Diurnal variations of hormonal secretion, alertness and cognition in extreme chronotypes under different lighting conditions
Jazyk angličtina Země Velká Británie, Anglie Médium electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
27646174
PubMed Central
PMC5028769
DOI
10.1038/srep33591
PII: srep33591
Knihovny.cz E-zdroje
- MeSH
- afekt MeSH
- bdění MeSH
- cirkadiánní rytmus fyziologie účinky záření MeSH
- dospělí MeSH
- hormony metabolismus MeSH
- hydrokortison metabolismus MeSH
- kognice * MeSH
- lidé MeSH
- melatonin metabolismus MeSH
- mladiství MeSH
- mladý dospělý MeSH
- osvětlení * škodlivé účinky MeSH
- pozornost * MeSH
- sliny metabolismus MeSH
- spánek fyziologie MeSH
- Check Tag
- dospělí MeSH
- lidé MeSH
- mladiství MeSH
- mladý dospělý MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- hormony MeSH
- hydrokortison MeSH
- melatonin MeSH
Circadian rhythms in physiology and behavior are modulated by external factors such as light or temperature. We studied whether self-selected office lighting during the habitual waking period had a different impact on alertness, cognitive performance and hormonal secretion in extreme morning and evening chronotypes (N = 32), whose preferred bed- and wake-up times differed by several hours. The self-selected lighting condition was compared with constant bright light and a control condition in dim light. Saliva samples for hormonal analyses, subjective ratings of alertness, wellbeing, visual comfort and cognitive performance were regularly collected. Between the self-selected and the bright, but not the dim lighting condition, the onset of melatonin secretion in the evening (as marker for circadian phase) was significantly different for both chronotypes. Morning chronotypes reported a faster increase in sleepiness during the day than evening chronotypes, which was associated with higher cortisol secretion. Wellbeing, mood and performance in more difficult cognitive tasks were better in bright and self-selected lighting than in dim light for both chronotypes, whereas visual comfort was best in the self-selected lighting. To conclude, self-selection of lighting at work might positively influence biological and cognitive functions, and allow for inter-individual differences.
Czech Technical University Prague UCEEB Trinecka 1024 273 43 Bustehrad Czech Republic
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Moore R. Y. & Eichler V. B. Loss of a circadian adrenal corticosterone rhythm following suprachiasmatic lesions in the rat. Brain Research 42, 201–206 (1972). PubMed
Husse J., Eichele G. & Oster H. Synchronization of the mammalian circadian timing system: Light can control peripheral clocks independently of the SCN clock: alternate routes of entrainment optimize the alignment of the body’s circadian clock network with external time. Bioessays 37, 1119–1128 (2015). PubMed PMC
Cajochen C. Alerting effects of light. Sleep Medicine Reviews 11, 453–464 (2007). PubMed
Lewy A. et al.. Melatonin marks circadian phase position and resets the endogenous circadian pacemaker in humans. Vol. 183 (John Wiley & Sons, 1995). PubMed
Khalsa S., Jewett M., Cajochen C. & Czeisler C. A phase response curve to single bright light pulses in human subjects. Journal of Physiology (London) 549.3, 945–952 (2003). PubMed PMC
Horne J. & Östberg O. A self-assessment questionnaire to determine morningness-eveningness in human circadian rhythms. International Journal of Chronobiology 4, 97–110 (1976). PubMed
Roenneberg T., Wirz-Justice A. & Merrow M. Life between clocks: daily temporal patterns of human chronotypes. Journal of Biological Rhythms 18, 80–90 (2003). PubMed
Kerkhof G., Korving H., Willemse-vd Geest H. & Rietveld W. Diurnal differences between morning-type and evening-type subjects in self-rated alertness, body temperature and the visual and auditory evoked potential. Neuroscience Letters 1, 11–15 (1980). PubMed
Katzenberg D. et al.. A CLOCK polymorphism associated with human diurnal preference. Sleep 21, 569–576 (1998). PubMed
Reid K. J. et al.. Familial advanced sleep phase syndrome. Archives Neurology 58, 1089–1094 (2001). PubMed
Archer S. et al.. Polymorphism in the PER3 promoter associates with diurnal preference and delayed sleep phase disorder. Sleep 33, 695–701 (2010). PubMed PMC
Hida A. et al.. Screening of clock gene polymorphisms demonstrates association of a PER3 polymorphism with morningness-eveningness preference and circadian rhythm sleep disorder. Scientific Reports 4, 6309 (2014). PubMed PMC
Brown S. et al.. Molecular insights into human daily behavior. Proceedings of the National Academy of Sciences of the USA 105, 1602–1607 (2008). PubMed PMC
Duffy J., Rimmer D. & Czeisler C. Association of intrinsic circadian period with morningness-eveningness, usual wake time, and circadian phase. Behavioral Neuroscience 115, 895–899 (2001). PubMed
