Carbachol Induces Phase-dependent Phase Shifts of Per1 Transcription Rhythms in Cultured Suprachiasmatic Nucleus Slices

J Biol Rhythms. 2017 Apr;32(2):101-108. doi: 10.1177/0748730417691205. Epub 2017 Feb 1.

Abstract

Among nonphotic stimulants, a classic cholinergic agonist, carbachol, is known to have a strong and unique phase-resetting effect on the circadian clock: Intracerebroventricular carbachol treatment causes phase delays during the subjective early night and phase advances in the subjective late night, but the effects of this drug on the suprachiasmatic nucleus (SCN) in vivo and in vitro are still controversial. In the present study, we succeeded in reproducing the biphasic phase-shifting effect of carbachol on clock gene expression in organotypic SCN slices prepared from mice carrying a Per1-promoter fused luciferase gene ( Per1-luc). Since this biphasic effect of carbachol in Per1-luc SCN was prevented by atropine but not by mecamylamine, we concluded that these phase shifts were muscarinic receptor-dependent. Next, we analyzed the expression of muscarinic receptors in the SCN by in situ hybridization and found that M3 and M4 subtypes were expressed in SCN cells. These signals appeared neonatally and reached adult levels at postnatal day 10. Together, these findings suggest that carbachol has a phase-dependent phase-shifting effect on the SCN clock through muscarinic receptor subtypes expressed in the SCN.

Keywords: Per1; carbachol; mice; muscarinic receptor; slice culture; suprachiasmatic nucleus.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Animals, Newborn
  • Atropine / pharmacology
  • Carbachol / pharmacology*
  • Cholinergic Agonists / pharmacology*
  • Circadian Clocks / drug effects
  • Circadian Rhythm / drug effects*
  • Gene Expression
  • Luciferases / genetics
  • Mecamylamine / pharmacology
  • Mice
  • Motor Activity
  • Muscarinic Antagonists / pharmacology
  • Nicotinic Antagonists / pharmacology
  • Organ Culture Techniques
  • Period Circadian Proteins / genetics*
  • Promoter Regions, Genetic
  • Receptors, Muscarinic / genetics
  • Receptors, Muscarinic / metabolism
  • Suprachiasmatic Nucleus / drug effects*
  • Suprachiasmatic Nucleus / physiology*
  • Transcription, Genetic*

Substances

  • Cholinergic Agonists
  • Muscarinic Antagonists
  • Nicotinic Antagonists
  • Per1 protein, mouse
  • Period Circadian Proteins
  • Receptors, Muscarinic
  • Mecamylamine
  • Atropine
  • Carbachol
  • Luciferases