The day/night difference in the circadian clock's response to acute lipopolysaccharide and the rhythmic Stat3 expression in the rat suprachiasmatic nucleus
Jazyk angličtina Země Spojené státy americké Médium electronic-ecollection
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
30265676
PubMed Central
PMC6161871
DOI
10.1371/journal.pone.0199405
PII: PONE-D-18-15844
Knihovny.cz E-zdroje
- MeSH
- cirkadiánní rytmus účinky léků MeSH
- krysa rodu Rattus MeSH
- lipopolysacharidy toxicita MeSH
- lokomoce účinky léků MeSH
- MAP kinasový signální systém účinky léků MeSH
- mitogenem aktivovaná proteinkinasa 3 metabolismus MeSH
- nucleus suprachiasmaticus metabolismus patologie MeSH
- potkani Wistar MeSH
- regulace genové exprese účinky léků MeSH
- transkripční faktor STAT3 biosyntéza MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- lipopolysacharidy MeSH
- mitogenem aktivovaná proteinkinasa 3 MeSH
- Stat3 protein, rat MeSH Prohlížeč
- transkripční faktor STAT3 MeSH
The circadian clock in the suprachiasmatic nucleus (SCN) regulates daily rhythms in physiology and behaviour and is an important part of the mammalian homeostatic system. Previously, we have shown that systemic inflammatory stimulation with lipopolysaccharide (LPS) induced the daytime-dependent phosphorylation of STAT3 in the SCN. Here, we demonstrate the LPS-induced Stat3 mRNA expression in the SCN and show also the circadian rhythm in Stat3 expression in the SCN, with high levels during the day. Moreover, we examined the effects of LPS (1mg/kg), applied either during the day or the night, on the rhythm in locomotor activity of male Wistar rats. We observed that recovery of normal locomotor activity patterns took longer when the animals were injected during the night. The clock genes Per1, Per2 and Nr1d1, and phosphorylation of kinases ERK1/2 and GSK3β are sensitive to external cues and function as the molecular entry for external signals into the circadian clockwork. We also studied the immediate changes in these clock genes expressions and the phosphorylation of ERK1/2 and GSK3β in the suprachiasmatic nucleus in response to daytime or night-time inflammatory stimulation. We revealed mild and transient changes with respect to the controls. Our data stress the role of STAT3 in the circadian clock response to the LPS and provide further evidence of the interaction between the circadian clock and immune system.
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