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Author Bukalev, A.V.; Vinogradova, I.A.; Zabezhinskii, M.A.; Semenchenko, A.V.; Anisimov, V.N.
Title Light pollution increases morbidity and mortality rate from different causes in female rats Type Journal Article
Year 2013 Publication Advances in Gerontology Abbreviated Journal Adv Gerontol
Volume 3 Issue 3 Pages 180-188
Keywords light-at-night; spontaneous tumors; nontumor pathology epiphysis; rats; animals; mammals
Abstract The influence of different light regimes (constant light, LL; constant darkness, DD; standard light regime, LD, 12 hours light/12 hours darkness; and natural lighting of the northwest of Russia (NL) on non-tumor pathology revealed in the post-mortem examination of female rats has been studied. It was found that keeping 25-days-old animals under LL and NL conditions led to an increase in the number of infectious diseases and the substantially faster development of spontaneous tumors (2.9 and 3.3 diseases per one rat, respectively), variety of nontumor pathology found in dead rats, compared with the animals in standard (standard light) regime (1.72 diseases per one rat). Light deprivation (DD) led to a substantial reduction in the development of new growth, as well as nontumor and infectious diseases (1.06 diseases per one rat), compared to the same parameters in a standard light regime.
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Corporate Author Thesis
Publisher Place of Publication Editor
Language Summary Language Original Title (down)
Series Editor Series Title Abbreviated Series Title
Series Volume Series Issue Edition
ISSN 2079-0570 ISBN Medium
Area Expedition Conference
Notes Approved no
Call Number IDA @ john @ Serial 89
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Author Bedrosian, T.A.; Fonken, L.K.; Walton, J.C.; Nelson, R.J.
Title Chronic exposure to dim light at night suppresses immune responses in Siberian hamsters Type Journal Article
Year 2011 Publication Biology Letters Abbreviated Journal Biol Lett
Volume 7 Issue 3 Pages 468-471
Keywords Animals; Blood Bactericidal Activity/immunology; Circadian Rhythm; Cricetinae; Fever/immunology; Hypersensitivity, Delayed/immunology; *Immunity; Light/*adverse effects; Lipopolysaccharides; Locomotion; Phodopus/*immunology
Abstract Species have been adapted to specific niches optimizing survival and reproduction; however, urbanization by humans has dramatically altered natural habitats. Artificial light at night (LAN), termed 'light pollution', is an often overlooked, yet increasing disruptor of habitats, which perturbs physiological processes that rely on precise light information. For example, LAN alters the timing of reproduction and activity in some species, which decreases the odds of successful breeding and increases the threat of predation for these individuals, leading to reduced fitness. LAN also suppresses immune function, an important proxy for survival. To investigate the impact of LAN in a species naive to light pollution in its native habitat, immune function was examined in Siberian hamsters derived from wild-caught stock. After four weeks exposure to dim LAN, immune responses to three different challenges were assessed: (i) delayed-type hypersensitivity (DTH), (ii) lipopolysaccharide-induced fever, and (iii) bactericide activity of blood. LAN suppressed DTH response and reduced bactericide activity of blood after lipopolysaccharide treatment, in addition to altering daily patterns of locomotor activity, suggesting that human encroachment on habitats via night-time lighting may inadvertently compromise immune function and ultimately fitness.
Address Department of Neuroscience, The Ohio State University Medical Center, Columbus, OH 43210, USA. tracy.bedrosian@osumc.edu
Corporate Author Thesis
Publisher Place of Publication Editor
Language English Summary Language Original Title (down)
Series Editor Series Title Abbreviated Series Title
Series Volume Series Issue Edition
ISSN 1744-9561 ISBN Medium
Area Expedition Conference
Notes PMID:21270021; PMCID:PMC3097873 Approved no
Call Number IDA @ john @ Serial 90
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Author Fonken, L.K.; Kitsmiller, E.; Smale, L.; Nelson, R.J.
