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Neurotherapeutic potential of erythropoietin after ischemic injury of the central nervous system

机译:中枢神经系统缺血性损伤后促红细胞生成素的神经治疗潜力

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摘要

Erythropoietin (EPO) is one of the most successful biopharmaceuticals in history and is used for treating anemia of different origins.However,it became clear that EPO could also work in a neuroprotective,antiapoptotic,antioxidative,angiogenetic and neurotropic way.It causes stimulation of cells to delay cell apoptosis,especially in the central nervous system.In rodent models of focal cerebral ischemia,EPO showed an impressive reduction of infarct size by 30% and improvement of neurobehavioral outcome by nearly 40%.A large animal model dealing with ischemia and reperfusion of the spinal cord showed that EPO could reduce the risk of spinal cord injury significantly.In addition,some clinical studies tested whether EPO works in real live clinical settings.One of the most promising studies showed the innocuous ness and improvements in follow-up,outcome scales and in infarct size,of EPO-use in humans suffering from ischemic stroke.Another study ended unfortunately in a negative outcome and an increased overall death rate in the EPO group.The most possible reason was the involvement of patients undergoing simultaneously systemic thrombolysis with recombinant tissue plasminogen activator.An experimental study on rats demonstrated that administration of EPO might exacerbate tissue plasminogen activator-induced brain hemorrhage without reducing the ischemic brain damage.This case shows clearly how useful animal models can be to check negative side effects of a treatment before going into clinical trials.Other groups looked in human trials at the effects of EPO on the outcome after ischemic stroke,relation to circulating endothelial progenitor cells,aneurysmal subarachnoid hemorrhage,traumatic brain injury,hemoglobin transfusion thresholds and elective first-time coronary artery bypass surgery.Most of the results were pos itive,but are based mostly on small group sizes.However,some of the most neglected facts when focusing on experimental setups of ischemia of the central nervous system are issues like age and comorbidities.It might be extremely worthy to consider these points for future projects,because EPO might influence all these factors.
机译:促红细胞生成素(EPO)是历史上最成功的生物药物之一,用于治疗不同来源的贫血。然而,很明显,EPO也可以以神经保护,抗凋亡,抗氧化,血管生成和神经营养的方式起作用。 EPO在局灶性脑缺血的啮齿动物模型中显示梗塞面积显着减少了30%,神经行为预后改善了近40%。脊髓的再灌注显示EPO可以显着降低脊髓损伤的风险。此外,一些临床研究测试了EPO是否可在实际的临床环境中起作用。最有前途的研究之一表明其无毒无害并改善了随访缺血性中风的人使用EPO的结果,结局范围和梗死面积。不幸的是,另一项研究以阴性结果告终。 n EPO组的总死亡率增加。最可能的原因是同时进行全身溶栓的重组组织纤溶酶原激活物参与的患者。对大鼠的实验研究表明,EPO的给药可能加重组织纤溶酶原激活物诱发的脑出血而不减少这种情况清楚地表明了动物模型在进行临床试验之前可以用来检查治疗的不良副作用的可能性。其他组在人体试验中研究了EPO对缺血性中风后与循环的关系的影响内皮祖细胞,蛛网膜下腔出血,脑外伤,血红蛋白输注阈值和择期首次冠状动脉搭桥手术。大多数结果是阳性的,但主要基于小组人数。然而,一些最被忽略的事实当专注于中央神经缺血的实验装置时我们的系统存在诸如年龄和合并症等问题。由于EPO可能会影响所有这些因素,因此在将来的项目中考虑这些要点可能是非常值得的。

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  • 来源
    《中国神经再生研究(英文版)》 |2019年第8期|1309-1312|共4页
  • 作者单位

    Department of Vascular and Endovascular Surgery, Heinrich-Heine-University of Düisseldorf, Düsseldorf, Germany;

    Department of Vascular and Endovascular Surgery, Heinrich-Heine-University of Düisseldorf, Düsseldorf, Germany;

    Department of Vascular and Endovascular Surgery, Heinrich-Heine-University of Düisseldorf, Düsseldorf, Germany;

    Department of Vascular and Endovascular Surgery, Heinrich-Heine-University of Düisseldorf, Düsseldorf, Germany;

    Department of Vascular and Endovascular Surgery, Heinrich-Heine-University of Düisseldorf, Düsseldorf, Germany;

  • 收录信息 中国科学引文数据库(CSCD);
  • 原文格式 PDF
  • 正文语种 eng
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  • 入库时间 2022-08-19 04:25:49
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