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Examining the Effects of Oxygen Exposure on the Developing Brain Through Murine Models

Year 2024, Volume: 4 Issue: 1, 15 - 25, 29.03.2024
https://doi.org/10.5281/zenodo.10894221

Abstract

Hyperoxia is one of the key players contributing preterm brain injury. Researchers typically use rodent models to pinpoint the underlying pathologic alterations in hyperoxic brain damage. When evaluating the neurological effects of neonatal hyperoxic brain injury in an experimental model, choosing the appropriate assessment techniques is crucial. The goal of this article is to review the behavioral and learning tests that can be used to determine the impact of hyperoxia on the developing brain. Injuries to the nervous system can be recovered very quickly in newborn rodents. Thus, the timing of evaluation tests are very critical. A model that is appropriate for the brain's developmental processes and accurately simulates the damage in humans should be utilized in studies on neonatal hyperoxic brain injury, and the right test should be chosen at the appropriate time. In the first twenty days, physical and motor development tests, and subsequent evaluation of damaged brain structures are relevant. The open field and forced swim tests can be used to assess the animal's locomotor activity and depressive condition, while the watermaze, passive avoidance and new object recognition tests can be used to assess cognitive abilities. In laboratory mice and rats, physical development and motor reflex development tests can be started right after birth, while learning and memory tests can be done from 4 weeks at the earliest. Correlations between motor development, behavior, memory tests, and results of cellular/ molecular studies should be made and interpreted carefully.

References

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Yenidoğan Rodent Modellerinde Hiperoksik Beyin Hasarının Değerlendirilmesi

Year 2024, Volume: 4 Issue: 1, 15 - 25, 29.03.2024
https://doi.org/10.5281/zenodo.10894221

Abstract

Hiperoksi, preterm beyin hasarına katkıda bulunan önemli postnatal faktörlerden biridir. Hiperoksinin neden preterm beyin dokusunda yol açtığı olduğu patolojik süreçlerin aydınlatılabilmesi için deneysel kemirgen modelleri sıklıkla kullanılmaktadır. Bu derleme, yenidoğan hiperoksik beyin hasarının değerlendirmesinde, araştırmacıların davranış ve öğrenme testleri ile ilgili seçimlerine ışık tutmayı hedeflemektedir. Yenidoğan kemirgen modellerinde, hayvanların nörolojik hasarlarından hızla iyileşme konusunda yüksek yeteneğe sahip olduğu göz ardı edilmemeli ve değerlendirme testlerinin yapılma zamanı iyi belirlenmelidir. Beynin gelişimsel süreçlerine uygun, insanlardaki hasarı daha iyi yansıtacak hayvan modeli kullanılmalı, doğru değerlendirme testi seçilmeli ve seçilen testler doğru zamanda uygulanmalıdır. Yaşamın ilk yirmi gününde fiziksel ve motor gelişim testleri kullanılmalı, daha sonraki süreçte beyin olgunlaşmasına paralel olarak davranış ve bellek testleri ile değerlendirilme yapılmalıdır. Lokomotor aktivite ve depresyon varlığı açısından açık alan testi, bilişsel işlevlerin değerlendirilmesi için yeni obje tanıma, su labirenti ve pasif kaçınma testleri seçilebilir. Motor gelişim, davranış ve bellek testleri, hücresel ve moleküler değişiklikler ile korele edilerek yorumlanmalıdır.

