The Development of Circadian Rhythms: From Animals to Humans

Sleep Medicine Clinics

Volumn 2, Issue 3, 2007, Pages 331-341

  Rivkees, Scott A ^a  

^a YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARGIPRESSIN; ESTROGEN; FLUORODEOXYGLUCOSE F 18; GONADOTROPIN; GROWTH HORMONE; HYDROCORTISONE; MELATONIN; MELATONIN RECEPTOR; PROGESTERONE; TESTOSTERONE; THYROTROPIN; VASOACTIVE INTESTINAL POLYPEPTIDE;

BABOON; BIOLOGICAL RHYTHM; BRAIN REGION; BRAIN VENTRICLE; CHILD DEVELOPMENT; CIRCADIAN RHYTHM; FUNCTIONAL MAGNETIC RESONANCE IMAGING; HORMONE RELEASE; HUMAN; ILLUMINATION; INFANT; LIGHT DARK CYCLE; NERVOUS SYSTEM DEVELOPMENT; NEWBORN; NONHUMAN; OPTIC CHIASM; PHOTOSENSITIVITY; POSITRON EMISSION TOMOGRAPHY; PRIMATE; PRIORITY JOURNAL; REVIEW; SLEEP WAKING CYCLE; SQUIRREL MONKEY; SUPRACHIASMATIC NUCLEUS; UTERUS CONTRACTILITY;

EID: 57149147345     PISSN: 1556407X     EISSN: 15564088     Source Type: Journal    
DOI: 10.1016/j.jsmc.2007.05.010     Document Type: Review

References (84)

