Cited by 198Circadian rhythm and melatoninDietary Effects on HealthNutrition, Genetics, and Disease

The DOI matches its Crossref record; 101 of the 101 references it cites were found in a registry or an index.

Nutrients, Clock Genes, and Chrononutrition

Open access

Oike, Hideaki, Oishi, Katsutaka, Kobori, Masuko·2014·Current Nutrition Reports

DOI 10.1007/s13668-014-0082-6PMC PMC4118017

Open this paper in CoChat — free account Open PDF

Abstract

Circadian clocks that comprise clock genes exist throughout the body and control daily physiological events. The central clock that dominates activity rhythms is entrained by light/dark cycles, whereas peripheral clocks regulating local metabolic rhythms are determined by feeding/fasting cycles. Nutrients reset peripheral circadian clocks and the local clock genes control downstream metabolic processes. Metabolic states also affect the clockworks in feedback manners. Because the circadian system organizes whole energy homeostasis, including food intake, fat accumulation, and caloric expenditure, the disruption of circadian clocks leads to metabolic disorders. Recent findings show that time-restricted feeding during the active phase amplifies circadian clocks and improves metabolic disorders induced by a high-fat diet without caloric reduction, whereas unusual/irregular food intake induces various metabolic dysfunctions. Such evidence from nutrition studies that consider circadian system (chrononutrition) has rapidly accumulated. We review molecular relationships between circadian clocks and nutrition as well as recent chrononutrition findings.

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

Integrity signals

Registry

Crossref · 10.1007/s13668-014-0082-6

Cites

101 of 101 references verified0 citation errors · 0 not checkable

Statistics

Fig. 1 Schematic representation of the circadian clock system and chrononutrition. Light/dark cycles entrain the central clock in the suprachiasmatic nucleus (SCN) dominating activity rhythms, whereas feeding cues determine the phase of peripheral clocks that dominate local metabolic rhythms. Both nutrients and meal timing can affect the clock system, thus “chrononutrition” has two aspects: 1) nutrients/food components regulate the clock system, e.g., caffeine prolongs the period of circadian clocks and the locomotor activity rhythm, and high-fat diets alter the rhythms of lipogenesis, circulating lipids, locomotor activity, and feeding behavior; 2) meal-timing affects output of the clock system, e.g., skipping breakfast and nocturnal eating increases risk of obesity, whereas time-restricted feedings prevent metabolic disorders induced by high-fat diets. Regular/time-restricted feedings synchronize and amplify the rhythms of clock system, whereas irregular/unusual feedings cause desynchronization and attenuate the rhythms, probably leading to metabolic disordersCC BY · PubMed Central

