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nisomycin治疗实验性自身免疫性脑脊髓炎

Preliminary effect of anisomycin on Experimental Autoimmune Encephalolmylitis

中文摘要英文摘要

目的:使用anisomycin体内治疗实验性自身免疫性脑脊髓炎(EAE),观察anisomycin的治疗效果。方法:用200 μg MOG35-55免疫雌性C57BL/6小鼠诱导EAE模型。将小鼠随机分为对照组、EAE组和anisomycin治疗组,10只/组。于免疫后第12 d注射30 mg/kg的anisomycin,连续治疗7 d;对照组和EAE组注射等体积的PBS,观察小鼠的临床评分和体重变化。在免疫后第18 d,取小鼠脑组织进行HE染色。结果:EAE组和anisomycin治疗组小鼠发生EAE的潜伏期分别是第12 d和第13 d;与对照组比较,实验组小鼠先后出现进食减少、体重下降、后肢无力,严重者后肢完全瘫痪; anisomycin治疗组小鼠的临床体征较EAE组明显减轻; anisomycin治疗组和EAE组的脑组织HE染色表现为小血管周围炎症细胞浸润,呈袖套状。Anisomycin治疗组的炎症细胞浸润较EAE组明显减轻。结论:anisomycin能明显缓解EAE的临床体征和炎症细胞浸润。

Objective:Anisomycin was used to treat Experimental Allergic Encephalomylitis in vivo to observe in vivo effect. Methods: Each female C57BL/6 mouse was immunized subcutaneously with 200 μg of MOG35-55. All mice were randomly distributed into three groups: normal control, EAE and anisomycin groups. The mice were intraperitoneally treated with anisomycin for one week. And the control group and the EAE group were injected intraperitoneally with an equal volume of PBS. The mouse brains were taken out at eighteen days after the immune to observe histopathological changes by HE staining. Results: Latency of the mice in the EAE or anisomycin group was 12 to 13 days. The mice had weight loss, hind limb weakness and hindquarter completely unable to performance. Clinical signs of the mice treated by anisomycin were significantly slighter than those of EAE mice. Brain tissues of EAE mice had EAE typical pathological changes, such as perivascular inflammatory cell infiltration in the "sleeve-like". Anisomycin treatment resulted in the reduction of inflammatory cell infiltration into the brain tissues, compared with the EAE group. Conclusion: Anisomycin has therapeutic effect on the EAE mice to some extent.

邢飞跃、孙曼曼、刘松

神经病学、精神病学基础医学药学

茴香霉素髓鞘少突胶质细胞糖蛋白实验性自身免疫性脑脊髓炎

anisomycinmyelin oligodendrocyte glycoproteinExperimental Autoimmune Encephalomyelitis

邢飞跃,孙曼曼,刘松.nisomycin治疗实验性自身免疫性脑脊髓炎[EB/OL].(2013-05-13)[2025-08-19].http://www.paper.edu.cn/releasepaper/content/201305-176.点此复制

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