Time to Network: The Molecular Blueprint of the Circadian Timing System in Plants

2015 ◽  
pp. 257-276 ◽  
Author(s):  
Selahattin Danisman ◽  
Julieta Mateos ◽  
Dorothee Staiger
2016 ◽  
Vol 8 (1) ◽  
pp. 14-22 ◽  
Author(s):  
Navin Adhikary ◽  
Santosh Lal Shrestha ◽  
Jia Zhong Sun

2020 ◽  
Vol 10 (3) ◽  
pp. 20190080 ◽  
Author(s):  
Gaby Illingworth

Sleep is vital for our physical, emotional and cognitive health. However, adolescents face many challenges where their sleep is concerned. This is reflected in their sleep patterns including the timing of their sleep and how much sleep they achieve on a regular basis: their sleep is characteristically delayed and short. Notably, insufficient sleep is associated with impairments in adolescent functioning. Endogenous and exogenous factors are known to affect sleep at this age. Alterations in the bioregulation of sleep, comprising the circadian timing system and the sleep/wake homeostatic system, represent the intrinsic mechanisms at work. Compounding this, environmental, psychosocial and lifestyle factors may contribute to shortened sleep. This review discusses the amount of sleep gained by adolescents and its implications, the challenges to adolescent sleep and the interventions introduced in an effort to prioritize sleep health in this important developmental period.


2014 ◽  
Vol 128 (3) ◽  
pp. 371-386 ◽  
Author(s):  
Amanda S. Damaggio ◽  
Michael R. Gorman

2009 ◽  
Vol 29 (1) ◽  
pp. 171-180 ◽  
Author(s):  
Alec J. Davidson ◽  
Oscar Castanon-Cervantes ◽  
Tanya L. Leise ◽  
Penny C. Molyneux ◽  
Mary E. Harrington

2019 ◽  
Vol 1 (3) ◽  
pp. 290-305 ◽  
Author(s):  
Jonathan Sun ◽  
Deborah A. M. Joye ◽  
Andrew H. Farkas ◽  
Michael R. Gorman

Exposure of mice to a 24 h light:dark:light:dark (LDLD) cycle with dimly illuminated nights induces the circadian timing system to program two intervals of activity and two intervals of rest per 24 h cycle and subsequently allows entrainment to a variety of extraordinary light regimens including 30 h LDLD cycles. Little is known about critical lighting requirements to induce and maintain this non-standard entrainment pattern, termed “bifurcation,” and to enhance the range of apparent entrainment. The current study determined the necessary duration of the photophase for animals to bifurcate and assessed whether requirements for maintenance differed from those for induction. An objective index of bifurcated entrainment varied with length of the photophase over 4–10 h durations, with highest values at 8 h. To assess photic requirements for the maintenance of bifurcation, mice from each group were subsequently exposed to the LDLD cycle with 4 h photophases. While insufficient to induce bifurcation, this photoperiod maintained bifurcation in mice transferred from inductive LDLD cycles. Entrainment to 30 h LDLD cycles also varied with photoperiod duration. These studies characterize non-invasive tools that reveal latent flexibility in the circadian control of rest/activity cycles with important translational potential for addressing needs of human shift-workers.


Sign in / Sign up

Export Citation Format

Share Document