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首页> 外文期刊>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)在轻度颅脑损伤并出血性休克模型中的神经保护作用

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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, 2.5mm deformation) followed by 50min of hemorrhagic hypotension (MAP 40mm Hg for 50min). Rats were randomly assigned to receive 5000U/kg of EPO, 30μg/kg of pHBSP, or an inactive substance every 12h for 3 days, starting at the end of resuscitation from the hemorrhagic hypotension, which was 110min post-injury. Both treatments reduced contusion volume at 2 weeks post-injury, from 20.8±2.8mm 3 in the control groups to 7.7±2. 0mm 3 in the EPO-treated group and 5.9±1.5mm 3 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。在轻度皮层撞击损伤(3m / sec,2.5mm变形)然后出血50分钟(MAP 40mm Hg持续50min)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。从出血性低血压复苏结束后(损伤后110分钟)开始,每12h将大鼠随机分配接受5000U / kg的EPO,30μg/ kg的pHBSP或无活性物质,持续3天。两种治疗方法均使受伤后2周的挫伤体积从对照组的20.8±2.8mm 3降低到7.7±2。 EPO治疗组为0mm 3,pHBSP治疗组为5.9±1.5mm 3(p = 0.001)。两种药物均可改善复苏后受伤大脑中脑血流的恢复,并导致束平衡和束行走测试的性能恢复更快。这些研究表明,在合并的脑损伤和低血压模型中,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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