Activation of MT2 melatonin receptors in rat suprachiasmatic nucleus phase advances the circadian clock

Amanda E. Hunt, Walid M. Al-Ghoul, Martha U. Gillette, Margarita L. Dubocovich

Research output: Contribution to journalArticle

Abstract

The aim of this study was to identify the melatonin receptor type(s) (MT1 or MT2) mediating circadian clock resetting by melatonin in the mammalian suprachiasmatic nucleus (SCN). Quantitative receptor autoradiography with 2-[125I]iodomelatonin and in situ hybridization histochemistry, with either 33P- or digoxigenin-labeled antisense MT1 and MT2 melatonin receptor mRNA oligonucleotide probes, revealed specific expression of both melatonin receptor types in the SCN of inbred Long-Evans rats. The melatonin receptor type mediating phase advances of the circadian rhythm of neuronal firing rate in the SCN slice was assessed using competitive melatonin receptor antagonists, the MT1/MT2 nonselective luzindole and the MT2-selective 4-phenyl-2-propionamidotetraline (4P-PDOT). Luzindole and 4P-PDOT (1 nM-1 μM) did not affect circadian phase on their own; however, they blocked both the phase advances (∼4 h) in the neuronal firing rate induced by melatonin (3 pM) at temporally distinct times of day [i.e., subjective dusk, circadian time (CT) 10; and dawn, CT 23], as well as the associated increases in protein kinase C activity. We conclude that melatonin mediates phase advances of the SCN circadian clock at both dusk and dawn via activation of MT2 melatonin receptor signaling.

Original languageEnglish (US)
Pages (from-to)C110-C118
JournalAmerican Journal of Physiology - Cell Physiology
Volume280
Issue number1 49-1
DOIs
StatePublished - 2001

Keywords

  • 4-phenyl-2-propionamidotetraline
  • Brain slice electrophysiology
  • Luzindole
  • Protein kinase C
  • Suprachiasmatic nucleus

ASJC Scopus subject areas

  • Clinical Biochemistry
  • Cell Biology
  • Physiology

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