Oxidative injury in the cerebral cortex and subplate neurons in periventricular leukomalacia

J Neuropathol Exp Neurol. 2008 Jul;67(7):677-86. doi: 10.1097/NEN.0b013e31817e5c5e.

Abstract

We previously identified immunocytochemical evidence of nitrative and oxidative injury in premyelinating oligodendrocytes in periventricular leukomalacia (PVL). Here, we tested the hypothesis that free radical injury occurs in the overlying cerebral cortex and subplate neurons in PVL. We immunostained for nitrotyrosine, malondialdehyde, and hydroxynonenal adducts and scored neuron staining density in PVL (n = 11) and non-PVL (n = 15) cases (postconceptional ages from 34 to 109 weeks). Analysis of covariance controlled for age. Mean malondialdehyde scores in PVL cases were increased over controls (p = 0.005). Hydroxynonenal scores increased with age only in PVL cases (diagnosis vs age interaction; p = 0.024). Nitrotyrosine scores were not significantly increased. In 11 PVL and 23 control cases between 20 and 183 postconceptional weeks, cells morphologically consistent with subplate and Cajal-Retzius neurons showed qualitatively increased free radical modification in PVL over control cases with statistically significant odds ratios for hydroxynonenal and nitrotyrosine in both subplate neurons and Cajal-Retzius cells. Glial fibrillary acidic protein and CD68 scores for reactive astrocytes and microglia, respectively, were not significantly increased, suggesting a minimal inflammatory response. Thus, oxidative/nitrative damage to cortical and "pioneer" neurons, although mild overall, may contribute to cortical volume loss and cognitive/behavioral impairment in survivors of prematurity.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Aldehydes / metabolism
  • Antigens, CD / metabolism
  • Antigens, Differentiation, Myelomonocytic / metabolism
  • Astrocytes / metabolism
  • Astrocytes / pathology
  • Brain Injuries / complications
  • Brain Injuries / pathology*
  • Cell Count / methods
  • Cerebral Cortex / injuries
  • Cerebral Cortex / pathology*
  • Female
  • Glial Fibrillary Acidic Protein / metabolism
  • Humans
  • Infant
  • Infant, Newborn
  • Leukomalacia, Periventricular / complications
  • Leukomalacia, Periventricular / pathology*
  • Logistic Models
  • Male
  • Neurons / pathology*
  • Oxidation-Reduction

Substances

  • Aldehydes
  • Antigens, CD
  • Antigens, Differentiation, Myelomonocytic
  • CD68 antigen, human
  • Glial Fibrillary Acidic Protein
  • 4-hydroxy-2-nonenal