Abstract
Tricyclic antidepressants and selective serotonin reuptake inhibitors are here shown to induce cell death in a neural cell line. The exposure to these drugs led to increased generation of reactive oxygen species and a concomitant reduction of intracellular glutathione levels. Furthermore, these antidepressants induced DNA fragmentation and increased the transcriptional and DNA-binding activity of NF-kappaB. In contrast, treatment with type A and B monoamine oxidase inhibitors did not induce changes in NF-kappaB activity and did not exert a detrimental influence on cell viability. These results indicate that some antidepressant drugs may cause both oxidative stress and changes in cellular antioxidative capacity, resulting in altered NF-kappaB activity and, ultimately, cell death.
MeSH terms
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Animals
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Antidepressive Agents / classification
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Antidepressive Agents / pharmacology*
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Antidepressive Agents, Tricyclic / pharmacology
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Apoptosis / drug effects*
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Cell Line
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Cell Survival / drug effects
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DNA Fragmentation
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Glutathione / metabolism
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Glutathione Disulfide / metabolism
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Hydrogen Peroxide / metabolism
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Monoamine Oxidase Inhibitors / pharmacology
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NF-kappa B / genetics*
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NF-kappa B / metabolism*
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Neurons / cytology
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Neurons / drug effects*
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Neurons / physiology
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Peroxides / metabolism
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Recombinant Fusion Proteins / biosynthesis
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Selective Serotonin Reuptake Inhibitors / pharmacology
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Transcription, Genetic / drug effects
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Transfection
Substances
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Antidepressive Agents
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Antidepressive Agents, Tricyclic
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Monoamine Oxidase Inhibitors
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NF-kappa B
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Peroxides
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Recombinant Fusion Proteins
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Serotonin Uptake Inhibitors
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Hydrogen Peroxide
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Glutathione
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Glutathione Disulfide