Effects of selective 5-HT1A agonist tandospirone on the rate and rhythmicity of binocular rivalry

Psychopharmacology (Berl). 2008 Jun;198(2):279-86. doi: 10.1007/s00213-008-1139-2. Epub 2008 Apr 12.

Abstract

Rationale: When dissimilar figures are presented to each eye individually, perception alternates spontaneously between each monocular view. This phenomenon, binocular rivalry, has been suggested to depend on serotonergic neural systems.

Objective: To investigate the relationship between binocular rivalry and serotonergic neural systems in more detail, we measured the perceptual alternation rate and rhythmicity of binocular rivalry under the influence of the 5-HT(1A) agonist tandospirone.

Materials and methods: Fifteen healthy volunteers were tested under placebo and 60 mg tandospirone conditions using the single-blind method. The perceptual alternation rate and rhythmicity of binocular rivalry were measured at pre-administration and at 90, 180, and 360 min post-administration.

Results: Compared to placebo, the administration of tandospirone decreased the rate and rhythmicity of perceptual switching significantly at 90 and 180 min post-administration in a manner that is consistent with its pharmacokinetics.

Conclusions: The present results suggest that the 5-HT(1A) neural pathways, mainly located in the mesolimbic system and brainstem, may play a crucial role as an oscillator in perceptual rivalry alternations.

Publication types

  • Randomized Controlled Trial

MeSH terms

  • Adult
  • Female
  • Functional Laterality / drug effects*
  • Humans
  • Isoindoles / pharmacokinetics
  • Isoindoles / pharmacology*
  • Limbic System / drug effects
  • Limbic System / physiology
  • Male
  • Photic Stimulation
  • Piperazines / pharmacokinetics
  • Piperazines / pharmacology*
  • Pyrimidines / pharmacokinetics
  • Pyrimidines / pharmacology*
  • Receptor, Serotonin, 5-HT1A / drug effects*
  • Serotonin Receptor Agonists / pharmacokinetics
  • Serotonin Receptor Agonists / pharmacology*
  • Visual Perception / drug effects*

Substances

  • Isoindoles
  • Piperazines
  • Pyrimidines
  • Serotonin Receptor Agonists
  • Receptor, Serotonin, 5-HT1A
  • tandospirone