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实验性切除横断及自体移植重建后兔坐骨神经再生的超微结构研究

Ultrastructural study of rabbit sciatic nerve regeneration following experimental excisional transection and autograft reconstruction.

作者信息

Achparaki-Alvanou A, Manthos A, Kontopoulos V, Kerameos-Foroglou C, Foroglou G

出版信息

Acta Neurochir (Wien). 1987;85(3-4):172-82. doi: 10.1007/BF01456115.

Abstract

This experimental study presents the ultrastructure of regenerating sciatic nerve of the rabbit, after transection and immediate end to end anastomosis, using perineural fascicular nerve autograft, in a sterile environment. Twenty-four hours, 1, 2, and 6 weeks after the anastomosis, the treated sciatic nerves were exposed and three segments were excised and studied. The first at the region of the graft and the others from the proximal and distal stump of the nerve, in the vicinity of the graft suture. The sections taken from the proximal part showed that the nerve structure was identical with the control. Degeneration and regeneration of nerve fibres were observed on the sections taken from the region of the grafts and from the distal parts. Macrophagic activity appeared mainly one week after the operation. Fibroblastic invasion started 24 hours after operation. A moderate amount of collagen fibres was gradually formed. The fibres were disposed in parallel with the neuraxon. Schwann cells were slightly affected initially but consequently they fully recovered and showed signs of extra-activity of the cytoplasm organelles, e.g., enlargement of the granular endoplasmic reticulum cisternae. The present study showed that the bridging of experimental gaps of rabbit's sciatic nerve, by means of autograft and by use of perineural suturing, was successful. The regenerating nerve fibres were growing through the graft towards the distal part of the nerve. In this process Schwann cells and fibroblastic activity play a key role, which is most favourably influenced by using the technique described in this paper.

摘要

本实验研究展示了在无菌环境下,采用神经束膜神经自体移植,对兔坐骨神经进行横断并立即端端吻合后再生坐骨神经的超微结构。吻合术后24小时、1周、2周和6周,暴露处理后的坐骨神经,切除三个节段进行研究。第一个节段取自移植部位,另外两个节段分别取自神经近端和远端残端,靠近移植缝线处。取自近端部分的切片显示神经结构与对照组相同。在取自移植部位和远端部分的切片上观察到神经纤维的变性和再生。巨噬细胞活性主要在术后1周出现。成纤维细胞浸润在术后24小时开始。逐渐形成适量的胶原纤维。这些纤维与神经轴突平行排列。雪旺细胞最初受到轻微影响,但随后完全恢复,并表现出细胞质细胞器超活性的迹象,如粗面内质网池扩大。本研究表明,通过自体移植和神经束膜缝合成功地桥接了兔坐骨神经的实验间隙。再生神经纤维通过移植体向神经远端生长。在此过程中,雪旺细胞和成纤维细胞活性起关键作用,采用本文所述技术对此影响最为有利。

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