Alcohol and nicotine interactions: pre-clinical models of dependence

Am J Drug Alcohol Abuse. 2017 Mar;43(2):146-154. doi: 10.1080/00952990.2016.1197232. Epub 2016 Oct 14.

Abstract

While the co-morbidity of alcohol (ethanol) and tobacco (nicotine) dependence is well described, the processes that underpin this strong connection are still under debate. With the increasing popularity of electronic cigarettes (e-cigarettes), it is now becoming more important to look to the neurobiological mechanisms involving alcohol and nicotine interactions to effectively treat a new generation of co-dependent individuals. Researchers have already recognized that the neuropathology produced by the combination of nicotine and ethanol is likely to produce an addictive nature very different to that of either one alone, and are employing a mixture of pre-clinical techniques to establish and investigate every stage in the development of both nicotine and ethanol-seeking behaviors. While it is agreed that multiple pathways orchestrate the complex reward profile of alcohol and nicotine co-addiction, several lines of evidence suggest the convergent site of action is within the mesolimbic dopaminergic system, at neuronal nicotinic acetylcholine receptors (nAChRs). A whole host of strategies are currently being employed to discover and unravel previously unknown or ill understood neurobiological processes in the brain, contributing greatly toward the development of novel pharmacotherapies with the aim of improving patient outcomes. This review intends to shed some light on the most influential and most recent pre-clinical work that is leading the charge in modeling this complicated relationship.

Keywords: Alcohol; addiction; nicotine; nicotinic receptors; pre-clinical.

Publication types

  • Review

MeSH terms

  • Alcoholism / complications
  • Alcoholism / physiopathology*
  • Animals
  • Behavior, Addictive / physiopathology*
  • Brain / physiopathology*
  • Disease Models, Animal
  • Dopaminergic Neurons / physiology
  • Drug Synergism*
  • Humans
  • Receptors, Nicotinic / drug effects
  • Tobacco Use Disorder / complications
  • Tobacco Use Disorder / physiopathology*

Substances

  • Receptors, Nicotinic