Evidence for the production of peroxynitrite in inflammatory CNS demyelination

被引:147
作者
Cross, AH
Manning, PT
Stern, MK
Misko, TP
机构
[1] GD SEARLE & CO,MOL PHARMACOL,INFLAMATORY DIS RES,ST LOUIS,MO 63167
[2] MONSANTO CO,MONSANTO CORP RES,ST LOUIS,MO 63167
关键词
peroxynitrite anion; nitric oxide; experimental autoimmune (allergic) encephalomyelitis; demyelination;
D O I
10.1016/S0165-5728(97)00145-8
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Peroxynitrite, which is generated by the reaction of nitric oxide (NO) with superoxide, is a strong oxidant that can damage subcellular organelles, membranes and enzymes through its actions on proteins, lipids, and DNA, including the nitration of tyrosine residues of proteins. Detection of nitrotyrosine (NT) serves as a biochemical marker of peroxynitrite-induced damage. In the present studies, NT was detected by immunohistochemistry in CNS tissues from mice with acute experimental autoimmune encephalomyelitis (EAE). NT immunoreactivity was displayed by many mononuclear inflammatory cells, including CD4+ cells. It was also observed in astrocytes near EAE lesions. Immunostaining for the inducible isoform of NO synthase (iNOS) was also observed, particularly during acute EAE. These data strongly suggest that peroxynitrite formation is a major consequence of NO produced via iNOS, and implicate this powerful oxidant in the pathogenesis of EAE. (C) 1997 Elsevier Science B.V.
引用
收藏
页码:121 / 130
页数:10
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