Effects of Atomoxetine on Motor and Cognitive Behaviors and Brain Electrophysiological Activity of Dopamine Transporter Knockout Rats

Biomolecules. 2022 Oct 14;12(10):1484. doi: 10.3390/biom12101484.

Abstract

Changes in dopaminergic and noradrenergic transmission are considered to be the underlying cause of attention deficit and hyperactivity disorder (ADHD). Atomoxetine (ATX) is a selective norepinephrine transporter (NET) inhibitor that is currently used for ADHD treatment. In this study, we aimed to evaluate the effect of atomoxetine on the behavior and brain activity of dopamine transporter knockout (DAT-KO) rats, which are characterized by an ADHD-like behavioral phenotype. Prepulse inhibition (PPI) was assessed in DAT-KO and wild type rats after saline and ATX injections, as well as behavioral parameters in the Hebb-Williams maze and power spectra and coherence of electrophysiological activity. DAT-KO rats demonstrated a pronounced behavioral and electrophysiological phenotype, characterized by hyperactivity, increased number of errors in the maze, repetitive behaviors and disrupted PPI, changes in cortical and striatal power spectra and interareal coherence. Atomoxetine significantly improved PPI and decreased repetitive behaviors in DAT-KO rats and influenced behavior of wild-type rats. ATX also led to significant changes in power spectra and coherence of DAT-KO and wild type rats. Assessment of noradrenergic modulation effects in DAT-KO provides insight into the intricate interplay of monoaminergic systems, although further research is still required to fully understand the complexity of this interaction.

Keywords: ADHD; atomoxetine; coherence; dopamine; dopamine transporter knockout (DAT-KO) rats; norepinephrine transporter (NET); power spectra; prepulse inhibition.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Atomoxetine Hydrochloride / pharmacology
  • Cognition
  • Corpus Striatum
  • Dopamine Plasma Membrane Transport Proteins* / genetics
  • Dopamine Plasma Membrane Transport Proteins* / metabolism
  • Norepinephrine / pharmacology
  • Norepinephrine Plasma Membrane Transport Proteins* / genetics
  • Norepinephrine Plasma Membrane Transport Proteins* / metabolism
  • Rats

Substances

  • Atomoxetine Hydrochloride
  • Dopamine Plasma Membrane Transport Proteins
  • Norepinephrine Plasma Membrane Transport Proteins
  • Norepinephrine

Grants and funding

This work was supported by the Russian Science Foundation grant number 21-75-20069. Z.F. and R.G. were supported by the project ID: 93018770 of the St. Petersburg State University, St. Petersburg, Russia.