Due to orbital mechanics, current space shuttle programs routinely require astronauts to repeatedly shift their sleep-wake schedules to an earlier hour during their approximately 2-week missions. This is achieved in some missions by imposing a sleep- wake schedule on a day length averaging 23.5-h. NASA's planned exploration class mission to Mars, currently scheduled for 2018, will require crew members to adapt to the 24.65-h Martian solar day throughout their approximately 540 day stay on Mars. However, the plasticity of the human circadian pacemaker's intrinsic period, which has recently been shown to average 24.1- 24.2 h immediately after release from entrainment to the 24-h day and which is a key determinant of the pacemaker's ability to adapt to such non-24-hour schedules, has not been systematically investigated. Data collected in animal studies provides considerable evidence that the intrinsic circadian period is affected by past history. Since the ability of astronauts to sustain a high level of performance during exploration class missions will be critically dependent upon the ability of the human circadian pacemaker to adapt to such non-24-hour day lengths, we propose to determine whether the intrinsic period of the human circadian pacemaker can be influenced by prior entrainment to non-24 hour day lengths. Specifically, we propose to test the following hypotheses: i) that entrainment of the human circadian pacemaker to a shorter- than-24-hour sleep-wake schedule will shorten the period of the circadian pacemaker; ii) that entrainment of the human circadian pacemaker to a longer-than-24-hour sleep-wake schedule will lengthen the period of the circadian pacemaker; iii) that the phase angle of entrainment to an imposed non-24-hour day will be strongly related to the period of the circadian pacemaker. The results of the proposed studies will answer fundamental questions on the mechanisms underlying circadian entrainment in humans and lead to the development of space flight countermeasures such as pre-adaptation of astronauts to non-24-hour days prior to space flight.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS041886-04
Application #
6785340
Study Section
Special Emphasis Panel (ZRG1-IFCN-3 (01))
Program Officer
Mitler, Merrill
Project Start
2001-09-04
Project End
2007-08-31
Budget Start
2004-09-01
Budget End
2007-08-31
Support Year
4
Fiscal Year
2004
Total Cost
$317,500
Indirect Cost
Name
Brigham and Women's Hospital
Department
Type
DUNS #
030811269
City
Boston
State
MA
Country
United States
Zip Code
02115
Burke, Tina M; Scheer, Frank A J L; Ronda, Joseph M et al. (2015) Sleep inertia, sleep homeostatic and circadian influences on higher-order cognitive functions. J Sleep Res 24:364-371
Lacoste, Alix M B; Schoppik, David; Robson, Drew N et al. (2015) A convergent and essential interneuron pathway for Mauthner-cell-mediated escapes. Curr Biol 25:1526-34
Chang, Anne-Marie; Buch, Alison M; Bradstreet, Dayna S et al. (2011) Human diurnal preference and circadian rhythmicity are not associated with the CLOCK 3111C/T gene polymorphism. J Biol Rhythms 26:276-9
Scheuermaier, Karine; Laffan, Alison M; Duffy, Jeanne F (2010) Light exposure patterns in healthy older and young adults. J Biol Rhythms 25:113-22
Scheer, Frank A J L; Wright Jr, Kenneth P; Kronauer, Richard E et al. (2007) Plasticity of the intrinsic period of the human circadian timing system. PLoS One 2:e721