The state of systemic circulation, collapsed or preserved defines the need for hyperoxic or normoxic resuscitation in neonatal mice with hypoxia-ischemia

Resuscitation. 2010 Feb;81(2):224-9. doi: 10.1016/j.resuscitation.2009.11.024. Epub 2009 Dec 31.

Abstract

Background: The return of spontaneous circulation (ROSC) is a primary goal of resuscitation. For neonatal resuscitation the International Liaison Committee on Resuscitation (ILCOR) recommends oxygen concentrations ranging from 21% to 100%.

Aims and methods: This study (a) compared the efficacy of resuscitation with room air (RA) or 100% O(2) in achieving ROSC in 46 neonatal mice with circulatory collapse induced by lethal hypoxia-ischemia (HI) and (b) determined whether re-oxygenation with RA or 100% O(2) alters the extent of HI cerebral injury in mice with preserved systemic circulation (n=31). We also compared changes in generation of reactive oxygen species (ROS) in cerebral mitochondria in response to re-oxygenation with RA or 100% O(2).

Result: In HI-mice with collapsed circulation re-oxygenation with 100% O(2) versus RA resulted in significantly greater rate of ROSC. In HI-mice with preserved systemic circulation and regional (unilateral) cerebral ischemia the restoration of cerebral blood flow was significantly faster upon re-oxygenation with 100% O(2), than RA. However, no difference in the extent of brain injury was detected. Regardless of the mode of re-oxygenation, reperfusion in these mice was associated with markedly accelerated ROS production in brain mitochondria.

Conclusion: In murine HI associated with circulatory collapse the resuscitation limited to re-oxygenation with 100% O(2) is superior to the use of RA in achievement of the ROSC. However, in HI-mice with preserved systemic circulation hyperoxic re-oxygenation has no benefit over the normoxic brain recovery.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Animals, Newborn
  • Blood Circulation*
  • Hypoxia-Ischemia, Brain / physiopathology*
  • Hypoxia-Ischemia, Brain / therapy*
  • Mice
  • Mice, Inbred C57BL
  • Oxygen Inhalation Therapy*
  • Resuscitation / methods*