The selective Rho-kinase inhibitor Fasudil is protective and therapeutic in experimental autoimmune encephalomyelitis

被引:70
作者
Sun, Xiaojia
Minohara, Motozumi
Kikuchi, Hitoshi
Ishizu, Takaaki
Tanaka, Masahito
Piao, Hua
Osoegawa, Manabu
Ohyagi, Yasumasa
Shimokawa, Hiroaki
Kira, Jun-ichi [1 ]
机构
[1] Kyushu Univ, Dept Neurol, Neurol Inst, Grad Sch Med Sci, Fukuoka 8128582, Japan
[2] Tohoku Univ, Grad Sch Med, Dept Cardiovasc Med, Sendai, Miyagi 980, Japan
关键词
Fasudil; Rho-kinase; multiple sclerosis; experimental autoimmune encephalomyelitis; IL-17;
D O I
10.1016/j.jneuroim.2006.06.027
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We studied the role of fasudil, a selective Rho-kinase inhibitor, in experimental autoimmune encephalomyelitis (EAE). Both parenteral and oral administration of fasudil prevented the development of EAE induced by proteolipid protein (PLP) p 139-151 in SJL/J mice. Specific proliferation of lymphocytes to PLP was significantly reduced, together with a downregulation of interleukin (IL)-17 and a marked decrease of the IFN-gamma/IL-4 ratio. Immunohistochemical examination also disclosed a marked decrease of inflammatory cell infiltration, and attenuated demyelination and acute axonal transaction. These results may provide a rationale of selective blockade of Rho-kinase by oral use of fasudil as a new therapy for multiple sclerosis. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:126 / 134
页数:9
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