Literature DB >> 20484691

Two components of nocturnal locomotor suppression by light.

Lawrence P Morin1, Pablo J Lituma, Keith M Studholme.   

Abstract

In nocturnal rodents, millisecond light ("flash") stimuli can induce both a large circadian rhythm phase shift and an associated state change from highly active to quiescence followed by behavioral sleep. Suppression of locomotion ("negative masking") is an easily measured correlate of the state change. The present mouse studies used both flashes and longer light stimuli ("pulses") to distinguish initiation from maintenance effects of light on locomotor suppression and to determine whether the locomotor suppression exhibits temporal integration as is thought to be characteristic of phase shift responses to pulse, but not flash, stimuli. In experiment 1, locomotor suppression increased with irradiance (0.01-100 microW/cm( 2)), in accordance with previous reports. It also increased with stimulus duration (3-3000 sec), but interpretation of this result is complicated by the ability of light to both initiate and maintain locomotor suppression. In experiment 2, an irradiance response curve was determined using a stimulus series of 10 flashes, 2 msec each, with total flash energy varying from 0.0025 to 110.0 J/m(2). This included a test for temporal integration in which the effects of two equal energy series of flashes that differed in the number of flashes per series (10 vs 100), were compared. The 10 flash series more effectively elicited locomotor suppression than the 100 flash series, a result consistent with prior observations involving flash-induced phase shifts. In experiment 3, exposure of mice to an 11-h light stimulus yielded irradiance-dependent locomotor suppression that was maintained for the entire stimulus duration by a 100-microW/cm(2) stimulus. Light has the ability to initiate a time-limited (30-40 min) interval of locomotor suppression (initiation effect) that can be extended by additional light (maintenance effect). Temporal integration resembling that seen in phase-shifting responses to light does not exist for either phase shift or locomotor suppression responses to flashes or for locomotor suppression responses to light pulses. The authors present an alternative interpretation of data thought to demonstrate temporal integration in the regulation of phase shift responses to light pulses.

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Year:  2010        PMID: 20484691      PMCID: PMC3063651          DOI: 10.1177/0748730410369890

Source DB:  PubMed          Journal:  J Biol Rhythms        ISSN: 0748-7304            Impact factor:   3.182


  22 in total

1.  Masking of locomotor activity in hamsters.

Authors:  U Redlin; N Mrosovsky
Journal:  J Comp Physiol A       Date:  1999-04       Impact factor: 1.836

2.  Masking by light in hamsters with SCN lesions.

Authors:  U Redlin; N Mrosovsky
Journal:  J Comp Physiol A       Date:  1999-04       Impact factor: 1.836

3.  Binocular contributions to the responsiveness and integrative capacity of the circadian rhythm system to light.

Authors:  Louise Muscat; Lawrence P Morin
Journal:  J Biol Rhythms       Date:  2005-12       Impact factor: 3.182

4.  Absence of normal photic integration in the circadian visual system: response to millisecond light flashes.

Authors:  Luis Vidal; Lawrence P Morin
Journal:  J Neurosci       Date:  2007-03-28       Impact factor: 6.167

5.  Classical and melanopsin photoreception in irradiance detection: negative masking of locomotor activity by light.

Authors:  Stewart Thompson; Russell G Foster; Edwin M Stone; Val C Sheffield; N Mrosovsky
Journal:  Eur J Neurosci       Date:  2008-04       Impact factor: 3.386

6.  Disruption of masking by hypothalamic lesions in Syrian hamsters.

Authors:  Xiaodong Li; Jenifer Gilbert; Fred C Davis
Journal:  J Comp Physiol A Neuroethol Sens Neural Behav Physiol       Date:  2004-09-24       Impact factor: 1.836

7.  Millisecond light pulses make mice stop running, then display prolonged sleep-like behavior in the absence of light.

Authors:  L P Morin; K M Studholme
Journal:  J Biol Rhythms       Date:  2009-12       Impact factor: 3.182

