| Literature DB >> 10998568 |
S V Spitsin1, G S Scott, R B Kean, T Mikheeva, D C Hooper.
Abstract
Peroxynitrite (ONOO(-)), the product of nitric oxide (NO(radical)) and superoxide (O(2)(-radical)), is believed to be a major contributor to immunotoxicity when produced by activated cells expressing inducible nitric oxide synthase (iNOS). Uric acid (UA) is a natural scavenger of ONOO(-) that is present at high levels in the sera of humans and other higher order primates relative to most lower mammals. We have previously shown that UA treatment is therapeutic in experimental allergic encephalomyelitis (EAE), a rodent model of multiple sclerosis (MS). In this study we have examined the effect of UA therapy on the dynamics of the appearance of iNOS-positive cells in central nervous system (CNS) tissue of mice subjected to the stimuli that cause EAE. The results indicate that UA prevents activated monocytes from entering CNS tissue where they may contribute to the pathogenesis of MS and other CNS diseases.Entities:
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Year: 2000 PMID: 10998568 DOI: 10.1016/s0304-3940(00)01446-4
Source DB: PubMed Journal: Neurosci Lett ISSN: 0304-3940 Impact factor: 3.046