Abstract
Continuous generation of new neurons has been demonstrated in the adult mammalian brain, and this process was shown to be stimulated by various pathologic conditions, including cerebral ischemia. Because brain oxygen deprivation is particularly frequent in neonates and represents the primary event of asphyxia, we analyzed long-term consequences of transient hypoxia in the newborn rat. Within 24 h after birth, animals were exposed to 100% N2 for 20 min at 36°C, and temporal changes in the vulnerable CA1 hippocampus were monitored. Cell density measurements revealed delayed cell death in the pyramidal cell layer reflecting apoptosis, as shown by characteristic nuclear morphology and expression levels of Bcl-2, Bax, and caspase-3. Neuronal loss was confirmed by reduced density of neuron-specific enolase (NSE)–labeled cells, and peaked by 1 wk post insult, to reach 27% of total cells. A gradual recovery then occurred, and no significant difference in cell density could be detected between controls and hypoxic rats at postnatal d 21. Repeated injections of bromodeoxyuridine (50 mg/kg) showed that newly divided cells expressing neuronal markers increased by 225% in the germinative subventricular zone, and they tended to migrate along the posterior periventricle toward the hippocampus. Therefore, transient hypoxia in the newborn rat triggered apoptosis in the CA1 hippocampus followed by increased neurogenesis and apparent anatomical recovery, suggesting that the developing brain may have a high capacity for self-repair.
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Abbreviations
- BrdU:
-
bromodeoxyuridine
- CO:
-
cytochrome oxidase
- DAPI:
-
4 6-diamidino-2-phenylindole
- DG:
-
dentate gyrus
- NSE:
-
neuron-specific enolase
- SVZ:
-
subventricular zone
References
Patel J, Edwards AD 1997 Prediction of outcome after perinatal asphyxia. Curr Opin Pediatr 9: 128–132
Berger R, Garnier Y 1999 Pathophysiology of perinatal brain damage. Brain Res Brain Res Rev 30: 107–134
Maneru C, Junque C, Botet F, Tallada M, Guardia J 2001 Neuropsychological long-term sequelae of perinatal asphyxia. Brain Inj 15: 1029–1039
Haddad GG, Jiang C 1993 O2deprivation in the central nervous system: on mechanisms of neuronal response, differential sensitivity and injury. Prog Neurobiol 40: 277–318
Walton M, Connor B, Lawlor P, Young D, Sirimanne E, Gluckman P, Cole G, Dragunow M 1999 Neuronal death and survival in two models of hypoxic-ischemic brain damage. Brain Res Brain Res Rev 29: 137–168
Nakajima W, Ishida A, Lange MS, Gabrielson KL, Wilson MA, Martin LJ, Blue ME, Johnston MV 2000 Apoptosis has a prolonged role in the degeneration after hypoxic ischemia in the newborn rat. J Neurosci 20: 7994–8004
Benchoua A, Guégan C, Couriaud C, Hosseini H, Sampaïo N, Morin D, Onténiente B 2001 Specific caspase pathways are activated in the two stages of cerebral infarction. J Neurosci 21: 7127–7134
Banasiak KJ, Haddad GG 1998 Hypoxia-induced apoptosis: effect of hypoxic severity and roles of p53 in neuronal cell death. Brain Res 797: 295–304
Bossenmeyer C, Chihab R, Muller S, Schroeder H, Daval JL 1998 Hypoxia/reoxygenation induces apoptosis through biphasic induction of protein synthesis in central neurons. Brain Res 787: 107–116
Bossenmeyer-Pourié C, Lièvre V, Grojean S, Koziel V, Pillot T, Daval JL 2002 Sequential expression patterns of apoptosis- and cell cycle-related proteins in neuronal response to severe or mild transient hypoxia. Neuroscience 114: 869–882
