Restricted feeding entrains liver clock without participation of the suprachiasmatic nucleus

R Hara, K Wan, H Wakamatsu, R Aida, T Moriya… - Genes to …, 2001 - Wiley Online Library
R Hara, K Wan, H Wakamatsu, R Aida, T Moriya, M Akiyama, S Shibata
Genes to Cells, 2001Wiley Online Library
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 …
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 7α‐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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