Literature DB >> 12443986

Attenuation of phase shifts to light by activity or neuropeptide Y: a time course study.

Gurprit S Lall1, Stephany M Biello.   

Abstract

Circadian rhythms in mammals can be synchronised to photic and non-photic stimuli. Interactions between photic and behavioural stimuli were investigated during the late subjective night, 6 h after activity onset in Syrian hamsters (CT18). Light pulses of 130 lx for 15 min at this time resulted in phase advance shifts. Novel wheel exposure, for a period of 3 h, following photic stimulation was able to attenuate the phase advancing effects of light. A time delay of up to 60 min between photic and behavioural stimuli also resulted in significant attenuation of light-induced phase shifts (P<0.05). A 90-min interval between stimuli resulted in no significant attenuation. Novel wheel exposure mediates its effects via the intergeniculate leaflet, which conveys information to the SCN and utilises neuropeptide Y (NPY) as its primary neurotransmitter. Phase shifts to light pulses given at CT18 were attenuated by NPY administration. Neuropeptide Y injections up to 60 min post-light exposure significantly attenuated phase shifts by 50% on average. However a 90-min interval between light and NPY microinjection did not significantly affect light-induced phase shifts. These results confirm previous work indicating that novel wheel exposure and NPY administration can modulate light-induced phase shifts during the late night. Further, they show for the first time that the time course for this interaction is similar between wheel running and NPY. Most significantly, our work indicates that the time course in vivo in the late night is similar to that shown previously in vitro during the early night.

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Year:  2002        PMID: 12443986     DOI: 10.1016/s0006-8993(02)03610-7

Source DB:  PubMed          Journal:  Brain Res        ISSN: 0006-8993            Impact factor:   3.252


  6 in total

1.  Combination of light and melatonin time cues for phase advancing the human circadian clock.

Authors:  Tina M Burke; Rachel R Markwald; Evan D Chinoy; Jesse A Snider; Sara C Bessman; Christopher M Jung; Kenneth P Wright
Journal:  Sleep       Date:  2013-11-01       Impact factor: 5.849

2.  Geniculohypothalamic GABAergic projections gate suprachiasmatic nucleus responses to retinal input.

Authors:  Lydia Hanna; Lauren Walmsley; Abigail Pienaar; Michael Howarth; Timothy M Brown
Journal:  J Physiol       Date:  2017-04-11       Impact factor: 5.182

3.  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

Review 4.  Circadian entrainment and its role in depression: a mechanistic review.

Authors:  G S Lall; L A Atkinson; S A Corlett; P J Broadbridge; D R Bonsall
Journal:  J Neural Transm (Vienna)       Date:  2012-07-14       Impact factor: 3.575

Review 5.  The dynamics of GABA signaling: Revelations from the circadian pacemaker in the suprachiasmatic nucleus.

Authors:  H Elliott Albers; James C Walton; Karen L Gamble; John K McNeill; Daniel L Hummer
Journal:  Front Neuroendocrinol       Date:  2016-11-25       Impact factor: 8.606

Review 6.  Using light to tell the time of day: sensory coding in the mammalian circadian visual network.

Authors:  Timothy M Brown
Journal:  J Exp Biol       Date:  2016-06-15       Impact factor: 3.312

  6 in total

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