Neonatal rat cardiomyocytes as an in vitro model for circadian rhythms in the heart. (November 2017)
- Record Type:
- Journal Article
- Title:
- Neonatal rat cardiomyocytes as an in vitro model for circadian rhythms in the heart. (November 2017)
- Main Title:
- Neonatal rat cardiomyocytes as an in vitro model for circadian rhythms in the heart
- Authors:
- du Pré, Bastiaan C.
Dierickx, Pieterjan
Crnko, Sandra
Doevendans, Pieter A.
Vos, Marc A.
Geijsen, Niels
Neutel, Didi
van Veen, Toon A.B.
van Laake, Linda W. - Abstract:
- Abstract: Circadian rhythms are biorhythms with a 24-hour period that are regulated by molecular clocks. Several clinical and animal models have been developed to analyze the role of these rhythms in cardiovascular physiology, disease and therapy, but a convenient in vitro model that mimics both molecular and functional circadian effects of the heart is not available. Therefore, we established a neonatal rat cardiomyocyte model that recapitulates in vivo circadian rhythmicity, as measured by anti-phasic oscillatory mRNA expression of two core clock genes, Bmal1 and Per2 and that shows functional dependence on the clock as indicated by an oscillating response in apoptosis induced by doxorubicin, hydroperoxide or hypoxia. In addition, perturbation of the cardiac clock by the use of several compounds including Resveratrol and Ex-527 was found to result in loss of functional rhythmicity. This indicates that neonatal rat cardiomyocytes are a good model to investigate the cardiac circadian clock as well as a system that allows for fast and easy preclinical testing of the influence of compounds on circadian rhythmicity that might have crucial effects on cardiac health. Highlights: Neonatal rat cardiomyocytes (nrCMs) possess a functional molecular circadian clock. nrCMs show 24-hour rhythmicity in beating frequency and induced damage response. Functional rhythmicity is lost upon clock disturbance by several compounds. nrCMs function as a good in vitro model for cardiac clockAbstract: Circadian rhythms are biorhythms with a 24-hour period that are regulated by molecular clocks. Several clinical and animal models have been developed to analyze the role of these rhythms in cardiovascular physiology, disease and therapy, but a convenient in vitro model that mimics both molecular and functional circadian effects of the heart is not available. Therefore, we established a neonatal rat cardiomyocyte model that recapitulates in vivo circadian rhythmicity, as measured by anti-phasic oscillatory mRNA expression of two core clock genes, Bmal1 and Per2 and that shows functional dependence on the clock as indicated by an oscillating response in apoptosis induced by doxorubicin, hydroperoxide or hypoxia. In addition, perturbation of the cardiac clock by the use of several compounds including Resveratrol and Ex-527 was found to result in loss of functional rhythmicity. This indicates that neonatal rat cardiomyocytes are a good model to investigate the cardiac circadian clock as well as a system that allows for fast and easy preclinical testing of the influence of compounds on circadian rhythmicity that might have crucial effects on cardiac health. Highlights: Neonatal rat cardiomyocytes (nrCMs) possess a functional molecular circadian clock. nrCMs show 24-hour rhythmicity in beating frequency and induced damage response. Functional rhythmicity is lost upon clock disturbance by several compounds. nrCMs function as a good in vitro model for cardiac clock interference. … (more)
- Is Part Of:
- Journal of molecular and cellular cardiology. Volume 112(2017)
- Journal:
- Journal of molecular and cellular cardiology
- Issue:
- Volume 112(2017)
- Issue Display:
- Volume 112, Issue 2017 (2017)
- Year:
- 2017
- Volume:
- 112
- Issue:
- 2017
- Issue Sort Value:
- 2017-0112-2017-0000
- Page Start:
- 58
- Page End:
- 63
- Publication Date:
- 2017-11
- Subjects:
- Circadian rhythms -- Heart -- In vitro -- Neonatal rat cardiomyocytes
Cardiology -- Periodicals
Heart Diseases -- Periodicals
Molecular Biology -- Periodicals
Cardiologie -- Périodiques
Cardiology
Electronic journals
Periodicals
616.12 - Journal URLs:
- http://www.sciencedirect.com/science/journal/00222828 ↗
http://www.clinicalkey.com/dura/browse/journalIssue/00222828 ↗
http://www.clinicalkey.com.au/dura/browse/journalIssue/00222828 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.yjmcc.2017.08.009 ↗
- Languages:
- English
- ISSNs:
- 0022-2828
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5020.690000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 4800.xml