1. Panda S., Hogenesch J.B., and Kay S.A. Circadian rhythms from flies to human. Nature 417 6886 (2002) 329-335
2. Ko C.H., and Takahashi J.S. Molecular components of the mammalian circadian clock. Hum Mol Genet 15 Spec No 2 (2006) R271-R277
3. Maywood E.S., O'Neill J., Wong G.K., et al. Circadian timing in health and disease. Prog Brain Res 153 (2006) 253-269
4. Moore-Ede M.C., Czeisler C.A., and Richardson G.S. Circadian timekeeping in health and disease. Part 1. Basic properties of circadian pacemakers. N Engl J Med 309 8 (1983) 469-476
5. Moore-Ede M.C., Czeisler C.A., and Richardson G.S. Circadian timekeeping in health and disease. Part 2. Clinical implications of circadian rhythmicity. N Engl J Med 309 9 (1983) 530-536
6. Arendt J. Melatonin and human rhythms. Chronobiol Int 23 1-2 (2006) 21-37
7. Tofler G.H., and Muller J.E. Triggering of acute cardiovascular disease and potential preventive strategies. Circulation 114 17 (2006) 1863-1872
8. Weaver D.R. The suprachiasmatic nucleus: a 25-year retrospective. J Biol Rhythms 13 2 (1998) 100-112
9. Ebisawa T. Circadian rhythms in the CNS and peripheral clock disorders: human sleep disorders and clock genes. J Pharmacol Sci 103 2 (2007) 150-154
10. Maemura K., Takeda N., and Nagai R. Circadian rhythms in the CNS and peripheral clock disorders: role of the biological clock in cardiovascular diseases. J Pharmacol Sci 103 2 (2007) 134-138
11. Ohdo S. Circadian rhythms in the CNS and peripheral clock disorders: chronopharmacological findings on antitumor drugs. J Pharmacol Sci 103 2 (2007) 155-158
12. Welsh D.K., Logothetis D.E., Meister M., et al. Individual neurons dissociated from rat suprachiasmatic nucleus express independently phased circadian firing rhythms. Neuron 14 4 (1995) 697-706
13. Liu C., Weaver D.R., Strogatz S.H., et al. Cellular construction of a circadian clock: period determination in the suprachiasmatic nuclei. Cell 91 6 (1997) 855-860
14. Morin L.P. The circadian visual system. Brain Res Brain Res Rev 19 1 (1994) 102-127
15. Morin L.P., and Allen C.N. The circadian visual system, 2005. Brain Res Brain Res Rev 51 1 (2006) 1-60
16. Kornhauser J.M., Mayo K.E., and Takahashi J.S. Light, immediate-early genes, and circadian rhythms. Behav Genet 26 3 (1996) 221-240
17. Watts A.G., Swanson L.W., and Sanchez-Watts G. Efferent projections of the suprachiasmatic nucleus: I. Studies using anterograde transport of Phaseolus vulgaris leucoagglutinin in the rat. J Comp Neurol 258 2 (1987) 204-229
18. Watts A.G., and Swanson L.W. Efferent projections of the suprachiasmatic nucleus: II. Studies using retrograde transport of fluorescent dyes and simultaneous peptide immunohistochemistry in the rat. J Comp Neurol 258 2 (1987) 230-252
19. Moore R.Y. Organization of the primate circadian system. J Biol Rhythms 8 Suppl (1993) S3-S9
20. Lydic R., Schoene W.C., Czeisler C.A., et al. Suprachiasmatic region of the human hypothalamus: homolog to the primate circadian pacemaker?. Sleep 2 3 (1980) 355-361
21. Lydic R., Albers H.E., Tepper B., et al. Three-dimensional structure of the mammalian suprachiasmatic nuclei: a comparative study of five species. J Comp Neurol 204 3 (1982) 225-237
22. Lushington K., Galka R., Sassi L.N., et al. Extraocular light exposure does not phase shift saliva melatonin rhythms in sleeping subjects. J Biol Rhythms 17 4 (2002) 377-386
23. Schwartz W.J., Reppert S.M., Eagan S.M., et al. In vivo metabolic activity of the suprachiasmatic nuclei: a comparative study. Brain Res 274 1 (1983) 184-187
24. Rivkees S.A., Hofman P.L., and Fortman J. Newborn primate infants are entrained by low intensity lighting. Proc Natl Acad Sci U S A 94 1 (1997) 292-297
25. Reppert S.M., Perlow M.J., Ungerleider L.G., et al. Effects of damage to the suprachiasmatic area of the anterior hypothalamus on the daily melatonin and cortisol rhythms in the rhesus monkey. J Neurosci 1 12 (1981) 1414-1425
26. Edgar D.M., Dement W.C., and Fuller C.A. Effect of SCN lesions on sleep in squirrel monkeys: evidence for opponent processes in sleep-wake regulation. J Neurosci 13 3 (1993) 1065-1079
27. Schwartz W.J., Busis N.A., and Hedley-Whyte E.T. A discrete lesion of ventral hypothalamus and optic chiasm that disturbed the daily temperature rhythm. J Neurol 233 1 (1986) 1-4
28. Rivkees S. Arrhythmicity in a child with septo-optic dysplasia and establishment of sleep-wake cyclicity with melatonin. J Pediatr 139 (2001) 463-465
