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Abstract
We compared the period of the rhythm of plasma melatonin, driven by the hypothalamic circadian pacemaker, to in vitro periodicity in cultured peripheral fibroblasts to assess the effects on these rhythms of a polymorphism of PER3 (rs57875989), which is associated with sleep timing. In vitro circadian period was determined using luminometry of cultured fibroblasts, in which the expression of firefly luciferase was driven by the promoter of the circadian gene Arntl (Bmal1). The period of the melatonin rhythm was assessed in a 9-d forced desynchrony protocol, minimizing confounding effects of sleep-wake and light-dark cycles on circadian rhythmicity. In vitro periods (32 participants, 24.61±0.33 h, mean±SD) were longer than in vivo periods (31 participants, 24.16±0.17 h; P<0.0001) but did not differ between PER3 genotypes (P>0.4). Analyses of replicate in vitro assessments demonstrated that circadian period was reproducible within individuals (intraclass correlation=0.62), but in vivo and in vitro period assessments did not correlate (P>0.9). In accordance with circadian entrainment theory, in vivo period correlated with the timing of melatonin (P<0.05) at baseline and with diurnal preference (P<0.05). Individual circadian rhythms can be reliably assessed in fibroblasts but may not correlate with physiological rhythms driven by the central circadian pacemaker.
Item Type: | Article |
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Additional Information: | Funding information: UK Biotechnology and Biological Sciences Research Council. Grant Number: BB/F022883/1 |
Uncontrolled Keywords: | Bmal1, Clock genes, Lentivirus, PER3, Sleep |
Subjects: | B900 Others in Subjects allied to Medicine C800 Psychology |
Department: | Faculties > Health and Life Sciences > Psychology |
Depositing User: | Rachel Branson |
Date Deposited: | 31 Aug 2021 14:46 |
Last Modified: | 31 Aug 2021 15:00 |
URI: | http://nrl.northumbria.ac.uk/id/eprint/47035 |
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