Abstract:
:We previously found increased microglial proliferation and pro-inflammatory cytokine release in infant mice compared to juvenile mice after hypoxia-ischemia (HI). The aim of the current study was to assess for differences in the effect of microglial suppression on HI-induced brain injury in infant and juvenile mice. HI was induced in neonatal (P9) and juvenile (P30) mice and minocycline or vehicle was administered at 2h and 24h post-HI. P9 minocycline-treated mice demonstrated early but transient improvements in neurologic injury, while P30 minocycline-treated mice demonstrated sustained improvements in cerebral atrophy and Morris Water Maze performance at 60days post-HI.
journal_name
J Neuroimmunoljournal_title
Journal of neuroimmunologyauthors
Cikla U,Chanana V,Kintner DB,Covert L,Dewall T,Waldman A,Rowley P,Cengiz P,Ferrazzano Pdoi
10.1016/j.jneuroim.2015.12.004subject
Has Abstractpub_date
2016-02-15 00:00:00pages
18-27eissn
0165-5728issn
1872-8421pii
S0165-5728(15)30097-7journal_volume
291pub_type
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