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Reduced brain edema and infarct volume in aquaporin-4 deficient mice after transient focal cerebral ischemia

机译:短暂性局灶性脑缺血后Aquaporin-4缺陷小鼠脑水肿和梗死面积减少

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摘要

Aquaporin-4 (AQP4) is a water channel expressed in astrocyte end-feet lining the blood-brain barrier. AQP4 deletion in mice is associated with improved outcomes in global cerebral ischemia produced by transient carotid artery occlusion, and focal cerebral ischemia produced by permanent middle cerebral artery occlusion (MCAO). Here, we investigated the consequences of 1-hour transient MCAO produced by intraluminal suture blockade followed by 23 hours of reperfusion. In nine AQP4+/+ and nine AQP4−/− mice, infarct volume was significantly reduced by an average of 39 ± 4 % at 24 hours in AQP4−/− mice, cerebral hemispheric edema was reduced by 23 ± 3 %, and Evans blue extravasation was reduced by 31 ± 2 % (mean ± SEM). Diffusion-weighted magnetic resonance imaging showed greatest reduction in apparent diffusion coefficient around the occlusion site after reperfusion, with remarkably lesser reduction in AQP4−/− mice. The reduced infarct volume in AQP4−/− mice following transient MCAO supports the potential utility of therapeutic AQP4 inhibition in stroke.
机译:Aquaporin-4(AQP4)是在血脑屏障内衬的星形胶质细胞末端表达的水通道。小鼠中的AQP4缺失与短暂性颈动脉闭塞产生的整体脑缺血和永久性大脑中动脉闭塞(MCAO)产生的局灶性脑缺血的预后有关。在这里,我们调查了腔内缝合阻断产生1小时瞬态MCAO的后果,然后再进行23小时再灌注。在9只AQP4 + / + 和9只AQP4 -/-小鼠中,AQP4 -中的梗塞体积在24小时平均平均减少了39±4%。 +/-小鼠,大脑半球水肿减少了23±3%,伊文思蓝外渗减少了31±2%(平均值±SEM)。扩散加权磁共振成像显示再灌注后闭塞部位周围的表观扩散系数最大降低,而AQP4 -/-小鼠的降低明显较少。短暂MCAO后,AQP4 -/-小鼠的梗死体积减少支持了卒中中治疗性AQP4抑制的潜在效用。

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