Strong resetting of the mammalian clock by constant light followed by constant darkness
Open accessAbstract
The mammalian molecular circadian clock in the suprachiasmatic nuclei (SCN) regulates locomotor activity rhythms as well as clocks in peripheral tissues (Reppert and Weaver, 2002; Ko and Takahashi, 2006). Constant light (LL) can induce behavioral and physiological arrhythmicity by desynchronizing clock cells in the SCN (Ohta et al., 2005). We examined how the disordered clock cells resynchronize by probing the molecular clock and measuring behavior in mice transferred from LL to constant darkness (DD). The circadian locomotor activity rhythms disrupted in LL become robustly rhythmic again from the beginning of DD, and the starting phase of the rhythm in DD is specific, not random, suggesting that the desynchronized clock cells are quickly reset in an unconventional manner by the L/D transition. By measuring mPERIOD protein rhythms, we showed that the SCN and peripheral tissue clocks quickly become rhythmic again in phase with the behavioral rhythms. We propose that this resetting mechanism may be different from conventional phase shifting, which involves light induction of Period genes (Albrecht et al., 1997; Shearman et al., 1997; Shigeyoshi et al., 1997). Using our functional insights, we could shift the circadian phase of locomotor activity rhythms by 12 h using a 15 h LL treatment: essentially producing phase reversal by a single light pulse, a feat that has not been reported previously in wild-type mice and that has potential clinical utility.
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Both the endogenous circadian timing system and exposure to ambient light influence cognition and affective state.
“Both the endogenous circadian timing system and exposure to ambient light are known to influence cognition and affective state (Chaudhury and Colwell, 2002; Chen et al., 2008; Gonzalez and Aston-Jones, 2008; Hampp et al., 2008; Ruby et al., 2008).”
From Biological rhythms, higher brain function, and behavior: Gaps, opportunities, and challenges (2009) · cites this paper as Chen et al., 2008
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Cites
Coordination of circadian timing in mammals
Reppert, S. M., & Weaver, D. R. (2002) · Nature · doi:10.1038/nature00965 · Cited by 4,379 · see citing works
The Geometry of Biological Time
Winfree, A. T. (1980) · doi:10.1007/978-3-662-22492-2 · Cited by 3,613 · see citing works
Damiola, F., Le Minh, N., Preitner, N., Kornmann, B., Fleury-Olela, F., & Schibler, U. (2000) · Genes & Development · doi:10.1101/gad.183500 · Cited by 2,394 · see citing works
Yoo, S.-H., Yamazaki, S., Lowrey, P. L., Shimomura, K., Ko, C. H., Buhr, E. D., Siepka, S. M., Hong, H.-K., Oh, W. J., Yoo, O. J., et al. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0308709101 · Cited by 2,329 · see citing works
Resetting central and peripheral circadian oscillators in transgenic rats
Yamazaki, S., Numano, R., Abe, M., Hida, A., Takahashi, R.-I., Ueda, M., Block, G. D., Sakaki, Y., Menaker, M., & Tei, H. (2000) · Science · doi:10.1126/science.288.5466.682 · Cited by 1,907 · see citing works
Resetting of circadian time in peripheral tissues by glucocorticoid signaling
Balsalobre, A., Brown, S. A., Marcacci, L., Tronche, F., Kellendonk, C., Reichardt, H. M., Schütz, G., & Schibler, U. (2000) · Science · doi:10.1126/science.289.5488.2344 · Cited by 1,859 · see citing works
