Neonatal hypoxic-ischemic brain injury leads to sex-specific deficits in rearing and climbing in adult mice

. 2020 Dec 31 ; 69 (Suppl 3) : S499-S512.

Jazyk angličtina Země Česko Médium print

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/pmid33476172

The study examined the morphological and long-term behavioral impacts of neonatal hypoxic-ischemic brain injury in a mouse model. We investigated the modification of different behavioral domains, such as spontaneous climbing, which represents fine motor skills. We also focused on sex-dependent differences during hypoxic-ischemic encephalopathy. The Rice-Vannucci model of hypoxia-ischemia was used, adjusted and adapted to 7-day-old C57BL/6NTac mice. The effects of induced hypoxia and ischemia were also studied separately. At postnatal day 60, mice underwent behavioral testing using the LABORAS apparatus. The perfusion for histological evaluation was performed one day after the behavioral analyses. In groups with separately induced hypoxia or ischemia, the observed alterations in behavior were not accompanied by morphological changes in the cortex or hippocampal formation. Female mice naturally climbed significantly more and hypoxic females reared less than hypoxic males (p<0.05). Male mice postnatally exposed to hypoxia-ischemia exhibited significantly lower vertical activity and higher horizontal activity (p<0.05). Mild hypoxic damage may not be morphologically detectable but may induce substantial behavioral changes in adult mice. There were significant differences between horizontal and vertical activity in reaction to hypoxia-ischemia. Our study indicates that the importance of behavioral testing is irreplaceable and may be reflected in neonatal medicine.

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BISWAL S, SHARMA D, KUMAR K, NAG TC, BARHWAL K, HOTA SK, KUMAR B. Global hypoxia induced impairment in learning and spatial memory is associated with precocious hippocampal aging. Neurobiol Learn Mem. 2016;133:157–170. doi: 10.1016/j.nlm.2016.05.011. PubMed DOI

BORBÉLYOVÁ V, JANIŠOVÁ K, MYSLIVEČEK J, RILJAK V. Sex-related differences in locomotion and climbing of C57Bl/6NTac mice in a novel environment. Physiol Res. 2019;68(Suppl 3):S353–S359. doi: 10.33549/physiolres.934348. PubMed DOI

CLOWRY GJ, BASUODAN R, CHAN F. What are the best animal models for testing early intervention in cerebral palsy? Front Neurol. 2014;5:258. doi: 10.3389/fneur.2014.00258. PubMed DOI PMC

COLVER A, FAIRHURST C, PHAROAH PO. Cerebral palsy. Lancet. 2014;383:1240–1249. doi: 10.1016/S0140-6736(13)61835-8. PubMed DOI

DAVIDSON JO, WASSINK G, Van den HEUIJ LG, BENNET L, GUNN AJ. Therapeutic hypothermia for neonatal hypoxic-ischemic encephalopathy - where to from here? Front Neurol. 2015;6:198. doi: 10.3389/fneur.2015.00198. PubMed DOI PMC

DERE E, RONNENBERG A, TAMPE B, ARINRAD S, SCHMIDT M, ZEISBERG E, EHRENREICH H. Cognitive, emotional and social phenotyping of mice in an observer-independent setting. Neurobiol Learn Mem. 2018;150:136–150. doi: 10.1016/j.nlm.2018.02.023. PubMed DOI

DERRICK M, ENGLOF I, DROBYSHEVSKY A, LUO K, YU L, TAN S. Intrauterine fetal demise can be remote from the inciting insult in an animal model of hypoxia-ischemia. Pediatr Res. 2012;72:154–160. doi: 10.1038/pr.2012.65. PubMed DOI PMC

DITELBERG JS, SHELDON RA, EPSTEIN CJ, FERRIERO DM. Brain injury after perinatal hypoxia-ischemia is exacerbated in copper/zinc superoxide dismutase transgenic mice. Pediatr Res. 1996;39:204–208. doi: 10.1203/00006450-199602000-00003. PubMed DOI

DOBBING J, SANDS J. Comparative aspects of the brain growth spurt. Early Hum Dev. 1979;3:79–83. doi: 10.1016/0378-3782(79)90022-7. PubMed DOI

DOUGLAS-ESCOBAR M, WEISS MD. Hypoxic-ischemic encephalopathy: a review for the clinician. JAMA Pediatr. 2015;169:397–403. doi: 10.1001/jamapediatrics.2014.3269. PubMed DOI

GENNARO M, MATTIELLO A, PIZZORUSSO T. Rodent models of developmental ischemic stroke for translational research: strengths and weaknesses. Neural Plast. 2019;2019:5089321. doi: 10.1155/2019/5089321. PubMed DOI PMC

