Antagonism of the serotonin (5-HT)-2 receptor and insulin sensitivity: implications for atypical antipsychotics

Psychosom Med. 2005 Sep-Oct;67(5):748-51. doi: 10.1097/01.psy.0000174994.91245.34.

Abstract

Objective: Both conventional and second-generation antipsychotics have been associated with an increased risk for impaired glucose tolerance and diabetes mellitus. Though this has been largely attributed to weight gain, there may also be a direct, receptor-mediated effect of antipsychotics on glucose tolerance. We tested the hypothesis that antagonism of the serotonin (5-HT)-2 receptor impairs insulin sensitivity.

Methods: Ten healthy male volunteers were included in a double-blind, placebo-controlled crossover study of a single dose of 40 mg of the 5-HT2 antagonist ketanserin versus placebo. Insulin sensitivity was measured by means of the euglycemic-hyperinsulinemic clamp technique. Subjects were treated with the alpha-1 adrenergic antagonist phenoxybenzamine in both parts of the study to control for ketanserin's effects at the level of this receptor.

Results: Compared with the placebo condition, subjects showed a significantly decreased insulin sensitivity after ketanserin (placebo: 9.4 +/- 3.6 mg/kg/min; ketanserin: 7.7 +/- 2.1 mg/kg/min; p = .047).

Conclusion: The selective 5-HT2 antagonist ketanserin impaired insulin sensitivity. This effect was possibly mediated by suppression of 5-HT(2A) receptor mediated glucose uptake in skeletal muscle.

Publication types

  • Comparative Study
  • Randomized Controlled Trial

MeSH terms

  • Adult
  • Antipsychotic Agents / adverse effects*
  • Blood Glucose / drug effects
  • Blood Glucose / metabolism
  • Blood Pressure / physiology
  • Body Mass Index
  • Diabetes Mellitus, Type 2 / blood
  • Diabetes Mellitus, Type 2 / chemically induced*
  • Diabetes Mellitus, Type 2 / metabolism
  • Double-Blind Method
  • Glucose / metabolism*
  • Glucose Clamp Technique
  • Glucose Tolerance Test
  • Glucose Transport Proteins, Facilitative / drug effects
  • Glucose Transport Proteins, Facilitative / metabolism
  • Humans
  • Insulin / blood
  • Insulin / metabolism*
  • Insulin Resistance
  • Ketanserin / pharmacology*
  • Male
  • Muscle, Skeletal / metabolism
  • Placebos
  • Risk Factors
  • Serotonin 5-HT2 Receptor Antagonists*
  • Serotonin Antagonists / pharmacology*

Substances

  • Antipsychotic Agents
  • Blood Glucose
  • Glucose Transport Proteins, Facilitative
  • Insulin
  • Placebos
  • Serotonin 5-HT2 Receptor Antagonists
  • Serotonin Antagonists
  • Ketanserin
  • Glucose