Cannabinoid-induced lower lip retraction in rats

Psychopharmacology (Berl). 2019 Apr;236(4):1199-1206. doi: 10.1007/s00213-018-5125-z. Epub 2018 Nov 20.

Abstract

Rationale: Lower lip retraction (LLR) in rats has been described as a distinctive effect of 5-HT1A agonists. In the course of evaluating behavioral effects of cannabinoid agonists in rats, LLR effects were evident following injection of several cannabinoid agonists.

Objectives: To pharmacologically characterize cannabinoid-induced LLR in rats.

Methods: Lower lip retraction was scored using a 3-point scale for up to 6 h after injection of the cannabinoid agonists Δ9-tetrahydrocannabinol (Δ9-THC, 1-10 mg/kg), AM7499 (0.01-1.0 mg/kg), or AM2389 (0.003-0.1 mg/kg), or, for comparison, the 5-HT1A agonist 8-OH-DPAT (0.01-0.3 mg/kg). Next, antagonist effects of rimonabant (1-10 mg/kg) and WAY100635 (0.3 mg/kg) on LLR produced by cannabinoid or 5-HT1A agonists were evaluated. Lastly, effects of 8-OH-DPAT were determined following pretreatment with AM2389 (0.003-0.01 mg/kg) or Δ9-THC (1 mg/kg).

Results: All three cannabinoid agonists produced LLR. Effects of AM2389 were attenuated by both rimonabant and WAY100635 whereas effects of 8-OH-DPAT were antagonized by WAY 100635 but not by rimonabant. Pretreatment with 1 mg/kg Δ9-THC or 0.01 mg/kg AM2389 shifted the 8-OH-DPAT dose-effect function for LLR to the left and isobolographic analysis of the data indicates CB1 and 5-HT1A interactions can be supraadditive.

Conclusions: Cannabinoid agonists produce LLR in rats, an effect heretofore ascribed only to activity at 5-HT1A receptors, via CB1 receptor-mediated actions. Co-administration of a cannabinoid agonist and the 5-HT1A agonist 8-OH-DPAT results in a synergistic effect on LLR.

Keywords: 8-OH-DPAT; AM2389; AM7499; Cannabinoid; Lower lip retraction; Δ9-THC.

MeSH terms

  • 8-Hydroxy-2-(di-n-propylamino)tetralin / pharmacology*
  • Animals
  • Benzopyrans / pharmacology
  • Cannabinoid Receptor Agonists / pharmacology*
  • Cannabinoids / pharmacology*
  • Dose-Response Relationship, Drug
  • Dronabinol / pharmacology
  • Female
  • Lip / drug effects*
  • Lip / physiology*
  • Rats
  • Rats, Sprague-Dawley
  • Receptor, Cannabinoid, CB1 / agonists
  • Receptor, Cannabinoid, CB1 / antagonists & inhibitors
  • Receptor, Cannabinoid, CB1 / metabolism
  • Receptor, Serotonin, 5-HT1A / metabolism
  • Serotonin Receptor Agonists / pharmacology*

Substances

  • 3-(1-hexylcyclobut-1-yl)-6a,7,8,9,10,10a-hexahydro-6,6-dimethyl-6H-dibenzo(b,d)pyran-1,9 diol
  • Benzopyrans
  • Cannabinoid Receptor Agonists
  • Cannabinoids
  • Receptor, Cannabinoid, CB1
  • Serotonin Receptor Agonists
  • Receptor, Serotonin, 5-HT1A
  • 8-Hydroxy-2-(di-n-propylamino)tetralin
  • Dronabinol