Aebischer P, Guénard V, Winn S R, Valentini R F, Galletti P M
Artificial Organ Laboratory, Brown University, Providence, RI 02912.
Brain Res. 1988 Jun 28;454(1-2):179-87. doi: 10.1016/0006-8993(88)90817-7.
The presence of a distal nerve segment is considered to be essential for peripheral nerve regeneration through impermeable synthetic guidance channels. The use of a perm-selective material may provide a more appropriate regenerating environment by allowing solute exchange across the wall of the channel. We compared perm-selective acrylic copolymer (AC) channels with impermeable silicone elastomer (SE) channels in terms of regeneration in the absence of a distal nerve stump. Cohorts of 6 animals received AC and SE channels for either 4 or 8 weeks, with the distal end of the polymer tube left open in half of the animals, and plugged with the same polymer ('capped') in the other half. Capped and uncapped AC channels contained regenerated nerve cables which extended fully to the distal end of the channel, whereas capped SE channels contained only 1 mm long granulomatous tissue cables, and uncapped SE channels showed small cables with only a few myelinated axons. The nerve cables regenerated in uncapped AC channels were smaller and contained fewer myelinated axons than those observed in capped AC channels. Capped AC channels sleeved with a tight-fitting silicone tube to render them impermeable, showed no regenerated tissue within their lumen. The use of a perm-selective channel may have allowed the influx of nutrients and growth factors from the external environment while concentrating factors released by the proximal nerve stump.
对于通过不可渗透的合成导向通道进行的周围神经再生而言,远端神经段的存在被认为是必不可少的。使用具有渗透选择性的材料可以通过允许溶质在通道壁上交换,从而提供一个更适宜的再生环境。我们比较了具有渗透选择性的丙烯酸共聚物(AC)通道与不可渗透的硅橡胶(SE)通道在不存在远端神经残端时的再生情况。每组6只动物分别植入AC通道和SE通道4周或8周,聚合物管的远端在一半动物中保持开放,另一半则用相同的聚合物堵塞(“封闭”)。封闭和未封闭的AC通道中都含有再生神经束,其完全延伸至通道的远端,而封闭的SE通道中仅含有1毫米长的肉芽肿组织束,未封闭的SE通道中则显示出只有少数有髓轴突的小束。未封闭的AC通道中再生的神经束比封闭的AC通道中的神经束更小,且有髓轴突更少。用紧密贴合的硅胶管包裹封闭的AC通道使其不可渗透,其管腔内未显示出再生组织。使用具有渗透选择性的通道可能允许营养物质和生长因子从外部环境流入,同时浓缩近端神经残端释放的因子。