Resetting process of peripheral circadian gene expression after the combined reversal of feeding schedule and light/dark cycle via a 24-h light period transition in rats

Physiological Research

Volumn 59, Issue 4, 2010, Pages 581-590

  Wu, T ^a   Ni, Y ^a   Zhuge, F ^a   Fu, Z ^a  

^a ZHEJIANG UNIVERSITY OF TECHNOLOGY   (China)

Author keywords

Heart; Light dark reversal; Liver; Peripheral clocks

Indexed keywords

BASIC HELIX LOOP HELIX TRANSCRIPTION FACTOR; BHLHB2 PROTEIN, RAT; CIRCADIAN RHYTHM SIGNALING PROTEIN; CRY1 PROTEIN, RAT; CRYPTOCHROME; HOMEODOMAIN PROTEIN; MESSENGER RNA; NR1D1 PROTEIN, RAT; NUCLEAR RECEPTOR NR1D1; PER1 PROTEIN, RAT; PER2 PROTEIN, RAT; TRANSCRIPTION FACTOR ARNTL;

ANIMAL; ARTICLE; ASSOCIATION; BIOLOGICAL RHYTHM; CIRCADIAN RHYTHM; FEEDING BEHAVIOR; GENE EXPRESSION REGULATION; GENETICS; HEART MUSCLE; JET LAG; LIVER; MALE; METABOLISM; PATHOPHYSIOLOGY; PHOTOPERIODICITY; PHOTOSTIMULATION; RAT; WISTAR RAT;

ANIMALS; ARNTL TRANSCRIPTION FACTORS; BASIC HELIX-LOOP-HELIX TRANSCRIPTION FACTORS; BIOLOGICAL CLOCKS; CIRCADIAN RHYTHM; CRYPTOCHROMES; CUES; FEEDING BEHAVIOR; GENE EXPRESSION REGULATION; HOMEODOMAIN PROTEINS; JET LAG SYNDROME; LIVER; MALE; MYOCARDIUM; NUCLEAR RECEPTOR SUBFAMILY 1, GROUP D, MEMBER 1; PERIOD CIRCADIAN PROTEINS; PHOTIC STIMULATION; PHOTOPERIOD; RATS; RATS, WISTAR; RNA, MESSENGER;

EID: 77958149666     PISSN: 08628408     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (24)

