4.5 Article

Prothrombolytic action of normobaric oxygen given alone or in combination with recombinant tissue-plasminogen activator in a rat model of thromboembolic stroke

Journal

JOURNAL OF APPLIED PHYSIOLOGY
Volume 112, Issue 12, Pages 2068-2076

Publisher

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/japplphysiol.00092.2012

Keywords

acute ischemic stroke; normobaric oxygen; thrombolysis; tissue-plasminogen activator

Funding

  1. University of Caen-Basse Normandie
  2. Centre de Recherche Centre Hospitalier Affilie Universitaire Hotel-Dieu de Levis
  3. Direction Generale de l'Armement of the French Ministry of Defence
  4. NNOXe Pharmaceuticals (Quebec City, QC, Canada)

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David HN, Haelewyn B, Degoulet M, Colomb DG Jr, Risso JJ, Abraini JH. Prothrombolytic action of normobaric oxygen given alone or in combination with recombinant tissue-plasminogen activator in a rat model of thromboembolic stroke. J Appl Physiol 112: 2068-2076, 2012. First published April 5, 2012; doi:10.1152/japplphysiol.00092.2012.-The potential benefit of 100 vol% normobaric oxygen (NBO) for the treatment of acute ischemic stroke patients is still a matter of debate. To advance this critical question, we studied the effects of intraischemic normobaric oxygen alone or in combination with recombinant tissue-plasminogen activator (rtPA) on cerebral blood flow and ischemic brain damage and swelling in a clinically relevant rat model of thromboembolic stroke. We show that NBO provides neuroprotection by achieving cerebral blood flow restoration equivalent to 0.9 mg/kg rtPA through probable direct interaction and facilitation of the fibrinolytic properties of endogenous tPA. In contrast, combined NBO and rtPA has no neuroprotective effect on ischemic brain damage despite producing cerebral blood flow restoration. These results 1) by providing a new mechanism of action of NBO highlight together with previous findings the way by which intraischemic NBO shows beneficial action; 2) suggest that NBO could be an efficient primary care therapeutic intervention for patients eligible for rtPA therapy; 3) indicate that NBO could be an interesting alternative for patients not eligible for rtPA therapy; and 4) caution the use of NBO in combination with rtPA in acute stroke patients.

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