دورية أكاديمية

Protective role of the cytokine-inducible isoform of nitric oxide synthase induction and nitrosative stress in experimental autoimmune encephalomyelitis of the DA rat.

التفاصيل البيبلوغرافية
العنوان: Protective role of the cytokine-inducible isoform of nitric oxide synthase induction and nitrosative stress in experimental autoimmune encephalomyelitis of the DA rat.
المؤلفون: Kahl KG; Department of Neurology, Julius-Maximilians-University, Würzburg, Germany., Zielasek J, Uttenthal LO, Rodrigo J, Toyka KV, Schmidt HH
المصدر: Journal of neuroscience research [J Neurosci Res] 2003 Jul 15; Vol. 73 (2), pp. 198-205.
نوع المنشور: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
اللغة: English
بيانات الدورية: Publisher: Wiley Interscience Country of Publication: United States NLM ID: 7600111 Publication Model: Print Cited Medium: Print ISSN: 0360-4012 (Print) Linking ISSN: 03604012 NLM ISO Abbreviation: J Neurosci Res Subsets: MEDLINE
أسماء مطبوعة: Publication: New York, NY : Wiley Interscience
Original Publication: New York, Liss.
مواضيع طبية MeSH: Cytokines/*biosynthesis , Encephalomyelitis, Autoimmune, Experimental/*enzymology , Nitric Oxide Synthase/*biosynthesis , Tyrosine/*analogs & derivatives , Tyrosine/*biosynthesis, Animals ; Encephalomyelitis, Autoimmune, Experimental/prevention & control ; Enzyme Induction/drug effects ; Enzyme Induction/physiology ; Enzyme Inhibitors/pharmacology ; Female ; Isoenzymes/antagonists & inhibitors ; Isoenzymes/biosynthesis ; Neuroprotective Agents/pharmacology ; Nitric Oxide Synthase/antagonists & inhibitors ; Nitric Oxide Synthase Type II ; Nitrosation/drug effects ; Rats
مستخلص: The pathogenic role of nitric oxide (NO) in multiple sclerosis (MS) remains controversial. Some groups have reported a pathogenic role of NO in experimental autoimmune encephalomyelitis (EAE), an animal model of some aspects of MS, whereas we and others have found a disease-suppressive effect of NO in EAE. Because the previously used EAE models have a mainly monophasic inflammatory disease course, distinct from MS, we here studied EAE in the DA rat, which better models the demyelinating and relapsing disease course of human MS. The induction of EAE in DA rats led to 1) severe inflammatory infiltrates mainly in the lumbar spinal cord; 2) an up-regulation of the activity of the cytokine-inducible isoform of NO synthases (NOS-II); and 3) increased tissue protein tyrosine nitration, as indicated by peroxynitrite (ONOO(-)), as a marker of nitrosative stress. Sources of superoxide metabolism, i.e., NADPH oxidase, myeloperoxidase, and superoxide dismutase, remained unchanged. Early treatment of animals with aminoguanidine, a relatively selective inhibitor of NOS-II, lowered nitrotyrosine immunoreactivity but at the same time led to more severe disease and pronounced inflammatory infiltrates in the lumbar spinal cord. Our results suggest a rather protective role of NOS-II induction and nitrosative stress in EAE in DA rats and support the hypothesis of a disease-mitigating immunomodulatory role of NO in this animal model of MS.
(Copyright 2003 Wiley-Liss, Inc.)
المشرفين على المادة: 0 (Cytokines)
0 (Enzyme Inhibitors)
0 (Isoenzymes)
0 (Neuroprotective Agents)
3604-79-3 (3-nitrotyrosine)
42HK56048U (Tyrosine)
EC 1.14.13.39 (Nitric Oxide Synthase)
EC 1.14.13.39 (Nitric Oxide Synthase Type II)
تواريخ الأحداث: Date Created: 20030702 Date Completed: 20030902 Latest Revision: 20131121
رمز التحديث: 20231215
DOI: 10.1002/jnr.10649
PMID: 12836162
قاعدة البيانات: MEDLINE
الوصف
تدمد:0360-4012
DOI:10.1002/jnr.10649