The cortical serotonin2 receptors studied with positron-emission tomography and [18F]-setoperone during depressive illness and antidepressant treatment with clomipramine

Biol Psychiatry. 1999 Jan 15;45(2):180-6. doi: 10.1016/s0006-3223(98)00007-9.

Abstract

Background: Changes in serotonin (5-HT)2 receptor densities were reported in depression by postmortem studies and following treatment with tricyclic antidepressants in animal studies. Here, 5-HT2 receptors were studied in vivo in depressed patients.

Methods: Cortical 5-HT2 receptors were investigated prospectively using positron-emission tomography and [18F]-setoperone in 7 depressed patients, before and after at least 3 weeks of clomipramine (CMI), 150 mg daily. They were compared to 7 age-matched controls.

Results: There was no significant difference between the untreated patients and the controls, except in the frontal region, where the [18F]-setoperone specific binding was slightly lower in patients. After CMI treatment, depression scores significantly improved and [18F]-setoperone specific binding decreased in cortical regions, suggesting receptor occupancy and/or receptor regulation, by CMI; however, no clinical score correlated with the 5-HT2 receptor measurements either in the untreated or in the treated conditions.

Conclusions: These data substantiate the view that tricyclic antidepressants such as clomipramine significantly interact with cortical 5-HT2 serotoninergic receptors in actual therapeutic situations.

Publication types

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

MeSH terms

  • Adult
  • Aged
  • Antidepressive Agents / pharmacology
  • Antidepressive Agents / therapeutic use*
  • Binding Sites / drug effects
  • Brain / diagnostic imaging*
  • Clomipramine / pharmacology
  • Clomipramine / therapeutic use*
  • Depressive Disorder / drug therapy*
  • Depressive Disorder / psychology
  • Female
  • Fluorine Radioisotopes* / metabolism
  • Humans
  • Male
  • Middle Aged
  • Pyrimidinones* / metabolism
  • Receptors, Serotonin / metabolism*
  • Tomography, Emission-Computed*

Substances

  • Antidepressive Agents
  • Fluorine Radioisotopes
  • Pyrimidinones
  • Receptors, Serotonin
  • setoperone
  • Clomipramine