Entrainment of the circadian clock in the liver by feeding
Stokkan, K.-A., Yamazaki, S., Tei, H., Sakaki, Y., & Menaker, M. (2001) · Science · doi:10.1126/science.291.5503.490 · Cited by 1,800 · see citing works
Molecular components of the mammalian circadian clock
Ko, C. H., & Takahashi, J. S. (2006) · Human Molecular Genetics · doi:10.1093/hmg/ddl207 · Cited by 1,657 · see citing works
Pittendrigh, C. S., & Daan, S. (1976) · Journal of Comparative Physiology ? A · doi:10.1007/bf01417860 · Cited by 1,636 · see citing works
Exogenous and Endogenous Components in Circadian RhythmsPreprint
Aschoff, J. (1960) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.1960.025.01.004 · Cited by 1,487 · see citing works
Molecular analysis of mammalian circadian rhythms
Reppert, S. M., & Weaver, D. R. (2001) · Annual Review of Physiology · doi:10.1146/annurev.physiol.63.1.647 · Cited by 1,444 · see citing works
Hattar, S., Lucas, R. J., Mrosovsky, N., Thompson, S., Douglas, R. H., Hankins, M. W., Lem, J., Biel, M., Hofmann, F., Foster, R. G., et al. (2003) · Nature · doi:10.1038/nature01761 · Cited by 1,245 · see citing works
Health disorders of shift workers
Knutsson, A. (2003) · Occupational Medicine · doi:10.1093/occmed/kqg048 · Cited by 1,218 · see citing works
A clockwork web: circadian timing in brain and periphery, in health and disease
Hastings, M. H., Reddy, A. B., & Maywood, E. S. (2003) · Nature reviews. Neuroscience · doi:10.1038/nrn1177 · Cited by 1,189 · see citing works
Posttranslational Mechanisms Regulate the Mammalian Circadian Clock
Lee, C., Etchegaray, J., Cagampang, F. R. A., Loudon, A. S. I., & Reppert, S. M. (2001) · Cell · doi:10.1016/s0092-8674(01)00610-9 · Cited by 1,158 · see citing works
Self-citationCircadian rhythms from flies to human
Panda, S., Hogenesch, J. B., & Kay, S. A. (2002) · Nature · doi:10.1038/417329a · Cited by 1,044 · see citing works
Circadian Gene Expression in Individual Fibroblasts
Nagoshi, E., Saini, C., Bauer, C. R., Laroche, T., Naef, F., & Schibler, U. (2004) · Cell · doi:10.1016/j.cell.2004.11.015 · Cited by 1,003 · see citing works
Bright Light Induction of Strong (Type 0) Resetting of the Human Circadian Pacemaker
Czeisler, C. A., Kronauer, R. E., Allan, J. S., Duffy, J. F., Jewett, M. E., Brown, E. N., & Ronda, J. M. (1989) · Science · doi:10.1126/science.2734611 · Cited by 946 · see citing works
Shigeyoshi, Y., Taguchi, K., Yamamoto, S., Takekida, S., Yan, L., Tei, H., Moriya, T., Shibata, S., Loros, J. J., Dunlap, J. C., et al. (1997) · Cell · doi:10.1016/s0092-8674(00)80494-8 · Cited by 891 · see citing works
A Differential Response of Two Putative Mammalian Circadian Regulators, mper1and mper2, to Light
Albrecht, U., Sun, Z. S., Eichele, G., & Lee, C. C. (1997) · Cell · doi:10.1016/s0092-8674(00)80495-x · Cited by 879 · see citing works
Self-citationPositional Syntenic Cloning and Functional Characterization of the Mammalian Circadian Mutation tau
Lowrey, P. L., Shimomura, K., Antoch, M. P., Yamazaki, S., Zemenides, P. D., Ralph, M. R., Menaker, M., & Takahashi, J. S. (2000) · Science · doi:10.1126/science.288.5465.483 · Cited by 860 · see citing works
Silver, R., LeSauter, J., Tresco, P. A., & Lehman, M. N. (1996) · Nature · doi:10.1038/382810a0 · Cited by 792 · see citing works
Two period Homologs: Circadian Expression and Photic Regulation in the Suprachiasmatic Nuclei
Shearman, L. P., Zylka, M. J., Weaver, D. R., Kolakowski, L. F., & Reppert, S. M. (1997) · Neuron · doi:10.1016/s0896-6273(00)80417-1 · Cited by 781 · see citing works
