Division of Neuroscience, Department of Histology and Embryology, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou 510080, China.
Neurosci Res. 2011 Jul;70(3):294-304. doi: 10.1016/j.neures.2011.03.010. Epub 2011 Apr 4.
Oligodendrocyte precursor cells (OPCs) are one of the potential treating tools for multiple sclerosis (MS). Therefore, the cell number and differentiation of OPCs in a demyelinated spinal cord are crucial for improvement of reparative process. In the present study, we investigated whether "Governor Vessel (GV)" electro-acupuncture (EA) could efficiently promote increase in cell number and differentiation of OPCs into oligodendrocytes, remyelination and functional recovery in the demyelinated spinal cord. The spinal cord of adult Sprague-Dawley rats was microinjected with ethidium bromide (EB) at T10, to establish a demyelinated model. Six groups of animals were performed for the experiment. After 15 days EA treatment, neurotrophin-3 (NT-3) level and number of NG2-positive OPCs were significantly increased. Compared with the sham group, more NG2-positive OPCs were distributed between neurofilament (NF)-positive nerve fibres or closely associated with them in the lesion site and nearby tissue. In rats given longer EA treatment for 30 days, the number of adenomatous polyposis coli (APC)-positive oligodendrocytes was increased. Concomitantly, the number of newly formed myelins was increased. This was coupled by increase in endogenous oligodendrocyte involved in myelin formation. Furthermore, behavioural test and spinal cord evoked potential detection demonstrated a significant functional recovery in the EA+EB day 30 group. Our results suggest EA treatment can promote NT-3 expression, increase the cell number and differentiation of endogenous OPCs, and remyelination in the demyelinated spinal cord as well as the functional improvement of demyelinated spinal cord.
少突胶质前体细胞 (OPC) 是多发性硬化症 (MS) 的潜在治疗工具之一。因此,脱髓鞘脊髓中 OPC 的数量和分化对于修复过程的改善至关重要。在本研究中,我们研究了“督脉(GV)”电针对促进脱髓鞘脊髓中 OPC 数量增加和分化为少突胶质细胞、髓鞘再生和功能恢复的作用。成年 Sprague-Dawley 大鼠的脊髓在 T10 处用溴化乙锭 (EB) 微注射,建立脱髓鞘模型。对 6 组动物进行了实验。EA 治疗 15 天后,神经营养因子-3 (NT-3) 水平和 NG2 阳性 OPC 数量显著增加。与假手术组相比,更多的 NG2 阳性 OPC 分布在神经丝 (NF) 阳性神经纤维之间或与其在病变部位和附近组织中紧密相关。在接受更长时间的 EA 治疗 30 天的大鼠中,腺瘤性结肠息肉病基因 (APC) 阳性少突胶质细胞的数量增加。同时,新形成的髓鞘数量增加。这与参与髓鞘形成的内源性少突胶质细胞的增加有关。此外,行为测试和脊髓诱发电位检测表明,在 EA+EB 第 30 天组中功能有显著恢复。我们的结果表明,EA 治疗可促进 NT-3 表达,增加脱髓鞘脊髓中内源性 OPC 的数量和分化,并促进脱髓鞘脊髓的髓鞘再生和功能改善。