Tamatani M, Ogawa S, Tohyama M 1998 Roles of Bcl-2 and caspases in hypoxia-induced neuronal cell death: a possible neuroprotective mechanism of peptide growth factors. Brain Res Mol Brain Res 58: 27–39
Tamatani M, Mitsuda N, Matsuzaki H, Okado H, Miyake SI, Vitek MP, Yamaguchi A, Tohyama M 2000 A pathway of neuronal apoptosis induced by hypoxia/reoxygenation: roles of nuclear factor-κB and Bcl-2. J Neurochem 75: 683–693
Gould E, Tanapat P 1997 Lesion-induced proliferation of neuronal progenitors in the dentate gyrus of the adult rat. Neuroscience 80: 427–436
Parent JM, Valentin VV, Lowenstein DH 2002 Prolonged seizures increase proliferating neuroblasts in the adult rat subventricular zone-olfactory bulb pathway. J Neurosci 22: 3174–3188
Liu J, Solway K, Messing RO, Sharp FR 1998 Increased neurogenesis in the dentate gyrus after transient global ischemia in gerbils. J Neurosci 18: 7768–7778
Jiang W, Gu W, Brännström T, Rosqvist R, Wester P 2001 Cortical neurogenesis in adult rats after transient middle cerebral artery occlusion. Stroke 32: 1201–1207
Kee NJ, Preston E, Wojtowicz JM 2001 Enhanced neurogenesis after transient global ischemia in the dentate gyrus of the rat. Exp Brain Res 136: 313–320
Zhang RL, Zhang ZG, Zhang L, Chopp M 2001 Proliferation and differentiation of progenitor cells in the cortex and the subventricular zone in the adult rat after focal cerebral ischemia. Neuroscience 105: 33–41
Zhu DA, Liu SH, Sun HS, Lu YM 2003 Expression of inducible nitric oxide synthase after focal cerebral ischemia stimulates neurogenesis in the adult rodent dentate gyrus. J Neurosci 23: 223–229
Gage FH 2000 Mammalian neural stem cells. Science 287: 1433–1438
Hastings NB, Tanapat P, Gould E 2001 Neurogenesis in the adult mammalian brain. Clin Neurosci Res 1: 175–182
Pencea V, Bingaman KD, Freedman LJ, Luskin MB 2001 Neurogenesis in the subventricular zone and rostral migratory stream of the neonatal and adult primate forebrain. Exp Neurol 172: 1–16
Seaberg RM, van der Kooy D 2002 Adult rodent neurogenic regions: the ventricular subependyma contains neural stem cells, but the dentate gyrus contains restricted progenitors. J Neurosci 22: 1784–1793
Magavi SS, Leavitt BR, Macklis JD 2000 Induction of neurogenesis in the neocortex of adult mice. Nature 405: 951–955
Yamamoto S, Yamamoto N, Kitamura T, Nakamura K, Nakafuku M 2001 Proliferation of parenchymal neural progenitors in response to injury in the adult rat spinal cord. Exp Neurol 172: 115–127
Grafe MR 1994 Developmental changes in the sensitivity of the neonatal rat brain. Brain Res 653: 161–166
Yager JY, Thornhill JA 1997 The effect of age on susceptibility to hypoxic-ischemic brain damage. Neurosci Biobehav Rev 21: 167–174
Li YB, Kaur C, Ling EA 1998 Neuronal degeneration and microglial reaction in the fetal and postnatal rat brain after transient maternal hypoxia. Neurosci Res 32: 137–148
Dell'Anna ME, Calzolari S, Molinari M, Iuvone L, Calimici R 1991 Neonatal anoxia induces transitory hyperactivity, permanent spatial memory deficits and CA1 cell density reduction in developing rats. Behav Brain Res 45: 125–134
Nyakas C, Buwalda B, Luiten PGM 1996 Hypoxia and brain development. Prog Neurobiol 49: 1–51
Pulsinelli WA, Brierley JB, Plum F 1982 Temporal profile of neuronal damage in a model of transient forebrain ischemia. Ann Neurol 11: 491–498
