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Opposing actions of neuropeptide Y and light on the expression of circadian clock genes in the mouse suprachiasmatic nuclei
Author(s) -
Maywood Elizabeth S.,
Okamura Hitoshi,
Hastings Michael H.
Publication year - 2002
Publication title -
european journal of neuroscience
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.346
H-Index - 206
eISSN - 1460-9568
pISSN - 0953-816X
DOI - 10.1046/j.0953-816x.2001.01852.x
Subject(s) - circadian rhythm , suprachiasmatic nucleus , light effects on circadian rhythm , entrainment (biomusicology) , endocrinology , biology , medicine , circadian clock , neuropeptide y receptor , neuropeptide , clock , period (music) , neuroscience , microbiology and biotechnology , rhythm , genetics , receptor , physics , acoustics
The circadian clockwork of the hypothalamic suprachiasmatic nuclei (SCN) is synchronized by light and by nonphotic cues. The core timing mechanism is cell‐autonomous, based on an autoregulatory transcriptional/translational feedback loop of circadian genes and their products. This study investigated the effects of neuropeptide Y (NPY), a potent nonphotic resetting cue, and its interaction with light in regulating clock gene expression in the SCN in vivo . Injection of NPY adjacent to the SCN and transfer to darkness 7 h before scheduled lights out, shifted the circadian activity–rest cycle. Exposure to light for 1 h immediately after NPY infusion blocked this behavioural response. NPY‐induced shifts were accompanied by suppression of both mPer1 and mPer2 mRNA in the SCN, assessed 3 h after infusion. mPer mRNAs were not altered 1 h after infusion. Levels of mClock mRNA or mCLOCK immunoreactivity in the SCN were not affected by NPY at either time point. In parallel to the behavioural response, the NPY‐induced suppression of mPer genes in the SCN was attenuated when a light pulse was delivered immediately after the infusion. These results identify mPer1 and mPer2 as molecular targets for both photic and nonphotic (NPY‐induced) resetting of the clockwork, and support a synthetic model of circadian entrainment based upon convergent up‐ and downregulation of mPer expression.