Tricyclic Antidepressants Amitriptyline and Desipramine Induced Neurotoxicity Associated with Parkinson's Disease

Mol Cells. 2015 Aug;38(8):734-40. doi: 10.14348/molcells.2015.0131. Epub 2015 Aug 4.

Abstract

Recent studies report that a history of antidepressant use is strongly correlated with the occurrence of Parkinson's disease (PD). However, it remains unclear whether antidepressant use can be a causative factor for PD. In the present study, we examined whether tricyclic antidepressants amitriptyline and desipramine can induce dopaminergic cell damage, both in vitro and in vivo. We found that amitriptyline and desipramine induced mitochondria-mediated neurotoxicity and oxidative stress in SH-SY5Y cells. When injected into mice on a subchronic schedule, amitriptyline induced movement deficits in the pole test, which is known to detect nigrostriatal dysfunction. In addition, the number of tyrosine hydroxylase-positive neurons in the substantia nigra pars compacta was reduced in amitriptyline-injected mice. Our results suggest that amitriptyline and desipramine may induce PD-associated neurotoxicity.

Keywords: Parkinson’s disease; amitriptyline; desipramine; neurotoxicity; tricyclic antidepressant.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphate / metabolism
  • Amitriptyline / pharmacology*
  • Amitriptyline / toxicity
  • Animals
  • Antidepressive Agents, Tricyclic / pharmacology*
  • Antioxidants / metabolism
  • Apoptosis / drug effects
  • Cell Line, Tumor
  • Desipramine / pharmacology*
  • Desipramine / toxicity
  • Dopaminergic Neurons / drug effects*
  • Humans
  • Male
  • Mice, Inbred C57BL
  • Mitochondria / drug effects
  • Parkinson Disease / metabolism*
  • Reactive Oxygen Species / metabolism

Substances

  • Antidepressive Agents, Tricyclic
  • Antioxidants
  • Reactive Oxygen Species
  • Amitriptyline
  • Adenosine Triphosphate
  • Desipramine