Acute light deprivation triggers anxiety-like and depressive behaviors in mice

Authors

  • Jiadai Zhong

DOI:

https://doi.org/10.61173/54a6z140

Keywords:

Light deprivation, Anxiety, Depression, Seasonal affective disorder, Mental health

Abstract

Light exposure plays a critical role in regulating circadian rhythms and mood-related behaviors. While chronic, constant light deprivation has been extensively studied pertaining to anxiety and depression, the impact of acute deprivation of light exposure remains poorly understood. This study investigated the acute light deprivation-induced effects on anxiety and depressive-like behaviors of male C57BL/6 mice. Six behavioral tests were employed to comprehensively assess anxiety-like and depressive-like levels, including the open field test (OFT), elevated zero maze (EZM), light-dark box test (LDT), sucrose splash test (SST), forced swim test (FST), and tail suspension test (TST). The results indicated that there was no significant difference in anxiety-related measures between the control and light-deprived mice. In contrast, depressive-like behaviors were significantly elevated in the light-deprived mice, as evidenced by reduced self-grooming behavior in the SST and increased immobility in stress-inducing environments in the FST and TST. These findings suggest that even short-term and moderate light deprivation can induce depressive phenotypes, emphasizing the sensitivity of mood regulation to environmental changes, especially light exposure, and highlighting the potential mental health risks faced by urban populations with restricted access to natural light. Further studies are warranted to elucidate the underlying neurobiological mechanisms.

References

[1] World Health Organisation. (2017). Depression and Other Common Mental Disorders Global Health Estimates. https:// iris.who.int/bitstream/handle/10665/254610/WHO-MSD-MER-

[2017] 2-eng.pdf

[2] Hirschfield, R. M. A. (2001). The Comorbidity of Major Depression and Anxiety Disorders. The Primary Care Companion to the Journal of Clinical Psychiatry, 03(06), 244–

[254] https://doi.org/10.4088/pcc.v03n0609

[3] Chodavadia, P., Teo, I., Poremski, D., Fung, D. S. S., & Finkelstein, E. A. (2023). Prevalence and economic burden of depression and anxiety symptoms among Singaporean adults: results from a 2022 web panel. BMC Psychiatry, 23(1). https:// doi.org/10.1186/s12888-023-04581-7

[4] Bedrosian, T. A., & Nelson, R. J. (2013). Influence of the modern light environment on mood. Molecular Psychiatry, 18(7), 751–757. https://doi.org/10.1038/mp.2013.70

[5] Olejniczak, I., Ripperger, J. A., Sandrelli, F., Schnell, A., Mansencal-Strittmatter, L., Wendrich, K., Hui, K. Y., Brenna, A., Ben Fredj, N., & Albrecht, U. (2021). Light affects behavioral despair involving the clock gene Period 1. PLOS Genetics, 17(7), e1009625. https://doi.org/10.1371/journal.pgen.1009625

[6] Welberg, L. (2011). The dark side of depression. Nature Reviews Neuroscience, 12(8), 435–435. https://doi.org/10.1038/ nrn3072

[7] Varela, P., João Carlos Escosteguy-Neto, Carolina Tesone Coelho, Araujo, E., Xavier, & Jair Guilherme Santos- Junior. (2014). Chronic light deprivation inhibits appetitive associative learning induced by ethanol and its respective c-Fos and pCREB expression. The International Journal of Neuropsychopharmacology, 17(11), 1815–1830. https://doi. org/10.1017/s1461145714000480

[8] Zhou, Y., Zhang, H., Liu, F., Lei, G., Liu, P., Jiao, T., & Dang, Y. (2018). Altered Light Conditions Contribute to Abnormalities in Emotion and Cognition Through HINT1 Dysfunction in C57BL/6 Mice. Frontiers in Behavioral Neuroscience, 12. https://doi.org/10.3389/fnbeh.2018.00110

[9] Gonzalez, M. M. C., & Aston-Jones, G. (2008). Light deprivation damages monoamine neurons and produces a depressive behavioral phenotype in rats. Proceedings of the National Academy of Sciences, 105(12), 4898–4903. https://doi. org/10.1073/pnas.0703615105

