Nest building is a novel method for indexing severity of alcohol withdrawal in mice

Behav Brain Res. 2016 Apr 1:302:182-90. doi: 10.1016/j.bbr.2016.01.023. Epub 2016 Jan 12.

Abstract

Withdrawal after chronic ethanol (EtOH) affects body temperature, goal-directed behavior and motor function in mice and increases general central nervous system excitability. Nest-building tests have been used to assay these states but to this point have not been employed as measures of EtOH withdrawal severity. We first refined nest-scoring methods using a genetically heterogeneous stock of mice (HS/Npt). Mice were then made physically dependent following three days of chronic EtOH vapor inhalation to produce average blood EtOH concentrations (BECs) of 1.89 mg/mL. EtOH withdrawal affected the progression of nest building over time when mice were tested 2-4 days after removal from three days of chronic exposure to EtOH. In a separate group of mice, chronic EtOH vapor inhalation (BECs 1.84 mg/mL) suppressed nest building over days 1-2 but not days 2-3 of withdrawal. In a following experiment, EtOH withdrawal dose-dependently slowed recovery of nest building for up to 32 h. Finally, we determined that long-lasting nest-building deficits extend to mice undergoing withdrawal from a high dose (4 g/kg) of acute EtOH. Sex differences for nest building were absent following EtOH exposure. In mice naïve to EtOH treatments, male mice had lower pre-test body temperatures and increased nest scores across a two-day testing period compared to females. These results suggest that nest building can be used to assess chronic and acute EtOH withdrawal severity in mice.

Keywords: Acute; Chronic; Ethanol; Mice; Nest; Withdrawal.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Alcohol-Induced Disorders / blood
  • Alcohol-Induced Disorders / etiology*
  • Alcohol-Induced Disorders / physiopathology*
  • Analysis of Variance
  • Animals
  • Body Temperature / drug effects
  • Central Nervous System Depressants / blood
  • Central Nervous System Depressants / toxicity*
  • Disease Models, Animal
  • Dose-Response Relationship, Drug
  • Drug Administration Routes
  • Ethanol / blood
  • Ethanol / toxicity*
  • Female
  • Male
  • Mice
  • Mice, Inbred Strains
  • Nesting Behavior / drug effects
  • Nesting Behavior / physiology*
  • Substance Withdrawal Syndrome / genetics
  • Substance Withdrawal Syndrome / physiopathology*
  • Time Factors

Substances

  • Central Nervous System Depressants
  • Ethanol