Department of Neurosciences, School of Medicine of Ribeirão Preto, University of São Paulo, Brazil.
BMC Neurosci. 2012 Aug 14;13:100. doi: 10.1186/1471-2202-13-100.
Axonal regeneration depends on many factors, such as the type of injury and repair, age, distance from the cell body and distance of the denervated muscle, loss of surrounding tissue and the type of injured nerve. Experimental models use tubulisation with a silicone tube to research regenerative factors and substances to induce regeneration. Agarose, collagen and DMEM (Dulbecco's modified Eagle's medium) can be used as vehicles. In this study, we compared the ability of these vehicles to induce rat sciatic nerve regeneration with the intent of finding the least active or inert substance. The experiment used 47 female Wistar rats, which were divided into four experimental groups (agarose 4%, agarose 0.4%, collagen, DMEM) and one normal control group. The right sciatic nerve was exposed, and an incision was made that created a 10 mm gap between the distal and proximal stumps. A silicone tube was grafted onto each stump, and the tubes were filled with the respective media. After 70 days, the sciatic nerve was removed. We evaluated the formation of a regeneration cable, nerve fibre growth, and the functional viability of the regenerated fibres.
Comparison among the three vehicles showed that 0.4% agarose gels had almost no effect on provoking the regeneration of peripheral nerves and that 4% agarose gels completely prevented fibre growth. The others substances were associated with profuse nerve fibre growth.
In the appropriate concentration, agarose gel may be an important vehicle for testing factors that induce regeneration without interfering with nerve growth.
轴突再生取决于许多因素,例如损伤和修复的类型、年龄、与细胞体的距离以及去神经肌肉的距离、周围组织的丧失以及受伤神经的类型。实验模型使用硅酮管进行管化,以研究再生因子和物质来诱导再生。琼脂糖、胶原蛋白和 DMEM(Dulbecco 改良 Eagle 培养基)可用作载体。在这项研究中,我们比较了这些载体诱导大鼠坐骨神经再生的能力,目的是找到最不活跃或惰性的物质。该实验使用了 47 只雌性 Wistar 大鼠,它们被分为四个实验组(琼脂糖 4%、琼脂糖 0.4%、胶原蛋白、DMEM)和一个正常对照组。暴露右侧坐骨神经,并在远端和近端残端之间做一个 10 毫米的切口。将硅酮管移植到每个残端上,并用各自的培养基填充管。70 天后,取出坐骨神经。我们评估了再生电缆的形成、神经纤维的生长以及再生纤维的功能活力。
三种载体之间的比较表明,0.4%琼脂糖凝胶几乎没有引发周围神经再生的作用,而 4%琼脂糖凝胶完全阻止了纤维生长。其他物质与丰富的神经纤维生长有关。
在适当的浓度下,琼脂糖凝胶可能是测试诱导再生的因素而不干扰神经生长的重要载体。