Publication

Light Environment Influences Developmental Programming of the Metabolic and Visual Systems in Mice

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Last modified
  • 05/23/2025
Type of Material
Authors
    Danielle A Clarkson-Townsend, Emory UniversityKatie L Bales, Atlanta VA Healthcare SystemCarmen Marsit, Emory UniversityMachelle Pardue, Emory University
Language
  • English
Date
  • 2021-04-01
Publisher
  • ASSOC RESEARCH VISION OPHTHALMOLOGY INC
Publication Version
Copyright Statement
  • 2021 The Authors
License
Final Published Version (URL)
Title of Journal or Parent Work
Volume
  • 62
Issue
  • 4
Start Page
  • 22
End Page
  • 22
Grant/Funding Information
  • Supported by funding from the National Institutes of Health (NIH-NICHD F31 HD097918 [to D.A.C.T.], NIH-NIEHS T32 ES012870 [to D.A.C.T.], NIH-NIEHS P30ES019776 [to C.J.M.], and NIH-NEI Core Grant P30EY006360) and the Department of Veterans Affairs (Rehabilitation Research and Development Senior Research Career Scientist Award RX003134 [to M.T.P.]).
Supplemental Material (URL)
Abstract
  • PURPOSE. Light is a salient cue that can influence neurodevelopment and the immune system. Light exposure out of sync with the endogenous clock causes circadian disruption and chronic disease. Environmental light exposure may contribute to developmental programming of metabolic and neurological systems but has been largely overlooked in Developmental Origins of Health and Disease (DOHaD) research. Here, we investigated whether developmental light exposure altered programming of visual and metabolic systems. METHODS. Pregnant mice and pups were exposed to control light (12:12 light:dark) or weekly light cycle inversions (circadian disruption [CD]) until weaning, after which male and female offspring were housed in control light and longitudinally measured to evaluate differences in growth (weight), glucose tolerance, visual function (optomotor response), and retinal function (electroretinogram), with and without high fat diet (HFD) challenge. Retinal microglia and macrophages were quantified by positive Iba1 and CD11b immunofluorescence. RESULTS. CD exposure caused impaired visual function and increased retinal immune cell expression in adult offspring. When challenged with HFD, CD offspring also exhibited altered retinal function and sex-specific impairments in glucose tolerance. CONCLUSIONS. Overall, these findings suggest that the light environment contributes to developmental programming of the metabolic and visual systems, potentially promoting a pro-inflammatory milieu in the retina and increasing the risk of visual disease later in life.
Author Notes
  • Machelle T. Pardue, Department of Biomedical Engineering, Georgia Institute of Technology and Emory University, 313 Ferst Drive, Room 4104 Atlanta, GA 30332, USA. Email: machelle.pardue@bme.gatech.edu
Keywords
Research Categories
  • Health Sciences, Public Health
  • Environmental Sciences
  • Engineering, Biomedical

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