Neurogenesis in rats after focal cerebral ischemia is enhanced by indomethacin

BD Hoehn, TD Palmer, GK Steinberg - Stroke, 2005 - Am Heart Assoc
BD Hoehn, TD Palmer, GK Steinberg
Stroke, 2005Am Heart Assoc
Background and Purpose—Newborn cells may participate in repair following ischemic brain
injury, but their survival and function may be influenced by inflammation. Methods—We
investigated the effects of indomethacin, a nonsteroidal antiinflammatory drug, on the fate of
newborn cells following transient focal ischemia. Results—Bromodeoxyuridine (BrdU)-
labeled cells, including migrating neuroblasts, were observed in the neighboring striatum
and overlying cortex 1 day poststroke. The density of BrdU+ cells labeled with doublecortin …
Background and Purpose— Newborn cells may participate in repair following ischemic brain injury, but their survival and function may be influenced by inflammation.
Methods— We investigated the effects of indomethacin, a nonsteroidal antiinflammatory drug, on the fate of newborn cells following transient focal ischemia.
Results— Bromodeoxyuridine (BrdU)-labeled cells, including migrating neuroblasts, were observed in the neighboring striatum and overlying cortex 1 day poststroke. The density of BrdU+ cells labeled with doublecortin, nestin, glial fibrillary acidic protein, or NG2 was increased at 14 and 28 days. Indomethacin increased BrdU+ cells of all lineages and reduced microglial/monocyte activation.
Conclusion— Indomethacin enhanced the accumulation of newborn cells following stroke.
Am Heart Assoc