[10] LeGates, T. A., Fernandez, D. C., & Hattar, S. (2014). Light as a central modulator of circadian rhythms, sleep and affect. Nature Reviews Neuroscience, 15(7), 443–454. https://doi. Dean&Francis ISSN 2959-409X org/10.1038/nrn3743

[11] Munir, S., & Abbas, M. (2022). Seasonal Depressive Disorder. PubMed; StatPearls Publishing. https://pubmed.ncbi. nlm.nih.gov/33760504/

[12] Volf, C., Bueno, B., Edwards, P., Hobday, R., Mäder, S., Matusiak, B. S., Wulff, K., Osterhaus, W., Manoli, G., Christina Della Giustina, Joshi, J., Kämpf, J. H., Vega, K., & Kueffer, C.

[2024] . Why daylight should be a priority for urban planning. Journal of Urban Management, 13(2). https://doi.org/10.1016/ j.jum.2024.02.002

[13] Brown, M. J., & Jacobs, D. E. (2011). Residential Light and Risk for Depression and Falls: Results from the LARES Study of Eight European Cities. Public Health Reports, 126(1_suppl), 131–140. https://doi.org/10.1177/00333549111260s117

[14] Kraeuter, A.-K., Guest, P. C., & Sarnyai, Z. (2018). The Open Field Test for Measuring Locomotor Activity and Anxiety- Like Behavior. Methods in Molecular Biology, 1916, 99–103. https://doi.org/10.1007/978-1-4939-8994-2_9

[15] Seibenhener, M. L., & Wooten, M. C. (2015). Use of the Open Field Maze to Measure Locomotor and Anxiety-like Behavior in Mice. Journal of Visualized Experiments, 96. https:// doi.org/10.3791/52434

[16] Tucker, L. B., & McCabe, J. T. (2021). Measuring Anxiety-Like Behaviors in Rodent Models of Traumatic Brain Injury. Frontiers in Behavioral Neuroscience, 15. https://doi. org/10.3389/fnbeh.2021.682935

[17] Bourin, M., & Hascoët, M. (2003). The mouse light/dark box test. European Journal of Pharmacology, 463(1-3), 55–65. https://doi.org/10.1016/s0014-2999(03)01274-3

[18] Campos-Cardoso, R., Lívea Dornela Godoy, Lazarini-Lopes, W., Novaes, L. S., Nilton, S., Perfetti Juliano Genaro, Garcia- Cairasco, N., Carolina Demarchi Munhoz, & Cláudia Maria Padovan. (2022). Exploring the light/dark box test: Protocols and implications for neuroscience research. Journal of Neuroscience Methods, 384, 109748–109748. https://doi.org/10.1016/ j.jneumeth.2022.109748

[19] Liu, D., Zheng, X., Hui, Y., Xu, Y., Du, J., Du, Z., Che, Y., Wu, F., Yu, G., Zhang, J., Gong, X., & Guo, G. (2024). Lateral hypothalamus orexinergic projection to the medial prefrontal cortex modulates chronic stress-induced anhedonia but not anxiety and despair. Translational Psychiatry, 14(1), 1–15. https://doi.org/10.1038/s41398-024-02860-9

[20] Bouguiyoud, N., Roullet, F., Bronchti, G., Frasnelli, J., & Al Aïn, S. (2022). Anxiety and Depression Assessments in a Mouse Model of Congenital Blindness. Frontiers in Neuroscience, 15. https://doi.org/10.3389/fnins.2021.807434

[21] Can, A., Dao, D. T., Arad, M., Terrillion, C. E., Piantadosi, S. C., & Gould, T. D. (2011). The Mouse Forced Swim Test. Journal of Visualized Experiments, 59(58). https://doi. org/10.3791/3638

[22] Kraeuter, A.-K., Guest, P. C., & Sarnyai, Z. (2018a). The Forced Swim Test for Depression-Like Behavior in Rodents. Methods in Molecular Biology, 1916, 75–80. https://doi. org/10.1007/978-1-4939-8994-2_5