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

In silico analysis enabling informed design for genome editing in medicinal cannabis; gene families and variant characterisation
Calamita, E., Schmid, M., Kunz, M., Ndebele-Murisa, M. R., Magadza, C. H. D., Nyambe, I., & Wehrli, B. (2019) · Figshare · doi:10.26181/6153922fe919c · Cited by 4,239
Obesity and Metabolic Syndrome in Circadian Clock Mutant Mice
Turek, F. W., Joshu, C., Kohsaka, A., Lin, E., Ivanova, G., McDearmon, E., Laposky, A., Losee-Olson, S., Easton, A., Jensen, D. R., et al. (2005) · Science · doi:10.1126/science.1108750 · Cited by 2,485
Restricted feeding uncouples circadian oscillators in peripheral tissues from the central pacemaker in the suprachiasmatic nucleus
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
Adverse metabolic and cardiovascular consequences of circadian misalignment
Scheer, F. A. J. L., Hilton, M. F., Mantzoros, C. S., & Shea, S. A. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0808180106 · Cited by 2,351
Clock Mutants of Drosophila melanogaster
Konopka, R. J., & Benzer, S. (1971) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.68.9.2112 · Cited by 2,287
Time-restricted feeding without reducing caloric intake prevents metabolic diseases in mice fed a high-fat diet
Hatori, M., Vollmers, C., Zarrinpar, A., DiTacchio, L., Bushong, E. A., Gill, S., Leblanc, M., Chaix, A., Joens, M., Fitzpatrick, J. A. J., et al. (2012) · Cell Metabolism · doi:10.1016/j.cmet.2012.04.019 · Cited by 1,986
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
High-Fat Diet Disrupts Behavioral and Molecular Circadian Rhythms in Mice
Kohsaka, A., Laposky, A. D., Ramsey, K. M., Estrada, C., Joshu, C., Kobayashi, Y., Turek, F. W., & Bass, J. (2007) · Cell Metabolism · doi:10.1016/j.cmet.2007.09.006 · Cited by 1,528
Transcriptional architecture and chromatin landscape of the core circadian clock in mammals
Koike, N., Yoo, S.-H., Huang, H.-C., Kumar, V., Lee, C., Kim, T.-K., & Takahashi, J. S. (2012) · Science · doi:10.1126/science.1226339 · Cited by 1,464
The NAD+-dependent deacetylase SIRT1 modulates CLOCK-mediated chromatin remodeling and circadian control
Nakahata, Y., Kaluzova, M., Grimaldi, B., Sahar, S., Hirayama, J., Chen, D., Guarente, L. P., & Sassone-Corsi, P. (2008) · Cell · doi:10.1016/j.cell.2008.07.002 · Cited by 1,427
SIRT1 regulates circadian clock gene expression through PER2 deacetylation
Asher, G., Gatfield, D., Stratmann, M., Reinke, H., Dibner, C., Kreppel, F., Mostoslavsky, R., Alt, F. W., & Schibler, U. (2008) · Cell · doi:10.1016/j.cell.2008.06.050 · Cited by 1,376
Circadian Control of the NAD + Salvage Pathway by CLOCK-SIRT1
Nakahata, Y., Sahar, S., Astarita, G., Kaluzova, M., & Sassone-Corsi, P. (2009) · Science · doi:10.1126/science.1170803 · Cited by 1,198
Circadian Clock Feedback Cycle Through NAMPT-Mediated NAD + Biosynthesis
Ramsey, K. M., Yoshino, J., Brace, C. S., Abrassart, D., Kobayashi, Y., Marcheva, B., Hong, H.-K., Chong, J. L., Buhr, E. D., Lee, C., et al. (2009) · Science · doi:10.1126/science.1171641 · Cited by 1,126
BMAL1 and CLOCK, two essential components of the circadian clock, are involved in glucose homeostasis
Rudic, R. D., McNamara, P., Curtis, A.-M., Boston, R. C., Panda, S., Hogenesch, J. B., & FitzGerald, G. A. (2004) · PLoS Biology · doi:10.1371/journal.pbio.0020377 · Cited by 1,059
Regulation of clock and NPAS2 DNA binding by the redox state of NAD cofactors
Rutter, J., Reick, M., Wu, L. C., & McKnight, S. L. (2001) · Science · doi:10.1126/science.1060698 · Cited by 1,059
Regulation of circadian behaviour and metabolism by REV-ERB-α and REV-ERB-β
Cho, H., Zhao, X., Hatori, M., Yu, R. T., Barish, G. D., Lam, M. T., Chong, L.-W., DiTacchio, L., Atkins, A. R., Glass, C. K., et al. (2012) · Nature · doi:10.1038/nature11048 · Cited by 1,037
AMPK regulates the circadian clock by cryptochrome phosphorylation and degradation
