Individual differences in orexin-I receptor modulation of motivation for the opioid remifentanil

Addict Biol. 2017 Mar;22(2):303-317. doi: 10.1111/adb.12323. Epub 2015 Nov 24.

Abstract

Orexin-1 receptors (Ox1Rs) have been implicated in the motivation for drugs of abuse. Here, we utilized a within-session behavioral-economics threshold procedure to screen for individual differences in economic demand for the ultra-short-acting opioid remifentanil and to test whether antagonism of Ox1Rs reduces remifentanil demand. The behavioral-economics procedure revealed robust individual differences in free consumption of remifentanil (Q0 parameter; hedonic set point). Rats with low baseline Q0 (low takers) displayed high demand elasticity (α parameter; reduced responding as drug price increased indicating low motivation for drug), whereas subjects with a higher Q0 (high takers) exhibit low demand elasticity (low α) by continuing to self-administer remifentanil despite increased cost (reflecting higher motivation for drug). In a punished responding paradigm utilizing footshock, subjects that were classified as high takers at baseline withstood twice as much shock as low takers to continue self-administering remifentanil. Interestingly, Ox1R antagonism with SB-334867 reduced Q0 and increased α in low takers but not in high takers. Similarly, the Ox1R antagonist attenuated cue-induced, but not drug-induced, reinstatement of remifentanil seeking in low takers but had no significant effect on reinstatement of drug seeking in high takers. Together, these data reveal a novel role of orexins in demand for remifentanil: Ox1Rs modulate demand in low takers but not in individuals that exhibit addictive-like behaviors (high takers). Finally, the behavioral assays in this study can serve as a novel laboratory model for studying individual differences in opioid use disorders.

Keywords: Addiction; behavioral economics; drug abuse; orexin; remifentanil; self-administration.

MeSH terms

  • Analgesics, Opioid / pharmacology*
  • Animals
  • Bacterial Outer Membrane Proteins
  • Behavior, Animal / drug effects*
  • Benzoxazoles / pharmacology
  • Conditioning, Operant
  • Economics, Behavioral
  • Escherichia coli Proteins
  • Individuality*
  • Lipoproteins
  • Male
  • Motivation / drug effects*
  • Naphthyridines
  • Orexin Receptor Antagonists / pharmacology*
  • Orexin Receptors / drug effects*
  • Orexin Receptors / metabolism
  • Piperidines / pharmacology*
  • Rats
  • Rats, Sprague-Dawley
  • Remifentanil
  • Self Administration
  • Urea / analogs & derivatives
  • Urea / pharmacology

Substances

  • 1-(2-methylbenzoxazol-6-yl)-3-(1,5)naphthyridin-4-yl urea
  • Analgesics, Opioid
  • Bacterial Outer Membrane Proteins
  • Benzoxazoles
  • Escherichia coli Proteins
  • Hcrtr1 protein, rat
  • Lipoproteins
  • Naphthyridines
  • NlpE protein, E coli
  • Orexin Receptor Antagonists
  • Orexin Receptors
  • Piperidines
  • Urea
  • Remifentanil