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Restricted feeding uncouples circadian oscillators in peripheral tissues from the central pacemaker in the suprachiasmatic nucleus
Open accessAbstract
In mammals, circadian oscillators exist not only in the suprachiasmatic nucleus, which harbors the central pacemaker, but also in most peripheral tissues. It is believed that the SCN clock entrains the phase of peripheral clocks via chemical cues, such as rhythmically secreted hormones. Here we show that temporal feeding restriction under light–dark or dark–dark conditions can change the phase of circadian gene expression in peripheral cell types by up to 12 h while leaving the phase of cyclic gene expression in the SCN unaffected. Hence, changes in metabolism can lead to an uncoupling of peripheral oscillators from the central pacemaker. Sudden large changes in feeding time, similar to abrupt changes in the photoperiod, reset the phase of rhythmic gene expression gradually and are thus likely to act through a clock-dependent mechanism. Food-induced phase resetting proceeds faster in liver than in kidney, heart, or pancreas, but after 1 wk of daytime feeding, the phases of circadian gene expression are similar in all examined peripheral tissues.
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In the citing paper
“However, food intake during the biological night can uncouple peripheral clocks from the SCN (31, 32), confirming that meal timing acts as a zeitgeber for circadian clocks.”
From Meal timing and its role in obesity and associated diseases (2024) · cites this paper as [32]
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“In nocturnal rodents, feeding during the daytime hours for a week completely altered the phase of the circadian expression of clock and clock-controlled genes in the peripheral tissues [261,262].”
From Effects of diet, lifestyle, Chrononutrition and alternative dietary interventions on postprandial Glycemia and insulin resistance (2022) · cites this paper as [262]
In the citing paper
“Exogenous, behavioral time cues associated with externally imposed schedules thus have the capacity to drive endogenous rhythmicity in metabolism, likely by impacting on peripheral oscillators (17, 18) and dissociating them from the rhythm of the central SCN pacemaker.”
From Separation of circadian- and behavior-driven metabolite rhythms in humans provides a window on peripheral oscillators and metabolism (2018) · cites this paper as [17]
In the citing paper
“A few years later it became clear that the feeding/fasting cycle is the main Zeitgeber in terms of the synchronization of these so-called peripheral clocks [6].”
From Circadian control of glucose metabolism (2014) · cites this paper as [6]
In the citing paper
“In animals, timed feeding is a strong resetting cue for peripheral clocks (51,52).”
From Role of the circadian system in cardiovascular disease (2018) · cites this paper as [51]
In the citing paper
“Feeding rodents only during the rest phase—as similarly occurs during night work when they eat during their night shift—can phase shift peripheral oscillators in the liver, pancreas, kidney, and heart while it has no effect on the phase of the SCN (Damiola et al., 2000; Stokkan et al., 2001).”
From The impact of the circadian timing system on cardiovascular and metabolic function (2012) · cites this paper as Damiola et al., 2000
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Citations
Cites
Molecular Bases for Circadian Clocks
Dunlap, J. C. (1999) · Cell · doi:10.1016/s0092-8674(00)80566-8 · Cited by 2,900
A Serum Shock Induces Circadian Gene Expression in Mammalian Tissue Culture Cells
Balsalobre, A., Damiola, F., & Schibler, U. (1998) · Cell · doi:10.1016/s0092-8674(00)81199-x · Cited by 2,001
Self-citationRoles of PPARs in health and disease
Kersten, S., Desvergne, B., & Wahli, W. (2000) · Nature · doi:10.1038/35013000 · Cited by 1,956
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
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
Self-citationTransplanted Suprachiasmatic Nucleus Determines Circadian Period
Ralph, M. R., Foster, R. G., Davis, F. C., & Menaker, M. (1990) · Science · doi:10.1126/science.2305266 · Cited by 1,853
Sleep Homeostasis and Models of Sleep Regulation
Borb, A. A., & Achermann, P. (1999) · Journal of Biological Rhythms · doi:10.1177/074873099129000894 · Cited by 1,546
Mammalian Cry1 and Cry2 are essential for maintenance of circadian rhythms
Horst, G. T. J. V. D., Muijtjens, M., Kobayashi, K., Takano, R., Kanno, S.-I., Takao, M., Wit, J. D., Verkerk, A., Eker, A. P. M., Leenen, D. V., et al. (1999) · Nature · doi:10.1038/19323 · Cited by 1,402
Neural regulation of circadian rhythms.
