Hashimoto Tadashi, Suzuki Yoshihisa, Suzuki Kyoko, Nakashima Toshihide, Tanihara Masao, Ide Chizuka
Production and Development Department, Kuraray Medical Inc., Kurashiki, Okayama, 710-8622, Japan.
J Mater Sci Mater Med. 2005 Jun;16(6):503-9. doi: 10.1007/s10856-005-0524-1.
We have developed a nerve regeneration material consisting of alginate gel crosslinked with covalent bonds. in the first part of this study, we attempted to analyze nerve regeneration through alginate gel in the early stages within 2 weeks. in the second part, we tried to regenerate cat peripheral nerve by using alginate tubular or non-tubular nerve regeneration devices, and compared their efficacies. Four days after surgery, regenerating axons grew without Schwann cell investment through the partially degraded alginate gel, being in direct contact with the alginate without a basal lamina covering. One to 2 weeks after surgery, regenerating axons were surrounded by common Schwann cells, forming small bundles, with some axons at the periphery being partly in direct contact with alginate. At the distal stump, numerous Schwann cells had migrated into the alginate 8-14 days after surgery. Remarkable restorations of the 50-mm gap in cat sciatic nerve were obtained after a long term by using tubular or non-tubular nerve regeneration material consisting mainly of alginate gel. However, there was no significant difference between both groups at electrophysiological and morphological evaluation. Although, nowadays, nerve regeneration materials being marketed mostly have a tubular structure, our results suggest that the tubular structure is not indispensable for peripheral nerve regeneration.
我们研发了一种由共价键交联藻酸盐凝胶组成的神经再生材料。在本研究的第一部分,我们试图分析在2周内早期通过藻酸盐凝胶的神经再生情况。在第二部分,我们尝试使用藻酸盐管状或非管状神经再生装置再生猫的周围神经,并比较它们的效果。术后4天,再生轴突通过部分降解的藻酸盐凝胶生长,没有施万细胞包绕,直接与没有基膜覆盖的藻酸盐接触。术后1至2周,再生轴突被普通施万细胞包围,形成小束,一些外周轴突部分直接与藻酸盐接触。在远端残端,术后8 - 14天有大量施万细胞迁移到藻酸盐中。通过使用主要由藻酸盐凝胶组成的管状或非管状神经再生材料,长期后猫坐骨神经50毫米间隙得到了显著修复。然而,在电生理和形态学评估中两组之间没有显著差异。尽管如今市场上销售的神经再生材料大多具有管状结构,但我们的结果表明管状结构对于周围神经再生并非必不可少。