DOI QR코드

DOI QR Code

Influence of various photoperiods on stress hormone production, immune function, and hematological parameters in ICR mice

광주기 변화에 따른 마우스의 스트레스 호르몬, 면역기능 및 혈액학적 지표에 미치는 영향

  • Received : 2015.04.01
  • Accepted : 2015.06.01
  • Published : 2015.06.30

Abstract

In the present study, the effects of different photoperiods on stress, immunity, and hematological parameters in ICR mice were evaluated. Fifty male ICR mice 7 weeks old (body weight, $27.3{\pm}2.5g$) were divided into five groups: DP-0 (0/24-h light/dark cycle), DP-6 (6/18-h light/dark cycle), DP-12 (12/12-h light/dark cycle), DP-18 (18/6-h light/dark cycle), and DP-24 (24/0-h light/dark cycle). During the experimental period, no significant differences in body weight or feed intake were observed between the groups. Hematological analysis revealed that white blood cell, red blood cell, and hemoglobin values for the DP-0 group were significantly different compared to those of the other groups. After 28 days, no significant difference in serum cortisol concentration was observed among the groups, but serum cortisol levels increased in a light exposure-dependent manner. Total serum immunoglobulin G (IgG) concentrations of the DP-0 and PD-6 groups were significantly increased compared to those of the other groups (p < 0.05), and serum total IgG levels decreased in a light exposure-dependent manner. Results of the present study indicated that various photoperiods affect hematological parameters and total serum IgG levels in ICR mice while having no significant effects on body weight, feed intake, or cortisol levels.

