Cerebral white matter injury of the premature infant - More common than you think

Pediatrics

Volumn 112, Issue 1 I, 2003, Pages 176-180

  Volpe, Joseph J ^a  

^a BOSTON CHILDREN S HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BRAIN INFECTION; BRAIN INJURY; BRAIN ISCHEMIA; DIFFUSION WEIGHTED IMAGING; NEUROPATHOLOGY; NOTE; NUCLEAR MAGNETIC RESONANCE IMAGING; PATHOGENESIS; PREMATURITY; PRIORITY JOURNAL; WHITE MATTER;

ANIMALS; BODY WATER; BRAIN DAMAGE, CHRONIC; DIFFUSION; FEMALE; HUMANS; HYPOXIA-ISCHEMIA, BRAIN; INFANT, LOW BIRTH WEIGHT; INFANT, NEWBORN; INFANT, PREMATURE; LEUKOMALACIA, PERIVENTRICULAR; MAGNETIC RESONANCE IMAGING; MODELS, ANIMAL; NEUROGLIA; PREGNANCY; PREGNANCY COMPLICATIONS, INFECTIOUS; RATS; REACTIVE NITROGEN SPECIES; REACTIVE OXYGEN SPECIES; REPERFUSION INJURY; TERMINOLOGY;

EID: 0038080904     PISSN: 00314005     EISSN: None     Source Type: Journal    
DOI: 10.1542/peds.112.1.176     Document Type: Note

References (62)

