Triarhou L C, Herndon R M
Arch Neurol. 1986 Feb;43(2):121-5. doi: 10.1001/archneur.1986.00520020015008.
Adult male Sprague-Dawley rats were injected intraspinally with 2 microL of 1% lysolecithin to induce demyelination. This was followed by systemic treatment with dexamethasone acetate for two weeks. Control groups were injected with lysolecithin but not treated. The animals were perfused at 8, 12, 28, and 60 days postoperatively, and the spinal cords were processed and examined histopathologically. The intraspinal injection of lysolecithin produced a focal area of primary demyelination followed by remyelination. In the steroid-treated groups, there was a suppression of the mononuclear phagocytic response, accompanied by slow clearance of the disrupted myelin sheaths and an apparent reduction in lesion size. Remyelination was substantially retarded in comparison with the controls. The findings suggest that steroids interfere with the process of remyelination, as they are known to do with myelination during development. Thus, dexamethasone appears to have a dual effect, decreasing demyelination but delaying remyelination.
成年雄性Sprague-Dawley大鼠经脊髓内注射2微升1%的溶血卵磷脂以诱导脱髓鞘。随后进行为期两周的醋酸地塞米松全身治疗。对照组注射溶血卵磷脂但不进行治疗。术后第8、12、28和60天对动物进行灌注,对脊髓进行处理并进行组织病理学检查。脊髓内注射溶血卵磷脂产生了一个原发性脱髓鞘的局部区域,随后进行了再髓鞘化。在类固醇治疗组中,单核吞噬细胞反应受到抑制,伴有受损髓鞘清除缓慢和病变大小明显减小。与对照组相比,再髓鞘化明显延迟。研究结果表明,类固醇会干扰再髓鞘化过程,正如已知它们在发育过程中干扰髓鞘形成一样。因此,地塞米松似乎具有双重作用,减少脱髓鞘但延迟再髓鞘化。