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首页> 外文期刊>Stroke: A Journal of Cerebral Circulation >Effect of brain-derived neurotrophic factor treatment and forced arm use on functional motor recovery after small cortical ischemia.
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Effect of brain-derived neurotrophic factor treatment and forced arm use on functional motor recovery after small cortical ischemia.

机译:小皮层缺血后脑源性神经营养因子治疗和强制手臂使用对功能性运动恢复的影响。

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BACKGROUND AND PURPOSE: Both the administration of growth factors and physical therapy such as forced arm use (FAU) are promising approaches to enhance recovery after stroke. We explored the effects of these therapies on behavioral recovery and molecular markers of regeneration after experimental ischemia. METHODS: Rats were subjected to photothrombotic ischemia: sham (no ischemia), control (ischemia), brain-derived neurotrophic factor (BDNF; ischemia plus BDNF, 20 microg), and FAU (ischemia plus FAU, 1-sleeve plaster cast ipsilateral limb). Animals survived 1 or 6 weeks and underwent behavioral testing (Rotarod, beam balance, adhesive removal, plantar test, neuroscore). After the rats were killed, brain sections were immunostained for semiquantitative analysis of MAP1B, MAP2, synaptophysin, GFAP expression, and quantification of infarct volumes. RESULTS: Infarct volumes were not different between the groups 1 or 6 weeks after ischemia. BDNF-treated animals had better functional motor recovery (Rotarod, beam balance, neuroscore) compared with all other groups (P<0.05). There was no significant adverse effect of early FAU treatment on motor recovery, although sensorimotor function (adhesive removal test) was impaired (P<0.05). There were no differences between groups as measured by nociception of the left and right forepaw (plantar test). BDNF treatment transiently induced MAP1B expression in the ischemic border zone and synaptophysin expression within the contralateral cortex 6 weeks after ischemia (P<0.05). Both BDNF and FAU reduced astrogliosis compared with controls (P<0.05). CONCLUSIONS: Postischemic intravenous BDNF treatment improves functional motor recovery after photothrombotic stroke and induces widespread neuronal remodeling. Early FAU treatment after stroke does not increase infarct size, impairs sensorimotor function, but leaves motor function unchanged. Postischemic astrogliosis was reduced by both treatments.
机译:背景与目的:生长因子的管理和物理疗法(如强制使用手臂(FAU))都是提高中风后恢复能力的有前途的方法。我们探讨了这些疗法对实验性缺血后行为恢复和再生的分子标志物的影响。方法:对大鼠进行光血栓性缺血:假(无缺血),对照(缺血),脑源性神经营养因子(BDNF;缺血加BDNF,20微克)和FAU(缺血加FAU,1袖石膏石膏同侧肢体) )。动物存活了1或6周,并进行了行为测试(Rotarod,束平衡,粘着剂去除,足底测试,神经评分)。处死大鼠后,对脑切片进行免疫染色,以进行MAP1B,MAP2,突触素,GFAP表达和梗死体积定量的半定量分析。结果:缺血1周或6周后两组之间的梗死体积无差异。与所有其他组相比,BDNF处理的动物具有更好的功能性运动恢复(Rotarod,束平衡,神经评分)(P <0.05)。尽管感觉运动功能(粘着力去除试验)受损(P <0.05),但早期FAU治疗对运动恢复没有明显的不良影响。通过左右前脚的伤害感受来测量,两组之间没有差异(足底试验)。 BDNF治疗在缺血6周后短暂诱导缺血边界区的MAP1B表达和对侧皮质内突触素表达(P <0.05)。与对照组相比,BDNF和FAU均能减少星形胶质细胞增多症(P <0.05)。结论:缺血后静脉内BDNF治疗可改善光血栓性中风后的运动功能恢复,并引起广泛的神经元重塑。中风后的早期FAU治疗不会增加梗塞面积,不会损害感觉运动功能,但会使运动功能保持不变。两种治疗均能减少缺血性星形胶质细胞增生。

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