Melanopsin is required for non-image-forming photic responses in blind mice
Panda, S., Provencio, I., Tu, D. C., Pires, S. S., Rollag, M. D., Castrucci, A. M., Pletcher, M. T., Sato, T. K., Wiltshire, T., Andahazy, M., et al. (2003) · Science · doi:10.1126/science.1086179 · Cited by 711 · see citing works
Intercellular Coupling Confers Robustness against Mutations in the SCN Circadian Clock Network
Liu, A. C., Welsh, D. K., Ko, C. H., Tran, H. G., Zhang, E. E., Priest, A. A., Buhr, E. D., Singer, O., Meeker, K., Verma, I. M., et al. (2007) · Cell · doi:10.1016/j.cell.2007.02.047 · Cited by 694 · see citing works
Multiple signaling pathways elicit circadian gene expression in cultured Rat-1 fibroblasts
Balsalobre, A., Marcacci, L., & Schibler, U. (2000) · Current Biology · doi:10.1016/s0960-9822(00)00758-2 · Cited by 485 · see citing works
Constant light desynchronizes mammalian clock neurons
Ohta, H., Yamazaki, S., & McMahon, D. G. (2005) · Nature Neuroscience · doi:10.1038/nn1395 · Cited by 405 · see citing works
Entrainment of Circadian Programs
Johnson, C. H., Elliott, J. A., & Foster, F. (2003) · Chronobiology International · doi:10.1081/cbi-120024211 · Cited by 380 · see citing works
<i>mPer1</i> and <i>mPer2</i> Are Essential for Normal Resetting of the Circadian Clock
Albrecht, U., Zheng, B., Larkin, D., Sun, Z. S., & Lee, C. C. (2001) · Journal of Biological Rhythms · doi:10.1177/074873001129001791 · Cited by 375 · see citing works
Self-citationOverview of circadian rhythms.
Vitaterna, M. H., Takahashi, J. S., & Turek, F. W. (2001) · PubMed · Cited by 353 · see citing works
Stopping Time: The Genetics of Fly and Mouse Circadian Clocks
Allada, R., Emery, P., Takahashi, J. S., & Rosbash, M. (2001) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.24.1.1091 · Cited by 315 · see citing works
Circadian timekeeping in BALB/c and C57BL/6 inbred mouse strains
Schwartz, W., & Zimmerman, P. (1990) · Journal of Neuroscience · doi:10.1523/jneurosci.10-11-03685.1990 · Cited by 315 · see citing works
A functional analysis of circadian pacemakers in nocturnal rodents
Daan, S., & Pittendrigh, C. S. (1976) · Journal of Comparative Physiology A · doi:10.1007/bf01417858 · Cited by 301 · see citing works
Adrenergic regulation of clock gene expression in mouse liver
Terazono, H., Mutoh, T., Yamaguchi, S., Kobayashi, M., Akiyama, M., Udo, R., Ohdo, S., Okamura, H., & Shibata, S. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0936797100 · Cited by 293 · see citing works
Vitaterna, M. H., Ko, C. H., Chang, A., Buhr, E. D., Fruechte, E. M., Schook, A. C., Antoch, M. P., Turek, F. W., & Takahashi, J. S. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0603601103 · Cited by 222 · see citing works
Suprachiasmatic nucleus: a central autonomic clock
Ueyama, T., Krout, K. E., Nguyen, X. V., Karpitskiy, V. V., Kollert, A., Mettenleiter, T. C., & Loewy, A. D. (1999) · Nature Neuroscience · doi:10.1038/15973 · Cited by 188 · see citing works
Redlin, U. (2001) · Chronobiology International · doi:10.1081/cbi-100107511 · Cited by 170 · see citing works
Low-Zeddies, S. S., & Takahashi, J. S. (2001) · Cell · doi:10.1016/s0092-8674(01)00294-x · Cited by 147 · see citing works
Comas, M., Beersma, D. G. M., Spoelstra, K., & Daan, S. (2006) · Journal of Biological Rhythms · doi:10.1177/0748730406292446 · Cited by 109 · see citing works
The Suprachiasmatic Nucleus: A Clock of Multiple Components
