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GSK249320,一种针对轴突生长抑制分子髓鞘相关糖蛋白的单克隆抗体,可改善实验性中风啮齿动物的预后。

GSK249320, A Monoclonal Antibody Against the Axon Outgrowth Inhibition Molecule Myelin-Associated Glycoprotein, Improves Outcome of Rodents with Experimental Stroke.

作者信息

Cash Diana, Easton Alanna C, Mesquita Michel, Beech John, Williams Steve, Lloyd Andrew, Irving Elaine, Cramer Steven C

机构信息

King's College London, Institute of Psychiatry, UK.

Phastar, Chiswick, London, UK.

出版信息

J Neurol Exp Neurosci. 2016;2(2):28-33. Epub 2016 Nov 21.

Abstract

Myelin-associated glycoprotein (MAG) is an inhibitor of axon growth. MAG levels increase after stroke. GSK249320 is a monoclonal antibody that neutralizes MAG-mediated inhibition and so may promote axon outgrowth and improve post-stroke outcomes. The current study tested the hypothesis that GSK249320 initiated 24 hours or 7 days after experimental stroke improves behavioural outcomes. Rats with right middle cerebral artery occlusion for 90 minutes were randomized to receive 6 weeks of intravenous (a) GSK249320 starting 24 hours post-stroke, (b) GSK249320 starting 7 days post-stroke, or (c) vehicle. Behavioral testing was performed over 7 weeks. Serial MRI demonstrated no differences in infarct volume across groups. Animals treated with GSK249320 24 hours post-stroke showed larger increases in Neuroscore (time X group, p = 0.0008) and staircase test (main effect of group, p = 0.0214) as compared to controls, but animals treated 7 days post-stroke showed no significant behavioral benefit. No significant results were found for the sticky tape or cylinder tests. A separate set of animals with experimental stroke received a single intravenous dose of GSK249320 or vehicle at 1 hour, 24 hours, 48 hours or 1 week post-stroke, and immunohistochemistry methods were used to measure GSK249320 distribution; GSK249320 was found in the ipsilesional hemisphere only, the extent of which increased with later times of injection. These data suggest that intravenous GSK249320 penetrates the lesion site and is associated with a small effect on functional outcomes when initiated 24 hours post-stroke and so support the translational potential of this monoclonal antibody as a restorative therapy for patients with stroke.

摘要

髓磷脂相关糖蛋白(MAG)是轴突生长的抑制剂。中风后MAG水平会升高。GSK249320是一种单克隆抗体,可中和MAG介导的抑制作用,因此可能促进轴突生长并改善中风后的预后。本研究检验了以下假设:实验性中风后24小时或7天开始使用GSK249320可改善行为结果。将右侧大脑中动脉闭塞90分钟的大鼠随机分为三组,分别接受为期6周的静脉注射:(a)中风后24小时开始注射GSK249320;(b)中风后7天开始注射GSK249320;(c)注射赋形剂。行为测试持续7周。连续MRI显示各组梗死体积无差异。与对照组相比,中风后24小时接受GSK24932治疗的动物在神经评分(时间×组,p = 0.0008)和阶梯试验(组的主效应,p = 0.0214)方面有更大的改善,但中风后7天接受治疗的动物未显示出明显的行为益处。在胶带或圆筒试验中未发现显著结果。另一组患有实验性中风的动物在中风后1小时、24小时、48小时或1周接受单次静脉注射GSK249320或赋形剂,并采用免疫组织化学方法测量GSK249320的分布;仅在同侧半球发现了GSK249320,其范围随注射时间的延迟而增加。这些数据表明,静脉注射GSK249320可穿透病变部位,中风后24小时开始使用时对功能结果有轻微影响,因此支持这种单克隆抗体作为中风患者恢复性治疗的转化潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d348/5179224/ee96712f2fb2/nihms835005f1.jpg

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