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Evidence for oxidative damage in a murine leukemia virus‐induced neurodegeneration
Author(s) -
Wilt Susan G.,
Dugger Natalie V.,
Hitt Nancy D.,
Hoffman Paul M.
Publication year - 2000
Publication title -
journal of neuroscience research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.72
H-Index - 160
eISSN - 1097-4547
pISSN - 0360-4012
DOI - 10.1002/1097-4547(20001101)62:3<440::aid-jnr14>3.0.co;2-m
Subject(s) - neurodegeneration , oxidative stress , microglia , neuropathology , lipid peroxidation , oxidative phosphorylation , biology , gliosis , immunology , pathology , medicine , neuroscience , biochemistry , inflammation , disease
Vacuolation in cellular organelles within the central nervous system is a common manifestation of oxidative injury. We found that the spongiform vacuolation observed in PVC‐211 murine leukemia virus (PVC‐MuLV) neurodegeneration was associated with oxidative damage as detected by immunoreactivity for 3‐nitrotyrosine and protein carbonyl groups. This oxidative injury was present in brain before or concomitant with the appearance of activated microglia, vacuolation, and gliosis that characterize PVC‐MuLV neuropathology. Treatment of infected F344 rat pups with the antioxidant vitamin E transiently protected and prolonged the latency of PVC‐MuLV neurodegeneration. Taken together, these findings implicate oxidative damage and lipid peroxidation in the pathogenesis of PVC‐MuLV neurodegeneration. This animal model may be useful for studies of mechanisms and potential therapies for progressive neurodegeneration following a well‐defined insult. J. Neurosci. Res. 62:440–450, 2000. Published 2000 Wiley‐Liss, Inc.