Rusak, B., & Zucker, I. (1979) · Physiological Reviews · doi:10.1152/physrev.1979.59.3.449 · Cited by 1,402
Interacting molecular loops in the mammalian circadian clock
Shearman, L. P., Sriram, S., Weaver, D. R., Maywood, E. S., Chaves, I., Zheng, B., Kume, K., Lee, C. C., van der, G. T. J., Horst, et al. (2000) · Science · doi:10.1126/science.288.5468.1013 · Cited by 1,367
Flagged first, then by citations
Cited by
Sorted by citations
Items 401–500 of 1,014
The Cerebellum Harbors a Circadian Oscillator Involved in Food Anticipation
Mendoza, J., Pévet, P., Felder‐Schmittbuhl, M., Bailly, Y. J. R., & Challet, É. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.5855-09.2010 · Cited by 122
Ekmekçioğlu, C., & Touitou, Y. (2010) · Obesity Reviews · doi:10.1111/j.1467-789x.2010.00716.x · Cited by 122
Timing of food intake: identifying contributing factors to design effective interventions
Dashti, H. S., Scheer, F. A. J. L., Saxena, R., & Garaulet, M. (2019) · Advances in Nutrition · doi:10.1093/advances/nmy131 · Cited by 121
MicroRNAs shape circadian hepatic gene expression on a transcriptome-wide scale
Du, N., Arpat, A. B., Matos, M. D., & Gatfield, D. (2014) · eLife · doi:10.7554/elife.02510 · Cited by 123
Functional neuroanatomy of sleep and circadian rhythms
Rosenwasser, A. M. (2009) · Brain Research Reviews · doi:10.1016/j.brainresrev.2009.08.001 · Cited by 127
The role of circadian rhythmicity in reproduction
Kennaway, D. J. (2005) · Human Reproduction Update · doi:10.1093/humupd/dmh054 · Cited by 120
Kornmann, B. (2001) · Nucleic Acids Research · doi:10.1093/nar/29.11.e51 · Cited by 119
Self-citationInteractions between metabolism and circadian clocks: reciprocal disturbances
Delezie, J., & Challet, É. (2011) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2011.06246.x · Cited by 124
Circadian Metabolism: From Mechanisms to Metabolomics and Medicine
Brown, S. A. (2016) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2016.03.015 · Cited by 122
Ramsey, K. M., Marcheva, B., Kohsaka, A., & Bass, J. T. (2007) · Annual Review of Nutrition · doi:10.1146/annurev.nutr.27.061406.093546 · Cited by 120
Cancer Inhibition through Circadian Reprogramming of Tumor Transcriptome with Meal Timing
Li, X., Delaunay, F., Dulong, S., Claustrat, B., Zampera, S., Fujii, Y., Teboul, M., Beau, J., & Lévi, F. (2010) · Cancer Research · doi:10.1158/0008-5472.can-09-4235 · Cited by 123
Mammalian circadian systems: Organization and modern life challenges
Finger, A., & Kramer, A. (2021) · Acta Physiologica · doi:10.1111/apha.13548 · Cited by 117
Cistromic Reprogramming of the Diurnal Glucocorticoid Hormone Response by High-Fat Diet
Quagliarini, F., Mir, A. A., Balázs, K., Wierer, M., Dyar, K. A., Jouffe, C., Makris, K., Hawe, J. S., Heinig, M., Filipp, F. V., et al. (2019) · Molecular Cell · doi:10.1016/j.molcel.2019.10.007 · Cited by 116
Mindikoglu, A. L., Abdulsada, M. M., Jain, A., Choi, J. M., Jalal, P. K., Devaraj, S., Mezzari, M. P., Petrosino, J. F., Opekun, A. R., & Jung, S. Y. (2020) · Journal of Proteomics · doi:10.1016/j.jprot.2020.103645 · Cited by 121
Sympathetic input modulates, but does not determine, phase of peripheral circadian oscillators
Vujović, N., Davidson, A. J., & Menaker, M. (2008) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00498.2007 · Cited by 116
