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Enhanced Oligodendrogenesis and Recovery of Neurological Function by Erythropoietin After Neonatal Hypoxic/Ischemic Brain Injury
Author(s) -
Masanori Iwai,
R. Anne Stetler,
Juan Xing,
Xiaoming Hu,
Yanqin Gao,
Wenting Zhang,
Jun Chen,
Guodong Cao
Publication year - 2010
Publication title -
stroke
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.397
H-Index - 319
eISSN - 1524-4628
pISSN - 0039-2499
DOI - 10.1161/strokeaha.109.570325
Subject(s) - medicine , erythropoietin , white matter , neurogenesis , neuroprotection , hypoxia (environmental) , ischemia , anesthesia , neuroscience , magnetic resonance imaging , biology , chemistry , organic chemistry , oxygen , radiology
Neuronal replacement has recently gained attention as a potential therapeutic target under ischemic conditions. However, the oligodendrogenic infrastructure is equally critical for restoration of brain function and is also sensitive to ischemic injury. Erythropoietin (EPO) is a neuroprotective molecule that stimulates neuronal replacement after neonatal hypoxia/ischemia (H/I) when delivered soon after the onset of reperfusion. Because EPO can improve recovery of neurological function in the absence of tissue protection, we hypothesize that EPO may improve neurological function via enhancement of white matter recovery after H/I. Thus, we sought to determine the effects of delayed administration of EPO on white matter injury and recovery of neurological function after neonatal H/I.

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