Dc. Hooper et al., LOCAL NITRIC-OXIDE PRODUCTION IN VIRAL AND AUTOIMMUNE-DISEASES OF THECENTRAL-NERVOUS-SYSTEM, Proceedings of the National Academy of Sciences of the United Statesof America, 92(12), 1995, pp. 5312-5316
Because of the short half-life of NO, previous studies implicating NO
in central nervous system pathology during infection had to rely on th
e demonstration of elevated levels of NO synthase mRNA or enzyme expre
ssion or NO metabolites such as nitrate and nitrite in the infected br
ain, To more definitively investigate the potential causative role of
NO in lesions of the central nervous system in animals infected with n
eurotropic viruses or suffering from experimental allergic encephaliti
s, we have determined directly the levels of NO present in the central
nervous system of such animals. Using spin trapping of NO and electro
n paramagnetic resonance spectroscopy, we confirm here that copious am
ounts of NO (up to 30-fold more than control) are elaborated in the br
ains of rats infected with rabies virus or borna disease virus, as wel
l as in the spinal cords of rats that had received myelin basic protei
n-specific T cells.