Wang Wei, Li Dongsheng, Li Qing, Wang Lei, Bai Guang, Yang Tao, Li Qiang, Zhu Zhitu, Sun Hongzhi
Department of General Surgery, The First Affiliated Hospital, Liaoning Medical University, Jinzhou, China.
Department of Renal Medicine, The Third Affiliated Hospital, Liaoning Medical University, Jinzhou, China.
Arch Med Sci. 2015 Apr 25;11(2):433-7. doi: 10.5114/aoms.2015.50976. Epub 2015 Apr 23.
Erythropoietin (EPO) has been shown to have beneficial effects on peripheral nerve damage, but its mechanism of action remains incompletely understood. In this study we hypothesized that EPO promotes peripheral nerve repair via neurotrophic factor upregulation.
Thirty adult male Wistar rats were employed to establish a sciatic nerve injury model. They were then randomly divided into two groups to be subjected to different treatment: 0.9% saline (group A) and 5000 U/kg EPO (group B). The walking behavior of rats was evaluated by footprint analysis, and the nerve regeneration was assessed by electron microscopy. The expression of insulin-like growth factor-1 (IGF-1) in the injured sciatic nerves was detected by immunohistochemical analysis.
Compared to saline treatment, EPO treatment led to the growth of myelin sheath, the recovery of normal morphology of axons and Schwann cells, and higher density of myelinated nerve fibers. Erythropoietin treatment promoted the recovery of SFI in the injured sciatic nerves. In addition, EPO treatment led to increased IGF-1 expression in the injured sciatic nerves.
Erythropoietin may promote peripheral nerve repair in a rat model of sciatic nerve injury through the upregulation of IGF-1 expression. These findings reveal a novel mechanism underlying the neurotrophic effects of EPO.
促红细胞生成素(EPO)已被证明对周围神经损伤具有有益作用,但其作用机制仍不完全清楚。在本研究中,我们假设EPO通过上调神经营养因子促进周围神经修复。
选用30只成年雄性Wistar大鼠建立坐骨神经损伤模型。然后将它们随机分为两组进行不同处理:0.9%生理盐水(A组)和5000 U/kg EPO(B组)。通过足迹分析评估大鼠的行走行为,并通过电子显微镜评估神经再生。通过免疫组织化学分析检测损伤坐骨神经中胰岛素样生长因子-1(IGF-1)的表达。
与生理盐水处理相比,EPO处理导致髓鞘生长、轴突和施万细胞正常形态的恢复以及有髓神经纤维密度更高。促红细胞生成素处理促进了损伤坐骨神经中SFI的恢复。此外,EPO处理导致损伤坐骨神经中IGF-1表达增加。
促红细胞生成素可能通过上调IGF-1表达促进坐骨神经损伤大鼠模型的周围神经修复。这些发现揭示了EPO神经营养作用的一种新机制。