Differential induction of NF-kappaB activity and neural cell death by antidepressants in vitro

Eur J Neurosci. 2000 Dec;12(12):4331-7. doi: 10.1046/j.0953-816x.2000.01352.x.

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

  • Animals
  • Antidepressive Agents / classification
  • Antidepressive Agents / pharmacology*
  • Antidepressive Agents, Tricyclic / pharmacology
  • Apoptosis / drug effects*
  • Cell Line
  • Cell Survival / drug effects
  • DNA Fragmentation
  • Glutathione / metabolism
  • Glutathione Disulfide / metabolism
  • Hydrogen Peroxide / metabolism
  • Monoamine Oxidase Inhibitors / pharmacology
  • NF-kappa B / genetics*
  • NF-kappa B / metabolism*
  • Neurons / cytology
  • Neurons / drug effects*
  • Neurons / physiology
  • Peroxides / metabolism
  • Recombinant Fusion Proteins / biosynthesis
  • Selective Serotonin Reuptake Inhibitors / pharmacology
  • Transcription, Genetic / drug effects
  • Transfection

Substances

  • Antidepressive Agents
  • Antidepressive Agents, Tricyclic
  • Monoamine Oxidase Inhibitors
  • NF-kappa B
  • Peroxides
  • Recombinant Fusion Proteins
  • Serotonin Uptake Inhibitors
  • Hydrogen Peroxide
  • Glutathione
  • Glutathione Disulfide