Lamia, K. A., Sachdeva, U. M., DiTacchio, L., Williams, E. C., Alvarez, J. G., Egan, D. F., Vasquez, D. S., Juguilon, H., Panda, S., Shaw, R. J., et al. (2009) · Science · doi:10.1126/science.1172156 · Cited by 958
Circadian timing of food intake contributes to weight gain
Arble, D. M., Bass, J., Laposky, A. D., Vitaterna, M. H., & Turek, F. W. (2009) · Obesity · doi:10.1038/oby.2009.264 · Cited by 953
Timing to perfection: the biology of central and peripheral circadian clocks
Albrecht, U. (2012) · Neuron · doi:10.1016/j.neuron.2012.04.006 · Cited by 915
Light at night increases body mass by shifting the time of food intake
Fonken, L. K., Workman, J. L., Walton, J. C., Weil, Z. M., Morris, J. S., Haim, A., & Nelson, R. J. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1008734107 · Cited by 796
Time of feeding and the intrinsic circadian clock drive rhythms in hepatic gene expression.
Vollmers, C., Gill, S., DiTacchio, L., Pulivarthy, S. R., Le, H. D., & Panda, S. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0909591106 · Cited by 765
Circadian Rhythms in Man: A self-sustained oscillator with an inherent frequency underlies human 24-hour periodicity
Aschoff, J. (1965) · Science · doi:10.1126/science.148.3676.1427 · Cited by 752
Molecular components of the mammalian circadian clock
Buhr, E. D., & Takahashi, J. S. (2013) · Handbook of experimental pharmacology · doi:10.1007/978-3-642-25950-0_1 · Cited by 738
Reprogramming of the Circadian Clock by Nutritional Challenge
Eckel‐Mahan, K. L., Patel, V. R., de Mateo, S., Orozco-Solís, R., Ceglia, N., Sahar, S., Dilag-Penilla, S. A., Dyar, K. A., Baldi, P., & Sassone‐Corsi, P. (2013) · Cell · doi:10.1016/j.cell.2013.11.034 · Cited by 737
Association between Eating Patterns and Obesity in a Free-living US Adult Population
Ma, Y. (2003) · American Journal of Epidemiology · doi:10.1093/aje/kwg117 · Cited by 725
Rev-erbα, a Heme Sensor That Coordinates Metabolic and Circadian Pathways
Yin, L., Wu, N., Curtin, J. C., Qatanani, M., Szwergold, N. R., Reid, R. A., Waitt, G. M., Parks, D. J., Pearce, K. H., Wisely, G. B., et al. (2007) · Science · doi:10.1126/science.1150179 · Cited by 707
A circadian rhythm orchestrated by histone deacetylase 3 controls hepatic lipid metabolism
Feng, D., Liu, T., Sun, Z., Bugge, A., Mullican, S. E., Alenghat, T., Liu, X. S., & Lazar, M. A. (2011) · Science · doi:10.1126/science.1198125 · Cited by 701
Transcriptional coactivator PGC-1α integrates the mammalian clock and energy metabolism
Liu, C., Li, S., Liu, T., Borjigin, J., & Lin, J. D. (2007) · Nature · doi:10.1038/nature05767 · Cited by 643
Timing of food intake predicts weight loss effectiveness
Garaulet, M., Gómez-Abellán, P., Alburquerque-Béjar, J. J., Lee, Y.-C., Ordovás, J. M., & Scheer, F. A. J. L. (2013) · International Journal of Obesity · doi:10.1038/ijo.2012.229 · Cited by 639
High Caloric intake at breakfast vs. dinner differentially influences weight loss of overweight and obese women
Jakubowicz, D., Barnea, M., Wainstein, J., & Froy, O. (2013) · Obesity · doi:10.1002/oby.20460 · Cited by 593
Restricted feeding entrains liver clock without participation of the suprachiasmatic nucleus
Hara, R., Wan, K., Wakamatsu, H., Aida, R., Moriya, T., Akiyama, M., & Shibata, S. (2001) · Genes to Cells · doi:10.1046/j.1365-2443.2001.00419.x · Cited by 569
Disruption of circadian clocks has ramifications for metabolism, brain, and behavior
Karatsoreos, I. N., Bhagat, S., Bloss, E. B., Morrison, J. H., & McEwen, B. S. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1018375108 · Cited by 547
Rev-erbα and Rev-erbβ coordinately protect the circadian clock and normal metabolic functionPreprint
Bugge, A. K., Feng, D., Everett, L. J., Briggs, E. R., Mullican, S. E., Wang, F., Jager, J., & Lazar, M. A. (2012) · Genes & Development · doi:10.1101/gad.186858.112 · Cited by 514
Circadian Rhythms and Metabolic Syndrome
Maury, E., Ramsey, K. M., & Bass, J. T. (2010) · Circulation Research · doi:10.1161/circresaha.109.208355 · Cited by 509
PER2 controls lipid metabolism by direct regulation of PPARγ
