LIGHT EXPOSURE’S EFFECTS ON INACTIVE STATE DURATION AND SLEEP LATENCY IN ZEBRAFISH (DANIO RERIO) LARVAE INSOMNIA MODEL
DOI:
https://doi.org/10.21776/ub.mnj.2022.008.02.11Keywords:
Insomnia, zebrafish, inactive state duration and sleep latencyAbstract
Background: Insomnia is defined as difficulty falling or staying asleep or a sleep state that cannot restore the body's condition. The zebrafish (Danio rerio) is a vertebrate model that has been extensively studied to study sleep and neurological disorders. One of the most widely used methods to examine the effect of the light-dark cycle on the circadian system is by exposing animals and humans to pulse wave light.
Objective: To see the effect of light exposure on zebrafish larvae by looking at inactive state duration and sleep latency in zebrafish (Danio rerio) larvae insomnia model.
Methods: This study used four groups of zebrafish larvae i.e : (1) normal group (2) minutes of light exposure and 2 minutes off (2/2)), (3) Four minutes of light exposure and 1 minute off (4/1), and (4) 24 hours on (24/0). Observation of larval movement was carried out on 5, 6, and 7 dpf (day post fertilization). Observation time was 30 minutes before and after turned off of light exposure.
Results: There were significant differences on days 5, 6, and 7 between the normal group and the three light treatment groups on inactive state duration and sleep latency in dark and light conditions with p-values (p<0.05) and (p< 0.031), but there was no significant difference among groups of light exposure 2 minutes on 2 minutes off, 4 minutes on 1 minute off, and 24 hours on. The 24-hour on treatment showed the most inactive state duration among the light treatments, while the sleep latency was found in the 24-hour treatment.
Conclusion: Light treatment of 2 minutes on 2 minutes off, 4 minutes on 1 minute off, and 24 hours on can cause insomnia, but the most substantial insomnia effect is obtained from the 24-hour treatment.
References
Ali MK, Nicholson HL. Increasing zebrafish (Danio rerio) numbers in a limited tank space reduces night-time fish sleep-like states and induces aggressive behavior. World J Depress Anxiety; 2018. 1(1):1–6.
Blume C, Garbazza C, & Spitschan M. Effects of light on human circadian rhythms, sleep, and mood. Somnology; 2019. 23(3), 147–156.
DOI: 10.1007/s11818-019-00215-x
Bringmann, H. Genetic sleep deprivation: using sleep mutants to study sleep functions. EMBO Reports; 2019. 20(3), 1–14. DOI: 10.15252/embr.201846807
Levitas-Djerbi T and Appelbaum L. Modeling sleep and neuropsychiatric disorders in zebrafish. Current opinion in neurobiology; 2017. 44:89-93.
DOI: 10.1016/j.conb.2017.02.017
Chiu CN and Prober DA. Regulation of zebrafish sleep and arousal states current and prospective approaches. Front. Neural Circuits; 2013. 7(58): 1–14. DOI: 10.3389/fncir.2013.00058
Abbott SM, Reid KJ and Zee PC. Circadian disorders of the sleep-wake cycle. Principles and Practice of Sleep Medicine. Elsevier; 2017. 414-423.
Cao R. mTOR Signaling, Translational Control, and the Circadian Clock. Frontiers in Genetics; 2018. 9:367. DOI: 10.3389/fgene.2018.00367
Cheng RK, Jesuthasan SJ & Penney TB. Zebrafish forebrain and temporal conditioning. Philosophical Transactions of the Royal Society B: Biological Sciences; 2014. 369(1637).
DOI: 10.1098/rstb.2012.0462
Qiu MH, Yao QL, Vetrivelan R, Chen MC, & Lu J. Nigrostriatal dopamine acting on globus pallidus regulates sleep. Cerebral Cortex; 2016. 26(4):1430–1439. DOI: 10.1093/cercor/bhu241.
Vaz RL, Outeiro TF & Ferreira JJ. Zebrafish as an animal model for drug discovery in parkinson’s disease and other movement disorders: A systematic review. Frontiers in Neurology; 2018. 9(Jun).
DOI: 10.3389/fneur.2018.00347
Cunnington D, Junge MF and Fernando AT. Insomnia: Prevalence, consequences, and effective treatment. Medical Journal of Australia; 2013. 199:S36-S40. DOI: 10.5694/mja13.10718
Rihel J, Prober DA & Schier AF. (2010). Monitoring sleep and arousal in zebrafish. Methods in Cell Biology Elsevier Inc; 2010. Third Edit, Vol. 100 Issue C. DOI: 10.1016/B978-0-12-384892-5.00011-6
Dohnt H, Gradisar M and Short MA. Insomnia and its symptoms in adolescents: Comparing DSM-IV and ICSD-II diagnostic criteria. Journal of Clinical Sleep Medicine; 2012. 8(3):295-299.
DOI: 10.5664/jcsm.1918
Praveena Devi CB, Samreen S, Kusuma Kumari N, B Praveena Devi CC & Sharma J. A review on insomnia: The sleep disorder. The Pharma Innovation Journal; 2018. 7(12):227–230. Available from: https://www.researchgate.net/publication/329673515
Pinheiro-da-Silva J, Silva PF, Nogueira MB and Luchiari AC. Sleep deprivation effects on object discrimination task in zebrafish (Danio rerio). Animal Cognition; 2017. 20(2): 159–169.
DOI: 10.1007/s10071-016-1034-x
Priscila JP, Silva F, Borges M & Luchiari AC. Sleep deprivation effects on object discrimination tasks in zebrafish (Danio rerio). Animal Cognition; 2016. DOI: 10.1007/s10071-016-1034-x
Kumari Y, Choo B, Shaikh M, Othman I. Melatonin receptor agonist Piper betle L. Ameliorates dexamethasone‑induced early life stress in adult zebrafish. Exp Ther Med. Published online; 2019. 1407-1416. DOI:10.3892/etm.2019.7685
Yokogawa T, Marin W, Faraco J, Pézeron G, Appelbaum L, Zhang J, Rosa F, Mourrain P and Mignot E. Characterization of sleep in zebrafish and insomnia in hypocretin receptor mutants. PLoS Biology; 2017. 5(10):e277.
DOI: 10.1371/journal.pbio.0050277
Prober DA, Rihel J, Onah AA, Sung RJ, Schier AF. Hypocretin/orexin overexpression induces an insomnia-like phenotype in zebrafish. J Neurosci; 2006. 26(51):13400–10.
DOI: 10.1523/JNEUROSCI.4332-06.2006
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