HAGBERG H, EDWARDS AD, GROENENDAAL F. Perinatal brain damage: the term infant. Neurobiol Dis. 2016;92:102–112. doi: 10.1016/j.nbd.2015.09.011. PubMed DOI PMC

HILL CA, FITCH RH. Sex differences in mechanisms and outcome of neonatal hypoxia-ischemia in rodent models: implications for sex-specific neuroprotection in clinical neonatal practice. Neurol Res Int. 2012;2012:867531. doi: 10.1155/2012/867531. PubMed DOI PMC

HUANG HZ, WEN XH, LIU H. Sex differences in brain MRI abnormalities and neurodevelopmental outcomes in a rat model of neonatal hypoxia-ischemia. Int J Neurosci. 2016;126:647–657. doi: 10.3109/00207454.2015.1047016. PubMed DOI

JOHNSTON MV, HAGBERG H. Sex and the pathogenesis of cerebral palsy. Dev Med Child Neurol. 2007;49:74–78. doi: 10.1017/S0012162207000199.x. PubMed DOI

LAN WC, PRIESTLEY M, MAYORAL SR, TIAN L, SHAMLOO M, PENN AA. Sex-specific cognitive deficits and regional brain volume loss in mice exposed to chronic, sublethal hypoxia. Pediatr Res. 2011;70:15–20. doi: 10.1203/PDR.0b013e31821b98a3. PubMed DOI PMC

LIU L, OZA S, HOGAN D, PERIN J, RUDAN I, LAWN JE, COUSENS S, MATHERS C, BLACK RE. Global, regional, and national causes of child mortality in 2000–13, with projections to inform post-2015 priorities: an updated systematic analysis. Lancet. 2015;385:430–440. doi: 10.1016/S0140-6736(14)61698-6. PubMed DOI

MURDEN S, BORBÉLYOVÁ V, LAŠTŮVKA Z, MYSLIVEČEK J, OTÁHAL J, RILJAK V. Gender differences involved in the pathophysiology of the perinatal hypoxic-ischemic damage. Physiol Res. 2019;68(Suppl 3):S207–S217. doi: 10.33549/physiolres.934356. PubMed DOI

NEVISON CM, HURST JL, BARNARD CJ. Why do male ICR(CD-1) mice perform bar-related (stereotypic) behaviour? Behav Processes. 1999;47:95–111. doi: 10.1016/S0376-6357(99)00053-4. PubMed DOI

NORTHINGTON FJ. Brief update on animal models of hypoxic-ischemic encephalopathy and neonatal stroke. ILAR J. 2006;47:32–38. doi: 10.1093/ilar.47.1.32. PubMed DOI

PERALS D, GRIFFIN AS, BARTOMEUS I, SOL D. Revisiting the open-field test: what does it really tell us about animal personality? Anim Behav. 2017;123:69–79. doi: 10.1016/j.anbehav.2016.10.006. DOI

PERLMAN JM, WYLLIE J, KATTWINKEL J, ATKINS DL, CHAMEIDES L, GOLDSMITH JP, GUINSBURG R, HAZINSKI MF, MORLEY C, RICHMOND S, SIMON WM, SINGHAL N, SZYLD E, TAMURA M, VELAPHI S. Part 11: neonatal resuscitation: 2010 International consensus on cardiopulmonary resuscitation and emergency cardiovascular care science with treatment recommendations. Circulation. 2010;122(16 Suppl 2):S516–S538. doi: 10.1161/CIRCULATIONAHA.110.971127. PubMed DOI

PIETROPAOLO S, MINTZ M, FELDON J, YEE BK. The behavioral sequela following the prevention of home-cage grid-climbing activity in C57BL/6 mice. Behav Neurosci. 2007;121:345–355. doi: 10.1037/0735-7044.121.2.345. PubMed DOI

RICE JE, 3RD, VANNUCCI RC, BRIERLEY JB. The influence of immaturity on hypoxic-ischemic brain damage in the rat. Ann Neurol. 1981;9:131–141. doi: 10.1002/ana.410090206. PubMed DOI

RILJAK V, KRAF J, DARYANANI A, JIRUŠKA P, OTÁHAL J. Pathophysiology of perinatal hypoxic-ischemic encephalopathy - biomarkers, animal models and treatment perspectives. Physiol Res. 2016;65(Suppl 5):S533–S545. doi: 10.33549/physiolres.933541. PubMed DOI

