Lykissas Marios G, Sakellariou Ekaterini, Vekris Marios D, Kontogeorgakos Vasilios A, Batistatou Anna K, Mitsionis Gregory I, Beris Alexandros E
Department of Orthopaedic Surgery, University of Ioannina, School of Medicine, Ioannina, P.C. 45110, Greece.
J Neurosci Methods. 2007 Aug 15;164(1):107-15. doi: 10.1016/j.jneumeth.2007.04.008. Epub 2007 Apr 19.
The aim of the present study is to evaluate the effects of erythropoietin to the collateral sprouting by using systemically delivered erythropoietin in an end-to-side nerve repair model. Forty-five rats were evaluated in four groups: (A) end-to-side neurorrhaphy only, (B) end-to-side neurorrhaphy and erythropoietin administration, (C) end-to-end neurorrhaphy and (D) nerve stumps buried into neighboring muscles. In all animals, the contralateral healthy side served as control. Functional assessment of nerve regeneration was performed at intervals up to 5 months using the Peroneal Function Index. Evaluation 150 days after surgery included peroneal and tibial nerve morphometric examination, and wet weights of the tibialis anterior muscle. During the first three weeks after surgery, when erythropoietin was regularly administered, functional evaluation showed that erythropoietin may facilitate peripheral nerve regeneration. However, there was rapid deterioration in the functional recovery when erythropoietin's administration was discontinued. As a consequence, at the end of this study, erythropoietin failed to maintain its initial stimulating effect in axonal regeneration. The results of wet muscle weights revealed statistically significant differences between Groups A and C, and Group B. Furthermore, data on axonal counting showed significant difference between Groups A and C, and Group B. Erythropoietin appears to facilitate peripheral nerve regeneration at the initial phase of its administration. Further investigation will be necessary to optimise the conditions (dose, mode of administration) in order to maintain its effects.
本研究的目的是通过在端侧神经修复模型中全身应用促红细胞生成素,评估其对侧支芽生的影响。45只大鼠被分为四组进行评估:(A)仅行端侧神经缝合术;(B)端侧神经缝合术并给予促红细胞生成素;(C)端端神经缝合术;(D)将神经断端埋入邻近肌肉。在所有动物中,对侧健康侧作为对照。使用腓总神经功能指数,每隔一段时间对神经再生进行功能评估,直至5个月。术后150天的评估包括腓总神经和胫神经的形态学检查,以及胫前肌的湿重。在术后前三周定期给予促红细胞生成素时,功能评估显示促红细胞生成素可能促进周围神经再生。然而,当停止给予促红细胞生成素时,功能恢复迅速恶化。因此,在本研究结束时,促红细胞生成素未能维持其对轴突再生的初始刺激作用。湿肌肉重量结果显示,A组与C组以及B组之间存在统计学显著差异。此外,轴突计数数据显示,A组与C组以及B组之间存在显著差异。促红细胞生成素在给药初期似乎促进周围神经再生。为了维持其效果,有必要进一步研究以优化条件(剂量、给药方式)。