Protective effects of caffeine on chronic hypoxia-induced perinatal white matter injury

Stephen A. Back, Andrew Craig, Ning Ling Luo, Jennifer Ren, Ravi Shankar Akundi, Ivy Ribeiro, Scott A. Rivkees

Research output: Contribution to journalArticle

125 Scopus citations

Abstract

Objective: Periventricular white matter injury (PWMI) is the major cause of cerebral palsy and cognitive impairment in prematurely born infants. PWMI is characterized by reductions in cerebral myelination and cerebrocortical volumes and is associated with secondary ventriculomegaly. In neonatal rodents, these features of PWMI can be induced by rearing in chronic hypoxia or by activation of A1 adenosine receptors. We determined: (1) whether altered maturation or development of one or more oligodendrocyte (OL) lineage stages plays a role in the pathogenesis of the myelination disturbances associated with exposure to chronic hypoxia, and (2) whether blockade of A1 adenosine receptor action with the adenosine antagonist caffeine can prevent hypoxia-induced white matter injury. Methods: Ventriculomegaly and reduced cerebral myelination were generated in mice reared in hypoxia (10% oxygen) from postnatal days 3 (P3) through 12. Results: Hypomyelination was related to abnormal OL lineage progression and a reduction in the OL progenitor pool. Myelination was enhanced and ventriculomegaly reduced in hypoxia-exposed neonatal pups treated with caffeine from P3 to P12. Interpretation: These observations support that hypoxia inhibits OL maturation and that caffeine administration during early postnatal development may have utility in the prevention of PWMI.

Original languageEnglish (US)
Pages (from-to)696-705
Number of pages10
JournalAnnals of Neurology
Volume60
Issue number6
DOIs
StatePublished - Dec 1 2006

ASJC Scopus subject areas

  • Neurology
  • Clinical Neurology

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    Back, S. A., Craig, A., Luo, N. L., Ren, J., Akundi, R. S., Ribeiro, I., & Rivkees, S. A. (2006). Protective effects of caffeine on chronic hypoxia-induced perinatal white matter injury. Annals of Neurology, 60(6), 696-705. https://doi.org/10.1002/ana.21008