Endocannabinoid-Epigenetic Cross-Talk: A Bridge toward Stress Coping

There is no argument with regard to the physical and psychological stress-related nature of neuropsychiatric disorders. Yet, the mechanisms that facilitate disease onset starting from molecular stress responses are elusive. Environmental stress challenges individuals’ equilibrium, enhancing homeosta...

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Main Authors: Francesco Rusconi, Tiziana Rubino, Elena Battaglioli
Format: Article
Language:English
Published: MDPI AG 2020-08-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/21/17/6252
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spelling doaj-62a2cf454e094108920049a571d22bfa2020-11-25T03:53:12ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672020-08-01216252625210.3390/ijms21176252Endocannabinoid-Epigenetic Cross-Talk: A Bridge toward Stress CopingFrancesco Rusconi0Tiziana Rubino1Elena Battaglioli2Department of Medical Biotechnology and Translational Medicine, Università degli Studi di Milano—Via Fratelli Cervi 93, 20090 Segrate (MI), ItalyDepartment of Biotechnology and Life Sciences, Università degli Studi dell’Insubria—Busto Arsizio (VA), 21052 Busto Arsizio, ItalyDepartment of Medical Biotechnology and Translational Medicine, Università degli Studi di Milano—Via Fratelli Cervi 93, 20090 Segrate (MI), ItalyThere is no argument with regard to the physical and psychological stress-related nature of neuropsychiatric disorders. Yet, the mechanisms that facilitate disease onset starting from molecular stress responses are elusive. Environmental stress challenges individuals’ equilibrium, enhancing homeostatic request in the attempt to steer down arousal-instrumental molecular pathways that underlie hypervigilance and anxiety. A relevant homeostatic pathway is the endocannabinoid system (ECS). In this review, we summarize recent discoveries unambiguously listing ECS as a stress coping mechanism. As stress evokes huge excitatory responses in emotional-relevant limbic areas, the ECS limits glutamate release via 2-arachydonilglycerol (2-AG) stress-induced synthesis and retrograde cannabinoid 1 (CB1)-receptor activation at the synapse. However, ECS shows intrinsic vulnerability as 2-AG overstimulation by chronic stress rapidly leads to CB1-receptor desensitization. In this review, we emphasize the protective role of 2-AG in stress-response termination and stress resiliency. Interestingly, we discuss ECS regulation with a further nuclear homeostatic system whose nature is exquisitely epigenetic, orchestrated by Lysine Specific Demethylase 1. We here emphasize a remarkable example of stress-coping network where <i>transcriptional</i> homeostasis subserves synaptic and behavioral adaptation, aiming at reducing psychiatric effects of traumatic experiences.https://www.mdpi.com/1422-0067/21/17/6252endocannabinoid systemepigeneticshomeostasispsychiatric disorders2-arachidonoylglycerol (2-AG)Lysine Specific Demethylase 1
collection DOAJ
language English
format Article
sources DOAJ
author Francesco Rusconi
Tiziana Rubino
Elena Battaglioli
spellingShingle Francesco Rusconi
Tiziana Rubino
Elena Battaglioli
Endocannabinoid-Epigenetic Cross-Talk: A Bridge toward Stress Coping
International Journal of Molecular Sciences
endocannabinoid system
epigenetics
homeostasis
psychiatric disorders
2-arachidonoylglycerol (2-AG)
Lysine Specific Demethylase 1
author_facet Francesco Rusconi
Tiziana Rubino
Elena Battaglioli
author_sort Francesco Rusconi
title Endocannabinoid-Epigenetic Cross-Talk: A Bridge toward Stress Coping
title_short Endocannabinoid-Epigenetic Cross-Talk: A Bridge toward Stress Coping
title_full Endocannabinoid-Epigenetic Cross-Talk: A Bridge toward Stress Coping
title_fullStr Endocannabinoid-Epigenetic Cross-Talk: A Bridge toward Stress Coping
title_full_unstemmed Endocannabinoid-Epigenetic Cross-Talk: A Bridge toward Stress Coping
title_sort endocannabinoid-epigenetic cross-talk: a bridge toward stress coping
publisher MDPI AG
series International Journal of Molecular Sciences
issn 1661-6596
1422-0067
publishDate 2020-08-01
description There is no argument with regard to the physical and psychological stress-related nature of neuropsychiatric disorders. Yet, the mechanisms that facilitate disease onset starting from molecular stress responses are elusive. Environmental stress challenges individuals’ equilibrium, enhancing homeostatic request in the attempt to steer down arousal-instrumental molecular pathways that underlie hypervigilance and anxiety. A relevant homeostatic pathway is the endocannabinoid system (ECS). In this review, we summarize recent discoveries unambiguously listing ECS as a stress coping mechanism. As stress evokes huge excitatory responses in emotional-relevant limbic areas, the ECS limits glutamate release via 2-arachydonilglycerol (2-AG) stress-induced synthesis and retrograde cannabinoid 1 (CB1)-receptor activation at the synapse. However, ECS shows intrinsic vulnerability as 2-AG overstimulation by chronic stress rapidly leads to CB1-receptor desensitization. In this review, we emphasize the protective role of 2-AG in stress-response termination and stress resiliency. Interestingly, we discuss ECS regulation with a further nuclear homeostatic system whose nature is exquisitely epigenetic, orchestrated by Lysine Specific Demethylase 1. We here emphasize a remarkable example of stress-coping network where <i>transcriptional</i> homeostasis subserves synaptic and behavioral adaptation, aiming at reducing psychiatric effects of traumatic experiences.
topic endocannabinoid system
epigenetics
homeostasis
psychiatric disorders
2-arachidonoylglycerol (2-AG)
Lysine Specific Demethylase 1
url https://www.mdpi.com/1422-0067/21/17/6252
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