RILJAK V, LAŠTŮVKA Z, MYSLIVEČEK J, BORBÉLYOVÁ V, OTÁHAL J. Early postnatal hypoxia induces behavioral deficits but not morphological damage in the hippocampus in adolescent rats. Physiol Res. 2020;69:165–179. doi: 10.33549/physiolres.934234. PubMed DOI PMC

RUMAJOGEE P, BREGMAN T, MILLER SP, YAGER JY, FEHLINGS MG. Rodent hypoxia-ischemia models for cerebral palsy research: a systematic review. Front Neurol. 2016;7:57. doi: 10.3389/fneur.2016.00057. PubMed DOI PMC

SANCHES EF, ARTENI N, NICOLA F, ARISTIMUNHA D, NETTO CA. Sexual dimorphism and brain lateralization impact behavioral and histological outcomes following hypoxia-ischemia in P3 and P7 rats. Neuroscience. 2015;290:581–593. doi: 10.1016/j.neuroscience.2014.12.074. PubMed DOI

SHELDON RA, SEDIK C, FERRIERO DM. Strain-related brain injury in neonatal mice subjected to hypoxia-ischemia. Brain Res. 1998;810:114–122. doi: 10.1016/S0006-8993(98)00892-0. PubMed DOI

SHELDON RA, WINDSOR C, FERRIERO DM. Strain-related differences in mouse neonatal hypoxia-ischemia. Dev Neurosci. 2018;40:490–496. doi: 10.1159/000495880. PubMed DOI PMC

SHETTY J. Neonatal seizures in hypoxic-ischaemic encephalopathy--risks and benefits of anticonvulsant therapy. Dev Med Child Neurol. 2015;57:40–43. doi: 10.1111/dmcn.12724. PubMed DOI

TAGIN M, ABDEL-HADY H, UR RAHMAN S, AZZOPARDI DV, GUNN AJ. Neuroprotection for perinatal hypoxic ischemic encephalopathy in low- and middle-income countries. J Pediatr. 2015;167:25–28. doi: 10.1016/j.jpeds.2015.02.056. PubMed DOI

TEN VS, BRADLEY-MOORE M, GINGRICH JA, STARK RI, PINSKY DJ. Brain injury and neurofunctional deficit in neonatal mice with hypoxic-ischemic encephalopathy. Behav Brain Res. 2003;145:209–219. doi: 10.1016/S0166-4328(03)00146-3. PubMed DOI

VALUSKOVA P, RILJAK V, FORCZEK ST, FARAR V, MYSLIVECEK J. Variability in the drug response of M(4) muscarinic receptor knockout mice during day and night time. Front Pharmacol. 2019;10:237–237. doi: 10.3389/fphar.2019.00237. PubMed DOI PMC

Van de WEERD HA, BULTHUIS RJ, BERGMAN AF, SCHLINGMANN F, TOLBOOM J, Van LOO PL, REMIE R, BAUMANS V, Van ZUTPHEN LF. Validation of a new system for the automatic registration of behaviour in mice and rats. Behav Processes. 2001;53:11–20. doi: 10.1016/S0376-6357(00)00135-2. PubMed DOI

VANNUCCI RC, VANNUCCI SJ. Perinatal hypoxic-ischemic brain damage: evolution of an animal model. Dev Neurosci. 2005;27:81–86. doi: 10.1159/000085978. PubMed DOI

VANNUCCI SJ, HAGBERG H. Hypoxia-ischemia in the immature brain. J Exp Biol. 2004;207:3149–3154. doi: 10.1242/jeb.01064. PubMed DOI

WOLF S, HAINZ N, BECKMANN A, MAACK C, MENGER MD, TSCHERNIG T, MEIER C. Brain damage resulting from postnatal hypoxic-ischemic brain injury is reduced in C57BL/6J mice as compared to C57BL/6N mice. Brain Res. 2016;1650:224–231. doi: 10.1016/j.brainres.2016.09.013. PubMed DOI

ZHAO L, MULLIGAN MK, NOWAK TS., JR Substrain- and sex-dependent differences in stroke vulnerability in C57BL/6 mice. J Cereb Blood Flow Metab. 2019;39:426–438. doi: 10.1177/0271678X17746174. PubMed DOI PMC

ZHU C, WANG X, BLOMGREN K. Cerebral hypoxia-ischemia in neonatal rats or mice: a model of perinatal brain injury. In: CHEN J, XU ZC, XU XM, ZHANG JH, editors. Animal Models of Acute Neurological Injuries. Humana Press; Totowa: 2009. pp. 221–230. DOI

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