29. Friedman D.I., Johnson J.K., Chorsky R.L., et al. Labeling of human retinohypothalamic tract with the carbocyanine dye, DiI. Brain Res 560 1-2 (1991) 297-302
30. Sadun A.A., Schaechter J.D., and Smith L.E. A retinohypothalamic pathway in man: light mediation of circadian rhythms. Brain Res 302 2 (1984) 371-377
31. Campbell S.S., and Murphy P.J. Extraocular circadian phototransduction in humans. Science 279 5349 (1998) 396-399
32. Hebert M., Martin S.K., and Eastman C.I. Nocturnal melatonin secretion is not suppressed by light exposure behind the knee in humans. Neurosci Lett 274 2 (1999) 127-130
33. Foster R.G. Shedding light on the biological clock. Neuron 20 5 (1998) 829-832
34. Jean-Louis G., Kripke D.F., Cole R.J., et al. No melatonin suppression by illumination of popliteal fossae or eyelids. J Biol Rhythms 15 3 (2000) 265-269
35. Weitzman E.D., Czeisler C.A., Zimmerman J.C., et al. Biological rhythms in man: relationship of sleep-wake, cortisol, growth hormone, and temperature during temporal isolation. Adv Biochem Psychopharmacol 28 (1981) 475-499
36. Czeisler C.A., and Klerman E.B. Circadian and sleep-dependent regulation of hormone release in humans. Recent Prog Horm Res 54 (1999) 97-130
37. Reppert S.M., Weaver D.R., and Rivkees S.A. Maternal communication of circadian phase to the developing mammal. Psychoneuroendocrinology 13 1-2 (1988) 63-78
38. Reppert S.M. Interaction between the circadian clocks of mother and fetus. Ciba Found Symp 183 (1995) 198-207 [discuss:198-207]
39. van Eerdenburg F.J., and Rakic P. Early neurogenesis in the anterior hypothalamus of the rhesus monkey. Brain Res Dev Brain Res 79 2 (1994) 290-296
40. Nowell-Morris L., and Faherenbruch C.E. Practical and evolutionary considerations for the use of nonhuman primate model in prenatal research (1985), Alan R. Liss, New York
41. Reppert S.M., Weaver D.R., Rivkees S.A., et al. Putative melatonin receptors in a human biological clock. Science 242 4875 (1988) 78-81
42. Rivkees S.A., and Lachowicz J.E. Functional D1 and D5 dopamine receptors are expressed in the suprachiasmatic, supraoptic, and paraventricular nuclei of primates. Synapse 26 1 (1997) 1-10
43. Reppert S.M., and Schwartz W.J. Functional activity of the suprachiasmatic nuclei in the fetal primate. Neurosci Lett 46 2 (1984) 145-149
44. Jolly A. Hour of birth in primates and man. Folia Primatol 18 1 (1972) 108-121
45. Swaab D.F. Development of the human hypothalamus. Neurochem Res 20 5 (1995) 509-519
46. Glotzbach S.F., Sollars P., and Pagano M. Development of the human retinohypothalamic tract. Soc Neurosci 18 (1992) 857
47. Rivkees S.A., and Hao H. Developing circadian rhythmicity. Semin Perinatol 24 4 (2000) 232-242
48. Boivin D.B., Duffy J.F., Kronauer R.E., et al. Dose-response relationships for resetting of human circadian clock by light. Nature 379 6565 (1996) 540-542
49. Shanahan T.L., and Czeisler C.A. Physiological effects of light on the human circadian pacemaker. Semin Perinatol 24 4 (2000) 299-320
50. Hao H., and Rivkees S.A. The biological clock of very premature primate infants is responsive to light. Proc Natl Acad Sci U S A 96 5 (1999) 2426-2429
51. Seron-Ferre M., Ducsay C.A., and Valenzuela G.J. Circadian rhythms during pregnancy. Endocr Rev 14 5 (1993) 594-609
52. Seron-Ferre M., Torres-Farfan C., Forcelledo M.L., et al. The development of circadian rhythms in the fetus and neonate. Semin Perinatol 25 6 (2001) 363-370
53. Parmelee Jr. A.H. Sleep cycles in infants. Dev Med Child Neurol 11 6 (1969) 794-795
54. Meier-Koll A., Hall U., Hellwig U., et al. A biological oscillator system and the development of sleep-waking behavior during early infancy. Chronobiologia 5 4 (1978) 425-440
55. Kleitman J., and Engelman T.G. Sleep characteristics of infants. J Appl Physiol 6 (1953) 127-134
56. Darnall R.A., Ariagno R.L., and Kinney H.C. The late preterm infant and the control of breathing, sleep, and brainstem development: a review. Clin Perinatol 33 4 (2006) 883-914 [abstract x]
57. Jenni O.G., Deboer T., and Achermann P. Development of the 24-h rest-activity pattern in human infants. Infant Behav Dev 29 2 (2006) 143-152
58. McKay S.M., and Angulo-Barroso R.M. Longitudinal assessment of leg motor activity and sleep patterns in infants with and without down syndrome. Infant Behav Dev 29 2 (2006) 153-168
