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Differential degeneration patterns of the proximal and distal stumps in a sciatic gap-injury model in the rabbit highlight the role of gap-length in preventing regeneration

机译:兔坐骨神经间隙损伤模型中近端和远端残端的差异性变性模式突出了间隙长度在预防再生中的作用

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The study showed that in gaps longer that 20 mm, the distal stump is too far to provide a contingent of Schwann cells able to reach the axonal sprouting in the proximal stump. At the level of proximal stump, axons degenerate until newly re-growing freshly myelinated axons appear after 3 or 4 months. These new axons may progress aligned with the length of the guide for a limited distance. We then confirmed, in a larger animal model, that regeneration in longer gaps fails because the distance does not allow a timely match between proximal sprouts and distal Schwann cells. Our study, however, may suggest an un-expected advantage of longer conduits in being used to control or prevent regeneration from a proximal stump of an amputated nerve; sprouts are allowed to degenerate and new axons are not engulfed by fibroblast/myofibroblasts. This may be useful in control or prevention of amputation neuroma.
机译:研究表明,在间隙长于20毫米的情况下,远端残端太远,以至于无法提供能够到达近端残端轴突萌发的许旺细胞。在近端残端水平,轴突变性,直到3或4个月后新近重新生长的新鲜有髓神经的轴突出现。这些新的轴突可能会在一定距离内与导板的长度对齐。然后,我们在较大的动物模型中确认,在较长的间隙中再生失败,因为该距离不允许近端新芽与远端施旺细胞之间的及时匹配。然而,我们的研究可能提示更长的导管在控制或预防截肢神经近端残端的再生中具有意想不到的优势。允许芽变质,新的轴突不被成纤维细胞/成肌纤维细胞吞噬。这在控制或预防截肢神经瘤中可能有用。

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