Chronic exposure to melatonin receptor agonists does not alter their effects on suprachiasmatic nucleus neurons

Shui Wang Ying, Benjamin Rusak, Elisabeth Mocaër

Résultat de recherche: Articleexamen par les pairs

32 Citations (Scopus)

Résumé

Previous studies have demonstrated that melatonin and a novel melatonin receptor agonist, S20098 (N-[2-(7-methoxy-1-naphthyl) ethyl] acetamide), regulate neuronal firing activity of photically responsive cells in the suprachiasmatic nucleus in vivo. In the present study, we used several different methods to investigate the effects of chronic daily treatment with melatonin, S20098 (1.0 mg/kg, s.c.) or control vehicle for 14 d on responsiveness of suprachiasmatic nucleus cells to these agonists. Both chronic and acute application of drugs were carried out during the day-night transition period. We confirmed that suprachiasmatic nucleus cells from control animals were most sensitive at this circadian phase. Chronic drug treatments did not alter sensitivity of photically responsive suprachiasmatic nucleus cells to S20098 or melatonin given intraperitoneally (i.p.) or iontophoretically in vivo. Suprachiasmatic nucleus cells studied in brain slice preparations also responded similarly to micropressure ejections of melatonin receptor agonists regardless of drug pretreatment. These results indicate that chronic melatonin receptor agonist pretreatment does not result in desensitization of suprachiasmatic nucleus neuronal responses to these agonists during the daily phase of maximum melatonin sensitivity.

Langue d'origineEnglish
Pages (de-à)29-37
Nombre de pages9
JournalEuropean Journal of Pharmacology
Volume342
Numéro de publication1
DOI
Statut de publicationPublished - janv. 19 1998

Note bibliographique

Funding Information:
This research was supported by contracts from Servier, Canada and Institut de Recherches Internationales Servier, and a grant from NSERC of Canada. We are grateful to Donna Goguen and Victoria Muise for their excellent technical assistance.

ASJC Scopus Subject Areas

  • Pharmacology

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