Peripheral Circadian Clocks in the Vasculature
Reilly, D. F., Westgate, E. J., & FitzGerald, G. A. (2007) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.107.144923 · Cited by 117
Hypothalamic clocks and rhythms in feeding behaviour
Bechtold, D. A., & Loudon, A. S. I. (2013) · Trends in Neurosciences · doi:10.1016/j.tins.2012.12.007 · Cited by 121
Spencer, R. L., Chun, L. E., Hartsock, M. J., & Woodruff, E. R. (2017) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2017.12.005 · Cited by 125
Entrainment of the mouse circadian clock: Effects of stress, exercise, and nutrition
Tahara, Y., & Shibata, S. (2017) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2017.12.026 · Cited by 120
Regulation of alternative splicing by the circadian clock and food related cues
McGlincy, N. J., Valomon, A., Chesham, J. E., Maywood, E. S., Hastings, M. H., & Ule, J. (2012) · Genome biology · doi:10.1186/gb-2012-13-6-r54 · Cited by 115
Requirement for NF-κB in maintenance of molecular and behavioral circadian rhythms in micePreprint
Hong, H., Maury, E., Ramsey, K. M., Perelis, M., Marcheva, B., Omura, C., Kobayashi, Y., Guttridge, D. C., Barish, G. D., & Bass, J. T. (2018) · Genes & Development · doi:10.1101/gad.319228.118 · Cited by 117
Durgan, D. J., Tsai, J.-Y., Grenett, M. H., Pat, B., Ratcliffe, W. F., Villegas‐Montoya, C., Garvey, M. E., Nagendran, J., Dyck, J. R. B., Bray, M. S., et al. (2011) · Chronobiology International · doi:10.3109/07420528.2010.550406 · Cited by 114
Chang, L., Xiong, W., Zhao, X., Fan, Y., Guo, Y., Garcia-Barrio, M. T., Zhang, J., Jiang, Z., Lin, J. D., & Chen, Y. (2018) · Circulation · doi:10.1161/circulationaha.117.029972 · Cited by 113
Spatiotemporal Metabolic Liver Zonation and Consequences on Pathophysiology
Martini, T., Naef, F., & Tchorz, J. S. (2023) · Annual Review of Pathology: Mechanisms of Disease · doi:10.1146/annurev-pathmechdis-031521-024831 · Cited by 113
The Light Responsive Transcriptome of the Zebrafish: Function and Regulation
Weger, B. D., Weger, M., Otto, G., Mracek, P., Armant, O., Dolle, D. D., Lahiri, K., Vallone, D., Ettwiller, L. M., Geisler, R., et al. (2011) · PLoS ONE · doi:10.1371/journal.pone.0017080 · Cited by 115
Borengasser, S. J., Kang, P., Faske, J. B., Gómez-Acevedo, H., Blackburn, M. L., Badger, T. M., & Shankar, K. (2014) · PLoS ONE · doi:10.1371/journal.pone.0084209 · Cited by 116
Velarde, E., Haque, R., Iuvone, P. M., Azpeleta, C., Alonso-Gómez, A. L., & Delgado, M. J. (2009) · Journal of Biological Rhythms · doi:10.1177/0748730408329901 · Cited by 112
Experimental and clinical aspects of melatonin and clock genes in diabetes
Peschke, E., Bähr, I., & Mühlbauer, E. (2015) · Journal of Pineal Research · doi:10.1111/jpi.12240 · Cited by 116
Rev‐erbα gives a time cue to metabolism
Duez, H., & Staels, B. (2007) · FEBS Letters · doi:10.1016/j.febslet.2007.08.032 · Cited by 114
Circadian rhythm and its role in malignancy
Rana, S., & Mahmood, S. (2010) · Journal of Circadian Rhythms · doi:10.1186/1740-3391-8-3 · Cited by 113
Kudo, T., Akiyama, M., Kuriyama, K., Sudo, M., Moriya, T., & Shibata, S. (2004) · Diabetologia · doi:10.1007/s00125-004-1461-0 · Cited by 112
The days and nights of cancer cells.