Keywords

References

  1. Bashiri F, Hassan CRC. Light pollution and its effect on the environment. Int J Fundam Phys Sci 2014, 4, 8-12.
  2. Boon P, Visser H, Daan S. Effect of photoperiod on body mass, and daily energy intake and energy expenditure in young rats. Physiol Behav 1997, 62, 913-919. https://doi.org/10.1016/S0031-9384(97)00271-0
  3. Chung MK, Choi YJ, Jung KH, Kim EA, Chung HM, Lee SH, Yoon TK, Chai YG. Expression of the circadian clock genes in the mouse gonad. Balsaenggwa Saengsig 2004, 8, 57-64.
  4. Cohen M, Lippman M, Chabner B. Role of pineal gland in aetiology and treatment of breast cancer. Lancet 1978, 2, 814-816.
  5. Demas GE, Nelson RJ. Photoperiod and temperature interact to affect immune parameters in adult male deer mice (Peromyscus maniculatus). J Biol Rhythms 1996, 11, 94-102. https://doi.org/10.1177/074873049601100202
  6. Drazen DL, Demas GE, Nelson RJ. Leptin effects on immune function and energy balance are photoperiod dependent in Siberian hamsters (Phodopus sungorus). Endocrinology 2001, 142, 2768-2775. https://doi.org/10.1210/endo.142.7.8271
  7. Guenther A, Trillmich F. Photoperiod influences the behavioral and physiological phenotype during ontogeny. Behav Ecol 2013, 24, 402-411. https://doi.org/10.1093/beheco/ars177
  8. Gunduz B. Serum leptin profiles, food intake, and body weight in melatonin-implanted Syrian hamsters (Mesocricetus auratus) exposed to long and short photoperiods. Turk J Biol 2014, 38, 185-192. https://doi.org/10.3906/biy-1308-40
  9. Haim A, Yukler A, Harel O, Schwimmer H, Fares F. Effects of chronobiology on prostate cancer cells growth in vivo. Sleep Sci 2010, 3, 32-35.
  10. Heideman PD, Sylvester CJ. Reproductive photoresponsiveness in unmanipulated male Fischer 344 laboratory rats. Biol Reprod 1997, 57, 134-138. https://doi.org/10.1095/biolreprod57.1.134
  11. Ki KS, Cho W. Effects of light pollution and environmental factors on dawn song initiation time of great tit (Parus major). Korean J Environ Ecol 2014, 28, 411-418. https://doi.org/10.13047/KJEE.2014.28.4.411
  12. Kong HJ, Kim JT. Light pollution of outdoor lighting in coastal area-ocused on Busan city. J Korean Inst Illum Electr Install Eng 2010, 24, 18-26.
  13. Krol E, Duncan JS, Redman P, Morgan PJ, Mercer JG, Speakman JR. Photoperiod regulates leptin sensitivity in field voles, Microtus agrestis. J Comp Physiol B 2006, 176, 153-163. https://doi.org/10.1007/s00360-005-0037-8
  14. Le Tallec T, Perret M, Thery M. Light pollution modifies the expression of daily rhythms and behavior patterns in a nocturnal primate. PLoS One 2013, 8, e79250. https://doi.org/10.1371/journal.pone.0079250
  15. Lee PJ. Design of multi-purpose guide light for light pollution protection. J Knowl Inf Technol Syst 2012, 7, 125-134.
  16. Lee SB. Ecological impact assessment of light pollution. pp. 1-2, Korea Environment Institute, Seoul, 2010.
  17. Longcore T, Rich C. Ecological light pollution. Front Ecol Environ 2004, 2, 191-198. https://doi.org/10.1890/1540-9295(2004)002[0191:ELP]2.0.CO;2
  18. Mira A, Mathias ML. Seasonal effects on the hematology and blood plasma proteins of two species of mice Mus musculus domesticus and M. spretus (Rodentia: Muridae) from Portugal. Hystrix 1993, 5, 63-72.
  19. Nelson RJ, Demas GE, Klein SL. Photoperiodic mediation of seasonal breeding and immune function in rodents: a multifactorial approach. Am Zool 1998, 38, 226-237. https://doi.org/10.1093/icb/38.1.226
  20. Nelson RJ, Moffatt CA, Goldman BD. Reproductive and nonreproductive responsiveness to photoperiod in laboratory rats. J Pineal Res 1994, 17, 123-131. https://doi.org/10.1111/j.1600-079X.1994.tb00123.x
  21. Niekamp SR, Sutherland MA, Dahl GE, Salak-Johnson JL. Immune responses of piglets to weaning stress: impacts of photoperiod. J Anim Sci 2007, 85, 93-100. https://doi.org/10.2527/jas.2006-153
  22. Olayaki LA, Salman TM, Jimoh AAG, Iduh G, Soladoye AO. Effects of photoperiod on some haematological indices in rats. Niger J Health Biomed Sci 2008, 7, 11-14.
  23. Ono H, Hoshino Y, Yasuo S, Watanabe M, Nakane Y, Murai A, Ebihara S, Korf HW, Yoshimura T. Involvement of thyrotropin in photoperiodic signal transduction in mice. Proc Natl Acad Sci U S A 2008, 105, 18238-18242. https://doi.org/10.1073/pnas.0808952105
  24. Pittendrigh CS. Temporal organization: reflections of a Darwinian clock-watcher. Annu Rev Physiol 1993, 55, 16-54.
  25. Pyter LM, Adelson JD, Nelson RJ. Short days increase hypothalamic-pituitary-adrenal axis responsiveness. Endocrinology 2007, 148, 3402-3409. https://doi.org/10.1210/en.2006-1432
  26. Rajkhowa R. Light pollution and impact of light pollution. Int J Sci Res 2014, 3, 861-867.
  27. Reppert SM, Weaver DR. Molecular analysis of mammalian circadian rhythms. Annu Rev Physiol 2001, 63, 647-676. https://doi.org/10.1146/annurev.physiol.63.1.647
  28. Ronchi E, Spencer RL, Krey LC, McEwen BS. Effects of photoperiod on brain corticosteroid receptors and the stress response in the golden hamster (Mesocricetus auratus). Brain Res 1998, 780, 348-351. https://doi.org/10.1016/S0006-8993(97)01303-6
  29. Sohn CH. Anatomy and physiology in human circadian rhythms. Sleep Med Psychophysiol 1998, 5, 1-11.
  30. Tavolaro FM, Thomson LM, Ross AW, Morgan PJ, Helfer G. Photoperiodic effects on seasonal physiology, reproductive status and hypothalamic gene expression in young male F344 rats. J Neuroendocrinol 2015, 27, 79-87. https://doi.org/10.1111/jne.12241
  31. Trivedi AK, Kumar V. Melatonin: an internal signal for daily and seasonal timing. Indian J Exp Biol 2014, 52, 425-437.
  32. Vinogradova IA, Iliukha VA, Khizhkin EA, Uzenbaeva LB, Il'na TN, Bukalev AV, Goranski AI, Matveeva IuP, Iunash VD, Lotosh TA. Light pollution, desynchronosis and aging: the state of problem and solutions. Adv Gerontol 2014, 27, 265-268.
  33. Walton JC, Grier AJ, Weil ZM, Nelson RJ. Photoperiod and stress regulation of corticosteroid receptor, brain-derived neurotrophic factor, and glucose transporter GLUT3 mRNA in the hippocampus of male Siberian hamsters (Phodopus sungorus). Neuroscience 2012, 213, 106-111. https://doi.org/10.1016/j.neuroscience.2012.03.043
  34. Weinstein MP, Turner RE, Ibanez C. The global sustainability transition: it is more than changing light bulbs. Sustainabil Sci Pract Policy 2013, 9, 4-15.

Cited by

  1. The preventive role of Spirulina platensis (Arthrospira platensis) in immune and oxidative insults in a stress-induced rat model vol.65, pp.2, 2021, https://doi.org/10.2478/jvetres-2021-0033