Emens J. et al.. Phase angle of entrainment in morning- and evening- types under naturalistic conditions. Chronobiology International 26, 474–493 (2009). PubMed PMC
Mongrain V., Lavoie S., Selmaoui B., Paquet J. & Dumont M. Phase relationships between sleep - wake cycle and underlying circadian rhythms in morningness - eveningness. Journal of Biological Rhythms 19, 248–257 (2004). PubMed
Taillard J., Phillip P., Coste O., Sagaspe P. & Bioulac B. The circadian and homeostaic modulation of sleep pressure during wakefulness differs between morning and evening chronotypes. Journal of Sleep Research 12, 275–282 (2003). PubMed
Mongrain V., Carrier J. & Dumont M. Circadian and homeostatic sleep regulation in morningness–eveningness. Journal of Sleep Research 15, 162–166 (2006). PubMed
Horne J., Brass C. & Petitt A. Circadian performance differences between morning and evening ‘types’. Ergonomics 23, 29–36 (1980). PubMed
Schmidt C. et al.. Homeostatic sleep pressure and responses to sustained attention in the suprachiasmatic area. Science 324, 516–519 (2009). PubMed
Schmidt C. et al.. Pushing the limits. Chronotype- and time-of-day modulate working memory-dependent cerebral activity. Frontiers in Neurology 6 (2015). PubMed PMC
Goulet G., Mongrain V., Desrosiers C., Paquet J. & Dumont M. Daily light exposure in morning-type and evening-type individuals. Journal of Biological Rhythms 22, 151–158 (2007). PubMed
Roenneberg T., Kumar C. J. & Merrow M. The human circadian clock entrains to sun time. Current Biology 17, R44–R45 (2007). PubMed
Duffy J., Dijk D., Hall E. & Czeisler C. Relationship of endogenous circadian melatonin and temperature rhythms to self-reported preference for morning or evening activity in young and older people. Journal of Investigative Medicine 47, 141–150 (1999). PubMed PMC
Baehr E., Revelle W. & Eastman C. Individual differences in the phase and amplitude of the human circadian temperature rhythm: with an emphasis on morningness–eveningness. Journal of Sleep Research 9, 117–127 (2000). PubMed
Gunn P., Middleton B., Davies S., Revell V. & Skene D. Sex differences in the circadian profiles of melatonin and cortisol in plasma and urine matrices under constant routine conditions. Chronobiology International 33, 39–50 (2016). PubMed PMC
Santhi N. et al.. Sex differences in the circadian regulation of sleep and waking cognition in humans. Proc Natl Acad Sci USA 113, E2730–E2739 (2016). PubMed PMC
Cain S. et al.. Sex differences in phase angle of entrainment and melatonin amplitude in humans. Journal of Biological Rhythms 25, 288–296 (2010). PubMed PMC
Zeitzer J., Dijk D., Kronauer R., Brown E. & Czeisler C. Sensitivity of the human circadian pacemaker to nocturnal light: melatonin phase resetting and suppression. Journal of Physiology 526, 695–702 (2000). PubMed PMC
Kudielka B., Federenko I., Hellhammer D. & Wüst S. Morningness and eveningness: The free cortisol rise after awakening in ‘early birds’ and ‘night owls’. Biological Psychology 72, 141–146 (2006). PubMed
Taillard J. et al.. Time course of neurobehavioral alertness during extended wakefulness in morning- and evening-type healthy sleepers. Chronobiology International 28, 520–527 (2011). PubMed
Wittmann M., Dinrich J., Merrow M. & Roenneberg T. Social jetlag: misalignement of biological and social time. Chronobiology International 23, 497–509 (2006). PubMed
Begeman S., Beld G. & Tenner A. Daylight, artificial light and people in an office environment, overview of visual and biological responses. International Journal of Industrial Ergonomics 20, 231–239 (1997).
van der Meijden W. et al.. Individual differences in sleep timing relate to melanopsin-based phototransduction in healthy adolescents and young adults. Sleep 39, 1305–1310 (2016). PubMed PMC
Maierova L., Borisuit A., Scartezzini J. & Münch M. In CLIMA. (11th REHVA World Congress & 8th International Conference on IAQVEC, Prague, Czech Republic, 16–19 June, 2013).
Zijlstra F. Efficiency in Work Behavior: A Design Approach for Modern Tools. (Delft University Press, 1993).
Phipps-Nelson J., Redman J., Dijk D.-J. & M R. S. Daytime exposure to bright light, as compared to dim light, decreases sleepiness and improves psychomotor vigilance performance. Sleep 26, 695–700 (2003). PubMed
Cajochen C., Zeitzer J. M., Czeisler C. A. & Dijk D. J. Dose- response relationship for light intensity and ocular and electroencephalographic correlates of human-alertness. Behavioral Brain Research 115, 75–83 (2000). PubMed
Danilenko K., Verevkin E., Antyufeev V., Wirz-Justice A. & Cajochen C. The hockey-stick method to estimate evening dim light melatonin onset (DLMO) in humans. Chronobiology International 31, 349–355 (2014). PubMed