Canaple, L., Kakizawa, T., & Laudet, V. (2003) · PubMed · Cited by 108
Adamovich, Y., Ladeuix, B., Sobel, J., Manella, G., Neufeld-Cohen, A., Assadi, M. H., Golik, M., Kuperman, Y., Tarasiuk, A., Koeners, M. P., et al. (2019) · Cell Metabolism · doi:10.1016/j.cmet.2019.01.007 · Cited by 108
Pan, X., Terada, T., Okuda, M., & Inui, K. (2004) · Journal of Nutrition · doi:10.1093/jn/134.9.2211 · Cited by 109
The hypothalamic clock and its control of glucose homeostasis
Kalsbeek, A., Yi, C., la Fleur, S. E., & Fliers, E. (2010) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2010.02.005 · Cited by 112
Nuclear receptors rock around the clock
Zhao, X., Cho, H., Yu, R. T., Atkins, A. R., Downes, M., & Evans, R. M. (2014) · EMBO Reports · doi:10.1002/embr.201338271 · Cited by 109
Sherman, H., Frumin, I., Gutman, R., Chapnik, N., Lorentz, A., Meylan, J., le Coutre, J., & Froy, O. (2010) · Journal of Cellular and Molecular Medicine · doi:10.1111/j.1582-4934.2010.01160.x · Cited by 109
Relevance of animal models to human eating disorders and obesity
Casper, R. C., Sullivan, E. L., & Tecott, L. H. (2008) · Psychopharmacology · doi:10.1007/s00213-008-1102-2 · Cited by 111
Oishi, K., Kasamatsu, M., & Ishida, N. (2004) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2004.03.055 · Cited by 107
Role of clock genes in gastrointestinal motility
Hoogerwerf, W. A. (2010) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00147.2010 · Cited by 107
Challet, É. (2003) · Frontiers in bioscience · doi:10.2741/1039 · Cited by 111
Circadian rhythms and tumor growth
Greene, M. W. (2012) · Cancer Letters · doi:10.1016/j.canlet.2012.01.001 · Cited by 105
Molecular aspects of circadian pharmacology and relevance for cancer chronotherapy
Ozturk, N., Ozturk, D., Kavakli, I. H., & Okyar, A. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18102168 · Cited by 106
Andreani, T., Itoh, T. Q., Yildirim, E., Hwangbo, D., & Allada, R. (2015) · Sleep Medicine Clinics · doi:10.1016/j.jsmc.2015.08.007 · Cited by 114
Time-Restricted Feeding Shifts the Skin Circadian Clock and Alters UVB-Induced DNA Damage
Wang, H., Spyk, E. N. V., Liu, Q., Geyfman, M., Salmans, M., Kumar, V., Ihler, A., Li, N., Takahashi, J. S., & D, B. A. M. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.07.022 · Cited by 105
Injection of LPS Causes Transient Suppression of Biological Clock Genes in Rats
Okada, K., Yano, M., Doki, Y., Azama, T., Iwanaga, H., Miki, H., Nakayama, M., Miyata, H., Takiguchi, S., Fujiwara, Y., et al. (2008) · Journal of Surgical Research · doi:10.1016/j.jss.2007.01.010 · Cited by 105
Krugluger, W., Brandstaetter, A., Kállay, E., Schueller, J., Krexner, E., Kriwanek, S., Bonner, E., & Cross, H. S. (2007) · Cancer Research · doi:10.1158/0008-5472.can-07-0133 · Cited by 106