Lee, H. S., Billings, H., & Lehman, M. N. (2003) · Journal of Biological Rhythms · doi:10.1177/0748730403259106 · Cited by 89 · see citing works
Sudo, M., Sasahara, K., Moriya, T., Akiyama, M., Hamada, T., & Shibata, S. (2003) · Neuroscience · doi:10.1016/s0306-4522(03)00457-3 · Cited by 88 · see citing works
Light-Induced Phase Shifts in tau Mutant Hamsters
Shimomura, K., & Menaker, M. (1994) · Journal of Biological Rhythms · doi:10.1177/074873049400900201 · Cited by 87 · see citing works
Effects of Preparation Time on Phase of Cultured Tissues Reveal Complexity of Circadian Organization
Yoshikawa, T., Yamazaki, S., & Menaker, M. (2005) · Journal of Biological Rhythms · doi:10.1177/0748730405280775 · Cited by 83 · see citing works
Skopik, S. D., & Pittendrigh, C. S. (1967) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.58.5.1862 · Cited by 81 · see citing works
Muñoz, M., Peirson, S. N., Hankins, M. W., & Foster, F. (2005) · Journal of Biological Rhythms · doi:10.1177/0748730404272858 · Cited by 49 · see citing works
Multiple Photopigments Entrain the Mammalian Circadian Oscillator
Panda, S. (2007) · Neuron · doi:10.1016/j.neuron.2007.02.017 · Cited by 32 · see citing works
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Physiology of Circadian Entrainment
Golombek, D. A., & Rosenstein, R. E. (2010) · Physiological Reviews · doi:10.1152/physrev.00009.2009 · Cited by 1,103 · see citing works
Tranah, G. J., Blackwell, T., Stone, K. L., Ancoli‐Israel, S., Paudel, M. L., Ensrud, K. E., Cauley, J. A., Redline, S., Hillier, T. A., Cummings, S. R., et al. (2011) · Annals of Neurology · doi:10.1002/ana.22468 · Cited by 525 · see citing works
Insulin/IGF-1 Drives PERIOD Synthesis to Entrain Circadian Rhythms with Feeding Time
Crosby, P., Hamnett, R., Putker, M., Hoyle, N. P., Reed, M., Karam, C. J., Maywood, E. S., Stangherlin, A., Chesham, J. E., Hayter, E. A., et al. (2019) · Cell · doi:10.1016/j.cell.2019.02.017 · Cited by 309 · see citing works
Light and Cognition: Roles for Circadian Rhythms, Sleep, and Arousal
Fisk, A. S., Tam, S. K. E., Brown, L. A., Vyazovskiy, V. V., Bannerman, D. M., & Peirson, S. N. (2018) · Frontiers in Neurology · doi:10.3389/fneur.2018.00056 · Cited by 278 · see citing works
Coomans, C. P., van den Berg, S. A. A., Houben, T., van Klinken, J., van den Berg, R., Pronk, A. C. M., Havekes, L. M., Romijn, J. A., van Dijk, K. W., Biermasz, N. R., et al. (2013) · The FASEB Journal · doi:10.1096/fj.12-210898 · Cited by 252 · see citing works
Chen, R., Schirmer, A. E., Lee, Y., Lee, H.-M., Kumar, V., Yoo, S. H., Takahashi, J. S., & Lee, C. (2009) · Molecular Cell · doi:10.1016/j.molcel.2009.10.012 · Cited by 225 · see citing works
Self-citationBunney, B. G., & Bunney, W. E. (2013) · Biological Psychiatry · doi:10.1016/j.biopsych.2012.07.020 · Cited by 181 · see citing works
Environmental 24-hr Cycles Are Essential for Health
Lucassen, E. A., Coomans, C. P., van Putten, M., de Kreij, S. R., van Genugten, J. H. L. T., Sutorius, R. P. M., de Rooij, K. E., van der Velde, M., Verhoeve, S. L., Smit, J. W. A., et al. (2016) · Current Biology · doi:10.1016/j.cub.2016.05.038 · Cited by 129 · see citing works
miRNAs Are Required for Generating a Time Delay Critical for the Circadian Oscillator
Chen, R., D'Alessandro, M. R., & Lee, C. (2013) · Current Biology · doi:10.1016/j.cub.2013.08.005 · Cited by 127 · see citing works
Self-citationBiological rhythms, higher brain function, and behavior: Gaps, opportunities, and challenges