1. Volpe JJ. Neurology of the Newborn, 4th ed. Philadelphia, PA: WB Saunders; 2001
2. Bracewell M, Marlow N. Patterns of motor disability in very preterm children. MRRD Res Rev. 2002;8:241-248
3. Aylward GP. Cognitive and neuropsychological outcomes: more than IQ scores. MRDD Res Rev. 2002;8:234-240
4. Wood NS, Markow N, Costeloe K, Gibson AT, Wilkinson AR. Neurologic and developmental disability after extremely preterm birth. N Engl J Med. 2000;343:378-384
5. Hack M, Wilson-Costello D, Friedman H, Taylor GH, Schluchter M, Fanaroff AA. Neurodevelopment and predictors of outcomes of children with birth weights of less than 1000 g. Arch Pediatr Adolesc Med. 2000;154:725-731
6. Counsell SJ, Allsop JM, Harrison MC, et al. Diffusion-weighted imaging of the brain in preterm infants with focal and diffuse white matter abnormality. Pediatrics. 2003;112:1-7
7. Banker BQ, Larroche JC. Periventricular leukomalacia of infancy. Arch Neurol. 1962;7:386-410
8. Inder TE, Anderson NJ, Spencer C, Wells SJ, Volpe J White matter injury in the premature infant: a comparison between serial cranial ultrasound and MRI at term. AJNR. 2003. In press
9. Maalouf EF, Duggan PJ, Counsell S, et al. Comparison of findings on cranial ultrasound and magnetic resonance imaging in preterm infants. Pediatrics. 2001;107:719-727
10. Gilles FH, Leviton A, Dooling EC. The Developing Human Brain: Growth and Epidemiologic Neuropathology. Boston, MA: John Wright, Inc; 1983
11. Gilles FH, Murphy SF. Perinatal telencephalic leucoencephalopathy. J Neurol Neurosurg Psychiatry. 1969;32:404-413
12. Maalouf EF, Duggan PJ, Rutherford MA, et al. Magnetic resonance imaging of the brain in a cohort of extremely preterm infants. J Pediatr. 1999;135:351-357
13. Neil JJ, Shiran SI, McKinstry RC, et al. Normal brain in human newborns: apparent diffusion coefficient and diffusion anisotropy measured by using diffusion tensor MR imaging. Radiology. 1998;209:57-66
14. Huppi PS, Maier SE, Peled S, et al. Microstructural development of human newborn cerebral white matter assessed in vivo by diffusion tensor magnetic resonance imaging. Pediatr Res. 1998;44:584-590
15. Back SA, Luo NL, Borenstein NS, Levine JM, Volpe JJ, Kinney HC. Late oligodendrocyte progenitors coincide with the developmental window of vulnerability for human perinatal white matter injury. J Neurosci. 2001;21:1302-1312
16. Back SA, Luo NL, Borenstein NS, Volpe JJ, Kinney HC. Arrested oligodendrocyte lineage progression during human cerebral white matter development: dissociation between the timing of progenitor differentiation and myelinogenesis. J Neuropathol Exper Neurol. 2002;61:197-211
17. Kinney HC, Brody BA, Kloman AS, Gilles FH. Sequence of central nervous system myelination in human infancy. II. Patterns of myelination in autopsied infants. J Neuropathol Exp Neurol. 1988;47:217-234
18. Wimberger DM, Roberts TP, Barkovich AJ, Prayer LM, Moseley ME, Kucharczyk J. Identification of "premyelination" by diffusion-weighted MRI. J Comput Assist Tomogr. 1995;19:28-33
19. Hildebrand C, Waxman SG. Postnatal differentiation of rat optic nerve fibers: electron microscopic observations on the development of nodes of Ranvier and axoglial relations. J Comp Neurol. 1984;224:25-37
20. Fields RD, Waxman SG. Regional membrane heterogeneity in premyelinated CNS axons: factors influencing the binding of sterol-specific probes. Brain Res. 1988;443:231-242
21. Black JA, Waxman SG, Ransom BR, Feliciano MD. A quantitative study of developing axons and glia following altered gliogenesis in rat optic nerve. Brain Res. 1986;380:122-135
22. Waxman SG, Black JA, Kocsis JD, Ritchie JM. Low density of sodium channels supports action potential conduction in axons of neonatal rat optic nerve. Proc Natl Acad Sci USA. 1989;86:1406-1410
23. Haynes RL, Folkerth RD, Keefe R, et al. Nitrosative and oxidative injury to premyelinating oligodendrocytes is accompanied by microglial activation in periventricular leukomalacia in the human premature infant. J Neuropath Exp Neurol. 2003. In press
24. Inder TE, Huppi PS, Warfield S, et al. Periventricular white matter injury in the premature infant is associated with a reduction in cerebral cortical gray matter volume at term. Ann Neurol. 1999;46:755-760
25. Inder TE, Mocatta T, Darlow B, Spencer C, Volpe JJ. Elevated free radical products in the cerebrospinal fluid of VLBW infants with cerebral white matter injury. Pediatr Res. 2002;52:213-218
26. Volpe JJ. Neurobiology of periventricular leukomalacia in the premature infant. Pediatr Res. 2001;50:553-562
27. Hagberg H, Peebles D, Mallard C. Models of white matter injury: comparison of infectious, hypoxic-ischemic, and excitotoxic insults. MRDD Res Rev. 2002;8:30-38
28. Skoff RP, Bessert DA, Barks JDE, Song DK, Cerghet M, Silverstein FS. Hypoxic-ischemic injury results in acute disruption of myelin gene expression and death of oligodendroglial precursors in neonatal mice. Int J Devl Neurosci. 2001;19:197-208
29. Cai ZW, Pang Y, Xiao F, Rhodes PG. Chronic ischemia preferentially causes white matter injury in the neonatal rat brain. Brain Res. 2001;898:126-135
30. Levison SW, Rothstein RP, Romanko MJ, Snyder MJ, Meyers RL, Vannucci SJ. Hypoxia-ischemia depletes the rat perinatal subventricular zone of oligodendrocyte progenitors and neural stem cells. Dev Neurosci. 2001;23:234-247
