Ohnishi A, Yamamoto T, Her Q, Han M, Murai Y, Ikeda M
Department of Neurology, School of Medicine, University of Occupational and Environmental Health, Kitakyushu, Japan.
J UOEH. 1996 Dec 1;18(4):261-71. doi: 10.7888/juoeh.18.261.
Brain-derived neurotrophic factor (BDNF) is produced in Schwann cells and fibroblasts in the peripheral nerve, and is considered to play an important role in survival, maintenance, development and repair of the peripheral neuron. In this study, the effect of human recombinant BDNF on the regeneration of nerve fibers following a crush injury to the sciatic nerves of Sprague-Dawley rats was evaluated. In the experimental group, 20 mg/kg of BDNF was injected subcutaneously three times a week for 4 weeks in seven rats. In the control group, only the dissolving solution used in the experimental group was injected similarly in seven rats as in the experimental group. The various morphometric parameters were evaluated in the peroneal, sural and tibial nerves and the nerve to soleus muscle distal to the crush site. There were no statistically significant differences in the change of body weight, the improvement of the width between the first and fifth toes on the side of the crush, the density of total myelinated fibers (numbers per mm2), the total number of myelinated fibers (number per nerve), maximum and median diameters of myelinated fibers, the density of unmyelinated fibers, and the electron microscopic parameters of axon and myelin sheath. On the other hand, the number of myelin lamellae in relation to the transverse axonal area was significantly greater in the experimental group than in the control group. Therefore, BDNF may promote the myelination. However, such an effect on myelination seems not to be clinically significant, because such an effect was not demonstrated in other morphometric evaluations reflecting the myelination condition. Therefore, taking all the data obtained in this study into consideration, we concluded that there was no definite evidence that BDNF promoted the regeneration of nerve fibers at least under these experimental conditions.
脑源性神经营养因子(BDNF)在外周神经的施万细胞和成纤维细胞中产生,被认为在周围神经元的存活、维持、发育和修复中发挥重要作用。在本研究中,评估了人重组BDNF对Sprague-Dawley大鼠坐骨神经挤压伤后神经纤维再生的影响。在实验组中,7只大鼠每周皮下注射3次20mg/kg的BDNF,共4周。在对照组中,7只大鼠以与实验组相同的方式仅注射实验组中使用的溶解液。在腓总神经、腓肠神经和胫神经以及挤压部位远端至比目鱼肌的神经中评估各种形态学参数。在体重变化、挤压侧第一和第五趾之间宽度的改善、有髓纤维总数密度(每平方毫米数量)、有髓纤维总数(每条神经数量)、有髓纤维的最大和中位直径、无髓纤维密度以及轴突和髓鞘的电子显微镜参数方面,均无统计学显著差异。另一方面,实验组中与横向轴突面积相关的髓鞘板层数明显多于对照组。因此,BDNF可能促进髓鞘形成。然而,这种对髓鞘形成的影响在临床上似乎并不显著,因为在反映髓鞘形成状况的其他形态学评估中未显示出这种效果。因此,综合本研究获得的所有数据,我们得出结论,至少在这些实验条件下,没有确凿证据表明BDNF促进了神经纤维的再生。