Benca, R., Duncan, M. J., Frank, E., McClung, C., Nelson, R. J., & Vicentic, A. (2009) · Brain Research Reviews · doi:10.1016/j.brainresrev.2009.09.005 · Cited by 125 · see citing works
Tamm, A., Lagerquist, O., Ley, A. L., & Collins, D. F. (2009) · Journal of Biological Rhythms · doi:10.1177/0748730409334135 · Cited by 109 · see citing works
Xin, H., Deng, F., Zhou, M., Huang, R., Ma, X., Tian, H., Tan, Y. H., Chen, X., Deng, D., Shui, G., et al. (2021) · iScience · doi:10.1016/j.isci.2021.102335 · Cited by 60 · see citing works
Unfried, C., Ansari, N., Yasuo, S., Korf, H., & von Gall, C. (2009) · Endocrinology · doi:10.1210/en.2009-0609 · Cited by 59 · see citing works
Circadian rhythms in skin and other elastic tissues
Sherratt, M. J., Hopkinson, L., Naven, M. A., Hibbert, S. A., Ozols, M., Eckersley, A., Newton, V. L., Bell, M., & Meng, Q. (2019) · Matrix Biology · doi:10.1016/j.matbio.2019.08.004 · Cited by 53 · see citing works
Stability of Wake-Sleep Cycles Requires Robust Degradation of the PERIOD Protein
D'Alessandro, M. R., Beesley, S., Kim, J. K., Jones, Z., Chen, R., Wi, J., Kyle, K. E., Vera, D. L., Pagano, M., Nowakowski, R. S., et al. (2017) · Current Biology · doi:10.1016/j.cub.2017.10.014 · Cited by 52 · see citing works
Self-citationA tunable artificial circadian clock in clock-defective mice
D'Alessandro, M. R., Beesley, S., Kim, J. K., Chen, R., Abich, E., Cheng, W. Y., Yi, P., Takahashi, J. S., & Lee, C. (2015) · Nature Communications · doi:10.1038/ncomms9587 · Cited by 52 · see citing works
Self-citationIs sleep disruption a risk factor for Alzheimer's disease?
Macedo, A. C., Balouch, S., & Tabet, N. (2017) · Journal of Alzheimer’s Disease · doi:10.3233/jad-161287 · Cited by 49 · see citing works
Yamamuro, D., Takahashi, M., Nagashima, S., Wakabayashi, T., Yamazaki, H., Takei, A., Takei, S., Sakai, K., Ebihara, K., Iwasaki, Y., et al. (2020) · PLoS ONE · doi:10.1371/journal.pone.0234439 · Cited by 45 · see citing works
The noradrenaline reuptake inhibitor atomoxetine phase-shifts the circadian clock in mice
O'Keeffe, S., Thome, J., & Coogan, A. N. (2011) · Neuroscience · doi:10.1016/j.neuroscience.2011.11.002 · Cited by 43 · see citing works
CRYPTOCHROMES confer robustness, not rhythmicity, to circadian timekeeping
Putker, M., Wong, D., Seinkmane, E., Rzechorzek, N. M., Zeng, A., Hoyle, N. P., Chesham, J. E., Edwards, M. D., Feeney, K. A., Fischer, R., et al. (2021) · The EMBO Journal · doi:10.15252/embj.2020106745 · Cited by 41 · see citing works
Phase-Shifting the Fruit Fly Clock without Cryptochrome
Kistenpfennig, C., Hirsh, J., Yoshii, T., & Helfrich‐Förster, C. (2012) · Journal of Biological Rhythms · doi:10.1177/0748730411434390 · Cited by 36 · see citing works
Fathallah‐Shaykh, H. M., Bona, J. L., & Kadener, S. (2009) · Biophysical Journal · doi:10.1016/j.bpj.2009.08.018 · Cited by 32 · see citing works
Getting lost: the fungal hijacking of ant foraging behaviour in space and time
Trinh, T., Ouellette, R., & de Bekker, C. (2021) · Animal Behaviour · doi:10.1016/j.anbehav.2021.09.003 · Cited by 28 · see citing works
Parkinson's Disease, Lights and Melanocytes: Looking Beyond the Retina
Willis, G. L., Moore, C., & Armstrong, S. M. (2014) · Scientific Reports · doi:10.1038/srep03921 · Cited by 20 · see citing works
Tuning up an aged clock: Circadian clock regulation in metabolism and aging
Sato, S., Solanas, G., Sassone‐Corsi, P., & Benitah, S. A. (2021) · Translational Medicine of Aging · doi:10.1016/j.tma.2021.11.003 · Cited by 21 · see citing works
