Literature DB >> 7656684

A non-photic gateway to the circadian clock of hamsters.

N Mrosovsky1.   

Abstract

This paper considers the neural mechanisms underlying a particular kind of non-photic phase shifting, that produced by novelty-induced wheel running in the hamster. The projection from the intergeniculate leaflet (IGL) to the suprachiasmatic nucleus (SCN) appears to be an important part of the mechanism mediating such phase shifts. A number of experiments support this view. First, expression of immediate-early genes in the IGL is induced by non-photic phase-shifting stimuli. Second, Fos-like immunoreactivity in the IGL co-localizes with neuropeptide Y (NPY) immunoreactivity. Third, direct application of NPY to the SCN produces phase shifts which do not depend on the hamsters becoming active following the injections. Fourth, blocking the normal actions of NPY at the SCN blocks or greatly attenuates the phase shifting that is normally produced by novelty-induced wheel running. Progress on the physiological basis of phase shifts associated with activity, or a correlate, depends on understanding the behavioural aspects of this phenomenon. The activity-shift response curve is especially useful.

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Mesh:

Year:  1995        PMID: 7656684     DOI: 10.1002/9780470514597.ch9

Source DB:  PubMed          Journal:  Ciba Found Symp        ISSN: 0300-5208


  12 in total

1.  The hamster circadian rhythm system includes nuclei of the subcortical visual shell.

Authors:  E G Marchant; L P Morin
Journal:  J Neurosci       Date:  1999-12-01       Impact factor: 6.167

Review 2.  The rhythmic GABAergic system.

Authors:  D P Cardinali; D A Golombek
Journal:  Neurochem Res       Date:  1998-05       Impact factor: 3.996

3.  Dim nighttime illumination alters photoperiodic responses of hamsters through the intergeniculate leaflet and other photic pathways.

Authors:  J A Evans; S N Carter; D A Freeman; M R Gorman
Journal:  Neuroscience       Date:  2011-12-02       Impact factor: 3.590

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.  Pituitary adenylate cyclase-activating peptide (PACAP) in the retinohypothalamic tract: a potential daytime regulator of the biological clock.

Authors:  J Hannibal; J M Ding; D Chen; J Fahrenkrug; P J Larsen; M U Gillette; J D Mikkelsen
Journal:  J Neurosci       Date:  1997-04-01       Impact factor: 6.167

6.  Pituitary adenylate cyclase activating peptide phase shifts circadian rhythms in a manner similar to light.

Authors:  M E Harrington; S Hoque; A Hall; D Golombek; S Biello
Journal:  J Neurosci       Date:  1999-08-01       Impact factor: 6.167

7.  Circadian phase shifts to neuropeptide Y In vitro: cellular communication and signal transduction.

Authors:  S M Biello; D A Golombek; K M Schak; M E Harrington
Journal:  J Neurosci       Date:  1997-11-01       Impact factor: 6.167

8.  The role of the intergeniculate leaflet in entrainment of circadian rhythms to a skeleton photoperiod.

Authors:  K Edelstein; S Amir
Journal:  J Neurosci       Date:  1999-01-01       Impact factor: 6.167

Review 9.  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

10.  Nocturnal to Diurnal Switches with Spontaneous Suppression of Wheel-Running Behavior in a Subterranean Rodent.

Authors:  Patricia Tachinardi; Øivind Tøien; Veronica S Valentinuzzi; C Loren Buck; Gisele A Oda
Journal:  PLoS One       Date:  2015-10-13       Impact factor: 3.240

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