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The vascular clock system generates the intrinsic circadian rhythm of vascular contractility

Many of the cardiovascular parameters or incidences of coronary artery diseases display circadian variations. These day/night time variances may be attributable to the diurnal change in vascular contractility. However, the molecular mechanism of the vascular clock system which generates the circadia...

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Autor principal: Saito, Toshiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Japan Society of Smooth Muscle Research 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5137311/
https://www.ncbi.nlm.nih.gov/pubmed/26935878
http://dx.doi.org/10.1540/jsmr.51.95
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author Saito, Toshiro
author_facet Saito, Toshiro
author_sort Saito, Toshiro
collection PubMed
description Many of the cardiovascular parameters or incidences of coronary artery diseases display circadian variations. These day/night time variances may be attributable to the diurnal change in vascular contractility. However, the molecular mechanism of the vascular clock system which generates the circadian variation of vascular contractility has remained largely unknown. Recently we found the existence of the intrinsic circadian rhythm in vascular contractility. A clock gene Rorα in vascular smooth muscle cells (VSMC) provokes the diurnal oscillatory change in the expression of Rho-associated kinase 2 (ROCK2), which induces the time-of-day-dependent variation in the agonist-induced phosphorylation of myosin light chain (MLC) and myofilament Ca(2+) sensitization. In this review, we introduce our recent findings with reference to the molecular basis of the biological clock system and the current literature concerning cardiovascular chronobiology.
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spelling pubmed-51373112017-02-14 The vascular clock system generates the intrinsic circadian rhythm of vascular contractility Saito, Toshiro J Smooth Muscle Res Invited Review Many of the cardiovascular parameters or incidences of coronary artery diseases display circadian variations. These day/night time variances may be attributable to the diurnal change in vascular contractility. However, the molecular mechanism of the vascular clock system which generates the circadian variation of vascular contractility has remained largely unknown. Recently we found the existence of the intrinsic circadian rhythm in vascular contractility. A clock gene Rorα in vascular smooth muscle cells (VSMC) provokes the diurnal oscillatory change in the expression of Rho-associated kinase 2 (ROCK2), which induces the time-of-day-dependent variation in the agonist-induced phosphorylation of myosin light chain (MLC) and myofilament Ca(2+) sensitization. In this review, we introduce our recent findings with reference to the molecular basis of the biological clock system and the current literature concerning cardiovascular chronobiology. Japan Society of Smooth Muscle Research 2016-03-02 2015 /pmc/articles/PMC5137311/ /pubmed/26935878 http://dx.doi.org/10.1540/jsmr.51.95 Text en ©2015 The Japan Society of Smooth Muscle Research http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License.
spellingShingle Invited Review
Saito, Toshiro
The vascular clock system generates the intrinsic circadian rhythm of vascular contractility
title The vascular clock system generates the intrinsic circadian rhythm of vascular contractility
title_full The vascular clock system generates the intrinsic circadian rhythm of vascular contractility
title_fullStr The vascular clock system generates the intrinsic circadian rhythm of vascular contractility
title_full_unstemmed The vascular clock system generates the intrinsic circadian rhythm of vascular contractility
title_short The vascular clock system generates the intrinsic circadian rhythm of vascular contractility
title_sort vascular clock system generates the intrinsic circadian rhythm of vascular contractility
topic Invited Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5137311/
https://www.ncbi.nlm.nih.gov/pubmed/26935878
http://dx.doi.org/10.1540/jsmr.51.95
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