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利巴韦林与替唑呋林联合治疗对实验性自身免疫性脑脊髓炎发展的治疗效果:临床与组织病理学评估

Therapeutic effects of combined treatment with ribavirin and tiazofurin on experimental autoimmune encephalomyelitis development: clinical and histopathological evaluation.

作者信息

Stojkov Danijela, Lavrnja Irena, Pekovic Sanja, Dacic Sanja, Bjelobaba Ivana, Mostarica-Stojkovic Marija, Stosic-Grujicic Stanislava, Jovanovic Sasa, Nedeljkovic Nadezda, Rakic Ljubisav, Stojiljkovic Mirjana

机构信息

Department of Neurobiology, Institute for Biological Research Sinisa Stankovic, Bulevar Despota Stefana 142, Belgrade, 11000, Serbia.

出版信息

J Neurol Sci. 2008 Apr 15;267(1-2):76-85. doi: 10.1016/j.jns.2007.10.010. Epub 2007 Nov 8.

Abstract

Experimental autoimmune encephalomyelitis (EAE) is an animal model of multiple sclerosis (MS) and the helpful tool in preclinical testing of various substances considered for treatment of this human CNS disease. Ribavirin (R) and tiazofurin (T) are purine nucleoside analogues, with the broad spectrum of anti-viral, anti-tumoral and anti-inflammatory properties. We proposed that combined treatment with RT, administrated during the effector phase of EAE, would attenuate disease severity, both clinically and pathologically. Ribavirin was given daily at a dosage of 30 mg/kg and tiazofurin was given at a dosage of 10 mg/kg every other day for 15 days. We detected amelioration of clinical signs and faster recovery in the RT group compared to the control group. Immunohistochemical analyses revealed that RT treatment decrease the number of T cells, macrophages and microglia. In the controls, we detected reactive type of microglia, while in the RT group we noticed ramified/resting form. Demyelination areas and axonal damage were not recorded in the RT group, in contrast to the control group where multiple areas of demyelination zones and axonal loss were found. RT combination treatment suppresses ongoing EAE, prevents demyelination and axonal loss, and therefore may well be the potential therapy for the treatment of MS.

摘要

实验性自身免疫性脑脊髓炎(EAE)是多发性硬化症(MS)的动物模型,也是用于治疗这种人类中枢神经系统疾病的各种物质临床前测试的有用工具。利巴韦林(R)和替唑呋林(T)是嘌呤核苷类似物,具有广泛的抗病毒、抗肿瘤和抗炎特性。我们提出,在EAE的效应期给予RT联合治疗,将在临床和病理上减轻疾病严重程度。利巴韦林每天以30mg/kg的剂量给药,替唑呋林每隔一天以10mg/kg的剂量给药,共15天。与对照组相比,我们在RT组中检测到临床症状改善且恢复更快。免疫组织化学分析显示,RT治疗减少了T细胞、巨噬细胞和小胶质细胞的数量。在对照组中,我们检测到反应性小胶质细胞,而在RT组中我们注意到分支状/静止型小胶质细胞。与对照组发现多个脱髓鞘区和轴突丢失的情况相反,RT组未记录到脱髓鞘区域和轴突损伤。RT联合治疗可抑制正在进行的EAE,预防脱髓鞘和轴突丢失,因此很可能是治疗MS的潜在疗法。

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