Yohimbine produces antinociception in the formalin test in rats: involvement of serotonin(1A) receptors

Psychopharmacology (Berl). 2000 Mar;149(1):93-7. doi: 10.1007/s002139900343.

Abstract

Rationale: Previous studies have suggested that the alpha2-adrenergic receptor antagonist yohimbine produced antinociceptive effects in the formalin test in rats. However, yohimbine is also an agonist at serotonin (5-HT)1A receptors, suggesting the possibility that the antinociceptive effects of yohimbine might be mediated via these receptors.

Objective: The purpose of the present studies was to evaluate the potential role of 5-HT(1A) receptors in mediating the antinociceptive effects of yohimbine.

Methods: The antinociceptive effects of yohimbine were evaluated using the formalin test in rats.

Results: Yohimbine (2.5-10 mg/kg s.c.) produced dose-related antinociception during both phase I and phase II of the formalin test, and was approximately equipotent and equiefficacious to morphine. The selective 5-HT(1A) receptor antagonist WAY 100,635 (0.03-3.0 mg/kg s.c.) produced a partial reversal of yohimbine. In comparison, the selective 5-HT(1A) receptor agonist (+/-)8-hydroxy-dipropylaminotetralin HBr (8OH-DPAT; 1.0 mg/kg s.c.) also produced a dose-related antinociception in the formalin test, although 8OH-DPAT was completely reversed by WAY 100,635 (3.0 mg/kg s.c.). The antinociceptive effects of yohimbine were not antagonized by the 5-HT(1B/1D) antagonist GR 127935 (1.0 mg/kg and 3.0 mg/kg s.c.), the 5-HT2 antagonist LY53857 (1.0 mg/kg s.c.), or the 5-HT3 antagonist zatosetron (3.0 mg/kg s.c.).

Conclusions: The present results demonstrate that yohimbine produces a dose-related antinociception in the formalin test in rats which is mediated in part by the agonistic actions at 5-HT(1A) receptors.

MeSH terms

  • 8-Hydroxy-2-(di-n-propylamino)tetralin / pharmacology
  • Adrenergic alpha-Antagonists / pharmacology*
  • Animals
  • Benzofurans / pharmacology
  • Bridged Bicyclo Compounds, Heterocyclic / pharmacology
  • Dose-Response Relationship, Drug
  • Ergolines / pharmacology
  • Formaldehyde
  • Male
  • Nociceptors / drug effects*
  • Oxadiazoles / pharmacology
  • Pain / chemically induced
  • Pain / prevention & control*
  • Pain Measurement
  • Piperazines / pharmacology
  • Pyridines / pharmacology
  • Rats
  • Rats, Sprague-Dawley
  • Receptor, Serotonin, 5-HT1D
  • Receptors, Serotonin / drug effects
  • Receptors, Serotonin / physiology
  • Receptors, Serotonin, 5-HT1
  • Serotonin Antagonists / pharmacology
  • Serotonin Receptor Agonists / pharmacology
  • Time Factors
  • Yohimbine / pharmacology*

Substances

  • Adrenergic alpha-Antagonists
  • Benzofurans
  • Bridged Bicyclo Compounds, Heterocyclic
  • Ergolines
  • Oxadiazoles
  • Piperazines
  • Pyridines
  • Receptor, Serotonin, 5-HT1D
  • Receptors, Serotonin
  • Receptors, Serotonin, 5-HT1
  • Serotonin Antagonists
  • Serotonin Receptor Agonists
  • Formaldehyde
  • GR 127935
  • Yohimbine
  • N-(2-(4-(2-methoxyphenyl)-1-piperazinyl)ethyl)-N-(2-pyridinyl)cyclohexanecarboxamide
  • 8-Hydroxy-2-(di-n-propylamino)tetralin
  • zatosetron
  • LY 53857