References

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  • Back, S. A., Luo, N. L., Borenstein, N. S., Levine, J. M., Volpe, J. J., & Kinney, H. C. (2001). Late Oligodendrocyte Progenitors Coincide with the Developmental Window of Vulnerability for Human Perinatal White Matter Injury. The Journal of Neuroscience, 21(4), 1302–1312. https://doi.org/10.1523/JNEUROSCI.21-04-01302.2001
  • Back, S. A., Riddle, A., & McClure, M. M. (2007). Maturation-dependent vulnerability of perinatal white matter in premature birth. Stroke, 38(2 Suppl), 724–730. https://doi.org/10.1161/01.STR.0000254729.27386.05
  • Balasubramaniam, J., Xue, M., & Del Bigio, M. (2005). Long-term motor deficit following periventricular hemorrhage in neonatal rats: A potential model for human cerebral palsy. Journal of Cerebral Blood Flow & Metabolism, 25(1_suppl), S242–S242. https://doi.org/10.1038/sj.jcbfm.9591524.0242
  • Bandstra, E. S., Morrow, C. E., Mansoor, E., & Accornero, V. H. (2010). Prenatal drug exposure: Infant and toddler outcomes. Journal of Addictive Diseases, 29(2), 245–258. https://doi.org/10.1080/10550881003684871
  • Brehmer, F., Bendix, I., Prager, S., van de Looij, Y., Reinboth, B. S., Zimmermanns, J., Schlager, G. W., Brait, D., Sifringer, M., Endesfelder, S., Sizonenko, S., Mallard, C., Bührer, C., Felderhoff-Mueser, U., & Gerstner, B. (2012). Interaction of Inflammation and Hyperoxia in a Rat Model of Neonatal White Matter Damage. PLoS ONE, 7(11), e49023. https://doi.org/10.1371/journal.pone.0049023
  • Cameron, N. M., Shahrokh, D., Del Corpo, A., Dhir, S. K., Szyf, M., Champagne, F. A., & Meaney, M. J. (2008). Epigenetic programming of phenotypic variations in reproductive strategies in the rat through maternal care. Journal of Neuroendocrinology, 20(6), 795–801. https://doi.org/10.1111/j.1365-2826.2008.01725.x
  • Champagne, F. A. (2009). Nurturing nature: Social experiences and the brain. Journal of Neuroendocrinology, 21(10), 867–868. https://doi.org/10.1111/j.1365-2826.2009.01901.x
  • Chawanpaiboon, S., Vogel, J. P., Moller, A.-B., Lumbiganon, P., Petzold, M., Hogan, D., Landoulsi, S., Jampathong, N., Kongwattanakul, K., Laopaiboon, M., Lewis, C., Rattanakanokchai, S., Teng, D. N., Thinkhamrop, J., Watananirun, K., Zhang, J., Zhou, W., & Gülmezoglu, A. M. (2019). Global, regional, and national estimates of levels of preterm birth in 2014: A systematic review and modelling analysis. The Lancet. Global Health, 7(1), e37–e46. https://doi.org/10.1016/S2214-109X(18)30451-0
  • Clancy, B., Finlay, B. L., Darlington, R. B., & Anand, K. J. S. (2007). Extrapolating brain development from experimental species to humans. Neurotoxicology, 28(5), 931–937. https://doi.org/10.1016/j.neuro.2007.01.014
  • Corti, S., Nizzardo, M., Nardini, M., Donadoni, C., Salani, S., Ronchi, D., Saladino, F., Bordoni, A., Fortunato, F., Del Bo, R., Papadimitriou, D., Locatelli, F., Menozzi, G., Strazzer, S., Bresolin, N., & Comi, G. P. (2008). Neural stem cell transplantation can ameliorate the phenotype of a mouse model of spinal muscular atrophy. The Journal of Clinical Investigation, 118(10), 3316–3330. https://doi.org/10.1172/JCI35432
  • Dean, J. M., Moravec, M. D., Grafe, M., Abend, N., Ren, J., Gong, X., Volpe, J. J., Jensen, F. E., Hohimer, A. R., & Back, S. A. (2011). Strain-specific differences in perinatal rodent oligodendrocyte lineage progression and its correlation with human. Developmental Neuroscience, 33(3–4), 251–260. https://doi.org/10.1159/000327242
