Mitogen-activated protein kinase is a functional component of the autonomous circadian system in the suprachiasmatic nucleus

Makoto Akashi, Naoto Hayasaka, Shin Yamazaki, Koichi Node

Research output: Contribution to journalArticle

35 Citations (Scopus)

Abstract

The suprachiasmatic nucleus (SCN) is the master circadian pacemaker driving behavioral and physiological rhythms in mammals. Circadian activation of mitogen-activated protein kinase [MAPK; also known as ERK (extracellular signal-regulated kinase)] is observed in vivo in the SCN under constant darkness, although the biological significance of this remains unclear. To elucidate this question, we first examined whether MAPK was autonomously activated in ex vivo SCN slices. Moreover, we investigated the effect of MAPK inhibition on circadian clock gene expression and neuronal firing rhythms using SCN-slice culture systems. We show herein that MAPK is autonomously activated in the SCN, and our data demonstrate that inhibition of the MAPK activity results in dampened rhythms and reduced basal levels in circadian clock gene expression at the SCN single-neuron level. Furthermore, MAPK inhibition attenuates autonomous circadian neuronal firing rhythms in the SCN. Thus, our data suggest that light-independent MAPK activity contributes to the robustness of the SCN autonomous circadian system.

Original languageEnglish (US)
Pages (from-to)4619-4623
Number of pages5
JournalJournal of Neuroscience
Volume28
Issue number18
DOIs
StatePublished - Apr 30 2008

Fingerprint

Suprachiasmatic Nucleus
Mitogen-Activated Protein Kinases
Circadian Clocks
Gene Expression
Darkness
Extracellular Signal-Regulated MAP Kinases
Mammals
Neurons
Light

Keywords

  • Circadian rhythms
  • ERK
  • Suprachiasmatic nucleus
  • Tissue culture
  • Transcription
  • Transgenic

ASJC Scopus subject areas

  • Neuroscience(all)
  • Medicine(all)

Cite this

Mitogen-activated protein kinase is a functional component of the autonomous circadian system in the suprachiasmatic nucleus. / Akashi, Makoto; Hayasaka, Naoto; Yamazaki, Shin; Node, Koichi.

In: Journal of Neuroscience, Vol. 28, No. 18, 30.04.2008, p. 4619-4623.

Research output: Contribution to journalArticle

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