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
Language English Country Czech Republic Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
19929146
DOI
10.33549/physiolres.931818
PII: 931818
Knihovny.cz E-resources
- MeSH
- Biological Clocks genetics MeSH
- Period Circadian Proteins genetics MeSH
- Circadian Rhythm genetics MeSH
- Photoperiod * MeSH
- Homeodomain Proteins genetics MeSH
- Nuclear Receptor Subfamily 1, Group D, Member 1 genetics MeSH
- Liver metabolism MeSH
- Jet Lag Syndrome genetics physiopathology MeSH
- Cryptochromes genetics MeSH
- Rats MeSH
- RNA, Messenger metabolism MeSH
- Myocardium metabolism MeSH
- Cues MeSH
- Rats, Wistar MeSH
- Gene Expression Regulation MeSH
- Feeding Behavior * MeSH
- Photic Stimulation MeSH
- ARNTL Transcription Factors genetics MeSH
- Basic Helix-Loop-Helix Transcription Factors genetics MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Male MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Bhlhe40 protein, rat MeSH Browser
- Period Circadian Proteins MeSH
- Cry1 protein, rat MeSH Browser
- Homeodomain Proteins MeSH
- Nuclear Receptor Subfamily 1, Group D, Member 1 MeSH
- Cryptochromes MeSH
- RNA, Messenger MeSH
- Nr1d1 protein, rat MeSH Browser
- Per1 protein, rat MeSH Browser
- Per2 protein, rat MeSH Browser
- ARNTL Transcription Factors MeSH
- Basic Helix-Loop-Helix Transcription Factors MeSH
To investigate the effect of light cue on the resetting of the peripheral clocks, we examined the resetting processes of clock genes (Per1, Per2, Bmal1, Cry1, Dec1, and Rev-erbalpha) in the liver and heart of rats after the feeding and light-dark (LD) reversal via a 24-h light period transition. The liver clock was reset quickly within 3 days, while the heart clock needed a longer time course of 5-7 days to be completely re-entrained. Moreover, the re-entrainment of Per1 and Per2 in the liver clock was more rapid than that of the other four clock genes, suggesting the important role of these two clock genes in initiating the circadian resetting of the hepatic clock. However, the resetting rates of these two clock genes were as similar as the others in the heart clock. Therefore, the resetting mechanisms underlining these two peripheral clocks may be totally distinct. Furthermore, the re-entrainment of the liver and heart clocks were relatively lengthened after the feeding and LD reversal via a light period transition compared to a dark period transition, suggesting a simultaneous shift of feeding schedule and the LD cycle may facilitate the circadian resetting in rats.
College of Biological and Environmental Engineering Zhejiang University of Technology Zhejiang China
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