Grimaldi, B., Bellet, M. M., Katada, S., Astarita, G., Hirayama, J., Amin, R. H., Granneman, J. G., Piomelli, D., Leff, T., & Sassone-Corsi, P. (2010) · Cell Metabolism · doi:10.1016/j.cmet.2010.10.005 · Cited by 489
Obesity in mice with adipocyte-specific deletion of clock component Arntl
Paschos, G. K., Ibrahim, S., Song, W.-L., Kunieda, T., Grant, G., Reyes, T. M., Bradfield, C. A., Vaughan, C. H., Eiden, M., Masoodi, M., et al. (2012) · Nature Medicine · doi:10.1038/nm.2979 · Cited by 465
Breakfast Eating and Weight Change in a 5-Year Prospective Analysis of Adolescents: Project EAT (Eating Among Teens)
Timlin, M. T., Pereira, M. A., Story, M. T., & Neumark‐Sztainer, D. (2008) · PEDIATRICS · doi:10.1542/peds.2007-1035 · Cited by 432
Timing of food intake and obesity: a novel association
Garaulet, M., & Gómez-Abellán, P. (2014) · Physiology & Behavior · doi:10.1016/j.physbeh.2014.01.001 · Cited by 362
The mammalian clock component PERIOD2 coordinates circadian output by interaction with nuclear receptors
Schmutz, I., Ripperger, J. A., Baeriswyl-Aebischer, S., & Albrecht, U. (2010) · Genes & Development · doi:10.1101/gad.564110 · Cited by 361
Timed high-fat diet resets circadian metabolism and prevents obesity
Sherman, H., Genzer, Y., Cohen, R., Chapnik, N., Madar, Z., & Froy, O. (2012) · The FASEB Journal · doi:10.1096/fj.12-208868 · Cited by 360
Deficient of a Clock Gene, Brain and Muscle Arnt-Like Protein-1 (BMAL1), Induces Dyslipidemia and Ectopic Fat Formation
Shimba, S., Ogawa, T., Hitosugi, S., Ichihashi, Y., Nakadaira, Y., Kobayashi, M., Tezuka, M., Kosuge, Y., Ishige, K., Ito, Y., et al. (2011) · PLoS ONE · doi:10.1371/journal.pone.0025231 · Cited by 353
Poly(ADP-ribose) polymerase 1 participates in the phase entrainment of circadian clocks to feeding
Asher, G., Reinke, H., Altmeyer, M., Gutierrez-Arcelus, M., Hottiger, M. O., & Schibler, U. (2010) · Cell · doi:10.1016/j.cell.2010.08.016 · Cited by 340
Night eating syndrome and nocturnal snacking: association with obesity, binge eating and psychological distress
Colles, S. L., Dixon, J. B., & O'Brien, P. E. (2007) · International Journal of Obesity · doi:10.1038/sj.ijo.0803664 · Cited by 324
Food intake during the normal activity phase prevents obesity and circadian desynchrony in a rat model of night work
Salgado-Delgado, R., Angeles-Castellanos, M., Saderi, N., Buijs, R. M., & Escobar, C. (2010) · Endocrinology · doi:10.1210/en.2009-0864 · Cited by 323
Circadian Clocks and Metabolism
Marcheva, B., Ramsey, K. M., Peek, C. B., Affinati, A., Maury, E., & Bass, J. (2013) · Handbook of Experimental Pharmacology · doi:10.1007/978-3-642-25950-0_6 · Cited by 282
Timing of energy intake during the day is associated with the risk of obesity in adults
Wang, J. B., Patterson, R. E., Ang, A., Emond, J. A., Shetty, N., & Arab, L. (2014) · Journal of Human Nutrition and Dietetics · doi:10.1111/jhn.12141 · Cited by 270
The nuclear receptor Rev-erbα controls circadian thermogenic plasticity
Gerhart‐Hines, Z., Feng, D., Emmett, M. J., Everett, L. J., Loro, E., Briggs, E. R., Bugge, A. K., Hou, C., Ferrara, C., Seale, P., et al. (2013) · Nature · doi:10.1038/nature12642 · Cited by 265
The role of mPer2 clock gene in glucocorticoid and feeding rhythms
Yang, S., Liu, A., Weidenhammer, A., Cooksey, R. C., McClain, D., Kim, M. K., Aguilera, G., Abel, E. D., & Chung, J. H. (2009) · Endocrinology · doi:10.1210/en.2008-0705 · Cited by 263
Circadian Desynchrony Promotes Metabolic Disruption in a Mouse Model of Shiftwork
Barclay, J. L., Husse, J., Bode, B., Naujokat, N., Meyer-Kovac, J., Schmid, S. M., Lehnert, H., & Oster, H. (2012) · PLoS ONE · doi:10.1371/journal.pone.0037150 · Cited by 259
Detrimental effects of constant light exposure and high-fat diet on circadian energy metabolism and insulin sensitivity
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
Advances in understanding the peripheral circadian clocks
Richards, J., & Gumz, M. L. (2012) · The FASEB Journal · doi:10.1096/fj.12-203554 · Cited by 247