31. Liu Y, Silverstein FS, Skoff R, Barks JDE. Hypoxic-ischemic oligodendroglial injury in neontal rat brain. Pediatr Res. 2002;51:25-33
32. Petersson KH, Pinar H, Stopa EG, et al. White matter injury after cerebral ischemia in ovine fetuses. Pediatr Res. 2002;51:768-776
33. Back SA, Han BH, Luo NL, et al. Selective vulnerability of late oligodendrocyte progenitors to hypoxia-ischemia. J Neurosci. 2002;22:455-463
34. Ivacko JA, Sun R, Silverstein FS. Hypoxic-ischemic brain injury induces an acute microglial reaction in perinatal rats. Pediatr Res. 1995;39:39-47
35. Bona E, Andersson A-L, Blomgren K, et al. Chemokine and inflammatory cell response to hypoxia-ischemia in immature rats. Pediatr Res. 1999;45:500-509
36. Possel H, Noack H, Putzke J, Wolf G, Sies H. Selective upregulation of inducible nitric oxide synthase (INOS) by lipopolysaccharide (LPS) and cytokines in microglia: in vitro and in vivo studies. Glia. 2000;32:51-59
37. Chao CC, Hu S, Molitor TW, Shaskan EG, Peterson PK. Activated microglia mediate neuronal cell injury via a nitric oxide mechanism. J Immunol. 1992;149:2736-2741
38. Colton CA, Gilbert DL. Microglia, an in vivo source of reactive oxygen species in the brain. Adv Neurol. 1993;59:321-326
39. Back SA, Gan X, Li Y, Rosenberg PR, Volpe JJ. Maturation-dependent vulnerability of oligodendrocytes to oxidative stress-induced death caused by glutathione depletion. J Neurosci. 1998;18:6241-6253
40. Baud O, Haynes RL, Volpe JJ, Rosenberg PA. Developmental upregulation of manganese superoxide dismutase (MnSOD) expression in oligodendrocytes (OLs) confers resistance to nitric oxide toxicity. Abstr Soc Neurosci. 2003. In press
41. Mackenzie-Graham AJ, Mitrovic B, Smoll A, Merrill JE. Differential sensitivity to nitric oxide in immortalized, cloned murine oligodendrocyte cell lines. Dev Neurosci. 1994;16:162-171
42. Merrill JE, Ignarro LJ, Sherman MP, Melinek J, Lane TE. Microglial cell cytotoxicity of oligodendrocytes is mediated through nitric oxide. J Immunol. 1993;151:2132-2141
43. Yoshioka A, Bacskai B, Pleasure D. Pathophysiology of oligodendroglial excitotoxicity. J Neurosci Res. 1996;46:427-438
44. Sanchez-Gomez MV, Matute C. AMPA and kainate receptors each mediate excitotoxicity in oligodendroglial cultures. Neurobiol Dis. 1999;6:475-485
45. Follett PL, Rosenberg PA, Volpe JJ, Jensen FE. NBQX attenuates excitotoxic injury in developing white matter. J Neurosci. 2000;20:9235-9241
46. Yoshioka A, Yamaya Y, Saiki S, et al. Non-N-methyl-D-aspartate glutamate receptors mediate oxygen-glucose deprivation-induced oligodendroglial injury. Brain Res. 2000;854:207-215
47. Fern R, Moller T. Rapid ischemic cell death in immature oligodendrocytes: a fatal glutamate release feedback loop. J Neurosci. 2000;20:34-42
48. Matute C, Alberdi E, Domercq M, Perez-Cerda F, Perez-Samartin A, Sanchez-Gomez MV. The link between excitotoxic oligodendroglial death and demyelinating diseases. Trends Neurosci. 2001;24:224-230
49. Xu HY, Barks JDE, Liu YQ, Silverstein FS. AMPA-Induced suppression of oligodendroglial gene expression in neonatal rat brain. Brain Res Dev Brain Res. 2001;132:175-178
50. Liu H-N, Giasson BI, Mushynski WE, Almazan G. AMPA receptor-mediated toxicity in oligodendrocyte progenitors involves free radical generation and activation of JNK, calpain and caspase 3. J Neurochem. 2002;82:398-409
51. Rosenberg PA, Dai W, Gan XD, et al. Mature myelin basic protein expressing oligodendrocytes are insensitive to kainate toxicity. J Neurosci Res. 2003;71:237-245
52. Pang Y, Cai ZW, Rhodes PG. Effects of lipopolysaccharide on oligodendrocyte progenitor cells are mediated by astrocytes and microglia. J Neurosci 2000;62:510-520
53. Tahraoui SL, Marret S, Bodenant C, et al. Central role of microglia in neonatal excitotoxic lesions of the murine periventricular white matter. Brain Pathol. 2001;11:56-71
54. Colton CA, Gilbert DL. Production of superoxide anions by a CNS macrophage, the microglia. FEBS Lett. 1987;223:284-288
55. Klegeris A, McGeer PL. Rat brain microglia and peritoneal macrophages show similar responses to respiratory burst stimulants. J Neuroimmunol. 1994;53:83-90
56. Tanaka M, Sotomatsu A, Yoshida T, Hirai S, Nishida A. Detection of superoxide production of activated microglia using a sensitive and specific chemiluminescence assay and microglia-mediated PC12h cell death. J Neurochem. 1994;63:266-270
57. 1-42- and lipopolysaccharide-activated microglia. J Neurosci. 2002;22:3484-3492
58. Zhang GL, Ghosh S. Toll-like receptor-mediated NF-κB activation: a phylogenetically conserved paradigm in innate immunity. J Clin Invest. 2001;107:13-19
59. Hallman M, Ramet M, Ezekowitz RA. Toll-like receptors as sensors of pathogens. Pediatr Res. 2001;50:315-321
60. Lehnardt S, Lachance C, Patrizi S, et al. The toll-like receptor TLR4 is necessary for lipopolysaccharide-induced oligodendrocyte injury in the CNS. J Neurosci. 2002;22:2478-2486
61. Eklind S, Mallard C, Leverin A-L, et al. Bacterial endotoxin sensitizes the immature brain to hypoxic-ischaemic injury. Eur J Neurosci. 2001;13:1101-1106
62. Tsuji M, Saul JP, du Plessis A, et al. Cerebral intravascular oxygenation correlates with mean arterial pressure in critically ill premature infants. Pediatrics. 2000;106:625-632