Literature DB >> 22877660

Circadian system from conception till adulthood.

Alena Sumova1, Martin Sladek2, Lenka Polidarova2, Marta Novakova2, Pavel Houdek2.   

Abstract

In mammals, the circadian system is composed of the central clock in the hypothalamic suprachiasmatic nuclei and of peripheral clocks that are located in other neural structures and in cells of the peripheral tissues and organs. In adults, the system is hierarchically organized so that the central clock provides the other clocks in the body with information about the time of day. This information is needed for the adaptation of their functions to cyclically changing external conditions. During ontogenesis, the system undergoes substantial development and its sensitivity to external signals changes. Perinatally, maternal cues are responsible for setting the phase of the developing clock, while later postnatally, the LD cycle is dominant. The central clock attains its functional properties during a gradual and programmed process. Peripheral clocks begin to exhibit rhythmicity independent of each other at various developmental stages. During the early developmental stages, the peripheral clocks are set or driven by maternal feeding, but later the central clock becomes fully functional and begins to entrain the periphery. During the perinatal period, the central and peripheral clocks seem to be vulnerable to disturbances in external conditions. Further studies are needed to understand the processes of how the circadian system develops and what degree of plasticity and resilience it possesses during ontogenesis. These data may lead to an assessment of the contribution of disturbances of the circadian system during early ontogenesis to the occurrence of circadian diseases in adulthood.
Copyright © 2012 Elsevier B.V. All rights reserved.

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Year:  2012        PMID: 22877660     DOI: 10.1016/B978-0-444-59427-3.00005-8

Source DB:  PubMed          Journal:  Prog Brain Res        ISSN: 0079-6123            Impact factor:   2.453


  10 in total

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3.  Early rhythmicity in the fetal suprachiasmatic nuclei in response to maternal signals detected by omics approach.

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5.  Maternal obesity programs offspring non-alcoholic fatty liver disease through disruption of 24-h rhythms in mice.

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6.  In vivo initiation of clock gene expression rhythmicity in fetal rat suprachiasmatic nuclei.

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7.  Challenging the Integrity of Rhythmic Maternal Signals Revealed Gene-Specific Responses in the Fetal Suprachiasmatic Nuclei.

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10.  Circadian Modulation of Neurons and Astrocytes Controls Synaptic Plasticity in Hippocampal Area CA1.

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  10 in total

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