Title Dim nighttime light impairs cognition and provokes depressive-like responses in a diurnal rodent Type Journal Article
Year 2012 Publication Journal of Biological Rhythms Abbreviated Journal J Biol Rhythms
Volume 27 Issue 4 Pages 319-327
Keywords Analysis of Variance; Animals; CA1 Region, Hippocampal/cytology; CA3 Region, Hippocampal/cytology; Circadian Rhythm/*physiology; Cognition/*physiology/radiation effects; Corticosterone/blood; Dendrites/physiology/radiation effects; Dentate Gyrus/cytology; Depressive Disorder/*physiopathology; Food Preferences/physiology/radiation effects; Light; Male; Maze Learning/physiology/radiation effects; Motor Activity/physiology/radiation effects; Murinae/*physiology; Neurons/drug effects/physiology; *Photoperiod; Swimming/physiology
Abstract Circadian disruption is a common by-product of modern life. Although jet lag and shift work are well-documented challenges to circadian organization, many more subtle environmental changes cause circadian disruption. For example, frequent fluctuations in the timing of the sleep/wake schedule, as well as exposure to nighttime lighting, likely affect the circadian system. Most studies of these effects have focused on nocturnal rodents, which are very different from diurnal species with respect to their patterns of light exposure and the effects that light can have on their activity. Thus, the authors investigated the effect of nighttime light on behavior and the brain of a diurnal rodent, the Nile grass rat. Following 3 weeks of exposure to standard light/dark (LD; 14:10 light [~150 lux] /dark [0 lux]) or dim light at night (dLAN; 14:10 light [~150 lux] /dim [5 lux]), rats underwent behavioral testing, and hippocampal neurons within CA1, CA3, and the dentate gyrus (DG) were examined. Three behavioral effects of dLAN were observed: (1) decreased preference for a sucrose solution, (2) increased latency to float in a forced swim test, and (3) impaired learning and memory in the Barnes maze. Light at night also reduced dendritic length in DG and basilar CA1 dendrites. Dendritic length in the DG positively correlated with sucrose consumption in the sucrose anhedonia task. Nighttime light exposure did not disrupt the pattern of circadian locomotor activity, and all grass rats maintained a diurnal activity pattern. Together, these data suggest that exposure to dLAN can alter affective responses and impair cognition in a diurnal animal.
Address Department of Neuroscience, The Ohio State University Wexner Medical Center, Columbus, OH 43210, USA. fonken.1@osu.edu
Corporate Author Thesis
Publisher Place of Publication Editor
Language English Summary Language Original Title (down)
Series Editor Series Title Abbreviated Series Title
Series Volume Series Issue Edition
ISSN 0748-7304 ISBN Medium
Area Expedition Conference
Notes PMID:22855576 Approved no
Call Number IDA @ john @ Serial 91
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Author Summa, K.C.; Vitaterna, M.H.; Turek, F.W.
Title Environmental perturbation of the circadian clock disrupts pregnancy in the mouse Type Journal Article
Year 2012 Publication PloS one Abbreviated Journal PLoS One
Volume 7 Issue 5 Pages e37668
Keywords Animals; Circadian Rhythm/*physiology; *Environment; Female; Locomotion/physiology; Mice; Mice, Inbred C57BL; Photoperiod; Pregnancy; Pregnancy Outcome; Reproduction/*physiology
Abstract BACKGROUND: The circadian clock has been linked to reproduction at many levels in mammals. Epidemiological studies of female shift workers have reported increased rates of reproductive abnormalities and adverse pregnancy outcomes, although whether the cause is circadian disruption or another factor associated with shift work is unknown. Here we test whether environmental disruption of circadian rhythms, using repeated shifts of the light:dark (LD) cycle, adversely affects reproductive success in mice. METHODOLOGY/PRINCIPAL FINDINGS: Young adult female C57BL/6J (B6) mice were paired with B6 males until copulation was verified by visual identification of vaginal plug formation. Females were then randomly assigned to one of three groups: control, phase-delay or phase-advance. Controls remained on a constant 12-hr light:12-hr dark cycle, whereas phase-delayed and phase-advanced mice were subjected to 6-hr delays or advances in the LD cycle every 5-6 days, respectively. The number of copulations resulting in term pregnancies was determined. Control females had a full-term pregnancy success rate of 90% (11/12), which fell to 50% (9/18; p<0.1) in the phase-delay group and 22% (4/18; p<0.01) in the phase-advance group. CONCLUSIONS/SIGNIFICANCE: Repeated shifting of the LD cycle, which disrupts endogenous circadian timekeeping, dramatically reduces pregnancy success in mice. Advances of the LD cycle have a greater negative impact on pregnancy outcomes and, in non-pregnant female mice, require longer for circadian re-entrainment, suggesting that the magnitude or duration of circadian misalignment may be related to the severity of the adverse impact on pregnancy. These results explicitly link disruptions of circadian entrainment to adverse pregnancy outcomes in mammals, which may have important implications for the reproductive health of female shift workers, women with circadian rhythm sleep disorders and/or women with disturbed circadian rhythms for other reasons.
