首页> 美国卫生研究院文献>Journal of Neurotrauma >Neuroprotection with an Erythropoietin Mimetic Peptide (pHBSP) in a Model of Mild Traumatic Brain Injury Complicated by Hemorrhagic Shock
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Neuroprotection with an Erythropoietin Mimetic Peptide (pHBSP) in a Model of Mild Traumatic Brain Injury Complicated by Hemorrhagic Shock

机译:促红细胞生成素模拟肽(pHBSP)对轻度创伤性脑出血并发出血性休克的模型的神经保护作用

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摘要

Pyroglutamate helix B surface peptide (pHBSP) is an 11 amino acid peptide, designed to interact with a novel cell surface receptor, composed of the classical erythropoietin (EPO) receptor disulfide linked to the beta common receptor. pHBSP has the cytoprotective effects of EPO without stimulating erythropoiesis. Effects on early cerebral hemodynamics and neurological outcome at 2 weeks post-injury were compared in a rat model of mild cortical impact injury (3m/sec, 2.5 mm deformation) followed by 50 min of hemorrhagic hypotension (MAP 40 mm Hg for 50 min). Rats were randomly assigned to receive 5000 U/kg of EPO, 30 μg/kg of pHBSP, or an inactive substance every 12 h for 3 days, starting at the end of resuscitation from the hemorrhagic hypotension, which was 110 min post-injury. Both treatments reduced contusion volume at 2 weeks post-injury, from 20.8±2.8 mm3 in the control groups to 7.7±2.0 mm3 in the EPO-treated group and 5.9±1.5 mm3 in the pHBSP-treated group (p=0.001). Both agents improved recovery of cerebral blood flow in the injured brain following resuscitation, and resulted in more rapid recovery of performance on beam balancing and beam walking tests. These studies suggest that pHBSP has neuroprotective effects similar to EPO in this model of combined brain injury and hypotension. pHBSP may be more useful in the clinical situation because there is less risk of thrombotic adverse effects.
机译:焦谷氨酸螺旋B表面肽(pHBSP)是一种11个氨基酸的肽,旨在与新型细胞表面受体相互作用,该受体由与β共有受体连接的经典促红细胞生成素(EPO)受体二硫键组成。 pHBSP具有EPO的细胞保护作用,而不会刺激红细胞生成。在轻度皮层撞击性损伤(3m / sec,2.5µmm变形)随后50µmin的出血性低血压(MAP 40µmm Hg持续50µmin)的大鼠模型中比较了损伤后2周对早期脑血流动力学和神经系统预后的影响。 。从出血性低血压的复苏结束(受伤后110分钟)开始,将大鼠随机分配为每12h接受5000μU/ kg的EPO,30μg/ kg的pHBSP或无活性物质,持续3天。两种治疗方法均使损伤后2周的挫伤体积从对照组的20.8±2.8±mm 3 降低至EPO治疗组的7.7±2.0 mm 3 和5.9 pHBSP治疗组为±1.5mm 3 (p = 0.001)。两种药物均可改善复苏后受伤的大脑中脑血流的恢复,并导致光束平衡和光束行走测试的性能恢复更快。这些研究表明,在这种合并性脑损伤和低血压的模型中,pHBSP具有类似于EPO的神经保护作用。 pHBSP在临床情况中可能更有用,因为血栓性不良反应的风险较小。

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