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      Perinatal Stress Programs Sex Differences in the Behavioral and Molecular Chronobiological Profile of Rats Maintained Under a 12-h Light-Dark Cycle

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          Abstract

          Stress and the circadian systems play a major role in an organism’s adaptation to environmental changes. The adaptive value of the stress system is reactive while that of the circadian system is predictive. Dysfunctions in these two systems may account for many clinically relevant disorders. Despite the evidence that interindividual differences in stress sensitivity and in the functioning of the circadian system are related, there is limited integrated research on these topics. Moreover, sex differences in these systems are poorly investigated. We used the perinatal stress (PRS) rat model, a well-characterized model of maladaptive programming of reactive and predictive adaptation, to monitor the running wheel behavior in male and female adult PRS rats, under a normal light/dark cycle as well as in response to a chronobiological stressor (6-h phase advance/shift). We then analyzed across different time points the expression of genes involved in circadian clocks, stress response, signaling, and glucose metabolism regulation in the suprachiasmatic nucleus (SCN). In the unstressed control group, we found a sex-specific profile that was either enhanced or inverted by PRS. Also, PRS disrupted circadian wheel-running behavior by inducing a phase advance in the activity of males and hypoactivity in females and increased vulnerability to chronobiological stress in both sexes. We also observed oscillations of several genes in the SCN of the unstressed group in both sexes. PRS affected males to greater extent than females, with PRS males displaying a pattern similar to unstressed females. Altogether, our findings provide evidence for a specific profile of dysmasculinization induced by PRS at the behavioral and molecular level, thus advocating the necessity to include sex as a biological variable to study the set-up of circadian system in animal models.

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          Epigenetic programming by maternal behavior.

          Here we report that increased pup licking and grooming (LG) and arched-back nursing (ABN) by rat mothers altered the offspring epigenome at a glucocorticoid receptor (GR) gene promoter in the hippocampus. Offspring of mothers that showed high levels of LG and ABN were found to have differences in DNA methylation, as compared to offspring of 'low-LG-ABN' mothers. These differences emerged over the first week of life, were reversed with cross-fostering, persisted into adulthood and were associated with altered histone acetylation and transcription factor (NGFI-A) binding to the GR promoter. Central infusion of a histone deacetylase inhibitor removed the group differences in histone acetylation, DNA methylation, NGFI-A binding, GR expression and hypothalamic-pituitary-adrenal (HPA) responses to stress, suggesting a causal relation among epigenomic state, GR expression and the maternal effect on stress responses in the offspring. Thus we show that an epigenomic state of a gene can be established through behavioral programming, and it is potentially reversible.
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            Coordinated transcription of key pathways in the mouse by the circadian clock.

            In mammals, circadian control of physiology and behavior is driven by a master pacemaker located in the suprachiasmatic nuclei (SCN) of the hypothalamus. We have used gene expression profiling to identify cycling transcripts in the SCN and in the liver. Our analysis revealed approximately 650 cycling transcripts and showed that the majority of these were specific to either the SCN or the liver. Genetic and genomic analysis suggests that a relatively small number of output genes are directly regulated by core oscillator components. Major processes regulated by the SCN and liver were found to be under circadian regulation. Importantly, rate-limiting steps in these various pathways were key sites of circadian control, highlighting the fundamental role that circadian clocks play in cellular and organismal physiology.
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              Stress and the individual. Mechanisms leading to disease.

              This article presents a new formulation of the relationship between stress and the processes leading to disease. It emphasizes the hidden cost of chronic stress to the body over long time periods, which act as a predisposing factor for the effects of acute, stressful life events. It also presents a model showing how individual differences in the susceptibility to stress are tied to individual behavioral responses to environmental challenges that are coupled to physiologic and pathophysiologic responses. Published original articles from human and animal studies and selected reviews. Literature was surveyed using MEDLINE. Independent extraction and cross-referencing by us. Stress is frequently seen as a significant contributor to disease, and clinical evidence is mounting for specific effects of stress on immune and cardiovascular systems. Yet, until recently, aspects of stress that precipitate disease have been obscure. The concept of homeostasis has failed to help us understand the hidden toll of chronic stress on the body. Rather than maintaining constancy, the physiologic systems within the body fluctuate to meet demands from external forces, a state termed allostasis. In this article, we extend the concept of allostasis over the dimension of time and we define allostatic load as the cost of chronic exposure to fluctuating or heightened neural or neuroendocrine response resulting from repeated or chronic environmental challenge that an individual reacts to as being particularly stressful. This new formulation emphasizes the cascading relationships, beginning early in life, between environmental factors and genetic predispositions that lead to large individual differences in susceptibility to stress and, in some cases, to disease. There are now empirical studies based on this formulation, as well as new insights into mechanisms involving specific changes in neural, neuroendocrine, and immune systems. The practical implications of this formulation for clinical practice and further research are discussed.
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                Author and article information

                Contributors
                Journal
                Front Mol Neurosci
                Front Mol Neurosci
                Front. Mol. Neurosci.
                Frontiers in Molecular Neuroscience
                Frontiers Media S.A.
                1662-5099
                01 May 2019
                2019
                : 12
                : 89
                Affiliations
                [1] 1UMR 8576, Unité de Glycobiologie Structurale et Fonctionnelle, Campus Cité Scientifique, CNRS, University of Lille , Lille, France
                [2] 2University Lille – CNRS-UMR 8576, International Associated Laboratory (LIA) “Prenatal Stress and Neurodegenerative Diseases,” Sapienza University of Rome – IRCCS Neuromed , Rome, Italy
                [3] 3Division of Neonatology, Department of Pediatrics, University of Geneva , Geneva, Switzerland
                [4] 4Department of Psychiatry, College of Medicine, Psychiatric Institute, Center for Alcohol Research in Epigenetics, University of Illinois at Chicago , Chicago, IL, United States
                [5] 5Laboratory of Neuroendocrinology, The Rockefeller University , New York, NY, United States
                [6] 6Department of Physiology and Pharmacology “V. Erspamer,” Sapienza University of Rome , Rome, Italy
                [7] 7Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), NEUROMED , Pozzilli, Italy
                [8] 8Department of Science and Medical – Surgical Biotechnology, Sapienza University of Rome , Rome, Italy
                Author notes

                Edited by: Gi Hoon Son, Korea University, South Korea

                Reviewed by: Henrik Oster, Universität zu Lübeck, Germany; Han Kyoung Choe, Daegu Gyeongbuk Institute of Science and Technology (DGIST), South Korea

                *Correspondence: Stefania Maccari, stefania.maccari@ 123456univ-lille.fr

                These authors have contributed equally to this work

                Present address: Ferdinando Nicoletti and Stefania Maccari, Co-director of International Associated Laboratory (LIA), University of Lille 1 – CNRS and Sapienza University of Rome – IRCCS Neuromed, Rome, Italy

                Article
                10.3389/fnmol.2019.00089
                6504690
                ee7ab216-0900-4290-ad01-d9c292db2ddd
                Copyright © 2019 Morley-Fletcher, Mairesse, Van Camp, Reynaert, Gatta, Marrocco, Bouwalerh, Nicoletti and Maccari.

                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.

                History
                : 28 November 2018
                : 21 March 2019
                Page count
                Figures: 4, Tables: 1, Equations: 0, References: 71, Pages: 15, Words: 0
                Categories
                Neuroscience
                Original Research

                Neurosciences
                predictive adaptation,reactive adaptation,circadian rhythms,locomotor activity,chronobiological stressor,mrna expression

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