Intragastric self-infusion of ethanol in high- and low-drinking mouse genotypes after passive ethanol exposure

Genes Brain Behav. 2011 Apr;10(3):264-75. doi: 10.1111/j.1601-183X.2010.00664.x. Epub 2010 Dec 16.

Abstract

Two experiments examined the effect of 5 days of passive exposure to ethanol (or water) on later self-infusion of ethanol or water via surgically implanted intragastric (IG) catheters in mouse genotypes previously shown to drink high (C57BL/6J, HAP2) or low (DBA/2J, LAP2) amounts of ethanol in home-cage continuous-access two-bottle choice procedures. Intragastric ethanol self-infusion was affected by both genotype and a history of passive ethanol exposure, with greater intakes in the high-drinking genotypes and in groups that received passive exposure to ethanol. Passive ethanol exposure also increased preference for the flavor that signaled ethanol infusion (S+), eliminating genetic differences in this measure. The increases in ethanol intake and S+ preference induced by ethanol exposure might have been mediated jointly by development of tolerance to aversive post-absorptive ethanol effects and negative reinforcement because of alleviation of withdrawal. Bout analyses indicated that ethanol exposure increased ethanol self-infusion by increasing the total number of daily bouts rather than by increasing bout size. These analyses also showed that DBA/2J mice infused larger ethanol bouts and a greater percentage of their total intakes in large bouts than C57BL/6J mice. Overall, these studies suggest that the IG self-infusion procedure is a potentially useful new tool for studying genetic and environmental influences on excessive ethanol intake and preference in mice.

Publication types

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

MeSH terms

  • Administration, Mucosal
  • Alcohol Drinking / genetics*
  • Alcohol-Induced Disorders, Nervous System / genetics*
  • Alcoholism / genetics*
  • Animals
  • Central Nervous System Depressants / metabolism
  • Central Nervous System Depressants / pharmacology
  • Disease Models, Animal
  • Drug Administration Routes
  • Ethanol / metabolism
  • Ethanol / pharmacology*
  • Female
  • Genetic Predisposition to Disease / genetics*
  • Genotype
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Inbred DBA
  • Self Administration / methods
  • Species Specificity

Substances

  • Central Nervous System Depressants
  • Ethanol