Fibroblast growth factor-18 reduced infarct volumes and behavioral deficits after transient occlusion of the middle cerebral artery in rats

被引:39
作者
Ellsworth, JL
Garcia, R
Yu, J
Kindy, MS
机构
[1] Zymogenet Inc, Seattle, WA 98102 USA
[2] Med Univ S Carolina, Dept Physiol & Neurosci, Stroke Program, Charleston, SC 29425 USA
[3] Ralph H Johnson Vet Affairs Med Ctr, Charleston, SC USA
[4] Mol Therapeut Inc, Mt Pleasant, SC USA
关键词
animal models; growth factors; neuroprotection; rats;
D O I
10.1161/01.STR.0000071760.66720.5F
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background and Purpose-Fibroblast growth factor 18 (FGF18) is expressed in rodent brain and is a trophic factor for neuron-derived cells in culture. The purpose of the present study was to evaluate whether FGF18 was neuroprotective in a rat model of cerebral ischemia and to compare the results with those obtained with FGF2. Methods-Cerebral ischemia was produced in rats by a transient 2-hour occlusion of the middle cerebral artery (MCAo) with an intraluminal filament followed by 22-hour reperfusion. Starting 15 minutes after MCAo, FGF18 or FGF2 was administered by a 3-hour intravenous infusion. Infarct volumes and behavioral deficits were measured 24 hours after MCAo. Results-Infusion of FGF18 produced dose-dependent reductions in infarct volumes and improvements in tests of reference and working memory, motor ability, and exploratory behavior. FGF18 was more efficacious than FGF2 on virtually all measures examined. The reductions in infarct volume and behavioral deficit were associated with FGF-mediated increases in regional cerebral blood flow. Conclusions-These results demonstrate that FGF18 is an effective neuroprotective agent in a rat model of transient MCAo.
引用
收藏
页码:1507 / 1512
页数:6
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