Activation of 5′-AMP-activated Kinase with Diabetes Drug Metformin Induces Casein Kinase Iɛ (CKIɛ)-dependent Degradation of Clock Protein mPer2
Um, J. H., Yang, S., Yamazaki, S., Kang, H., Viollet, B., Foretz, M., & Chung, J. H. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.c700070200 · Cited by 244
The Implications of Multiple Circadian Clock Origins
Rosbash, M. (2009) · PLoS Biology · doi:10.1371/journal.pbio.1000062 · Cited by 239
A diurnal serum lipid integrates hepatic lipogenesis and peripheral fatty acid use
Liu, S., Brown, J. D., Stanya, K. J., Homan, E. A., Leidl, M., Inouye, K., Bhargava, P., Gangl, M. R., Dai, L., Hatano, B., et al. (2013) · Nature · doi:10.1038/nature12710 · Cited by 237
The Role of Sleep Duration in the Regulation of Energy Balance: Effects on Energy Intakes and Expenditure
St-Onge, M.-P. (2013) · Journal of Clinical Sleep Medicine · doi:10.5664/jcsm.2348 · Cited by 220
Quantitative analysis of light-phase restricted feeding reveals metabolic dyssynchrony in mice
Bray, M. S., Ratcliffe, W. F., Grenett, M. H., Brewer, R. A., Gamble, K. L., & Young, M. E. (2012) · International Journal of Obesity · doi:10.1038/ijo.2012.137 · Cited by 213
Chronobiology and nutrition
Tahara, Y., & Shibata, S. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.08.049 · Cited by 198
High-fat diet acutely affects circadian organisation and eating behavior
Pendergast, J. S., Branecky, K. L., Yang, W., Ellacott, K. L. J., Niswender, K. D., & Yamazaki, S. (2013) · European Journal of Neuroscience · doi:10.1111/ejn.12133 · Cited by 198
Circadian variation of diet-induced thermogenesis
Romon, M., Edme, J., Boulenguez, C., Lescroart, J., & Frimat, P. (1993) · The American Journal of Clinical Nutrition · doi:10.1093/ajcn/57.4.476 · Cited by 197
Breakfast Frequency and Quality May Affect Glycemia and Appetite in Adults and Children
Pereira, M. A., Erickson, E., McKee, P., Schrankler, K., Raatz, S. K., Lytle, L. A., & Pellegrini, A. D. (2010) · Journal of Nutrition · doi:10.3945/jn.109.114405 · Cited by 194
CLOCK, PER2 and BMAL1 DNA Methylation: Association with Obesity and Metabolic Syndrome Characteristics and Monounsaturated Fat Intake
Milagro, F., Gómez-Abellán, P., Campión, J., Martinez, J., Ordovás, J. M., & Garaulet, M. (2012) · Chronobiology International · doi:10.3109/07420528.2012.719967 · Cited by 191
The REV-ERBs and RORs: Molecular Links Between Circadian Rhythms and Lipid Homeostasis
Solt, L. A., Kojetin, D. J., & Burris, T. P. (2011) · Future Medicinal Chemistry · doi:10.4155/fmc.11.9 · Cited by 177
Shift work and cardiovascular risk factors: New knowledge from the past decade
Esquirol, Y., Perret, B., Ruidavets, J. B., Marquié, J. C., Diène, E., Niezborala, M., & Ferrières, J. (2011) · Archives of cardiovascular diseases · doi:10.1016/j.acvd.2011.09.004 · Cited by 173
Disrupted fat absorption attenuates obesity induced by a high‐fat diet in Clock mutant mice
Oishi, K., Atsumi, G.-I., Sugiyama, S., Kodomari, I., Kasamatsu, M., Machida, K., & Ishida, N. (2006) · FEBS Letters · doi:10.1016/j.febslet.2005.11.063 · Cited by 166
Self-citation
The Effects of Caffeine on Sleep inDrosophilaRequire PKA Activity, But Not the Adenosine Receptor
Wu, M. N., Ho, K. S., Crocker, A. J., Yue, Z., Koh, K., & Sehgal, A. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.1653-09.2009 · Cited by 130
Refeeding after Fasting Elicits Insulin-Dependent Regulation of Per2 and Rev-erbα with Shifts in the Liver Clock
Tahara, Y., Otsuka, M., Fuse, Y., Hirao, A., & Shibata, S. (2011) · Journal of Biological Rhythms · doi:10.1177/0748730411405958 · Cited by 125
Real-time monitoring in three-dimensional hepatocytes reveals that insulin acts as a synchronizer for liver clock
Yamajuku, D., Inagaki, T., Haruma, T., Okubo, S., Kataoka, Y., Kobayashi, S., Ikegami, K., Laurent, T., Kojima, T., Noutomi, K., et al. (2012) · Scientific Reports · doi:10.1038/srep00439 · Cited by 124
Gene- and tissue-specific alterations of circadian clock gene expression in streptozotocin-induced diabetic mice under restricted feeding