Sherwood NM, Timiras PS 1970 A Stereotaxic Atlas of the Developing Rat Brain. University of California Press, Berkeley, CA, 209
Wolvetang EJ, Johnson KL, Krauer K, Ralph SJ, Linnane AW 1994 Mitochondrial respiratory chain inhibitors induce apoptosis. FEBS Lett 339: 40–44
Park DS, Morris EJ, Greene LA, Geller HM 1997 G1/S cell cycle blockers and inhibitors of cyclin-dependent kinases suppress camptothecin-induced neuronal apoptosis. J Neurosci 17: 1256–1270
Bossenmeyer-Pourié C, Chihab R, Schroeder H, Daval JL 1999 Transient hypoxia may lead to neuronal proliferation in the developing mammalian brain: from apoptosis to cell cycle completion. Neuroscience 91: 221–231
Grojean S, Lièvre V, Koziel V, Vert P, Daval JL 2001 Bilirubin exerts additional toxic effects in hypoxic cultured neurons from the developing rat brain by the recruitment of glutamate neurotoxicity. Pediatr Res 49: 507–513
Bossenmeyer-Pourié C, Daval JL 1998 Prevention from hypoxia-induced apoptosis by preconditioning: a mechanistic approach in cultured neurons from fetal rat forebrain. Brain Res Mol Brain Res 58: 237–239
Wong-Riley MTT 1979 Changes in the visual system of monocularly sutured or enucleated cats demonstrable with cytochrome oxidase histochemistry. Brain Res 171: 11–28
Strazielle C, Dubois M, Eyer J, Lalonde R 2002 NFH-LacZ transgenic mice: regional brain activity of cytochrome oxidase. Exp Neurol 177: 521–530
Strazielle C, Krémarik P, Ghersi-Egea JF, Lalonde R 1998 Regional brain variations of cytochrome oxidase activity and motor coordination in Lurchermutant mice. Exp Brain Res 121: 35–45
Alling C 1985 Biochemical maturation of the brain and the concept of vulnerable period. In: Rydberg U (ed) Alcohol and the Developing Brain. Raven Press, New York, 5–10.
Morgane PJ, Austin-LaFrance RJ, Bronzino JD, Tonkiss J, Diaz-Cintra S, Cintra L, Kemper T, Galler JR 1993 Prenatal malnutrition and development of the brain. Neurosci Biobehav Rev 17: 91–128
Clancy B, Darlington RB, Finlay BL 2001 Translating developmental time across mammalian species. Neuroscience 105: 7–17
Avishai-Eliner S, Brunson KL, Sandman CA, Baram TZ 2002 Stressed-out, or in (utero). Trends Neurosci 25: 518–524
MacManus J, Linnik M 1997 Gene expression induced by cerebral ischemia: an apoptotic perspective. J Cereb Blood Flow Metab 17: 815–832
Chen J, Nagayama T, Jin K, Stetler RA, Zhu RL, Graham SH, Simon RP 1998 Induction of caspase-3-like protease may mediate delayed neuronal death in the hippocampus after transient cerebral ischemia. J Neurosci 18: 4914–4928
Isenmann S, Stoll G, Schroeter M, Krajewski S, Reed JC, Bahr M 1998 Differential regulation of Bax, Bcl-2, and Bcl-X proteins in focal cortical ischemia in the rat. Brain Pathol 8: 49–63
Bédard A, Lévesque M, Bernier PJ, Parent A 2002 The rostral migratory stream in adult squirrel monkeys: contribution of new neurons to the olfactory tubercle and involvement of the antiapoptotic protein Bcl-2. Eur J Neurosci 16: 1917–1924
Wong-Riley MTT 1989 Cytochrome oxidase: an endogenous metabolic marker for neuronal activity. Trends Neurosci 12: 94–101
Vila M, Levy R, Herrero MT, Ruberg M, Faucheux B, Obeso JA, Agid Y, Hirsch E 1997 Consequences of nigrostriatal denervation on the functioning of the basal ganglia in human and nonhuman primates: an in situhybridization study of cytochrome oxidase subunit I mRNA. J Neurosci 17: 765–773