The embryonic pineal gland of the chicken as a model for experimental jet lag
Kommedal, S., CSERNUS, V. J., & Nagy, A. D. (2013) · General and Comparative Endocrinology · doi:10.1016/j.ygcen.2013.04.006 · Cited by 18 · see citing works
Constant Light Dysregulates Cochlear Circadian Clock and Exacerbates Noise-Induced Hearing Loss
Yang, C., Hwang, C., Chuang, J., Lian, W., Wang, F., Huang, E. I., & Yang, M. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21207535 · Cited by 18 · see citing works
Protocol for setup and circadian analysis of inverted feeding in mice
Xin, H., Huang, R., Zhou, M., Bao, X., Chen, J., Zeng, F., Wan, X., Tong, S., Deng, F., Li, M., et al. (2021) · STAR Protocols · doi:10.1016/j.xpro.2021.100701 · Cited by 12 · see citing works
Circadian rhythm and myocardial infarction
Škrlec, I. (2019) · Medicina · doi:10.21860/medflum2019_216321 · Cited by 10 · see citing works
Circadian Rhythms in Older Adults
Tranah, G. J., Stone, K. L., & Ancoli‐Israel, S. (2016) · Elsevier eBooks · doi:10.1016/b978-0-323-24288-2.00154-9 · Cited by 10 · see citing works
Myocardial Infarction and Circadian Rhythm
Škrlec, I., Marić, S., & Včev, A. (2019) · IntechOpen eBooks · doi:10.5772/intechopen.83393 · Cited by 7 · see citing works
Lengthened circadian rhythms in mice with self-controlled ambient light intensity
Ogasawara, J., Matsumoto, N., Takeuchi, Y., Yamashiro, K., Yasui, M., & Ikegaya, Y. (2024) · Scientific Reports · doi:10.1038/s41598-024-58415-x · Cited by 8 · see citing works
Does a Red House Affect Rhythms in Mice with a Corrupted Circadian System?
Öztürk, M., Ingenwerth, M., Sager, M., von Gall, C., & Ali, A. A. H. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22052288 · Cited by 6 · see citing works
Jasińska, M., Jasek-Gajda, E., Ziaja, M., Litwin, J. A., LIS, G. J., & Pyza, E. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms252312870 · Cited by 5 · see citing works
Association Between Phase Shifts, Expression Levels, and Amplitudes in Peripheral Circadian Clocks
Barnea, M., Sherman, H., Genzer, Y., & Froy, O. (2013) · Chronobiology International · doi:10.3109/07420528.2012.754456 · Cited by 5 · see citing works
Prolonged Light Exposure Induces Circadian Impairment in Aquaporin-4-Knockout Mice
Murakami, A., Tsuji, K., Isoda, M., Matsuo, M., Abe, Y., Yasui, M., Okamura, H., & Tominaga, K. (2023) · Journal of Biological Rhythms · doi:10.1177/07487304221146242 · Cited by 5 · see citing works
Richardson, M. E. S., Browne, C.-A., & Mazariegos, C. I. H. (2023) · Scientific Reports · doi:10.1038/s41598-023-41029-0 · Cited by 4 · see citing works
Modeling of Regulatory Networks
Scribner, E. Y., & Fathallah‐Shaykh, H. M. (2010) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/b978-0-12-381270-4.00002-0 · Cited by 3 · see citing works
Oh, C. E., Lim, H. J., Park, J., Moon, E., & Park, J. K. (2022) · Clinical Psychopharmacology and Neuroscience · doi:10.9758/cpn.2022.20.4.649 · Cited by 2 · see citing works
Circadian responses to non-photic treatments in BTBR mice
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Krilis, G., Costello, H. M., Turner, F. S., Little, R., Komolova, A., Nespoux, J., Czopek, A., Dunbar, D. R., Bailey, M. A., & Ivy, J. R. (2025) · Cardiovascular Research · doi:10.1093/cvr/cvaf236 · Cited by 1 · see citing works
Areshidze, D. A., Kozlova, M. A., Anurkina, A. I., & Chernikov, V. P. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27062663 · Cited by 1 · see citing works
