Circadian and light regulation of oxytocin and parvalbumin protein levels in the ciliated ependymal layer of the third ventricle in the C57 mouse

K. Devarajan, E. G. Marchant, B. Rusak

Résultat de recherche: Articleexamen par les pairs

20 Citations (Scopus)

Résumé

The walls of the third ventricle have been proposed to serve as a bidirectional conduit for exchanges between the neural parenchyma and the cerebrospinal fluid. In immunohistochemical studies of mice, we observed that light exposure and circadian phase affected peptide staining surrounding the third ventricle at the level of the suprachiasmatic nuclei. Under high magnification, we observed robust staining for the neurohormone oxytocin and the calcium-binding protein parvalbumin associated with cilia extending into the third ventricle from the surrounding ventricular wall; no similar staining was observed for vasopressin or calbindin. Retinal illumination had opposite effects on levels of parvalbumin and oxytocin in the cilia: light exposure during late subjective night increased oxytocin staining, but decreased parvalbumin staining in the cilia. Preventing cellular transport with colchicine eliminated immunohistochemical staining for oxytocin in the cilia. There was also a significant daily rhythm of oxytocin immunostaining in the third ventricle wall, and in magnocellular neurons in the anterior hypothalamus. The results suggest that environmental lighting and circadian rhythms regulate levels of oxytocin in the cerebrospinal fluid, possibly by regulating movement of oxytocin through the third ventricle wall.

Langue d'origineEnglish
Pages (de-à)539-547
Nombre de pages9
JournalNeuroscience
Volume134
Numéro de publication2
DOI
Statut de publicationPublished - 2005

Note bibliographique

Funding Information:
We would like to thank Kazue Semba, Sue Carter and David Hopkins for their valuable advice and assistance. We are also grateful to Donna Goguen, Debbie Fice, Marc Goguen, Stephen Whitefield and Haiyun Zhang for their technical assistance. Supported by grants from the Canadian Institutes of Health Research (MOP53347) and NSERC of Canada (A0305). K.D. and E.M. were supported by undergraduate and postdoctoral awards from NSERC.

ASJC Scopus Subject Areas

  • General Neuroscience

PubMed: MeSH publication types

  • Journal Article
  • Research Support, Non-U.S. Gov't

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