Sokoloff L, Reivich M, Kennedy C, DesRosiers MH, Patlak CS, Pettigrew KD, Sakurada O, Shinohara M 1977 The [14C]deoxyglucose method for the measurement of local cerebral glucose utilization: theory, procedure, and normal values in the conscious and anesthetized albino rat. J Neurochem 28: 897–916
Dimlich RVW, Showers MJ, Shipley MT 1990 Densitometric analysis of cytochrome oxidase in ischemic rat brain. Brain Res 516: 181–191
Anderson A, Oviedo M, Adcock LM, Yamashita Y, Louis PT, Goddard-Finegold J 1996 Cytochrome oxidase is decreased in piglet hippocampus following hypoxia-ischemia. Metab Brain Dis 12: 61–68
Nakatsuka H, Ohta S, Tanaka J, Toku K, Kumon Y, Maeda N, Sakanaka M, Sakaki S 2000 Histochemical cytochrome coxidase activity and caspase-3 in gerbil hippocampal CA1 neurons after transient forebrain ischemia. Neurosci Lett 285: 127–130
Ikonomidou C, Turski L 1996 Neurodegenerative disorders: clues from glutamate and energy metabolism. Crit Rev Neurobiol 10: 239–263
Dave KR, Saul I, Busto R, Ginsberg MD, Sick TJ, Perez-Pinzon MA 2001 Ischemic preconditioning preserves mitochondrial function after global cerebral ischemia in rat hippocampus. J Cereb Blood Flow Metab 21: 1401–1410
Alvarez-Buylla A, Garcia-Verdugo JM 2002 Neurogenesis in adult subventricular zone. J Neurosci 22: 629–634
Rakic P 2002 Neurogenesis in adult primate neocortex: an evaluation of the evidence. Nat Rev Neurosci 3: 65–71
Levison SW, Rothstein RP, Romanko MJ, Snyder MJ, Meyers RL, Vannucci SJ 2001 Hypoxia/ischemia depletes the rat perinatal subventricular zone of oligodendrocyte progenitors and neural stem cells. Dev Neurosci 23: 234–247
Levison SW, Romanko MJ, Rothstein RP, Snyder MJ 2003 Recruitment of neural stem cells following perinatal hypoxic/ischemic insult. J Neurochem 85( suppl 2): 3
Kishi K 1987 Golgi studies on the development of granule cells of the rat olfactory bulb with reference to migration in the sub-ependymal layer. J Comp Neurol 258: 112–124
Luskin MB 1993 Restricted proliferation and migration of postnatally generated neurons derived from the forebrain subventricular zone. Neuron 11: 173–189
Schmidt W, Reymann KG 2002 Proliferating cells differentiate into neurons in the hippocampal CA1 region of gerbils after global cerebral ischemia. Neurosci Lett 334: 153–156
Arvidsson A, Collin T, Kirik D, Kokaia Z, Lindvall O 2002 Neuronal replacement from endogenous precursors in the adult brain after stroke. Nat Med 8: 963–970
Nakatomi H, Kuriu T, Okabe S, Yamamoto S, Hatano O, Kawahara N, Tamura A, Kirino T, Nakafuku M 2002 Regeneration of hippocampal pyramidal neurons after ischemic brain injury by recruitment of endogenous neural progenitors. Cell 110: 429–441
van Praag H, Schinder AF, Christie BR, Toni N, Palmer TD, Gage FH 2002 Functional neurogenesis in the adult hippocampus. Nature 415: 1030–1034
Kokaia Z, Lindvall O 2003 Neurogenesis after ischaemic brain insults. Curr Opin Neurobiol 13: 127–132
Acknowledgements
The authors thank B. Foliguet (Laboratoire de Microscopie Electronique, Faculté de Médecine, Nancy) for his help and free access to image processing system facilities.
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Daval, JL., Pourié, G., Grojean, S. et al. Neonatal Hypoxia Triggers Transient Apoptosis Followed by Neurogenesis in the Rat CA1 Hippocampus. Pediatr Res 55, 561–567 (2004). https://doi.org/10.1203/01.PDR.0000113771.51317.37
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DOI: https://doi.org/10.1203/01.PDR.0000113771.51317.37
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