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Author Watson, L.A.; Phillips, A.J.K.; Hosken, I.T.; McGlashan, E.M.; Anderson, C.; Lack, L.C.; Lockley, S.W.; Rajaratnam, S.M.W.; Cain, S.W. url  doi
openurl 
  Title Increased sensitivity of the circadian system to light in delayed sleep-wake phase disorder Type Journal Article
  Year 2018 Publication The Journal of Physiology Abbreviated Journal J Physiol  
  Volume in press Issue Pages  
  Keywords Human Health  
  Abstract KEY POINTS: This is the first study to demonstrate an altered circadian phase shifting response in a circadian rhythm sleep disorder. Patients with Delayed Sleep-Wake Phase Disorder (DSWPD) demonstrate greater sensitivity of the circadian system to the phase delaying effects of light. Increased circadian sensitivity to light is associated with later circadian timing within both control and DSWPD groups. DSWPD patients had a greater sustained pupil response after light exposure. Treatments for DSWPD should consider sensitivity of the circadian system to light as a potential underlying vulnerability, making patients susceptible to relapse. ABSTRACT: Patients with Delayed Sleep-Wake Phase Disorder (DSWPD) exhibit delayed sleep-wake behavior relative to desired bedtime, often leading to chronic sleep restriction and daytime dysfunction. The majority of DSWPD patients also display delayed circadian timing in the melatonin rhythm. Hypersensitivity of the circadian system to phase delaying light is a plausible physiological basis for DSWPD vulnerability. We compared the phase shifting response to a 6.5-h light exposure ( approximately 150 lux) between male patients with diagnosed DSWPD (n = 10; aged 22.4 +/- 3.3 years) and male healthy controls (n = 11; aged 22.4 +/- 2.4 years). Salivary dim light melatonin onset (DLMO) was measured under controlled conditions in dim light (<3 lux) before and after light exposure. Correcting for the circadian time of the light exposure, DSWPD patients exhibited 31.5% greater phase delay shifts than healthy controls. In both groups, a later initial phase of the melatonin rhythm was associated with greater magnitude of phase shifts, indicating that increased circadian sensitivity to light may be a factor that contributes to delayed phase, even in non-clinical groups. DSWPD patients also had reduced pupil size following the light exposure, and showed a trend towards increased melatonin suppression during light exposure. These findings indicate that, for patients with DSWPD, assessment of light sensitivity may be an important factor that can inform behavioral therapy, including minimization of exposure to phase-delaying night-time light. This article is protected by copyright. All rights reserved.  
  Address Monash Institute of Cognitive and Clinical Neurosciences, School of Psychological Sciences, Monash University, Melbourne, Victoria, Australia  
  Corporate Author Thesis  
  Publisher Place of Publication Editor  
  Language English Summary Language Original Title  
  Series Editor Series Title Abbreviated Series Title  
  Series Volume Series Issue Edition  
  ISSN 0022-3751 ISBN Medium  
  Area Expedition Conference  
  Notes PMID:30281150 Approved no  
  Call Number GFZ @ kyba @ Serial 2026  
Permanent link to this record
 

 
Author Leise, T.L.; Goldberg, A.; Michael, J.; Montoya, G.; Solow, S.; Molyneux, P.; Vetrivelan, R.; Harrington, M.E. url  doi
openurl 
  Title Recurring circadian disruption alters circadian clock sensitivity to resetting Type Journal Article
  Year 2018 Publication The European Journal of Neuroscience Abbreviated Journal Eur J Neurosci  
  Volume in press Issue Pages  
  Keywords Animals  
  Abstract A single phase advance of the light:dark (LD) cycle can temporarily disrupt synchrony of neural circadian rhythms within the suprachiasmatic nucleus (SCN) and between the SCN and peripheral tissues. Compounding this, modern life can involve repeated disruptive light conditions. To model chronic disruption to the circadian system, we exposed male mice to more than a month of a 20 h light cycle (LD10:10), which mice typically cannot entrain to. Control animals were housed under LD12:12. We measured locomotor activity and body temperature rhythms in vivo, and rhythms of PER2::LUC bioluminescence in SCN and peripheral tissues ex vivo. Unexpectedly, we discovered strong effects of the time of dissection on circadian phase of PER2::LUC bioluminescent rhythms, which varied across tissues. White adipose tissue was strongly reset by dissection, while thymus phase appeared independent of dissection timing. Prior light exposure impacted the SCN, resulting in strong resetting of SCN phase by dissection for mice housed under LD10:10, and weak phase shifts by time of dissection in SCN from control LD12:12 mice. These findings suggest that exposure to circadian disruption may desynchronize SCN neurons, increasing network sensitivity to perturbations. We propose that tissues with a weakened circadian network, such as the SCN under disruptive light conditions, or with little to no coupling, e.g., some peripheral tissues, will show increased resetting effects. In particular, exposure to light at inconsistent circadian times on a recurring weekly basis disrupts circadian rhythms and alters sensitivity of the SCN neural pacemaker to dissection time. This article is protected by copyright. All rights reserved.  
