Nitric Oxide Production in the Striatum and Cerebellum of a Rat Model of Preterm Global Perinatal Asphyxia

M. Barkhuizen, W. D. J. Van de Berg, J. De Vente, C. E. Blanco, A. W. D. Gavilanes, H. W. M. Steinbusch*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

5 Citations (Web of Science)

Abstract

Encephalopathy due to perinatal asphyxia (PA) is a major cause of neonatal morbidity and mortality in the period around birth. Preterm infants are especially at risk for cognitive, attention and motor impairments. Therapy for this subgroup is limited to supportive care, and new targets are thus urgently needed. Post-asphyxic excitotoxicity is partially mediated by excessive nitric oxide (NO) release. The aims of this study were to determine the timing and distribution of nitric oxide (NO) production after global PA in brain areas involved in motor regulation and coordination. This study focused on the rat striatum and cerebellum, as these areas also affect cognition or attention, in addition to their central role in motor control. NO/peroxynitrite levels were determined empirically with a fluorescent marker on postnatal days P5, P8 and P12. The distributions of neuronal NO synthase (nNOS), cyclic guanosine monophosphate (cGMP), astroglia and caspase-3 were determined with immunohis-tochemistry. Apoptosis was additionally assessed by measuring caspase-3-like activity from P2-P15. On P5 and P8, increased intensity of NO-associated fluorescence and cGMP immunoreactivity after PA was apparent in the striatum, but not in the cerebellum. No changes in nNOS immunoreactivity or astrocytes were observed. Modest changes in caspase-3-activity were observed between groups, but the overall time course of apoptosis over the first 11 days of life was similar between PA and controls. Altogether, these data suggest that PA increases NO/peroxynitrite levels during the first week after birth within the striatum, but not within the cerebellum, without marked astrogliosis. Therapeutic benefits of interventions that reduce endogenous NO production would likely be greater during this time frame.

Original languageEnglish
Pages (from-to)400-409
Number of pages10
JournalNeurotoxicity Research
Volume31
Issue number3
DOIs
Publication statusPublished - Apr 2017

Keywords

  • Asphyxia
  • Nitrosidative stress
  • cGMP
  • Neuronal
  • nitric oxide synthase
  • Peroxynitrite
  • Selective vulnerability
  • HYPOXIC-ISCHEMIC ENCEPHALOPATHY
  • CENTRAL-NERVOUS-SYSTEM
  • NEONATAL ENCEPHALOPATHY
  • SYNTHASE IMMUNOREACTIVITY
  • SELECTIVE VULNERABILITY
  • HUNTINGTONS-DISEASE
  • PREMATURE-INFANTS
  • BRAIN-DEVELOPMENT
  • CEREBRAL-PALSY
  • NEURONS

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