Address Center for Sleep and Circadian Biology, Department of Neurobiology, Northwestern University, Evanston, Illinois, United States of America
Corporate Author Thesis
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Language English Summary Language Original Title (down)
Series Editor Series Title Abbreviated Series Title
Series Volume Series Issue Edition
ISSN 1932-6203 ISBN Medium
Area Expedition Conference
Notes PMID:22649550; PMCID:PMC3359308 Approved no
Call Number IDA @ john @ Serial 92
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Author Fonken, L.K.; Lieberman, R.A.; Weil, Z.M.; Nelson, R.J.
Title Dim light at night exaggerates weight gain and inflammation associated with a high-fat diet in male mice Type Journal Article
Year 2013 Publication Endocrinology Abbreviated Journal Endocrinology
Volume 154 Issue 10 Pages 3817-3825
Keywords Adipose Tissue, White/*immunology/metabolism/pathology; Animals; Antigens, CD11b/biosynthesis/genetics/metabolism; Appetite Regulation/*radiation effects; Arcuate Nucleus/*immunology/metabolism/pathology; Behavior, Animal/radiation effects; Circadian Rhythm; Cytokines/biosynthesis/genetics/metabolism; Diet, High-Fat/*adverse effects; Feeding Behavior/radiation effects; Gene Expression Regulation; Glucose Intolerance/etiology/immunology/metabolism/pathology; I-kappa B Kinase/biosynthesis/genetics/metabolism; Insulin Resistance; Lighting/*adverse effects; Male; Mice; Microglia/immunology/metabolism/pathology; Nerve Tissue Proteins/biosynthesis/genetics/metabolism; Obesity/*etiology/immunology/metabolism/pathology; Random Allocation; *Weight Gain
Abstract Elevated nighttime light exposure is associated with symptoms of metabolic syndrome. In industrialized societies, high-fat diet (HFD) and exposure to light at night (LAN) often cooccur and may contribute to the increasing obesity epidemic. Thus, we hypothesized that dim LAN (dLAN) would provoke additional and sustained body mass gain in mice on a HFD. Male mice were housed in either a standard light/dark cycle or dLAN and fed either chow or HFD. Exposure to dLAN and HFD increase weight gain, reduce glucose tolerance, and alter insulin secretion as compared with light/dark cycle and chow, respectively. The effects of dLAN and HFD appear additive, because mice exposed to dLAN that were fed HFD display the greatest increases in body mass. Exposure to both dLAN and HFD also change the timing of food intake and increase TNFalpha and MAC1 gene expression in white adipose tissue after 4 experimental weeks. Changes in MAC1 gene expression occur more rapidly due to HFD as compared with dLAN; after 5 days of experimental conditions, mice fed HFD already increase MAC1 gene expression in white adipose tissue. HFD also elevates microglia activation in the arcuate nucleus of the hypothalamus and hypothalamic TNFalpha, IL-6, and Ikbkb gene expression. Microglia activation is increased by dLAN, but only among chow-fed mice and dLAN does not affect inflammatory gene expression. These results suggest that dLAN exaggerates weight gain and peripheral inflammation associated with HFD.
Address Department of Neuroscience, Wexner Medical Center, The Ohio State University, 636 Biomedical Research Tower, 460 West 12th Avenue, Columbus, Ohio 43210. fonken.1@osu.edu
Corporate Author Thesis
Publisher Place of Publication Editor
Language English Summary Language Original Title (down)
Series Editor Series Title Abbreviated Series Title
Series Volume Series Issue Edition
ISSN 0013-7227 ISBN Medium
Area Expedition Conference
Notes PMID:23861373 Approved no
Call Number IDA @ john @ Serial 93
Permanent link to this record