Literature DB >> 7732038

Blocking the phase-shifting effect of neuropeptide Y with light.

S M Biello1, N Mrosovsky.   

Abstract

Previous studies have indicated that the neuropeptide Y input from the intergeniculate leaflet of the lateral geniculate nucleus to the suprachiasmatic nucleus is the final part of a non-photic phase shifting pathway to pacemakers in hamsters, or that neuropeptide Y is necessary for other pathways to be effective. Experiments in which two stimuli are presented during the same circadian cycle have shown that phase shifts in response to at least two non-photic stimuli are attenuated by a subsequent light pulse during the subjective day. This study was conducted to investigate the neural site of the blocking effect of light on non-photic stimuli. Experiment 1 showed that phase shifts in response to induced wheel-running during the subjective day are greatly attenuated by a subsequent light pulse. Experiment 2 showed that phase shifts in response to injections of neuropeptide Y in the middle of the subjective day were also greatly reduced by a subsequent light pulse. These results provide some insight about the site of the blocking action of light on non-photic phase shifts. Because there is evidence indicating that neuropeptide Y may mediate phase shifts in response to induced activity, and because light was able to block phase shifts produced by neuropeptide Y, we conclude that, in blocking activity-induced shifts, light must act downstream from the release of neuropeptide Y into the suprachiasmatic nucleus.

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Year:  1995        PMID: 7732038     DOI: 10.1098/rspb.1995.0026

Source DB:  PubMed          Journal:  Proc Biol Sci        ISSN: 0962-8452            Impact factor:   5.349


  12 in total

1.  In vivo resetting of the hamster circadian clock by 5-HT7 receptors in the suprachiasmatic nucleus.

Authors:  J C Ehlen; G H Grossman; J D Glass
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Review 3.  Assessing ethanol's actions in the suprachiasmatic circadian clock using in vivo and in vitro approaches.

Authors:  Rebecca A Prosser; J David Glass
Journal:  Alcohol       Date:  2014-10-18       Impact factor: 2.405

4.  Glutamate blocks serotonergic phase advances of the mammalian circadian pacemaker through AMPA and NMDA receptors.

Authors:  R A Prosser
Journal:  J Neurosci       Date:  2001-10-01       Impact factor: 6.167

5.  Functional Significance of the Excitatory Effects of GABA in the Suprachiasmatic Nucleus.

Authors:  John K McNeill; James C Walton; H Elliott Albers
Journal:  J Biol Rhythms       Date:  2018-07-05       Impact factor: 3.182

6.  Systematic review of drugs that modify the circadian system's phase-shifting responses to light exposure.

Authors:  Robert Lee; Austin McGee; Fabian-Xosé Fernandez
Journal:  Neuropsychopharmacology       Date:  2021-12-27       Impact factor: 8.294

7.  Site-specific effects of gastrin-releasing peptide in the suprachiasmatic nucleus.

Authors:  George J Kallingal; Eric M Mintz
Journal:  Eur J Neurosci       Date:  2013-10-28       Impact factor: 3.386

8.  Gastrin releasing peptide and neuropeptide Y exert opposing actions on circadian phase.

Authors:  George J Kallingal; Eric M Mintz
Journal:  Neurosci Lett       Date:  2007-06-08       Impact factor: 3.046

9.  Juxtacellular recording/labeling analysis of physiological and anatomical characteristics of rat intergeniculate leaflet neurons.

Authors:  Stephen Thankachan; Benjamin Rusak
Journal:  J Neurosci       Date:  2005-10-05       Impact factor: 6.709

Review 10.  Synchronization of Biological Clock Neurons by Light and Peripheral Feedback Systems Promotes Circadian Rhythms and Health.

Authors:  Ashna Ramkisoensing; Johanna H Meijer
Journal:  Front Neurol       Date:  2015-06-05       Impact factor: 4.003

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