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Unbiased Quantification of Subplate Neuron Loss following Neonatal Hypoxia-Ischemia in a Rat Model
Author(s) -
Alexandra Mikhailova,
Naveena Sunkara,
Patrick S. McQuillen
Publication year - 2017
Publication title -
developmental neuroscience
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.893
H-Index - 82
eISSN - 1421-9859
pISSN - 0378-5866
DOI - 10.1159/000460815
Subject(s) - subplate , neuroscience , neuron , biology , ischemia , white matter , cerebral cortex , neural stem cell , hypoxia (environmental) , medicine , stem cell , magnetic resonance imaging , chemistry , microbiology and biotechnology , organic chemistry , radiology , oxygen
Cellular targets of neonatal hypoxia-ischemia (HI) include both oligodendrocyte and neuronal lineages with differences in the patterns of vulnerable cells depending upon the developmental stage at which the injury occurs. Injury to the developing white matter is a characteristic feature of human preterm brain injury. Data are accumulating, however, for neuronal injury in the developing cerebral cortex. In the most widely used rodent model of preterm HI brain injury, conflicting data have been reported regarding the sensitivity of subplate neurons to early neonatal HI, with some reports of selective vulnerability and others that find no increased loss of subplate neurons in comparison with other cortical layers. Methods used to identify subplate neurons and quantify their numbers vary across studies.

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