AI Article Synopsis

  • Artificial light at night (ALAN) has negative effects on health, disrupting sleep cycles and potentially contributing to mood, metabolic disorders, and cancer.
  • A study on female tumor-bearing mice found that ALAN exposure accelerated tumor growth and increased anxiety-like behaviors, while reducing preferences for sweet substances, indicating that ALAN negatively impacts both physical and affective health.
  • The findings suggest that while ALAN may hasten tumor development, it could paradoxically reduce anxiety in mice with tumors due to environmental changes.

Article Abstract

Artificial light at night (ALAN) is a pervasive phenomenon. Although initially assumed to be innocuous, recent research has demonstrated its deleterious effects on physiology and behavior. Exposure to ALAN is associated with disruptions to sleep/wake cycles, development of mood disorders, metabolic disorders, and cancer. However, the influence of ALAN on affective behavior in tumor-bearing mice has not been investigated. We hypothesize that exposure to ALAN accelerates mammary tumor growth and predict that ALAN exacerbates negative affective behaviors in tumor-bearing mice. Adult (>8 weeks) female C3H mice received a unilateral orthotropic injection of FM3A mouse mammary carcinoma cells (1.0 × 10 in 100 μL) into the fourth inguinal mammary gland. Nineteen days after tumor inoculation, mice were tested for sucrose preference (anhedonia-like behavior). The following day, mice were subjected to an open field test (anxiety-like behavior), followed by forced swim testing (depressive-like behavior). Regardless of tumor status, mice housed in ALAN increased body mass through the first ten days. Tumor-bearing ALAN-housed mice demonstrated reduced latency to tumor onset (day 5) and increased terminal tumor volume (day 21). Exposure to ALAN reduced sucrose preference independent of tumor status. Additionally, tumor-bearing mice housed in dark nights demonstrated significantly increased anxiety-like behavior that was normalized via housing in ALAN. Together, these data reaffirm the negative effects of ALAN on tumorigenesis and demonstrate the potential anxiolytic effect of ALAN in the presence of mammary tumors.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8508227PMC
http://dx.doi.org/10.3390/cancers13194860DOI Listing

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