Hypothermia and erythropoietin for neuroprotection after neonatal brain damage

Pediatr Res. 2013 Jan;73(1):18-23. doi: 10.1038/pr.2012.139. Epub 2012 Oct 19.

Abstract

Background: Both hypothermia and erythropoietin (EPO) are reported to have neuroprotective effects after perinatal hypoxia-ischemia (HI). We investigated a possible additive effect of the use of a combination of hypothermia-EPO in a rat model of neonatal HI.

Methods: At postnatal day 7, rats were subjected to HI and then randomized to 3 h of hypothermia, EPO, or both. Sensorimotor function was assessed by the cylinder-rearing test (CRT) at 2 and 5 wk after HI. Brain lesion volume and white matter loss were determined by hematoxylin-eosin and luxol fast blue staining, respectively.

Results: Multivariable analysis using general linear modeling showed that hypothermia, EPO, and the interaction hypothermia × gender were determinants of sensorimotor function, both at 2 and 5 wk after HI. Neuroprotective effects of hypothermia at 5 wk were more pronounced in females, showing 52% improvement in the CRT. Maximal improvement in males was 26% after combined treatment with hypothermia and EPO. Histological outcome was improved by hypothermia only with no additional effect of EPO or gender.

Conclusion: Hypothermia after HI improved sensorimotor function in females more than in males. There was a borderline additive effect of EPO when combined with hypothermia. Histology of brain lesion volume and white matter damage was improved only by hypothermia.

MeSH terms

  • Animals
  • Animals, Newborn
  • Blood Glucose
  • Body Temperature
  • Erythropoietin / therapeutic use*
  • Female
  • Histological Techniques
  • Hypothermia, Induced / methods*
  • Hypoxia-Ischemia, Brain / drug therapy*
  • Hypoxia-Ischemia, Brain / pathology
  • Hypoxia-Ischemia, Brain / therapy*
  • Linear Models
  • Male
  • Neuroprotective Agents / therapeutic use*
  • Rats
  • Sex Factors

Substances

  • Blood Glucose
  • Neuroprotective Agents
  • Erythropoietin