Oraebosi, M. I., Baucom, C., & Cao, R. (2026) · Diabetology · doi:10.3390/diabetology7070122 · Cited by 2 · see citing works
The roles of vasoactive intestinal polypeptide in circadian entrainment of suprachiasmatic nucleus
An, S. (2011) · Open Scholarship Institutional Repository (Washington University in St. Louis) · doi:10.7936/k7ff3qch
Richardson, K. (2010) · Palgrave Macmillan UK eBooks · doi:10.1057/9780230299245_3 · Cited by 1 · see citing works
Giannetto, C., Arfuso, F., Rizzo, M. A., Giudice, E., Calapai, F., Guercio, A., Macaluso, G., Giacchino, I., Piccione, G. G., & Cannella, V. (2024) · Chronobiology International · doi:10.1080/07420528.2024.2315217 · Cited by 1 · see citing works
Circadian Sleep-Wake Activity Patterns During Aging
Stone, K. L., & Tranah, G. J. (2017) · Healthy ageing and longevity · doi:10.1007/978-3-319-64543-8_13 · Cited by 1 · see citing works
Circadian and histaminergic regulation of the sleep-wakefulness cycle
Rozov, S. V. (2016) · Työväentutkimus Vuosikirja
Action, time, and uncertainty: two types of temporal uncertainty in cognitive motor control
Schüür, F. (2012) · UCL Discovery (University College London)
Richardson, M. E. S., Browne, C.-A., & Mazariegos, C. I. H. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.04.20.537697
Ambient Darkness and Consumer Behavior
Vo, K. (2023) · doi:10.12794/metadc2179328
Chrisp, R., Masterson, M., Pope, R., Roberts, C. J., Collins, H. M., Watson, D. J., O’Neil, D. S., Aagaard, K. M., Gibson, C. L., Heery, D. M., et al. (2025) · Scientific Reports · doi:10.1038/s41598-025-92938-1
Jandot, A., Calligaro, H., Dianak-Shoori, A., Tartour, K., Sandu, C., Haddjeri, N., Ribelayga, C., Ananthasubramaniam, B., Padmanabhan, K., Felder‐Schmittbuhl, M., et al. (2026) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-026-06298-8
- Authors
- Chen, R., Seo, D.-O., Bell, E., von Gall, C., & Lee, C.
- Affiliations
- Florida State University (US)
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2008-11-12
- Volume
- 28
- Issue
- 46
- Pages
- 11839-11847
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC2626189
- OpenAlex
- W2071360237
- Cited by
- 53
- References
- 46
- Citations by year
- 2026: 3 · 2025: 3 · 2024: 3 · 2023: 4 · 2022: 1 · 2021: 6 · 2020: 2 · 2019: 4 · 2018: 1 · 2017: 3 · 2016: 3 · 2015: 1 · 2014: 1 · 2013: 4 · 2012: 3
- FWCI
- 1.63
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Neuroscience (publishedVersion, cc-by-nc-sa)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- Funders
- National Institutes of Health
- National Institute of Neurological Disorders and Stroke (NS-053616, R01NS053616)
- Topics
- Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Circadian rhythm and melatonin
- Social Sciences › Psychology › Experimental and Cognitive Psychology › Sleep and Work-Related Fatigue
- Life Sciences › Neuroscience › Cognitive Neuroscience › Sleep and Wakefulness Research
- Keywords
- circadian clock, constant light, constant darkness, suprachiasmatic nucleus, clock resetting, phase reversal, locomotor activity rhythm, phase shifting, light pulses, mice
- MeSH terms
- Animals, Biological Clocks, Circadian Rhythm, Darkness, Light, Male, Mice, Inbred C57BL, Motor Activity, Nuclear Proteins, Photic Stimulation, Suprachiasmatic Nucleus, Transcription Factors, Cell Cycle Proteins, Mice, Period Circadian Proteins
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