The Role of Clock Genes in Pharmacology
Paschos, G. K., Baggs, J. E., Hogenesch, J. B., & FitzGerald, G. A. (2010) · The Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev.pharmtox.010909.105621 · Cited by 105
Perrin, L., Loizides‐Mangold, U., Skarupelova, S., Pulimeno, P., Chanon, S., Robert, M., Bouzakri, K., Modoux, C., Roux‐Lombard, P., Vidal, H., et al. (2015) · Molecular Metabolism · doi:10.1016/j.molmet.2015.07.009 · Cited by 107
The Circadian Clock, Shift Work, and Tissue-Specific Insulin Resistance
Oosterman, J. E., Wopereis, S., & Kalsbeek, A. (2020) · Endocrinology · doi:10.1210/endocr/bqaa180 · Cited by 109
Heat Stress and Animal Productivity
Aggarwal, A., & Upadhyay, R. C. (2012) · Springer eBooks · doi:10.1007/978-81-322-0879-2 · Cited by 111
Aoyama, S., & Shibata, S. (2017) · Frontiers in Neuroscience · doi:10.3389/fnins.2017.00063 · Cited by 108
Petrenko, V., Saini, C., Giovannoni, L., Gobet, C., Sage, D., Unser, M., Heddad-Masson, M., Gu, G., Bosco, D., Gachon, F., et al. (2017) · Genes & Development · doi:10.1101/gad.290379.116 · Cited by 108
Nutrient sensing and the circadian clock
Peek, C. B., Ramsey, K. M., Marcheva, B., & Bass, J. T. (2012) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2012.02.003 · Cited by 109
ZeitZeiger: supervised learning for high-dimensional data from an oscillatory system
Hughey, J., Hastie, T. J., & Butte, A. J. (2016) · Nucleic Acids Research · doi:10.1093/nar/gkw030 · Cited by 103
The RNA-Binding Protein NONO Coordinates Hepatic Adaptation to Feeding
Benegiamo, G., Mure, L. S., Erikson, G. A., Le, H. D., Moriggi, E., Brown, S. A., & Panda, S. (2018) · Cell Metabolism · doi:10.1016/j.cmet.2017.12.010 · Cited by 104
Evidence for widespread dysregulation of circadian clock progression in human cancer
Shilts, J., Chen, G., & Hughey, J. (2018) · PeerJ · doi:10.7717/peerj.4327 · Cited by 101
Circadian Clocks and Cancer: Timekeeping Governs Cellular Metabolism
Verlande, A., & Masri, S. (2019) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2019.05.001 · Cited by 104
Circadian autophagy rhythm: a link between clock and metabolism?
Ma, D., Li, S., Molusky, M. M., & Lin, J. D. (2012) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2012.03.004 · Cited by 106
Oxyntomodulin regulates resetting of the liver circadian clock by food
Landgraf, D., Tsang, A. H. K., Leliavski, A., Koch, C. E., Barclay, J. L., Drucker, D. J., & Oster, H. (2015) · eLife · doi:10.7554/elife.06253 · Cited by 106
Circadian regulation of gene expression in animals
Ripperger, J. A., & Schibler, U. (2001) · Current Opinion in Cell Biology · doi:10.1016/s0955-0674(00)00220-9 · Cited by 109
Self-citationThe Role of the Endocrine System in Feeding-Induced Tissue-Specific Circadian Entrainment