  • DeSesso, J. M., Scialli, A. R., & Holson, J. F. (1999). Apparent lability of neural tube closure in laboratory animals and humans. American Journal of Medical Genetics, 87(2), 143–162. https://doi.org/10.1002/(sici)1096-8628(19991119)87:2<143::aid-ajmg6>3.0.co;2-j
  • Di Florio, D. N., Sin, J., Coronado, M. J., Atwal, P. S., & Fairweather, D. (2020). Sex differences in inflammation, redox biology, mitochondria and autoimmunity. Redox Biology, 31, 101482. https://doi.org/10.1016/j.redox.2020.101482
  • Dobbing, J., & Sands, J. (1973). Quantitative growth and development of human brain. Archives of Disease in Childhood, 48(10), 757–767. https://doi.org/10.1136/adc.48.10.757
  • Dobbing, J., & Sands, J. (1979). Comparative aspects of the brain growth spurt. Early Human Development, 3(1), 79–83. https://doi.org/10.1016/0378-3782(79)90022-7
  • El-Khodor, B. F., Edgar, N., Chen, A., Winberg, M. L., Joyce, C., Brunner, D., Suárez-Fariñas, M., & Heyes, M. P. (2008). Identification of a battery of tests for drug candidate evaluation in the SMNDelta7 neonate model of spinal muscular atrophy. Experimental Neurology, 212(1), 29–43. https://doi.org/10.1016/j.expneurol.2008.02.025
  • Eltokhi, A., Kurpiers, B., & Pitzer, C. (2020). Behavioral tests assessing neuropsychiatric phenotypes in adolescent mice reveal strain- and sex-specific effects. Scientific Reports, 10(1), 11263. https://doi.org/10.1038/s41598-020-67758-0
  • Falsaperla, R., Giacchi, V., Saporito, M. A. N., Pavone, P., Puglisi, F., & Ruggieri, M. (2022). Pulse Oximetry Saturation (Spoxygen) Monitoring in the Neonatal Intensive Care Unit (NICU): The Challenge for Providers: A Systematic Review. Advances in Neonatal Care: Official Journal of the National Association of Neonatal Nurses, 22(3), 231–238. https://doi.org/10.1097/ANC.0000000000000914
  • Farber, J. M., Shapiro, B. K., Palmer, F. B., & Capute, A. J. (1985). The diagnostic value of the neurodevelopmental examination. Clinical Pediatrics, 24(7), 367–372. https://doi.org/10.1177/000992288502400701
  • Farrow, K. N., Lee, K. J., Perez, M., Schriewer, J. M., Wedgwood, S., Lakshminrusimha, S., Smith, C. L., Steinhorn, R. H., & Schumacker, P. T. (2012). Brief Hyperoxia Increases Mitochondrial Oxidation and Increases Phosphodiesterase 5 Activity in Fetal Pulmonary Artery Smooth Muscle Cells. Antioxidants & Redox Signaling, 17(3), 460–470. https://doi.org/10.1089/ars.2011.4184
  • Feather-Schussler, D. N., & Ferguson, T. S. (2016). A Battery of Motor Tests in a Neonatal Mouse Model of Cerebral Palsy. Journal of Visualized Experiments: JoVE, 117. https://doi.org/10.3791/53569
  • Felderhoff-Mueser, U., Bittigau, P., Sifringer, M., Jarosz, B., Korobowicz, E., Mahler, L., Piening, T., Moysich, A., Grune, T., Thor, F., Heumann, R., Bührer, C., & Ikonomidou, C. (2004). Oxygen causes cell death in the developing brain. Neurobiology of Disease, 17(2), 273–282. https://doi.org/10.1016/j.nbd.2004.07.019
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There are 49 citations in total.

Details

Primary Language English
Subjects Animal Biotechnology
Journal Section Derlemeler
Authors

Canberk Yılmaz 0000-0002-0049-7614

Defne Engür 0000-0003-0405-085X

Abdullah Kumral 0000-0003-0004-1761

Osman Yılmaz 0000-0001-7817-7576

Publication Date March 29, 2024
Submission Date April 24, 2023
Published in Issue Year 2024 Volume: 4 Issue: 1

Cite

EndNote Yılmaz C, Engür D, Kumral A, Yılmaz O (March 1, 2024) Examining the Effects of Oxygen Exposure on the Developing Brain Through Murine Models. Laboratuvar Hayvanları Bilimi ve Uygulamaları Dergisi 4 1 15–25.

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