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      Peripheral Skin Temperature and Circadian Biological Clock in Shift Nurses after a Day off

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          Abstract

          The circadian biological clock is essentially based on the light/dark cycle. Some people working with shift schedules cannot adjust their sleep/wake cycle to the light/dark cycle, and this may result in alterations of the circadian biological clock. This study explored the circadian biological clock of shift and daytime nurses using non-invasive methods. Peripheral skin temperature, cortisol and melatonin levels in saliva, and Per2 expression in pubic hair follicle cells were investigated for 24 h after a day off. Significant differences were observed in peripheral skin temperature and cortisol levels between shift and daytime nurses. No differences in melatonin levels were obtained. Per2 maximum values were significantly different between the two groups. Shift nurses exhibited lower circadian variations compared to daytime nurses, and this may indicate an adjustment of the circadian biological clock to continuous shift schedules. Non-invasive procedures, such as peripheral skin temperature measurement, determination of cortisol and melatonin in saliva, and analysis of clock genes in hair follicle cells, may be effective approaches to extensively study the circadian clock in shift workers.

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          Most cited references63

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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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            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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              A transcription factor response element for gene expression during circadian night.

              Mammalian circadian clocks consist of complex integrated feedback loops that cannot be elucidated without comprehensive measurement of system dynamics and determination of network structures. To dissect such a complicated system, we took a systems-biological approach based on genomic, molecular and cell biological techniques. We profiled suprachiasmatic nuclei and liver genome-wide expression patterns under light/dark cycles and constant darkness. We determined transcription start sites of human orthologues for newly identified cycling genes and then performed bioinformatical searches for relationships between time-of-day specific expression and transcription factor response elements around transcription start sites. Here we demonstrate the role of the Rev-ErbA/ROR response element in gene expression during circadian night, which is in phase with Bmal1 and in antiphase to Per2 oscillations. This role was verified using an in vitro validation system, in which cultured fibroblasts transiently transfected with clock-controlled reporter vectors exhibited robust circadian bioluminescence.
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                Author and article information

                Contributors
                Role: Academic Editor
                Journal
                Int J Mol Sci
                Int J Mol Sci
                ijms
                International Journal of Molecular Sciences
                MDPI
                1422-0067
                26 April 2016
                May 2016
                : 17
                : 5
                : 623
                Affiliations
                [1 ]Occupational Medicine, Department of Clinical and Molecular Sciences, Polytechnic University of Marche, Via Tronto 10/A, Ancona 60126, Italy; veronica.ciarapica@ 123456virgilio.it (V.C.); nicolamanzella@ 123456virgilio.it (N.M.); m.tomasetti@ 123456univpm.it (M.T.); simonagae87@ 123456hotmail.it (S.G.); monaco_federica@ 123456virgilio.it (F.M.); m.amati@ 123456univpm.it (M.A.); m.valentino@ 123456univpm.it (M.V.); l.santarelli@ 123456univpm.it (L.S.)
                [2 ]Healthcare Workers Service, ASUR Area 2, Loreto Hospital, Via S. Francesco 1, Loreto 60025, Italy; alfredo.copertaro@ 123456sanita.marche.it (A.C.); mariella.barbaresi@ 123456sanita.marche.it (M.B.)
                [3 ]Section of Occupational Medicine, Department of Internal Medicine and Systemic Diseases, University of Catania, Via Santa Sofia 78, Catania 95123, Italy; dottore.rapisarda@ 123456gmail.com
                Author notes
                [* ]Correspondence: m.bracci@ 123456univpm.it ; Tel.: +39-071-220-6063; Fax: +39-071-220-6062
                Article
                ijms-17-00623
                10.3390/ijms17050623
                4881449
                27128899
                89887fe9-bf12-4b3d-9b9c-1350d8e9128a
                © 2016 by the authors; licensee MDPI, Basel, Switzerland.

                This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC-BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 28 February 2016
                : 19 April 2016
                Categories
                Article

                Molecular biology
                skin temperature,circadian rhythm,cortisol,melatonin,per2 gene,circadian clocks,light dark cycle,circadian dysregulation,occupational health,shift work

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