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局部添加单唾液酸神经节苷脂GM1可刺激体内外周轴突再生。

Local addition of monosialoganglioside GM1 stimulates peripheral axon regeneration in vivo.

作者信息

Lainetti R D, Da-Silva C F

机构信息

Departamento de Histologia e Embriologia, Universidade de São Paulo, Brasil.

出版信息

Braz J Med Biol Res. 1993 Aug;26(8):841-5.

PMID:8298520
Abstract

Tubulization repair technique is a useful model to study peripheral nerve regeneration by offering quantifiable parameters to assess the possible effect of exogenously applied substances on nerve repair. In the present study we demonstrated that locally administered GM1 inside a tubular prosthesis at the time of implantation can significantly improve the repair process. The sciatic nerve of 8 male C57BL/6J mice, approximately 3 months old at the time of surgery and divided into two groups of 4 animals each, was transected and the proximal and distal nerve stumps were sutured into a polyethylene tube (PT), 0.76 mm internal diameter (ID), to bridge a nerve gap of 4 mm. The tubes contained 2 microliters of collagen type I (2.4 mg/ml) alone or in combination (1:1 volume ratio) with monosialoganglioside GM1 (10 mg/ml in the final solution). Four additional animals received a PT with 1.14 mm ID filled with 5.5 microliters of collagen/GM1 (at the same ratio and final concentration as above). After 6 weeks the PT with the regenerating nerve cables were processed for total myelinated axon counts with a computer-controlled system. GM1 significantly increased peripheral axon regeneration (3427 +/- 64 myelinated axons for the 0.76-mm PT and 3623 +/- 270 for the 1.14-mm PT, mean +/- SEM) compared to the group receiving collagen alone (2516 +/- 156) and this effect did not depend on tube diameter. This action is possibly due to a stimulating effect of GM1 on neurite outgrowth and sprouting.

摘要

微管修复技术是一种有用的模型,可通过提供可量化参数来评估外源性应用物质对神经修复的可能影响,从而用于研究周围神经再生。在本研究中,我们证明了在植入时将GM1局部施用于管状假体内部可显著改善修复过程。8只雄性C57BL/6J小鼠的坐骨神经在手术时约3个月大,分为两组,每组4只动物,将其切断,将近端和远端神经残端缝合到内径(ID)为0.76毫米的聚乙烯管(PT)中,以桥接4毫米的神经间隙。这些管子单独含有2微升I型胶原蛋白(2.4毫克/毫升),或与单唾液酸神经节苷脂GM1(最终溶液中为10毫克/毫升)以(1:1体积比)组合。另外4只动物接受内径为1.14毫米的PT,其中填充有5.5微升胶原蛋白/GM1(比例和最终浓度与上述相同)。6周后,对带有再生神经束的PT进行处理,使用计算机控制系统对总髓鞘轴突进行计数。与仅接受胶原蛋白的组(2516 +/- 156)相比,GM1显著增加了外周轴突再生(内径0.76毫米的PT为3427 +/- 64个有髓鞘轴突,内径1.14毫米的PT为3623 +/- 270个,平均值 +/- 标准误),并且这种作用不依赖于管的直径。这种作用可能是由于GM1对神经突生长和发芽的刺激作用。

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Local addition of monosialoganglioside GM1 stimulates peripheral axon regeneration in vivo.局部添加单唾液酸神经节苷脂GM1可刺激体内外周轴突再生。
Braz J Med Biol Res. 1993 Aug;26(8):841-5.
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Exogenous ganglioside stimulation of axonal regeneration after nerve transection and entubulation repair.
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