59. Kennaway D.J., Stamp G.E., and Goble F.C. Development of melatonin production in infants and the impact of prematurity. J Clin Endocrinol Metab 75 2 (1992) 367-369
60. Kennaway D.J., Goble F.C., and Stamp G.E. Factors influencing the development of melatonin rhythmicity in humans. J Clin Endocrinol Metab 81 4 (1996) 1525-1532
61. Beitins I.Z., Kowarski A., Migeon C.J., et al. Adrenal function in normal infants and in marasmus and kwashiorkor: cortisol secretion, diurnal variation of plasma cortisol, and urinary excretion of 17-hydroxycorticoids, free corticoids, and cortisol. J Pediatr 86 2 (1975) 302-308
62. Onishi S., Miyazawa G., Nishimura Y., et al. Postnatal development of circadian rhythm in serum cortisol levels in children. Pediatrics 72 3 (1983) 399-404
63. Price D.A., Close G.C., and Fielding B.A. Age of appearance of circadian rhythm in salivary cortisol values in infancy. Arch Dis Child 58 6 (1983) 454-456
64. Hellbrugge T., Lange J.E., and Rutenfranz J. Circadian periodicity of physiological functions in different stages of infancy and childhood. Ann N Y Acad Sci 117 (1964) 361-373
65. Parmelee Jr. A.H., Wenner W.H., Akiyama Y., et al. Sleep states in premature infants. Dev Med Child Neurol 9 1 (1967) 70-77
66. Rivkees S.A. Developing circadian rhythmicity: basic and clinical aspects. Pediatr Clin North Am 44 2 (1997) 467-487
67. D'Souza S.W., Tenreiro S., Minors D., et al. Skin temperature and heart rate rhythms in infants of extreme prematurity. Arch Dis Child 67 7 Spec No (1992) 784-788
68. Anders T.F., Keener M.A., and Kraemer H. Sleep-wake state organization, neonatal assessment and development in premature infants during the first year of life. II. Sleep 8 3 (1985) 193-206
69. Glotzbach S.F., Edgar D.M., Boeddiker M., et al. Biological rhythmicity in normal infants during the first 3 months of life. Pediatrics 94 4 Pt 1 (1994) 482-488
70. Glotzbach S.F., Edgar D.M., and Ariagno R.L. Biological rhythmicity in preterm infants prior to discharge from neonatal intensive care. Pediatrics 95 2 (1995) 231-237
71. Rivkees S.A., Mayes L., Jacobs H., et al. Rest-activity patterns of premature infants are regulated by cycled lighting. Pediatrics 113 4 (2004) 833-839
72. Mirmiran M., and Ariagno R.L. Influence of light in the NICU on the development of circadian rhythms in preterm infants. Semin Perinatol 24 4 (2000) 247-257
73. Mann N.P., Haddow R., Stokes L., et al. Effect of night and day on preterm infants in a newborn nursery: randomised trial. Br Med J (Clin Res Ed) 293 6557 (1986) 1265-1267
74. Brandon D.H., Holditch-Davis D., and Belyea M. Preterm infants born at less than 31 weeks' gestation have improved growth in cycled light compared with continuous near darkness. J Pediatr 140 2 (2002) 192-199
75. Mirmiran M., and Lunshof S. Perinatal development of human circadian rhythms. Prog Brain Res 111 (1996) 217-226
76. McGraw K., Hoffmann R., Harker C., et al. The development of circadian rhythms in a human infant. Sleep 22 3 (1999) 303-310
77. Ariagno R.L., and Mirmiran M. Shedding light on the very low birth weight infant. J Pediatr 139 4 (2001) 476-477
78. Glass P., Avery G.B., Subramanian K.N., et al. Effect of bright light in the hospital nursery on the incidence of retinopathy of prematurity. N Engl J Med 313 7 (1985) 401-404
79. Fielder A.R., and Moseley M.J. Environmental light and the preterm infant. Semin Perinatol 24 4 (2000) 291-298
80. Reynolds J.D., Hardy R.J., Kennedy K.A., et al. Lack of efficacy of light reduction in preventing retinopathy of prematurity: light reduction in retinopathy of prematurity (LIGHT-ROP) cooperative group. N Engl J Med 338 22 (1998) 1572-1576
81. Kennedy K.A., Fielder A.R., Hardy R.J., et al. Reduced lighting does not improve medical outcomes in very low birth weight infants. J Pediatr 139 4 (2001) 527-531
82. Als H., Lawhon G., Duffy F.H., et al. Individualized developmental care for the very low-birth-weight preterm infant: medical and neurofunctional effects. JAMA 272 11 (1994) 853-858
83. Ariagno R.L., Thoman E.B., Boeddiker M.A., et al. Developmental care does not alter sleep and development of premature infants. Pediatrics 100 6 (1997) E9
84. Symington A, Pinelli J. Developmental care for promoting development and preventing morbidity in preterm infants. Cochrane Database Syst Rev 2006;2:CD001814.