Phongsisay Vongsavanh, Susuki Keiichiro, Matsuno Kenjiro, Yamahashi Takuyu, Okamoto Saori, Funakoshi Kei, Hirata Koichi, Shinoda Motoo, Yuki Nobuhiro
Department of Neurology, Dokkyo Medical University, Kitakobayashi 880, Mibu, Shimotsuga, Tochigi 321-0293, Japan.
J Neuroimmunol. 2008 Dec 15;205(1-2):101-4. doi: 10.1016/j.jneuroim.2008.09.016. Epub 2008 Oct 29.
Complement-mediated disruption of voltage-gated sodium channels at the nodes of Ranvier acts in the development of acute motor axonal neuropathy. Nafamostat mesilate, a synthetic serine protease inhibitor, used in clinical practice for more than 20 years, has anti-complement activity. Acute motor axonal neuropathy rabbits obtained by GM1 ganglioside sensitization were or were not given nafamostat mesilate intravenously. Complement deposition and sodium channel disruption in the spinal anterior roots were significantly less frequent in the treated rabbits than in the controls. Nafamostat mesilate inhibited complement deposition and prevented sodium channel disruption. This provided the rationale for a clinical trial.
补体介导的郎飞结处电压门控钠通道破坏在急性运动轴索性神经病的发展中起作用。甲磺酸萘莫司他是一种合成的丝氨酸蛋白酶抑制剂,已在临床实践中使用20多年,具有抗补体活性。通过GM1神经节苷脂致敏获得的急性运动轴索性神经病兔静脉注射或未注射甲磺酸萘莫司他。与对照组相比,治疗组兔脊髓前根中的补体沉积和钠通道破坏明显较少。甲磺酸萘莫司他抑制补体沉积并防止钠通道破坏。这为一项临床试验提供了理论依据。