Oishi, K., Kasamatsu, M., & Ishida, N. (2004) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2004.03.055 · Cited by 107
Self-citation
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
Meal frequency patterns determine the phase of mouse peripheral circadian clocks
Kuroda, H., Tahara, Y., Saito, K., Ohnishi, N., Kubo, Y., Seo, Y., Otsuka, M., Fuse, Y., Ohura, Y., Hirao, A., et al. (2012) · Scientific Reports · doi:10.1038/srep00711 · Cited by 105
Association of Breakfast Skipping With Visceral Fat and Insulin Indices in Overweight Latino Youth
Alexander, K. E., Ventura, E. E., Spruijt‐Metz, D., Weigensberg, M. J., Goran, M. I., & Davis, J. N. (2009) · Obesity · doi:10.1038/oby.2009.127 · Cited by 105
A 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
Caffeine lengthens circadian rhythms in mice
Oike, H., Kobori, M., Suzuki, T., & Ishida, N. (2011) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2011.06.049 · Cited by 96
Self-citation
Entrainment in calorie-restricted mice: conflicting zeitgebers and free-running conditions
Challet, É., Solberg, L. C., & Turek, F. W. (1998) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1998.274.6.r1751 · Cited by 96
Chrono-biology, Chrono-pharmacology and Chrono-nutrition
Tahara, Y., & Shibata, S. (2014) · Journal of Pharmacological Sciences · doi:10.1254/jphs.13r06cr · Cited by 94
The adjustment and manipulation of biological rhythms by light, nutrition, and abused drugs
Shibata, S., Tahara, Y., & Hirao, A. (2010) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2010.06.003 · Cited by 91
The Time of Metabolism: NAD+, SIRT1, and the Circadian ClockPreprint
Bellet, M. M., Orozco-Solís, R., Sahar, S., Eckel‐Mahan, K. L., & Sassone‐Corsi, P. (2011) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.2011.76.010520 · Cited by 90
Short sleep duration is associated with decreased serum leptin, increased energy intake and decreased diet quality in postmenopausal women
Stern, J. H., Grant, A. S., Thomson, C. A., Tinker, L., Hale, L., Brennan, K. M., Woods, N. F., & Chen, Z. (2014) · Obesity · doi:10.1002/oby.20683 · Cited by 86
Combination of starvation interval and food volume determines the phase of liver circadian rhythm in Per2::Luc knock-in mice under two meals per day feeding
Hirao, A., Nagahama, H., Tsuboi, T., Hirao, M., Tahara, Y., & Shibata, S. (2010) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00330.2010 · Cited by 86
Differential Roles of Breakfast and Supper in Rats of a Daily Three-Meal Schedule Upon Circadian Regulation and Physiology
Wu, T., Sun, L., ZhuGe, F., Guo, X., Zhao, Z., Tang, R., Chen, Q., Chen, L., Kato, H., & Fu, Z. (2011) · Chronobiology International · doi:10.3109/07420528.2011.622599 · Cited by 86
Differential roles of breakfast only (one meal per day) and a bigger breakfast with a small dinner (two meals per day) in mice fed a high-fat diet with regard to induced obesity and lipid metabolism
Fuse, Y., Hirao, A., Kuroda, H., Otsuka, M., Tahara, Y., & Shibata, S. (2012) · Journal of Circadian Rhythms · doi:10.1186/1740-3391-10-4 · Cited by 80
Altered behavioral and metabolic circadian rhythms in mice with disrupted NAD+ oscillation
Sahar, S., Nin, V., Barbosa, M. T., Chini, E. N., & Sassone-Corsi, P. (2011) · Aging · doi:10.18632/aging.100368 · Cited by 79
Feeding Cues and Injected Nutrients Induce Acute Expression of Multiple Clock Genes in the Mouse Liver
Oike, H., Nagai, K., Fukushima, T., Ishida, N., & Kobori, M. (2011) · PLoS ONE · doi:10.1371/journal.pone.0023709 · Cited by 72
Self-citation
PPARα is a potential therapeutic target of drugs to treat circadian rhythm sleep disorders
Shirai, H., Oishi, K., Kudo, T., Shibata, S., & Ishida, N. (2007) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2007.04.002 · Cited by 70
Self-citation
Early nocturnal meal skipping alters the peripheral clock and increases lipogenesis in mice
Yoshida, C., Shikata, N., Seki, S., Koyama, N., & Noguchi, Y. (2012) · Nutrition & Metabolism · doi:10.1186/1743-7075-9-78 · Cited by 68
