Different mechanisms of adjustment to a change of the photoperiod in the suprachiasmatic and liver circadian clocks
Language English Country United States Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
20071612
DOI
10.1152/ajpregu.00561.2009
PII: 00561.2009
Knihovny.cz E-resources
- MeSH
- Biological Clocks MeSH
- Period Circadian Proteins genetics MeSH
- Circadian Rhythm physiology MeSH
- Photoperiod * MeSH
- Nuclear Receptor Subfamily 1, Group D, Member 1 genetics MeSH
- Liver physiology MeSH
- DNA, Complementary genetics MeSH
- Mice MeSH
- Suprachiasmatic Nucleus physiology MeSH
- Organ Specificity MeSH
- Motor Activity physiology MeSH
- Reverse Transcriptase Polymerase Chain Reaction MeSH
- Gene Expression Regulation MeSH
- Social Adjustment MeSH
- Light MeSH
- Darkness MeSH
- ARNTL Transcription Factors genetics MeSH
- Animals MeSH
- Check Tag
- Mice MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Bmal1 protein, mouse MeSH Browser
- Period Circadian Proteins MeSH
- Nuclear Receptor Subfamily 1, Group D, Member 1 MeSH
- DNA, Complementary MeSH
- Per2 protein, mouse MeSH Browser
- ARNTL Transcription Factors MeSH
Changes in photoperiod modulate the circadian system, affecting the function of the central clock located in the suprachiasmatic nucleus (SCN) of the hypothalamus. The aim of the present study was to elucidate the dynamics of adjustment to a change of a long photoperiod with 18 h of light to a short photoperiod with 6 h of light of clock gene expression rhythms in the mouse SCN and in the peripheral clock in the liver, as well as of the locomotor activity rhythm. Three, five, and thirteen days after the photoperiod change, daily profiles of Per1, Per2, and Rev-erbalpha expression in the rostral, middle, and caudal parts of the SCN and of Per2 and Rev-erbalpha in the liver were determined by in situ hybridization and real-time RT-PCR, respectively. The clock gene expression rhythms in the different SCN regions, desynchronized under the long photoperiod, attained synchrony gradually following the transition from long to short days, mostly via advancing the expression decline. The photoperiodic modulation of the SCN was due not only to the degree of synchrony among the SCN regions but also to different waveforms of the rhythms in the individual SCN parts. The locomotor activity rhythm adjusted gradually to short days by advancing the activity onset, and the liver rhythms adjusted by advancing the Rev-erbalpha expression rise and Per2 decline. These data indicate different mechanisms of adjustment to a change of the photoperiod in the central SCN clock and the peripheral liver clock.
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