Effects of orally-bioavailable short-acting kappa opioid receptor-selective antagonist LY2456302 on nicotine withdrawal in mice

Neuropharmacology. 2015 Oct:97:270-4. doi: 10.1016/j.neuropharm.2015.05.023. Epub 2015 Jun 1.

Abstract

Kappa opioid receptor (KOR) signaling has been implicated in mediating behavioral and biochemical effects associated with drug dependence. The most commonly used KOR antagonists, norbinaltorphimine (norBNI) and (3R)-7-Hydroxy-N{(1S)-1-{[(3R,4R)-4-(3-hydroxyphenyl)-3,4-dimethyl-1-piperidinyl]methyl}-2-methylpropyl}-1,2,3,4-tetrahydro-3-isoquinoline-carboxamide (JDTic), have provided a wealth of information in this area; however, the delayed onset and long-lasting effects of these antagonists complicate experimental design and interpretation of results, and make them less than ideal for clinical studies. Initial studies with the recently developed KOR antagonist, LY2456302, show that the compound is a short acting, high-affinity, selective KOR antagonist with therapeutic potential for mood disorders and ethanol use in animal models, and is well tolerated in humans. The goal of the current study was to evaluate the effectiveness of LY2456302 in alleviating the nicotine withdrawal syndrome in mice. Mice were chronically treated with nicotine for 14 days and physical and affective nicotine withdrawal signs were measured using a spontaneous nicotine withdrawal model and conditioned place aversion (CPA) following pre-treatment with LY2456302, administered orally. Vehicle treated nicotine withdrawn mice displayed significant anxiety-related behavior, somatic signs, hyperalgesia, and CPA. Similar to previous studies with norBNI and JDTic, LY2456302 alleviated the nicotine withdrawal syndrome, as evidenced by decreased expression of nicotine withdrawal induced anxiety-related behavior, somatic signs, and CPA, and increased hotplate latency in nicotine withdrawn mice following pre-treatment. Given the current results, and with its favorable pharmacokinetic and pharmacodynamic profile, LY2456302 may be a useful therapeutic agent for treatment of multiple aspects of the nicotine withdrawal syndrome.

Keywords: Kappa opioid receptor; Kappa opioid receptor antagonist; LY2456302; Nicotine dependence; Nicotine withdrawal.

Publication types

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

MeSH terms

  • Animals
  • Anxiety / drug therapy
  • Anxiety / physiopathology
  • Benzamides / pharmacology*
  • Conditioning, Psychological / drug effects
  • Conditioning, Psychological / physiology
  • Disease Models, Animal
  • Hot Temperature
  • Hyperalgesia / drug therapy
  • Hyperalgesia / physiopathology
  • Male
  • Mice, Inbred ICR
  • Narcotic Antagonists / pharmacology*
  • Nicotine / adverse effects
  • Nicotine / pharmacology
  • Nicotinic Agonists / adverse effects
  • Nicotinic Agonists / pharmacology
  • Pyrrolidines / pharmacology*
  • Receptors, Opioid, kappa / antagonists & inhibitors*
  • Receptors, Opioid, kappa / metabolism
  • Spatial Behavior / drug effects
  • Spatial Behavior / physiology
  • Substance Withdrawal Syndrome / drug therapy*
  • Substance Withdrawal Syndrome / physiopathology
  • Tobacco Use Disorder / drug therapy*
  • Tobacco Use Disorder / physiopathology

Substances

  • Benzamides
  • Narcotic Antagonists
  • Nicotinic Agonists
  • Pyrrolidines
  • Receptors, Opioid, kappa
  • Nicotine
  • Aticaprant