Resveratrol Regulates Circadian Clock Genes in Rat-1 Fibroblast Cells
Oike, H., & Kobori, M. (2008) · Bioscience Biotechnology and Biochemistry · doi:10.1271/bbb.80426 · Cited by 67
Self-citation
Effects of feeding schedule changes on the circadian phase of the cardiac autonomic nervous system and serum lipid levels
Yoshizaki, T., Tada, Y., Hida, A., Sunami, A., Yokoyama, Y., Yasuda, J., Nakai, A., Togo, F., & Kawano, Y. (2013) · European Journal of Applied Physiology · doi:10.1007/s00421-013-2702-z · Cited by 65
Circadian Periodicity in Neurospora : Alteration by Inhibitors of Cyclic AMP Phosphodiesterase
Feldman, J. F. (1975) · Science · doi:10.1126/science.173018 · Cited by 64
Thermoregulation Is Impaired in an Environment Without Circadian Time Cues
Fuller, C. A., Sulzman, F. M., & Moore‐Ede, M. C. (1978) · Science · doi:10.1126/science.414356 · Cited by 62
Food-anticipatory activity and liver per1-luc activity in diabetic transgenic rats
Davidson, A. J., Stokkan, K., Yamazaki, S., & Menaker, M. (2002) · Physiology & Behavior · doi:10.1016/s0031-9384(02)00680-7 · Cited by 59
Ketogenic Diet Disrupts the Circadian Clock and Increases Hypofibrinolytic Risk by Inducing Expression of Plasminogen Activator Inhibitor-1
Oishi, K., Uchida, D., Ohkura, N., Doi, R., Ishida, N., Kadota, K., & Horie, S. (2009) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.109.190140 · Cited by 59
Self-citation
Behavioral risk factors for overweight in early childhood; the ‘Be active, eat right’ study
Veldhuis, L., Vogel, I., Renders, C. M., van Rossem, L., Oenema, A., Hirasing, R. A., & Raat, H. (2012) · International Journal of Behavioral Nutrition and Physical Activity · doi:10.1186/1479-5868-9-74 · Cited by 57
High-salt diet advances molecular circadian rhythms in mouse peripheral tissues
Oike, H., Nagai, K., Fukushima, T., Ishida, N., & Kobori, M. (2010) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2010.09.072 · Cited by 49
Self-citation
FEEDING-INDUCED RAPID RESETTING OF THE HEPATIC CIRCADIAN CLOCK IS ASSOCIATED WITH ACUTE INDUCTION OFPER2ANDDEC1TRANSCRIPTION IN RATS
Wu, T., Ni, Y., Kato, H., & Fu, Z. (2010) · Chronobiology International · doi:10.3109/07420520903398625 · Cited by 45
Time-restricted feeding of rapidly digested starches causes stronger entrainment of the liver clock in PER2::LUCIFERASE knock-in mice
Itokawa, M., Hirao, A., Nagahama, H., Otsuka, M., Ohtsu, T., Furutani, N., Hirao, K., Hatta, T., & Shibata, S. (2013) · Nutrition Research · doi:10.1016/j.nutres.2012.12.004 · Cited by 41
Effects of cAMP, theophylline, imidazole, and 4-(3,4-dimethoxybenzyl)-2-imidazolidone on the leaf movement rhythm of Trifolium repens?a test of the cAMP-hypothesis of circadian rhythms
Bollig, I., Mayer, K., Mayer, W., & Engelmann, W. (1978) · Planta · doi:10.1007/bf00387893 · Cited by 39
The harmala alkaloid harmine is a modulator of circadian Bmal1 transcription
Onishi, Y., Oishi, K., Kawano, Y., & Yamazaki, Y. (2011) · Bioscience Reports · doi:10.1042/bsr20110002 · Cited by 38
Self-citation
Site-specific circadian expression of leptin and its receptor in human adipose tissue.
Gómez-Abellán, P., Santos, C. G., Madrid, J. A., Milagro, F. I., Campión, J., Martínez, J. A., Luján, J., Ordovás, J. M., & Garaulet, M. (2011) · PubMed · doi:10.1590/s0212-16112011000600029 · Cited by 25
Peroxisome proliferator-activated receptor α (PPARα) activation advances locomotor activity and feeding daily rhythms in mice
Gutman, R., Barnea, M., Haviv, L., Chapnik, N., & Froy, O. (2011) · International Journal of Obesity · doi:10.1038/ijo.2011.215 · Cited by 22
Dietary Obesity Caused by a Specific Circadian Eating Pattern
Hariri, N., & Thibault, L. (2011) · Chronobiology International · doi:10.3109/07420528.2010.548614 · Cited by 21
THE EFFECTS OF CAFFEINE AND THEOPHYLLINE ON THE PHOTOTACTIC RHYTHM OFCHLAMYDOMONAS REINHARDII
Goodenough, J., & Bruce, V. G. (1980) · Biological Bulletin · doi:10.2307/1540830 · Cited by 19

