Combined treatment with a selective PDE10A inhibitor TAK-063 and either haloperidol or olanzapine at subeffective doses produces potent antipsychotic-like effects without affecting plasma prolactin levels and cataleptic responses in rodents

Pharmacol Res Perspect. 2018 Feb;6(1):e00372. doi: 10.1002/prp2.372.

Abstract

Activation of indirect pathway medium spiny neurons (MSNs) via promotion of cAMP production is the principal mechanism of action of current antipsychotics with dopamine D2 receptor antagonism. TAK-063 [1-[2-fluoro-4-(1H-pyrazol-1-yl)phenyl]-5-methoxy-3-(1-phenyl-1H-pyrazol-5-yl)pyridazin-4(1H)-one] is a novel phosphodiesterase 10A inhibitor that activates both direct and indirect pathway MSNs through increasing both cAMP and cGMP levels by inhibition of their degradation. The activation of indirect pathway MSNs through the distinct mechanism of action of these drugs raises the possibility of augmented pharmacological effects by combination therapy. In this study, we evaluated the potential of combination therapy with TAK-063 and current antipsychotics, such as haloperidol or olanzapine after oral administration. Combined treatment with TAK-063 and either haloperidol or olanzapine produced a significant increase in phosphorylation of glutamate receptor subunit 1 in the rat striatum. An electrophysiological study using rat corticostriatal slices showed that TAK-063 enhanced N-methyl-D -aspartic acid receptor-mediated synaptic responses in both direct and indirect pathway MSNs to a similar extent. Further evaluation using pathway-specific markers revealed that coadministration of TAK-063 with haloperidol or olanzapine additively activated the indirect pathway, but not the direct pathway. Combined treatment with TAK-063 and either haloperidol or olanzapine at subeffective doses produced significant effects on methamphetamine- or MK-801-induced hyperactivity in rats and MK-801-induced deficits in prepulse inhibition in mice. TAK-063 at 0.1 mg/kg did not affect plasma prolactin levels and cataleptic response from antipsychotics in rats. Thus, TAK-063 may produce augmented antipsychotic-like activities in combination with antipsychotics without effects on plasma prolactin levels and cataleptic responses in rodents.

Keywords: TAK-063; antipsychotics; medium spiny neuron; phosphodiesterase 10A; schizophrenia.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Administration, Oral
  • Akathisia, Drug-Induced / blood
  • Akathisia, Drug-Induced / drug therapy*
  • Akathisia, Drug-Induced / etiology
  • Akathisia, Drug-Induced / physiopathology
  • Animals
  • Antipsychotic Agents / pharmacology*
  • Antipsychotic Agents / therapeutic use
  • Benzodiazepines / pharmacology
  • Benzodiazepines / therapeutic use
  • Catalepsy / blood
  • Catalepsy / chemically induced
  • Corpus Striatum / drug effects
  • Corpus Striatum / physiopathology
  • Dendritic Spines / drug effects
  • Dendritic Spines / physiology
  • Disease Models, Animal
  • Dopamine Antagonists / pharmacology*
  • Dopamine Antagonists / therapeutic use
  • Drug Synergism
  • Drug Therapy, Combination / methods
  • Haloperidol / pharmacology
  • Haloperidol / therapeutic use
  • Humans
  • Male
  • Methamphetamine / toxicity
  • Mice
  • Mice, Inbred ICR
  • Neurons / cytology
  • Neurons / drug effects
  • Neurons / physiology
  • Olanzapine
  • Phosphodiesterase Inhibitors / pharmacology*
  • Phosphodiesterase Inhibitors / therapeutic use
  • Prolactin / blood
  • Pyrazoles / pharmacology
  • Pyrazoles / therapeutic use
  • Pyridazines / pharmacology
  • Pyridazines / therapeutic use
  • Rats
  • Rats, Sprague-Dawley
  • Synaptic Potentials / drug effects
  • Treatment Outcome

Substances

  • 1-(2-fluoro-4-(1H-pyrazol-1-yl)phenyl)-5-methoxy-3-(1-phenyl-1H-pyrazol-5-yl)pyridazin-4(1H)-one
  • Antipsychotic Agents
  • Dopamine Antagonists
  • Phosphodiesterase Inhibitors
  • Pyrazoles
  • Pyridazines
  • Benzodiazepines
  • Methamphetamine
  • Prolactin
  • Haloperidol
  • Olanzapine