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      Multimodal Regulation of Circadian Glucocorticoid Rhythm by Central and Adrenal Clocks

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          Abstract

          Adrenal glucocorticoids (GCs) control a wide range of physiological processes, including metabolism, cardiovascular and pulmonary activities, immune and inflammatory responses, and various brain functions. During stress responses, GCs are secreted through activation of the hypothalamic–pituitary–adrenal axis, whereas circulating GC levels in unstressed states follow a robust circadian oscillation with a peak around the onset of the active period of a day. A recent advance in chronobiological research has revealed that multiple regulatory mechanisms, along with classical neuroendocrine regulation, underlie this GC circadian rhythm. The hierarchically organized circadian system, with a central pacemaker in the suprachiasmatic nucleus of the hypothalamus and local oscillators in peripheral tissues, including the adrenal gland, mediates periodicities in physiological processes in mammals. In this review, we primarily focus on our understanding of the circadian regulation of adrenal GC rhythm, with particular attention to the cooperative actions of the suprachiasmatic nucleus central and adrenal local clocks, and the clinical implications of this rhythm in human diseases.

          Abstract

          The present review mainly focuses on our understanding of the circadian regulation of adrenal glucocorticoids rhythm, particularly by the cooperative actions of the central and adrenal local clocks.

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          The orphan nuclear receptor REV-ERBalpha controls circadian transcription within the positive limb of the mammalian circadian oscillator.

          Mammalian circadian rhythms are generated by a feedback loop in which BMAL1 and CLOCK, players of the positive limb, activate transcription of the cryptochrome and period genes, components of the negative limb. Bmal1 and Per transcription cycles display nearly opposite phases and are thus governed by different mechanisms. Here, we identify the orphan nuclear receptor REV-ERBalpha as the major regulator of cyclic Bmal1 transcription. Circadian Rev-erbalpha expression is controlled by components of the general feedback loop. Thus, REV-ERBalpha constitutes a molecular link through which components of the negative limb drive antiphasic expression of components of the positive limb. While REV-ERBalpha influences the period length and affects the phase-shifting properties of the clock, it is not required for circadian rhythm generation.
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            Resetting of circadian time in peripheral tissues by glucocorticoid signaling.

            In mammals, circadian oscillators reside not only in the suprachiasmatic nucleus of the brain, which harbors the central pacemaker, but also in most peripheral tissues. Here, we show that the glucocorticoid hormone analog dexamethasone induces circadian gene expression in cultured rat-1 fibroblasts and transiently changes the phase of circadian gene expression in liver, kidney, and heart. However, dexamethasone does not affect cyclic gene expression in neurons of the suprachiasmatic nucleus. This enabled us to establish an apparent phase-shift response curve specifically for peripheral clocks in intact animals. In contrast to the central clock, circadian oscillators in peripheral tissues appear to remain responsive to phase resetting throughout the day.
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              Role of the CLOCK protein in the mammalian circadian mechanism.

              The mouse Clock gene encodes a bHLH-PAS protein that regulates circadian rhythms and is related to transcription factors that act as heterodimers. Potential partners of CLOCK were isolated in a two-hybrid screen, and one, BMAL1, was coexpressed with CLOCK and PER1 at known circadian clock sites in brain and retina. CLOCK-BMAL1 heterodimers activated transcription from E-box elements, a type of transcription factor-binding site, found adjacent to the mouse per1 gene and from an identical E-box known to be important for per gene expression in Drosophila. Mutant CLOCK from the dominant-negative Clock allele and BMAL1 formed heterodimers that bound DNA but failed to activate transcription. Thus, CLOCK-BMAL1 heterodimers appear to drive the positive component of per transcriptional oscillations, which are thought to underlie circadian rhythmicity.
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                Author and article information

                Contributors
                Journal
                J Endocr Soc
                J Endocr Soc
                jes
                Journal of the Endocrine Society
                Endocrine Society (Washington, DC )
                2472-1972
                01 May 2018
                06 April 2018
                : 2
                : 5
                : 444-459
                Affiliations
                [1 ]Department of Biomedical Sciences, College of Medicine, Korea University, Seoul, Korea
                [2 ]Department of Brain and Cognitive Sciences, Scranton College, Ewha Womans University, Seoul, Korea
                [3 ]Department of Brain and Cognitive Sciences, Daegu Gyeongbuk Institute of Science and Technology, Daegu, Korea
                [4 ]Korea Brain Research Institute, Daegu, Korea
                Author notes
                Correspondence:  Gi Hoon Son, PhD, Department of Biomedical Sciences, College of Medicine, Korea University, Inchon-ro 73, Seongbuk-gu, Seoul 02841, Korea. E-mail: songh@ 123456korea.ac.kr ; or Kyungjin Kim, PhD, Department of Brain and Cognitive Sciences, Daegu-Gyeongbuk Institute of Science and Technology, Techno Jungang-daero 333, Hyeonpung-myeon, Dalseong-gun, Daegu 42988, Korea. E-mail: kyungjin@ 123456dgist.ac.kr .
                Article
                js_201800021
                10.1210/js.2018-00021
                5915959
                b09e23e9-df98-4783-b615-55cabcc7ca95
                Copyright © 2018 Endocrine Society

                This article has been published under the terms of the Creative Commons Attribution Non-Commercial, No-Derivatives License (CC BY-NC-ND; https://creativecommons.org/licenses/by-nc-nd/4.0/).

                History
                : 24 January 2018
                : 03 April 2018
                Page count
                Pages: 16
                Funding
                Funded by: National Research Foundation of Korea 10.13039/501100003725
                Award ID: NRF-2015M3A9E7029176
                Award ID: NRF-2016M3C7A1904340
                Award ID: NRF-2014R1A6A3A04054863
                Award ID: NRF-20171A2A1A05001351
                Funded by: Korea University research grant
                Funded by: Daegu Gyeongbuk Institute of Science and Technology start-up research fund
                Award ID: 20180136
                Categories
                Mini-Review
                Adrenal

                circadian clock,adrenal gland,circadian rhythm,glucocorticoid,hypothalamic-pituitary-adrenal axis

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