Sorted by citations

Precision Nutrition: A Review of Personalized Nutritional Approaches for the Prevention and Management of Metabolic Syndrome
de Toro‐Martín, J., Arsenault, B. J., Després, J., & Vohl, M. (2017) · Nutrients · doi:10.3390/nu9080913 · Cited by 534
The Influence of Meal Frequency and Timing on Health in Humans: The Role of Fasting
Paoli, A., Tinsley, G. M., Bianco, A., & Moro, T. (2019) · Nutrients · doi:10.3390/nu11040719 · Cited by 415
Circadian and feeding rhythms differentially affect rhythmic mRNA transcription and translation in mouse liver
Atger, F., Gobet, C., Marquis, J., Martín, E., Wang, J., Weger, B. D., Lefebvre, G. C., Descombes, P., Naef, F., & Gachon, F. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1515308112 · Cited by 254
New Insights Into the Circadian Rhythm and Its Related Diseases
Xie, Y., Tang, Q., Chen, G., Xie, M., Yu, S., Zhao, J., & Chen, L. (2019) · Frontiers in Physiology · doi:10.3389/fphys.2019.00682 · Cited by 250
On the origin of obesity: identifying the biological, environmental and cultural drivers of genetic risk among human populations
Qasim, A., Turcotte, M., de Souza, R. J., Samaan, M. C., Champredon, D., Dushoff, J., Speakman, J. R., & Meyre, D. (2018) · Obesity Reviews · doi:10.1111/obr.12625 · Cited by 241

See all 198

Authors: Oike, H., Oishi, K., & Kobori, M.
Affiliations: National Agriculture and Food Research Organization (JP)
Tokyo University of Science (JP)
Corresponding author: Oike, Hideaki
ORCID: Oike, Hideaki
Oishi, Katsutaka
Kobori, Masuko
Venue: Current Nutrition Reports
Publisher: Springer Science and Business Media LLC
Published: 2014-04-27
Volume: 3
Issue: 3
Pages: 204-212
ISSN: 2161-3311 (ISSN-L)
DOI: 10.1007/s13668-014-0082-6
PMC: PMC4118017
OpenAlex: W2072829785
Cited by: 198
References: 101
Citations by year: 2026: 10 · 2025: 25 · 2024: 17 · 2023: 20 · 2022: 20 · 2021: 19 · 2020: 21 · 2019: 18 · 2018: 7 · 2017: 18 · 2016: 9 · 2015: 12 · 2014: 2
FWCI: 1.54
Type: journal article
Language: en
Open access: hybrid
doi.org
Licence: cc-by
creativecommons.org/licenses/by/4.0 (unspecified)
Locations: Current Nutrition Reports (publishedVersion, cc-by)
PubMed Central (publishedVersion, cc-by)
PubMed (publishedVersion)
Funders: Japan Society for the Promotion of Science (25560066, 25702005, 25350179)
Topics: Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Circadian rhythm and melatonin
Health Sciences › Medicine › Physiology (medical) › Dietary Effects on Health
Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Nutrition, Genetics, and Disease
Keywords: circadian clock, clock genes, chrononutrition, time-restricted feeding, metabolic disorders, high-fat diet, energy homeostasis, dietary intake, fat deposition, energy expenditure, circadian rhythm disruption

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

Nutrients, Clock Genes, and Chrononutrition

Abstract

Overview

Integrity signals

Figures

Verification

Claims the paper makes

Claims other papers make about this one

Self-check

Citations

Cites

Cited by

Related

Metadata

Record

About these checks