The DOI matches its Crossref record; 28 of the 28 references it cites were found in a registry or an index.
Restricted feeding entrains liver clock without participation of the suprachiasmatic nucleus
Abstract
BACKGROUND: There are two main stimuli that entrain the circadian rhythm, the light-dark cycle (LD) and restricted feeding (RF). Light-induced entrainment requires induction of the Per1 and Per2 genes in the suprachiasmatic nucleus (SCN), the locus of a main oscillator. In this experiment, we determined whether RF resets the expression of circadian clock genes in the mouse liver with or without participation of the SCN. RESULTS: Mice were allowed access to food for 4 h during the daytime (7 h advance of feeding time) under LD or constant darkness (DD). The peaks of mPer1, mPer2, D-site-binding protein (Dbp) and cholesterol 7alpha-hydroxylase (Cyp7A) mRNA in the liver were advanced 6-12 h after 6 days of RF, whereas those in SCN were unaffected. The advance of mPer expression in the liver by RF was still observed in SCN-lesioned mice. A 7 h advance in the LD cycle advanced the peaks of clock gene expression in both the liver and SCN, whereas, a shift in the LD did not move the phase of the liver clock when the shift was carried out under a fixed RF schedule during the night-time. CONCLUSIONS: These results suggest that restricted feeding strongly entrained the expression of circadian clock genes in the liver without the participation of an SCN clock function.
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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 [261]
In the citing paper
“Indeed, it was shown that rhythmic feeding is both necessary and sufficient to drive the circadian expression of liver genes [7,8]”
From Circadian control of glucose metabolism (2014) · cites this paper as [7]
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Modulation of metabolic and clock gene mRNA rhythms by pineal and retinal circadian oscillators
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“…oscillators (Yoo et al., 2004; Stratmann and Schibler, 2006), we have decided to focus on liver and heart, since these tissues are commonly studied in mammalian systems, where they have been shown to be regulated autonomously from SCN (Damiola et al., 2000; Hara et al., 2001; Stokkan et al., 2001).”
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“The SF regimen entrains circadian clocks in the liver, kidney, lung, heart, salivary gland, and pancreas (Challet et al., 2003; Damiola et al., 2000; Hara et al., 2001; Kobayashi et al., 2004; Schibler et al., 2003; Stokkan et al., 2001; Kuroda et al., 2012).”
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“…allowed to eat only during a portion of their resting time, entrains rhythms in clock gene expression in peripheral organs, e.g., in the liver, heart, intestine, etc., but does not affect rhythmicity in the SCN (Damiola et al., 2000; Sládek et al., 2007; Hara et al., 2001; Stokkan et al., 2001).”
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“In this way, the hepatic clock is entrained directly by time-restricted feeding cycles, not by lightdark phase cycles and this phenomenon is independent of the master clock located in the SCN [52, 53, 55].”
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“Studies reporting no changes on the SCN have exposed mice (not rats) to relatively brief (6–8 days in duration) intervals of daily feeding schedules (Damiola et al., 2000; Hara et al., 2001; Wakamatsu et al., 2001).”
BackgroundThe impact of meal timing on cardiometabolic syndrome indicators in shift workers
Molzof, H. E., Wirth, M. D., Burch, J. B., Shivappa, N., Hébert, J. R., Johnson, R. L., & Gamble, K. L. (2017) · Chronobiology International · doi:10.1080/07420528.2016.1259242 · Cited by 52
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“…of clock genes in peripheral tissues, such as in the intestine and liver, is also affected by food availability (Damiola et al., 2000; Stokkan et al., 2001; Hara et al., 2001; Stephan, 2002; Feillet et al., 2006; Mendoza, 2007; Hussain and Pan, 2009; Patton and Mistlberger, 2013; Hussain, 2014b).”
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Atger, F., Mauvoisin, D., Weger, B. D., Gobet, C., & Gachon, F. (2017) · Frontiers in Endocrinology · doi:10.3389/fendo.2017.00042 · Cited by 46
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“In rodents, daytime restricted feeding (RF) can entrain the circadian clock of many peripheral tissues and some extra-SCN brain regions independent of the SCN clock (Damiola et al., 2000; Hara et al., 2001; MinanaSolis et al., 2009; Stokkan et al., 2001; Wakamatsu et al., 2000).”
