Cited by 23Circadian rhythm and melatoninSleep and Wakefulness ResearchImpact of Light on Environment and Health

Transient anhedonia phenotype and altered circadian timing of behaviour during night-time dim light exposure in Per3−/− mice, but not wildtype mice

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Martynhak, Bruno Jacson, Hogben, Alexandra L., Zanos, Panos, Georgiou, Polymnia, Andreatini, Roberto, Kitchen, Ian, Archer, Simon N., von Schantz, Malcolm +2 more·2017·Scientific Reports

Abstract

Industrialisation greatly increased human night-time exposure to artificial light, which in animal models is a known cause of depressive phenotypes. Whilst many of these phenotypes are ‘direct’ effects of light on affect, an ‘indirect’ pathway via altered sleep-wake timing has been suggested. We have previously shown that the Period3 gene, which forms part of the biological clock, is associated with altered sleep-wake patterns in response to light. Here, we show that both wild-type and Per3−/− mice showed elevated levels of circulating corticosterone and increased hippocampal Bdnf expression after 3 weeks of exposure to dim light at night, but only mice deficient for the PERIOD3 protein (Per3−/−) exhibited a transient anhedonia-like phenotype, observed as reduced sucrose preference, in weeks 2–3 of dim light at night, whereas WT mice did not. Per3−/− mice also exhibited a significantly smaller delay in behavioural timing than WT mice during weeks 1, 2 and 4 of dim light at night exposure. When treated with imipramine, neither Per3−/− nor WT mice exhibited an anhedonia-like phenotype, and neither genotypes exhibited a delay in behavioural timing in responses to dLAN. While the association between both Per3−/− phenotypes remains unclear, both are alleviated by imipramine treatment during dim night-time light.

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  • Studies have reported no association between light at night and mood in C57Bl/6 mice, suggesting a potential strain-specific effect of light at night.

    “However, studies have also reported no association between LAN and mood in C57Bl/6 mice suggesting a potential strain specific effect of LAN96,97.”

    From Circadian rhythm disruption and mental health (2020) · cites this paper as [96]

    The Results (Sucrose preference; page unavailable) report no reduction in sucrose preference in wild-type mice during four weeks of dim light at night. The Discussion identifies the model as C57bl/6 and contrasts it with a different strain in which depressive-like behaviour had been reported. This supports a possible strain difference, but the study measured only sucrose preference during this exposure period, not an absence of any association between light at night and mood generally. (LLM, conf=0.84)

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Authors
Martynhak, B. J., Hogben, A. L., Zanos, P., Georgiou, P., Andreatini, R., Kitchen, I., Archer, S. N., von Schantz, M., Bailey, A., & van der Veen, D. R.
Affiliations
  • University of Surrey (GB)
  • Universidade Federal do Paraná (BR)
  • St George's, University of London (GB)
Venue
Scientific Reports
Published
2017-01-10
Volume
7
Issue
1
Pages
40399-40399
ISSN
2045-2322 (ISSN-L)
OpenAlex
W2570210165
Cited by
23
References
71
Citations by year
2025: 3 · 2024: 3 · 2023: 3 · 2022: 1 · 2021: 2 · 2020: 2 · 2019: 3 · 2018: 3 · 2017: 3
FWCI
1.85
Type
journal article
Language
en
Open access
Locations
  • Scientific Reports (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • Northumbria Research Link (Northumbria University) (acceptedVersion)
  • St George's Online Research Archive (St George's University of London) (acceptedVersion)
  • Surrey Research Insight Open Access (The University of Surrey) (submittedVersion)
Topics
  • Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Circadian rhythm and melatonin
  • Life Sciences › Neuroscience › Cognitive Neuroscience › Sleep and Wakefulness Research
  • Physical Sciences › Environmental Science › Global and Planetary Change › Impact of Light on Environment and Health
Keywords
circadian rhythm, dim light at night, artificial light exposure, anhedonia, sucrose preference, corticosterone, brain-derived neurotrophic factor, hippocampus, sleep timing, imipramine, depression, biological clock
MeSH terms
Animals, Circadian Rhythm, Gene Expression Regulation, Hippocampus, Humans, Imipramine, Motor Activity, Sleep, Sleep Wake Disorders, Photoperiod, Mice, Knockout, Brain-Derived Neurotrophic Factor, Mice, Period Circadian Proteins, Circadian Clocks, Anhedonia

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