Journal article icon

Journal article

Constant light desynchronises olfactory versus object and visuospatial recognition memory performance

Abstract:
Circadian rhythms optimise physiology and behaviour to the varying demands of the 24-hour day. The master circadian clock is located in the suprachiasmatic nuclei (SCN) of the hypothalamus and it regulates circadian oscillators in tissues throughout the body to prevent internal desynchrony. Here we demonstrate for the first time that, under standard 12-h:12-h light–dark cycles (LD), object, visuospatial, and olfactory recognition performance in C57BL/6J mice is consistently better at midday relative to midnight. However, under repeated exposure to constant light (rLL), recognition performance becomes desynchronised, with object and visuospatial performance better at subjective midday and olfactory performance better at subjective midnight. This desynchrony in behavioural performance is mirrored by changes in expression of the canonical clock genes Period1 and Period2 (Per1 and Per2) as well as the immediate-early gene Fos in the SCN, dorsal hippocampus, and olfactory bulb. Under rLL, rhythmic Per1 and Fos expression is attenuated in the SCN. By contrast, hippocampal gene expression remains rhythmic, mirroring object and visuospatial performance. Strikingly, Per1 and Fos expression in the olfactory bulb is reversed, mirroring the inverted olfactory performance. Temporal desynchrony among these regions does not result in arrhythmicity, as core body temperature and exploratory activity rhythms persist under rLL. Our data provide the first demonstration that abnormal lighting conditions can give rise to temporal desynchrony between autonomous circadian oscillators in different regions, with different consequences for performance across different sensory domains. Such a dispersed network of dissociable circadian oscillators may provide greater flexibility when faced with conflicting environmental signals.
Publication status:
Published
Peer review status:
Peer reviewed

Actions

Access Document

Files:
Publisher copy:
10.1523/JNEUROSCI.3213-16.2017

Authors

More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Experimental Psychology
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Clinical Neurosciences
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Clinical Neurosciences
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Clinical Neurosciences
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Clinical Neurosciences
Role:
Author


More from this funder
Funding agency for:
Foster, R
Peirson, S
Grant:
BB/I021086/1
BB/I021086/1
More from this funder
Funding agency for:
Hankins, M
Foster, R
Bannerman, D
Peirson, S
Grant:
098461/Z/12/Z
BB/I021086/1
087736
BB/I021086/1


Publisher:
Society for Neuroscience
Journal:
Journal of Neuroscience More from this journal
Volume:
37
Issue:
13
Pages:
3555-3567
Publication date:
2017-03-29
Acceptance date:
2017-02-04
DOI:
EISSN:
1529-2401
ISSN:
0270-6467


Keywords:
Pubs id:
pubs:679172
UUID:
uuid:a0abff97-954d-488f-ad6b-c6262cfcf23d
Local pid:
pubs:679172
Deposit date:
2017-02-21
ARK identifier:

Terms of use


Views and Downloads






If you are the owner of this record, you can report an update to it here: Report update to this record

TO TOP