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Silver, R., Balsam, P. D., Butler, M. P., & LeSauter, J. (2011) · Physiology & Behavior · doi:10.1016/j.physbeh.2011.05.034 · Cited by 44
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“By contrast, the profiles in the liver were completely phase-inverted as previously reported [15,16,17], which denoted that the liver clock was preferentially entrained by feeding-associated cues rather than light-related cues, whereas the response of the pituitary clock appeared more complex.”
BackgroundInfluentialTime-Restricted Feeding Alters the Innate Immune Response to Bacterial Endotoxin
Cissé, Y. M., Borniger, J. C., Lemanski, E. A., Walker, W. H., & Nelson, R. J. (2017) · The Journal of Immunology · doi:10.4049/jimmunol.1701136 · Cited by 43
“Phase shifts of circadian clocks in the liver (22, 23), kidney, heart, pancreas (54), and muscle (64) have been reported in response to time-restricted feeding.”
BackgroundThe Impact of Time of Day on Energy Expenditure: Implications for Long-Term Energy Balance
Shaw, E., Leung, G. K. W., Jong, J., Coates, A. M., Davis, R., Blair, M., Huggins, C. E., Dorrian, J., Banks, S., Kellow, N. J., et al. (2019) · Nutrients · doi:10.3390/nu11102383 · Cited by 45
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“After 5 days of the shift, when rats were left in DD and with food ad libitum, we observed that in the RFS-S group, the phase of the free-running rhythm started at the phase achieved after 5 days in the new cycle, suggesting a corresponding shift of the SCN.”
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“…to the extent that the working pattern decouples from the central master clock (SCN) to obey other synchronizing cues (Damiola et al., 2000; Hara et al., 2001; Schilber, 2009; Stokkan et al., 2001), and becomes tissue-specific for particular physiological processes (Betancor et al., 2014).”
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“Similar to food restriction, calorie restriction can also synchronize peripheral oscillators; however, unlike food restriction, calorie restriction can entrain the SCN [269-272].”
BackgroundHepatic nervous system and neurobiology of the liver
Jensen, K. J., Alpini, G., & Glaser, S. (2013) · Comprehensive physiology · doi:10.1002/j.2040-4603.2013.tb00506.x · Cited by 38
“Endogenous expression of Per1 has been shown to be flattened by restricted feeding (34).”
The role of the circadian timing system on drug metabolism and detoxification: an update
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“These pathways are essential and effective in synchronizing the circadian expression of peripheral clocks [6–9].”
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Peripheral Circadian Oscillators
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“Previously, it has been shown that SCN-lesioned mice exhibit arrhythmicity of behavioral rhythm and dispersed phase of liver rhythm (Yoo et al., 2004).”
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“…Per1 gene expression; in WT mice, inductive effects of TCDD on mammary gland expression of Cyp1A1 are low during the day and high at night corresponding respectively to times when the rhythmic peak and trough in tissue levels of Per1 mRNA are known to occur (Hara et al., 2001; Metz et al., 2006).”
BackgroundNeural regulation of the hepatic Circadian rhythm
Shibata, S. (2004) · The Anatomical Record Part A Discoveries in Molecular Cellular and Evolutionary Biology · doi:10.1002/ar.a.20095 · Cited by 39
“…adrenocorticotropic hormone, glucocorticoid (Moore, 1997; Meyer-Bernstein et al., 1999), and locomotor activity (Hara et al., 2001) and flattens the circadian expression rhythm of clock genes such as Per and Bmal1 in peripheral tissues such as the liver (Sakamoto et al., 1998; Hara et al., 2001).”
BackgroundInfluentialGuerrero‐Vargas, N. N., Zárate‐Mozo, C., Guzmán‐Ruiz, M. A., Cárdenas‐Rivera, A., & Escobar, C. (2020) · Journal of Neuroscience Research · doi:10.1002/jnr.24741 · Cited by 41
“Food intake during the normal rest phase induces circadian desynchrony by differentially shifting the phase of some peripheral oscillators, while others stay synchronized to the light–dark cycle (Hara et al., 2001; Wu et al., 2008).”
