Age-dependent changes in the circadian system of the mouse will be examined as a model of the same changes in man. The disintegration of the circadian rhythm of sleep-wakefulness in the age and exercise (wheel-running) restriction experiments documented in our previous grant will be studied in greater detail. The body temperature rhythm will be added to the existing automated EEG scoring system to enable assessment or the phase relationships among the sleep/wake, activity, and body temperature rhythms both during the aging process and during exercise restriction in young and aged mice. An additional activity measurement will be added to provide an index of activity during the exercise restriction experiments. We also intend to: 1) examine the temporal order among the sleep/wake, body temperature, activity and drinking rhythms in young and old animals as well as in exercise-restricted animals; 2) directly test the hypothesis that the age and exercise-restriction effects on the sleep/wake rhythm are mediated through the circadian system; 3) attempt to ameliorate the age-dependent decay in the sleep/wake rhythm by restricting wheel availability to a specific time of day; 4) evaluate whether the young mouse exhibits a circadian phase-dependent sensitivity to exercise restriction; 5) examine whether the deterioration of the sleep/wake rhythm in the aged animal is accompanied by a decrement in the benzodiazepine receptor rhythm; 6) measure local cerebral glucose metabolism using the [14C] 2-deoxyglucose technique in young and aged mice to attempt to identify the neural basis of the age-dependent decay or circadian organization, with particular attention to the metabolic activity of the suprachiasmatic nucleus (SCN); and 7) attempt to consolidate the sleep/wake rhythm in an animal whose circadian system has been experimentally disrupted by lesion of the SCN. We anticipate that these experiments will elucidate mechanisms underlying the age-dependent decay of circadian organization in the mouse and that these principles should be generalizable to sleep disturbances observed in aged humans.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Research Project (R01)
Project #
1R01AG006490-01
Application #
3562474
Study Section
(SSS)
Project Start
1986-09-01
Project End
1991-08-31
Budget Start
1986-09-01
Budget End
1987-08-31
Support Year
1
Fiscal Year
1986
Total Cost
Indirect Cost
Name
Stanford University
Department
Type
DUNS #
800771545
City
Stanford
State
CA
Country
United States
Zip Code
94305
Kas, M J; Edgar, D M (1999) A nonphotic stimulus inverts the diurnal-nocturnal phase preference in Octodon degus. J Neurosci 19:328-33
Kas, M J; Edgar, D M (1998) Crepuscular rhythms of EEG sleep-wake in a hystricomorph rodent, Octodon degus. J Biol Rhythms 13:9-17
Edgar, D M; Reid, M S; Dement, W C (1997) Serotonergic afferents mediate activity-dependent entrainment of the mouse circadian clock. Am J Physiol 273:R265-9
Bradbury, M J; Dement, W C; Edgar, D M (1997) Serotonin-containing fibers in the suprachiasmatic hypothalamus attenuate light-induced phase delays in mice. Brain Res 768:125-34
Glotzbach, S F; Edgar, D M; Ariagno, R L (1995) Biological rhythmicity in preterm infants prior to discharge from neonatal intensive care. Pediatrics 95:231-7
Seidel, W F; Maze, M; Dement, W C et al. (1995) Alpha-2 adrenergic modulation of sleep: time-of-day-dependent pharmacodynamic profiles of dexmedetomidine and clonidine in the rat. J Pharmacol Exp Ther 275:263-73
Edgar, D M (1994) Sleep-wake circadian rhythms and aging: potential etiologies and relevance to age-related changes in integrated physiological systems. Neurobiol Aging 15:499-501
Prosser, R A; Edgar, D M; Heller, H C et al. (1994) A possible glial role in the mammalian circadian clock. Brain Res 643:296-301
Glotzbach, S F; Edgar, D M; Boeddiker, M et al. (1994) Biological rhythmicity in normal infants during the first 3 months of life. Pediatrics 94:482-8
Dantz, B; Edgar, D M; Dement, W C (1994) Circadian rhythms in narcolepsy: studies on a 90 minute day. Electroencephalogr Clin Neurophysiol 90:24-35

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