Neurotrophins render neurons highly vulnerable to certain injuries. We examined the possibility that NT-4/5 would enhance free radical neurotoxicity in vivo as well as in vitro. Striatal neurons exposed to 10 μM Fe2+ or 1 mM L-buthionine-[S, R]-sulfoximine (BSO) underwent mild degeneration within 24 h. With concurrent addition of 10-100 ng/ml NT-4/5, neuronal death following exposure to Fe2+ or BSO was significantly increased and suppressed by addition of 100 μM trolox, an antioxidant. In the adult brain, the intrastriatal injections of 20 nmol Fe2+ revealed features of neuronal necrosis such as swelling cell body and mitochondria, fenestration of plasma membrane prior to nuclear membrane, and scattering condensation of nuclear chromatin. Cotreatment with 1.8 μg NT-4/5 augmented the striatal damage 24 h following the injections of Fe2+. This study implies that free radicals produce necrotic degeneration in vivo as well as in vitro that becomes more sensitive in the presence of neurotrophins. (C) 2000 Academic Press.
Bibliographical noteFunding Information:
We thank Genentech Inc. (South San Francisco, CA) for the generous gift of NT-4/5. This study was supported by the Korean Science and Engineering Foundation (KOSEF) through the BDRC at Ajou University (B.J.G.).
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