Sato, M., Murakami, M., Node, K., Matsumura, R., & Akashi, M. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.06.015 · Cited by 102
Genomic Convergence among ERRα, PROX1, and BMAL1 in the Control of Metabolic Clock Outputs
Dufour, C. R., Levasseur, M.-P., Pham, N. H. H., Eichner, L. J., Wilson, B. J., Charest-Marcotte, A., Duguay, D., Poirier-Héon, J.-F., Cermakian, N., & Giguère, V. (2011) · PLoS Genetics · doi:10.1371/journal.pgen.1002143 · Cited by 107
Truong, K. K., Lam, M. T. Y., Grandner, M. A., Sassoon, C. S. H., & Malhotra, A. (2016) · Annals of the American Thoracic Society · doi:10.1513/annalsats.201602-125fr · Cited by 105
Regulation and function of extra‐SCN circadian oscillators in the brain
Begemann, K., Neumann, A., & Oster, H. (2020) · Acta Physiologica · doi:10.1111/apha.13446 · Cited by 106
Time after time: inputs to and outputs from the mammalian circadian oscillators
Morse, D., & Sassone‐Corsi, P. (2002) · Trends in Neurosciences · doi:10.1016/s0166-2236(02)02274-9 · Cited by 103
Mostafaie, N., Kállay, E., Sauerzapf, E., Bonner, E., Kriwanek, S., Cross, H. S., Huber, K. R., & Krugluger, W. (2009) · Molecular Carcinogenesis · doi:10.1002/mc.20510 · Cited by 102
A Time to Fast, a Time to Feast: The Crosstalk between Metabolism and the Circadian Clock
Kovac, J., Husse, J., & Oster, H. (2009) · Molecules and Cells · doi:10.1007/s10059-009-0113-0 · Cited by 104
Metabolic Implications of Exposure to Light at Night: Lessons from Animal and Human Studies
Fleury, G., Masís‐vargas, A., & Kalsbeek, A. (2020) · Obesity · doi:10.1002/oby.22807 · Cited by 100
The circadian system and the balance of the autonomic nervous system
Buijs, R. M., Escobar, C., & Swaab, D. F. (2013) · Handbook of clinical neurology · doi:10.1016/b978-0-444-53491-0.00015-8 · Cited by 101
Kato, Y., Kawamoto, T., Fujimoto, K., & Noshiro, M. (2014) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/b978-0-12-405943-6.00010-5 · Cited by 100
STRUBBE, J. H., & van Dijk, G. (2002) · Neuroscience & Biobehavioral Reviews · doi:10.1016/s0149-7634(02)00016-7 · Cited by 100
Peripheral Circadian Oscillators
Cuninkova, L., & Brown, S. A. (2008) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1417.005 · Cited by 103
Sinturel, F., Gos, P., Petrenko, V., Hagedorn, C., Kreppel, F., Storch, K.-F., Knutti, D., Liani, A., Weitz, C. J., Emmenegger, Y., et al. (2021) · Genes & Development · doi:10.1101/gad.346460.120 · Cited by 100
Self-citationFoundations of circadian medicine
Kramer, A., Lange, T., Spies, C., Finger, A.-M., Berg, D., & Oster, H. (2022) · PLOS Biology · doi:10.1371/journal.pbio.3001567 · Cited by 99
“The dominant natural time signal (or zeitgeber) for the human circadian clock is light, but food signals can also entrain cellular circadian clocks in peripheral tissues [10].”