[23] Kaufman, J., DeLorenzo, C., Choudhury, S., & Parsey, R. V. (2016). The 5-HT1A receptor in Major Depressive Disorder. European Neuropsychopharmacology, 26(3), 397–410. https:// doi.org/10.1016/j.euroneuro.2015.12.039

[24] Steru, L., Chermat, R., Thierry, B., & Simon, P. (1985). The tail suspension test: A new method for screening antidepressants in mice. Psychopharmacology, 85(3), 367–370. https://doi. org/10.1007/bf00428203

[25] LeGates, T., Altimus, C., Wang, H., Lee, H.-K., Yang, S., Zhao, H., Kirkwood, A., Weber, T., & Hattar, S. (2012). Aberrant light directly impairs mood and learning through melanopsinexpressing neurons. Nature, 491(7425), 594–598. https://doi. org/10.1038/nature11673

[26] Asadian, N., Parsaie, H., Vafaei, A. A., Dadkhah, M., Omoumi, S., & Sedaghat, K. (2021). Chronic light deprivation induces different effects on spatial and fear memory and hippocampal BDNF/TRKB expression during light and dark phases of rat diurnal rhythm. Behavioural Brain Research, 418, 113638. https://doi.org/10.1016/j.bbr.2021.113638

[27] Lu, C., Lin, H.-Z., Li, Y.-Y., & Zhang, Y.-F. (2017). Light deprivation: An efficient way in inducing depression-like behavior animal models. Research and Review Insights, 1(2). https://doi.org/10.15761/rri.1000112

[28] Agata Gabryelska, Turkiewicz, S., Kaczmarski, P., Gajewski, A., Piotr Białasiewicz, Strzelecki, D., Maciej Chałubiński, & Marcin Sochal. (2024). Circadian clock dysregulation: a potential mechanism of depression in obstructive sleep apnea patients. Translational Psychiatry, 14(1). https://doi.org/10.1038/ s41398-024-03134-0

[29] Yagishita, S. (2019). Transient and sustained effects of dopamine and serotonin signaling in motivation‐related behavior. Psychiatry and Clinical Neurosciences, 74(2), 91–98. https://doi. org/10.1111/pcn.12942

[30] Afridi, R., & Suk, K. (2021). Neuroinflammatory Basis of Depression: Learning From Experimental Models. Frontiers in Cellular Neuroscience, 15. https://doi.org/10.3389/ fncel.2021.691067

[31] Strekalova, T., Liu, Y.-Z., Kiselev, D. A., Sharafuddin Khairuddin, Chiu, J. L., Lam, J., Chan, Y., Pavlov, D. A., Andrey Proshin, Lesch, K.-P., Anthony, D. C., & Lee Yong Lim. (2022). Chronic mild stress paradigm as a rat model of depression: facts, artifacts, and future perspectives. Psychopharmacology, 239(3), 663–693. https://doi.org/10.1007/s00213-021-05982-w Supplementary: Dean&Francis Jiadai Zhong Table 1. Anxiety-like behavioral tests Control Light deprivation OFT Total distance traveled (cm) 2938.42 2398.30 Time in the center area (s) 39.82 41.30 Distance traveled in the center (cm) 411.97 389.21 Number of center area entry 24.29 23.71 EZM Time in open arm (s) 116.66 77.71 Latency to 1st into the open arm (s) 16.07 11.36 Number of open arm entry (s) 16.29 16.00 LDT Time in light box (s) 186.77 187.04 Number of light box entry 14.86 17.00 Latency to 1st enter dark box (s) 14.06 12.89 Table 2. Depressive-like behavioral tests Control Light deprivation SST Time of grooming (s) 91.14 50.24 Number of grooming 25.43 15.57 FST Immobility time (s) 159.56 193.30 Latency to 1st into immobility (s) 67.00 54.87 Number of mobility 18.43 21.29 TST Immobility time (s) 138.79 211.96 Latency to 1st into immobility (s) 35.14 7.54 Number of mobility 19.29 29.29

Downloads

Published

2025-08-26