首页> 美国卫生研究院文献>Journal of Cerebral Blood Flow Metabolism >Acute hepatocyte growth factor treatment induces long-term neuroprotection and stroke recovery via mechanisms involving neural precursor cell proliferation and differentiation
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Acute hepatocyte growth factor treatment induces long-term neuroprotection and stroke recovery via mechanisms involving neural precursor cell proliferation and differentiation

机译:急性肝细胞生长因子治疗通过涉及神经前体细胞增殖和分化的机制诱导长期神经保护和中风恢复

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摘要

Hepatocyte growth factor (HGF) is an interesting candidate for acute stroke treatment as shown by continuous infusion or gene delivery protocols. However, little is known about HGF-mediated long-term effects. The present study therefore analyzed long-term effects of an acute intrastriatal HGF treatment (5 μg) after a 45-minute stroke, with regard to brain injury and neurologic recovery. Hepatocyte growth factor induced long-term neuroprotection as assessed by infarct volume and neuronal cell death analysis for as long as 4 weeks after stroke, which was associated with sustained neurologic recovery as evidenced by corner-turn and tight-rope tests. Analyzing underlying mechanisms of HGF-induced sustained neuroprotection, enhanced cell proliferation followed by increased neuronal differentiation of neural precursor cells (NPCs) was observed in the ischemic striatum of HGF-treated mice, which persisted for up to 4 weeks. In line with this, HGF promoted neurosphere formation as well as proliferation of NPC and decreased caspase-3-dependent hypoxic injury in vitro. Preservation of blood–brain barrier integrity 24 hours after stroke was furthermore noticed in animals receiving HGF, which was associated with the inhibition of matrix metalloproteases (MMP)-2 and MMP-9 at 4 and 24 hours, respectively. We suggest that sustained recruitment of proliferating cells together with improved neurovascular remodeling provides an explanation for HGF-induced long-term neuroprotection.
机译:如连续输注或基因递送方案所示,肝细胞生长因子(HGF)是急性中风治疗的有趣候选者。但是,对于HGF介导的长期作用知之甚少。因此,本研究分析了中风45分钟后急性纹状体内HGF治疗(5μg)的长期效果,涉及脑损伤和神经系统恢复。卒中后长达4周,通过梗死体积和神经元细胞死亡分析评估,肝细胞生长因子诱导了长期的神经保护作用,这与转弯和紧绳试验证明了持续的神经功能恢复有关。分析HGF诱导的持续神经保护的潜在机制,观察到在HGF治疗的小鼠的缺血纹状体中,细胞增殖增强,然后神经前体细胞(NPC)的神经元分化增加,这种现象持续了长达4周。与此相一致,在体外,HGF促进了神经球的形成以及NPC的增殖,并减少了caspase-3依赖性缺氧损伤。此外,在接受HGF的动物中发现中风后24小时仍能保持血脑屏障的完整性,这与分别在4小时和24小时时抑制基质金属蛋白酶(MMP)-2和MMP-9有关。我们建议持续增殖细胞的募集以及改善的神经血管重塑为HGF诱导的长期神经保护提供了解释。

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