress plays a role in etiopathogenesis of several diseases through this complex interplay. John Wiley and Sons Inc. 2020-12-08 /pmc/articles/PMC7882157/ /pubmed/33295155 http://dx.doi.org/10.1002/brb3.1960 Text en © 2020 The Authors. Brain and Behavior published by Wiley Periodicals LLC This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Zefferino, Roberto
Di Gioia, Sante
Conese, Massimo
Molecular links between endocrine, nervous and immune system during chronic stress
title Molecular links between endocrine, nervous and immune system during chronic stress
title_full Molecular links between endocrine, nervous and immune system during chronic stress
title_fullStr Molecular links between endocrine, nervous and immune system during chronic stress
title_full_unstemmed Molecular links between endocrine, nervous and immune system during chronic stress
title_short Molecular links between endocrine, nervous and immune system during chronic stress
title_sort molecular links between endocrine, nervous and immune system during chronic stress
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7882157/
https://www.ncbi.nlm.nih.gov/pubmed/33295155
http://dx.doi.org/10.1002/brb3.1960
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