ferrous-citrate and 6-hydroxy-2-5-7-8-tetramethylchroman-2-carboxylic-acid

Neurotrophic factors have been shown to potentiate necrotic neuronal death in cortical cultures. In this study we characterized the death induced by various oxidative insults and tested the effects of neurotrophic factors on that death. Treatment with fibroblast growth factor-2, neurotrophin-4, or insulin-like growth factor-1 potentiated neuronal cell death induced by iron-citrate (Fe) or buthionine sulfoximine (BSO), but not ethacrynic acid (EA). Neuronal death induced by each insult was blocked by the free radical scavenger, trolox. An analysis of the death indicated that Fe and BSO induced necrotic cell death, while EA induced apoptotic cell death. BSO and EA caused decreased cellular glutathione levels, whereas Fe had no effect on glutathione levels. Neurotrophic factors had no effect on the changes in glutathione. The results indicate that oxidative insults can induce either apoptotic or necrotic death and that the effects of neurotrophic factors are dependent on the type of cell death.

Topics: Animals; Buthionine Sulfoximine; Cell Death; Cells, Cultured; Cerebral Cortex; Chromans; Citric Acid; Ethacrynic Acid; Ferrous Compounds; Fetus; Fibroblast Growth Factor 2; Free Radical Scavengers; Insulin-Like Growth Factor I; Mice; Nerve Growth Factors; Neuroglia; Neurons; Oxidative Stress