Dopamine D₂/₃ occupancy of ziprasidone across a day: a within-subject PET study

Psychopharmacology (Berl). 2013 Jul;228(1):43-51. doi: 10.1007/s00213-013-3012-1. Epub 2013 Feb 17.

Abstract

Rationale: Ziprasidone is an atypical antipsychotic recommended to be administered twice daily.

Objectives: The purpose of this study was to investigate whether occupancy of the dopamine D2/3 receptors by ziprasidone is maintained across a day employing a within subject design.

Methods: Positron emission tomography (PET) scans with [(11)C]-raclopride were performed in 12 patients with schizophrenia while treated with ziprasidone 60 mg twice daily. Each patient completed [(11)C]-raclopride PET scans at 5, 13 and 23 h after the last dose of ziprasidone. Dopamine D2/3 receptor occupancy was estimated with reference to binding potential data of 44 age- and sex-matched control subjects in the caudate, putamen and ventral striatum.

Results: Eleven scans were available at each time point, and the mean occupancies at 5-, 13- and 23-h scans were 66, 39 and 2 % in the putamen; 62, 35 and -6 % in the caudate; and 68, 47 and 11 % in the ventral striatum, respectively. The time-course of receptor occupancy across the regions indicated an occupancy half-life of 8.3 h. The serum level of ziprasidone associated with 50 % D2/3 receptors occupancy was estimated to be 204 nmol/L (84 ng/ml). Prolactin levels were highest at 5-h post-dose and none showed hyperprolactinemia at 23-h scans.

Conclusions: The absence of ziprasidone striatal D2/3 receptor binding 23 h after taking 60 mg under steady-state conditions is consistent with its peripheral half-life. The results support our earlier report that ziprasidone 60 mg administered twice daily appears to be the minimal dose expected to achieve therapeutic central dopamine D2/3 receptor occupancy (i.e. 60 %).

Clinical trials registration: 24-Hour Time Course of Striatal Dopamine D2 Receptor Occupancy of Ziprasidone: A PET Study, www.clinicaltrials.gov/ct2/show/NCT00818298 , NCT00818298.

Publication types

  • Controlled Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Antipsychotic Agents / metabolism*
  • Antipsychotic Agents / pharmacokinetics
  • Antipsychotic Agents / therapeutic use
  • Brain / metabolism
  • Case-Control Studies
  • Dopamine Antagonists / metabolism
  • Dopamine Antagonists / therapeutic use
  • Female
  • Half-Life
  • Humans
  • Male
  • Middle Aged
  • Piperazines / metabolism*
  • Piperazines / pharmacokinetics
  • Piperazines / therapeutic use
  • Positron-Emission Tomography / methods
  • Prolactin / blood
  • Raclopride / metabolism
  • Receptors, Dopamine D2 / metabolism*
  • Receptors, Dopamine D3 / metabolism*
  • Schizophrenia / drug therapy
  • Thiazoles / metabolism*
  • Thiazoles / pharmacokinetics
  • Thiazoles / therapeutic use
  • Time Factors
  • Young Adult

Substances

  • Antipsychotic Agents
  • Dopamine Antagonists
  • Piperazines
  • Receptors, Dopamine D2
  • Receptors, Dopamine D3
  • Thiazoles
  • Raclopride
  • ziprasidone
  • Prolactin

Associated data

  • ClinicalTrials.gov/NCT00818298