BackgroundRegulation of circadian gene expression in the kidney by light and food cues in rats
Wu, T., Ni, Y., Dong, Y., Xu, J., Song, X., Kato, H., & Fu, Z. (2010) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00578.2009 · Cited by 37
“In the SCN clock, CLOCK and BMAL1 form heterodimers that bind to E-boxes in the promoter of various target genes, including those encoding for negative (e.g., Per1, Cry1) and positive (e.g., Bmal1) loop components, resulting in transcriptional activation (7, 13).”
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Time to learn: The role of the molecular circadian clock in learning and memory
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“Restriction of food availability to only the resting part of the day, that is, to its light phase in nocturnal rodents, is a potent entraining cue for the peripheral clocks, while the SCN clock remains dominantly synchronized with the LD cycle (Damiola et al., 2000; Hara et al., 2001; Stokkan et al., 2001; Wakamatsu e…”
BackgroundAn Endocrinologist's Guide to the Clock
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“Also consistent with previous work, nighttime restricted feeding induced a rhythm of PER2 expression in the DMH and these effects occurred without affecting the rhythm in the suprachiasmatic nucleus (SCN).”
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“…activity rhythm especially in rats (Mistlberger, 1994; Stephan, 2001) and do not affect the phase of clock genes in the SCN (Damiola et al., 2000; Hara et al., 2001; Wakamatsu et al., 2001), although entrainment to temporal restricted feeding has been recently reported in mice housed in constant…”
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Circadian rhythms: a possible new player in non-alcoholic fatty liver disease pathophysiology
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Transcriptional control of circadian metabolic rhythms in the liver
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Patterns of fos activation in rat raphe nuclei during feeding behavior
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Misalignment of Circadian Rhythms in Diet-Induced Obesity
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Multi-Modal Regulation of Circadian Physiology by Interactive Features of Biological Clocks
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Diurnal expression ofDnmt3bmRNA in mouse liver is regulated by feeding and hepatic clockwork
Maekawa, F., Shimba, S., Takumi, S., Sano, T., Suzuki, T., Bao, J., Ohwada, M., Ehara, T., Ogawa, Y., & Nohara, K. (2012) · Epigenetics · doi:10.4161/epi.21539 · Cited by 32
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“In adult rats, several reports have indicated that clock gene and protein rhythms in the SCN do not shift in relation to feeding schedules (Damiola et al., 2000; Hara et al., 2001).”
Modifications of local cerebral glucose utilization during circadian food-anticipatory activity
de Vasconcelos, A. P., Bartol-Munier, I., Feillet, C. A., Gourmelen, S., Pévet, P., & Challet, É. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2005.12.045 · Cited by 30
Metadata
- Authors
- Hara, R., Wan, K., Wakamatsu, H., Aida, R., Moriya, T., Akiyama, M., & Shibata, S.
- Affiliations
- Waseda University (JP)
- Corresponding author
- Shibata, Shigenobu
- ORCID
- Shibata, Shigenobu
- Venue
- Genes to Cells
- Publisher
- Wiley
- Published
- 2001-03
- Volume
- 6
- Issue
- 3
- Pages
- 269-278
- ISSN
- 1356-9597 (ISSN-L)
- 1365-2443
- OpenAlex
- W1965036088
- Cited by
- 569
- References
- 28
- Citations by year
- 2026: 12 · 2025: 12 · 2024: 17 · 2023: 20 · 2022: 27 · 2021: 24 · 2020: 24 · 2019: 18 · 2018: 23 · 2017: 36 · 2016: 20 · 2015: 29 · 2014: 26 · 2013: 21 · 2012: 29
- FWCI
- 5.94
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Genes to Cells (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Ministerul Cercetării, Inovării şi Digitalizării
- Topics
- Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Circadian rhythm and melatonin
- Health Sciences › Medicine › Physiology (medical) › Dietary Effects on Health
- Social Sciences › Psychology › Experimental and Cognitive Psychology › Sleep and Work-Related Fatigue
- Keywords
- feed restriction, circadian entrainment, liver clock, suprachiasmatic nucleus, clock genes, Per1, Per2, DBP, SCN lesions, light-dark cycle, constant darkness
- MeSH terms
- Animals, Biological Clocks, Feeding Methods, Gene Expression Regulation, Liver, Male, Nuclear Proteins, Suprachiasmatic Nucleus, Transcription Factors, Cell Cycle Proteins, Mice, Period Circadian Proteins
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