The D1/D2-like receptor antagonist flupentixol and the D2-like receptor antagonist L-741626 decrease operant responding for nicotine and food and locomotor activity in male and female rats

J Psychopharmacol. 2023 Feb;37(2):216-228. doi: 10.1177/02698811221147141. Epub 2023 Jan 21.

Abstract

Background: The reinforcing properties of nicotine play a critical role in smoking and vaping. There is a need for treatments that decrease the reinforcing properties of nicotine and thereby improve smoking and vaping rates. Dopamine plays a role in the reinforcing properties of nicotine, but little is known about the role of dopamine D2-like receptors in nicotine intake and whether there are sex differences in the effects of dopaminergic drugs on nicotine intake.

Aim: The goal of the present studies was to investigate the effects of the D1/D2-like receptor antagonist flupentixol and the D2-like receptor antagonist L-741626 on nicotine self-administration in male and female rats.

Methods: The effects of flupentixol and L-741626 on operant responding for nicotine and food and locomotor activity in a small open field were investigated.

Results: There were no sex differences in baseline nicotine intake. The D1/D2-like receptor antagonist flupentixol and the D2-like receptor antagonist L-741626 decreased operant responding for nicotine. Blockade of D1/D2-like receptors and blockade of D2-like receptors also decreased operant responding for food and decreased locomotor activity. Flupentixol induced a greater decrease in operant responding for food in males than females. However, in the other tests, there were no sex differences in the effects of the dopamine receptor antagonists.

Conclusions: Blockade of D1/D2-like receptors with flupentixol and D2-like receptors with L-741626 decreases nicotine and food intake in rats of both sexes. These compounds also decrease locomotor activity which might be indicative of a sedative effect.

Keywords: Nicotine; dopamine; dopamine receptors; rats; reward; self-administration.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Conditioning, Operant
  • Dopamine / pharmacology
  • Female
  • Flupenthixol* / pharmacology
  • Locomotion
  • Male
  • Nicotine* / pharmacology
  • Rats
  • Receptors, Dopamine D1
  • Receptors, Dopamine D2

Substances

  • Flupenthixol
  • Nicotine
  • 3-(4-(4-chlorophenyl-4-hydroxypiperidino)methyl)indole
  • Receptors, Dopamine D2
  • Dopamine
  • Receptors, Dopamine D1