8.  Melanopsin cells are the principal conduits for rod-cone input to non-image-forming vision.

Authors:  Ali D Güler; Jennifer L Ecker; Gurprit S Lall; Shafiqul Haq; Cara M Altimus; Hsi-Wen Liao; Alun R Barnard; Hugh Cahill; Tudor C Badea; Haiqing Zhao; Mark W Hankins; David M Berson; Robert J Lucas; King-Wai Yau; Samer Hattar
Journal:  Nature       Date:  2008-04-23       Impact factor: 49.962

9.  Targeted destruction of photosensitive retinal ganglion cells with a saporin conjugate alters the effects of light on mouse circadian rhythms.

Authors:  Didem Göz; Keith Studholme; Douglas A Lappi; Mark D Rollag; Ignacio Provencio; Lawrence P Morin
Journal:  PLoS One       Date:  2008-09-05       Impact factor: 3.240

10.  Inducible ablation of melanopsin-expressing retinal ganglion cells reveals their central role in non-image forming visual responses.

Authors:  Megumi Hatori; Hiep Le; Christopher Vollmers; Sheena Racheal Keding; Nobushige Tanaka; Thorsten Buch; Ari Waisman; Christian Schmedt; Timothy Jegla; Satchidananda Panda
Journal:  PLoS One       Date:  2008-06-11       Impact factor: 3.240

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  8 in total

1.  Separation of function for classical and ganglion cell photoreceptors with respect to circadian rhythm entrainment and induction of photosomnolence.

Authors:  L P Morin; K M Studholme
Journal:  Neuroscience       Date:  2011-10-04       Impact factor: 3.590

2.  Prolonged daily light exposure increases body fat mass through attenuation of brown adipose tissue activity.

Authors:  Sander Kooijman; Rosa van den Berg; Ashna Ramkisoensing; Mariëtte R Boon; Eline N Kuipers; Marieke Loef; Tom C M Zonneveld; Eliane A Lucassen; Hetty C M Sips; Iliana A Chatzispyrou; Riekelt H Houtkooper; Johanna H Meijer; Claudia P Coomans; Nienke R Biermasz; Patrick C N Rensen
Journal:  Proc Natl Acad Sci U S A       Date:  2015-05-11       Impact factor: 11.205

3.  Brief light stimulation during the mouse nocturnal activity phase simultaneously induces a decline in core temperature and locomotor activity followed by EEG-determined sleep.

Authors:  Keith M Studholme; Heinrich S Gompf; Lawrence P Morin
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2013-01-30       Impact factor: 3.619

4.  Drugs that prevent mouse sleep also block light-induced locomotor suppression, circadian rhythm phase shifts and the drop in core temperature.

Authors:  P Vivanco; K M Studholme; L P Morin
Journal:  Neuroscience       Date:  2013-09-19       Impact factor: 3.590

5.  Acute effects of light on the brain and behavior of diurnal Arvicanthis niloticus and nocturnal Mus musculus.

Authors:  Dorela D Shuboni; Shannon L Cramm; Lily Yan; Chidambaram Ramanathan; Breyanna L Cavanaugh; Antonio A Nunez; Laura Smale
Journal:  Physiol Behav       Date:  2014-10-28

6.  The acute effects of light on murine sleep during the dark phase: importance of melanopsin for maintenance of light-induced sleep.

Authors:  Fanuel Muindi; Jamie M Zeitzer; Damien Colas; H Craig Heller
Journal:  Eur J Neurosci       Date:  2013-03-20       Impact factor: 3.386

Review 7.  A Path to Sleep Is through the Eye

Authors:  Lawrence P Morin
Journal:  eNeuro       Date:  2015-03-26

8.  Loss of Melanopsin Photoreception and Antagonism of the Histamine H3 Receptor by Ciproxifan Inhibit Light-Induced Sleep in Mice.

Authors:  Fanuel Muindi; Damien Colas; Jesse Ikeme; Norman F Ruby; H Craig Heller
Journal:  PLoS One       Date:  2015-06-17       Impact factor: 3.240

  8 in total

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