1. ALBRECHT U, SUN ZS, EICHELE G, LEE CC: A differential response of two putative mammalian circadian regulators, mper1 and mper2, to light. Cell 91: 1055-1064, 1997.
2. ALBRECHT U, ZHENG B, LARKIN D, SUN ZS, LEE CC: mPer1 and mPer2 are essential for normal resetting of the circadian clock. J Biol Rhythms 16: 100-104, 2001.
3. BARRETT RK, TAKAHASHI JS: Temperature compensation and temperature entrainment of the chick pineal cell circadian clock. J Neurosci 15: 5681-5692, 1995.
4. DAMIOLA F, LE MINH N, PREITNER N, KORNMANN B, FLEURY-OLELA F, SCHIBLER U: Restricted feeding uncouples circadian oscillators in peripheral tissues from the central pacemaker in the suprachiasmatic nucleus. Genes Dev 14: 2950-2961, 2000.
5. DONG Y, WU T, NI Y, KATO H, FU Z: Effect of fasting on the peripheral circadian gene expression in rats. Biol Rhythm Res 41: 41-47, 2009.
6. DUNLAP JC: Molecular bases for circadian clocks. Cell 96: 271-290, 1999.
7. FEILLET CA, RIPPERGER JA, MAGNONE MC, DULLOO A, ALBRECHT U, CHALLET E: Lack of food anticipation in Per2 mutant mice. Curr Biol 16: 2016-2022, 2006.
8. GREEN CB, TAKAHASHI JS, BASS J: The meter of metabolism. Cell 134: 728-742, 2008.
9. HARA R, WAN K, WAKAMATSU H, AIDA R, MORIYA T, AKIYAMA M, SHIBATA S: Restricted feeding entrains liver clock without participation of the suprachiasmatic nucleus. Genes Cells 6: 269-278, 2001.
10. HASTINGS MH: Circadian clocks. Curr Biol 7: R670-R672, 1997.
11. ILLNEROVÁ H, VANECEK J, HOFFMANN K: Adjustment of the rat pineal N-acetyltransferase rhythm to eight-hour shifts of the light-dark cycle: advance of the cycle disturbs the rhythm more than delay. Brain Res 417: 167-171, 1987.
12. ISHIDA A, MUTOH T, UEYAMA T, BANDO H, MASUBUCHI S, NAKAHARA D, TSUJIMOTO G, OKAMURA H: Light activates the adrenal gland: timing of gene expression and glucocorticoid release. Cell Metab 2: 297-307, 2005.
13. LIU C, WEAVER DR, JIN X, SHEARMAN LP, PIESCHL RL, GRIBKOFF VK, REPPERT SM: Molecular dissection of two distinct actions of melatonin on the suprachiasmatic circadian clock. Neuron 19: 91-102, 1997.
14. ΔΔCt method. Methods 25: 402-408, 2001.
15. MIRANDA-ANAYA M, BARTELL PA, YAMAZAKI S, MENAKER M: Circadian rhythm of ERG in Iguana iguana: role of the pineal. J Biol Rhythms 15: 163-171, 2000.
16. REDDY AB, FIELD MD, MAYWOOD ES, HASTINGS MH: Differential resynchronisation of circadian clock gene expression within the suprachiasmatic nuclei of mice subjected to experimental jet lag. J Neurosci 22: 7326-7330, 2002.
17. SHIGEYOSHI Y, TAGUCHI K, YAMAMOTO S, TKEKIDA S, YAN L, TEI H, MORIYA T, SHIBATA S, LOROS JJ, DUNLAP JC, OKAMURA H: Light-induced resetting of a mammalian circadian clock is associated with rapid induction of the mPer1 transcript. Cell 91: 1043-1053, 1997.
18. STOKKAN KA, YAMAZAKI S, TEI H, SAKAKI Y, MENAKER M: Entrainment of the circadian clock in the liver by feeding. Science 291: 490-493, 2001.
19. SUJINO M, NAGANO M, FUJIOKA A, SHIGEYOSHI Y, INOUYE ST: Temporal profile of circadian clock gene expression in a transplanted suprachiasmatic nucleus and peripheral tissues. Eur J Neurosci 26: 2731-2738, 2007.
20. TAKAMURE M, MURAKAMI N, TAKAHASHI K, KURODA H, ETOH T: Rapid reentrainment of the circadian clock itself, but not the measurable activity rhythms to a new light-dark cycle in the rat. Physiol Behav 50: 443-449, 1991.
21. WAKAMATSU H, YOSHINOBU Y, AIDA R, MORIYA T, AKIYAMA M, SHIBATA S: Restricted-feeding-induced anticipatory activity rhythm is associated with a phase-shift of the expression of mPer1 and mPer2 mRNA in the cerebral cortex and hippocampus but not in the suprachiasmatic nucleus of mice. Eur J Neurosci 13: 1190-1196, 2001.
22. WU T, JIN Y, KATO H, FU Z: Light and food signals cooperate to entrain the rat pineal circadian system. J Neurosci Res 86: 3246-3255, 2008a.
23. WU T, JIN Y, NI Y, ZHANG D, KATO H, FU Z: Effects of light cues on re-entrainment of the food-dominated peripheral clocks in mammals. Gene 419: 27-34, 2008b.
24. WU T, DONG Y, YANG Z, KATO H, NI Y, FU Z: Differential resetting process of circadian system in rat pineal gland after the reversal of light/dark cycle via a 24-h light or dark period transition. Chronobiol Int 26: 793-807, 2009.