Serotonergic function in obsessive-compulsive disorder. Behavioral and neuroendocrine responses to oral m-chlorophenylpiperazine and fenfluramine in patients and healthy volunteers

Arch Gen Psychiatry. 1992 Jan;49(1):21-8. doi: 10.1001/archpsyc.1992.01820010021003.

Abstract

To evaluate serotonergic (5-hydroxytryptamine) function in obsessive-compulsive disorder, behavioral and neuroendocrine responses to m-chlorophenylpiperazine (m-CPP; 0.5 mg/kg orally) and fenfluramine hydrochloride (60 mg orally) were examined in 20 patients and 10 healthy controls under double-blind, placebo-controlled conditions. Following m-CPP, but not fenfluramine or placebo, 55% (11/20) of the patients with obsessive-compulsive disorder experienced a transient exacerbation of obsessive-compulsive disorder. Prolactin response was blunted in patients following m-CPP but not following fenfluramine. Patients with greater behavioral response to m-CPP had smaller prolactin responses. Cortisol response to m-CPP and fenfluramine did not significantly differ between the groups. Behavioral and neuroendocrine responses appeared divergent. This does not suggest simply upregulation or downregulation of 5-hydroxytryptamine receptors, but rather complex mechanisms involving multiple neurotransmitter and neuromodulator systems.

Publication types

  • Clinical Trial
  • Controlled Clinical Trial
  • Randomized Controlled Trial
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Administration, Oral
  • Adolescent
  • Adult
  • Double-Blind Method
  • Down-Regulation / drug effects
  • Female
  • Fenfluramine / pharmacology*
  • Humans
  • Hydrocortisone / blood
  • Male
  • Middle Aged
  • Obsessive-Compulsive Disorder / diagnosis
  • Obsessive-Compulsive Disorder / metabolism
  • Obsessive-Compulsive Disorder / physiopathology*
  • Piperazines / administration & dosage
  • Piperazines / pharmacology*
  • Placebos
  • Prolactin / blood
  • Receptors, Serotonin / drug effects
  • Serotonin / metabolism
  • Serotonin / physiology*
  • Up-Regulation / drug effects

Substances

  • Piperazines
  • Placebos
  • Receptors, Serotonin
  • Fenfluramine
  • Serotonin
  • Prolactin
  • 1-(3-chlorophenyl)piperazine
  • Hydrocortisone