Oxidative stress has been shown to be important in several neurodegenerativ
e disorders. Previous in vitro studies have already demonstrated the abilit
y of a prion protein fragment to induce oxidative stress in cultured cells.
By immunohistochemistry for nitrotyrosine (NT) and heme oxygenase-l as mar
kers for oxidative stress, we found widespread neuronal labeling for NT in
scrapie-infected mouse brains, in agreement with peroxynitrite mediated neu
ronal degeneration. Damage by free radicals is a likely cause for neurodege
neration in prion disease, and antioxidants are a potential therapy of thes
e disorders. (C) 2000 Academic Press.