  Address Neuroscience Program, Smith College, Northampton, MA, 01063, USA  
  Corporate Author Thesis  
  Publisher Place of Publication Editor  
  Language English Summary Language Original Title  
  Series Editor Series Title Abbreviated Series Title  
  Series Volume Series Issue Edition  
  ISSN 0953-816X ISBN Medium  
  Area Expedition Conference  
  Notes PMID:30269396 Approved no  
  Call Number GFZ @ kyba @ Serial 2036  
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Author Ma, Q.; Tan, Y.; Chen, X.; Chen, S.; Sun, Y.; Zhou, B. url  doi
openurl 
  Title Regulation of the MAPK signaling pathway by miR-421-5p in rats under light pollution Type Journal Article
  Year 2018 Publication International Journal of Molecular Medicine Abbreviated Journal Int J Mol Med  
  Volume in press Issue Pages in press  
  Keywords Animals  
  Abstract The present study aimed to explore the difference in the expression profiles of ovarian microRNA sequences in rats in a light pollution environment and rats in a normal light environment. Rats in the control group were exposed to 12h light/dark cycles, while rats in the model group were continuously exposed to 24h light. The ovaries were extracted from the two groups of rats, and Illumina HiSeq 2500 highthroughput sequencing technology was used to detect the differences in microRNA (miRNA) expression among the two groups. Fluorescence quantitative reverse transcriptionpolymerase chain reaction was used to verify the differential expression of miRNA. The present study was designed to experimentally validate the interaction between miR4215p and mitogenactivated protein kinase (MAPK) 7 by using the dualluciferase reporter system, and to explore the expression of proteins in the MAPK signaling pathway with a lentiviral vectormediated small hairpin RNA interference against microRNA4215p. The expression of 45 miRNAs was significantly different. In total, 13 miRNAs were upregulated, of which 5 miRNA sequences were known and 8 were predicted. Furthermore, 32 miRNAs were downregulated, of which 11 miRNA sequences were known and 21 were predicted. The results of the luciferase reporter assay confirmed the targeting association between miR4215p and MAPK7. The expression levels of MAPK and genes in its downstream signaling pathways, including cFos, CREB and cMyc, were downregulated when miR4215p was overexpressed and upregulated when miR4215p was silenced. The differential expression of miRNAs may serve an important role in the development of the ovary in a light pollution environment. miR4215p may regulate ovarian growth and development by targeting the MAPK signaling pathway in light polluted rat ovaries.  
  Address Nanjing University of Chinese Medicine, Nanjing, Jiangsu 210023, P.R. China  
  Corporate Author Thesis  
  Publisher Place of Publication Editor  
  Language English Summary Language Original Title  
  Series Editor Series Title Abbreviated Series Title  
  Series Volume Series Issue Edition  
  ISSN 1107-3756 ISBN Medium  
  Area Expedition Conference  
  Notes PMID:30221682 Approved no  
  Call Number GFZ @ kyba @ Serial 2005  
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Author Park, C.Y. url  doi
openurl 
  Title Night Light Pollution and Ocular Fatigue Type Journal Article
  Year 2018 Publication Journal of Korean Medical Science Abbreviated Journal J Korean Med Sci  
  Volume 33 Issue 38 Pages e257  
  Keywords Commentary; Human Health  
  Abstract  
  Address Department of Ophthalmology, Dongguk University, Ilsan Hospital, Goyang, Korea  
  Corporate Author Thesis  
  Publisher Place of Publication Editor  
  Language English Summary Language Original Title  
  Series Editor Series Title Abbreviated Series Title  
  Series Volume Series Issue Edition  
  ISSN 1011-8934 ISBN Medium  
  Area Expedition Conference  
  Notes PMID:30220898; PMCID:PMC6137033 Approved no  
  Call Number GFZ @ kyba @ Serial 2011  
Permanent link to this record
 

 
Author McGlashan, E.M.; Nandam, L.S.; Vidafar, P.; Mansfield, D.R.; Rajaratnam, S.M.W.; Cain, S.W. url  doi
openurl 
  Title The SSRI citalopram increases the sensitivity of the human circadian system to light in an acute dose Type Journal Article
  Year 2018 Publication Psychopharmacology Abbreviated Journal Psychopharmacology (Berl)  
  Volume in press Issue Pages in press  
  Keywords Human Health  
  Abstract RATIONALE: Disturbances of the circadian system are common in depression. Though they typically subside when depression is treated with antidepressants, the mechanism by which this occurs is unknown. Despite being the most commonly prescribed class of antidepressants, the effect of selective serotonin reuptake inhibitors (SSRIs) on the human circadian clock is not well understood. OBJECTIVE: To examine the effect of the SSRI citalopram (30 mg) on the sensitivity of the human circadian system to light. METHODS: This study used a double-blind, placebo-controlled, within-subjects, crossover design. Participants completed two melatonin suppression assessments in room level light (~ 100 lx), taking either a single dose of citalopram 30 mg or a placebo at the beginning of each light exposure. Melatonin suppression was calculated by comparing placebo and citalopram light exposure conditions to a dim light baseline. RESULTS: A 47% increase in melatonin suppression was observed after administration of an acute dose of citalopram, with all participants showing more suppression after citalopram administration (large effect, d = 1.54). Further, melatonin onset occurred later under normal room light with citalopram compared to placebo. CONCLUSIONS: Increased sensitivity of the circadian system to light could assist in explaining some of the inter-individual variability in antidepressant treatment responses, as it is likely to assist in recovery in some patients, while causing further disruption for others.  
  Address Monash Institute of Cognitive and Clinical Neurosciences, School of Psychological Sciences, Monash University, 18 Innovation Walk, Clayton, VIC, 3800, Australia. sean.cain@monash.edu  
  Corporate Author Thesis  
  Publisher Place of Publication Editor  
  Language English Summary Language Original Title  
  Series Editor Series Title Abbreviated Series Title  
  Series Volume Series Issue Edition  
  ISSN 0033-3158 ISBN Medium  
  Area Expedition Conference  
  Notes PMID:30219986 Approved no  
  Call Number GFZ @ kyba @ Serial 2012  
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