BackgroundJohnson, B. P., Walisser, J. A., Liu, Y., Shen, A. L., McDearmon, E. L., Moran, S. M., McIntosh, B. E., Vollrath, A. L., Schook, A. C., Takahashi, J. S., et al. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1421708111 · Cited by 103
Changes of Dietary Fat and Carbohydrate Content Alter Central and Peripheral Clock in Humans
Pivovarova‐Ramich, O., Jürchott, K., Rudovich, N. N., Hornemann, S., Lu, Y., Möckel, S., Murahovschi, V., Kessler, K., Seltmann, A., Maser‐Gluth, C., et al. (2015) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2014-3868 · Cited by 99
Patel, S. A., Velingkaar, N., Makwana, K., Chaudhari, A., & Kondratov, R. V. (2016) · Scientific Reports · doi:10.1038/srep25970 · Cited by 103
Feedback actions of locomotor activity to the circadian clock
Hughes, A. T. L., & Piggins, H. D. (2012) · Progress in brain research · doi:10.1016/b978-0-444-59427-3.00018-6 · Cited by 103
At the Interface of Lifestyle, Behavior, and Circadian Rhythms: Metabolic Implications
Bae, S.-A., Fang, M., Rustgi, V. K., Zarbl, H., & Androulakis, I. P. (2019) · Frontiers in Nutrition · doi:10.3389/fnut.2019.00132 · Cited by 103
Chronobiological Influence Over Cardiovascular Function
Rana, S., Prabhu, S. D., & Young, M. E. (2020) · Circulation Research · doi:10.1161/circresaha.119.313349 · Cited by 99
Interactions between light, mealtime and calorie restriction to control daily timing in mammals
Challet, É. (2010) · Journal of Comparative Physiology B · doi:10.1007/s00360-010-0451-4 · Cited by 105
Time-restricted feeding entrains daily rhythms of energy metabolism in mice
Satoh, Y., Kawai, H. F., Kudo, N., Kawashima, Y., & Mitsumoto, A. (2005) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00775.2005 · Cited by 99
Regulation of Circadian Gene Expression in Liver by Systemic Signals and Hepatocyte OscillatorsPreprint
Kornmann, B., Schaad, O., Reinke, H., Saini, C., & Schibler, U. (2007) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.2007.72.041 · Cited by 102
Self-citationA Balanced Diet Is Necessary for Proper Entrainment Signals of the Mouse Liver Clock
Hirao, A., Tahara, Y., Kimura, I., & Shibata, S. (2009) · PLoS ONE · doi:10.1371/journal.pone.0006909 · Cited by 98
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Metadata
- Authors
- Damiola, F., Le Minh, N., Preitner, N., Kornmann, B., Fleury-Olela, F., & Schibler, U.
- Affiliations
- University of Geneva (CH)
- Venue
- Genes & Development
- Publisher
- Cold Spring Harbor Laboratory
- Published
- 2000-12-01
- Volume
- 14
- Issue
- 23
- Pages
- 2950-2961
- ISSN
- 0890-9369 (ISSN-L)
- 1549-5477
- PMC
- PMC317100
- OpenAlex
- W2164628441
- Cited by
- 2,394
- References
- 62
- Citations by year
- 2026: 78 · 2025: 116 · 2024: 112 · 2023: 98 · 2022: 125 · 2021: 129 · 2020: 146 · 2019: 111 · 2018: 124 · 2017: 108 · 2016: 112 · 2015: 116 · 2014: 102 · 2013: 103 · 2012: 97
- Type
- posted content
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Genes & Development (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Archive ouverte UNIGE (University of Geneva) (publishedVersion, other-oa)
- Archive ouverte UNIGE (University of Geneva) (submittedVersion, cc-by)
- Funders
- National Science Foundation
- Louis-Jeantet Foundation
- Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung (47314)
- Bonizzi-Theler Stiftung
- 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 › Agricultural and Biological Sciences › Plant Science › Plant Molecular Biology Research
- Keywords
- circadian clock, feed restriction, suprachiasmatic nucleus, peripheral circadian oscillators, phase resetting, circadian gene expression, photoperiod, liver, kidney, heart, pancreas
- MeSH terms
- Animals, Aryl Hydrocarbon Hydroxylases, Biological Clocks, Body Temperature, Circadian Rhythm, Cytochrome P-450 Enzyme System, DNA-Binding Proteins, Eye Proteins, Feeding Behavior, Flavoproteins, Food, Food Deprivation, Mixed Function Oxygenases, Kinetics, Liver, Neurons, Nuclear Proteins, Proteins, Suprachiasmatic Nucleus, Transcription Factors, Photoreceptor Cells, Invertebrate, Receptors, Cytoplasmic and Nuclear, Cell Cycle Proteins, Drosophila Proteins, Receptors, G-Protein-Coupled, Mice, Cryptochromes, Period Circadian Proteins, Nuclear Receptor Subfamily 1, Group D, Member 1, Cytochrome P-450 CYP2A6
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