Ethanol Sensitivity in High Drinking in the Dark Selectively Bred Mice

John C. Crabbe, Lauren C. Kruse, Alexandre M. Colville, Andy J. Cameron, Stephanie E. Spence, Jason P. Schlumbohm, Lawrence C. Huang, Pamela Metten

Research output: Contribution to journalArticlepeer-review

16 Scopus citations

Abstract

Background: Mouse lines are being selectively bred in replicate for high blood ethanol concentrations (BECs) achieved after a short period of ethanol (EtOH) drinking early in the circadian dark phase. High Drinking in the Dark-1 (HDID-1) mice were in selected generation S18, and the replicate HDID-2 line in generation S11. Methods: To determine other traits genetically correlated with high DID, we compared naïve animals from both lines with the unselected, segregating progenitor stock, HS/Npt. Differences between HDID-1 and HS would imply commonality of genetic influences on DID and these traits. Results: HDID-1 mice showed less basal activity, greater EtOH stimulated activity, and greater sensitivity to EtOH-induced foot slips than HS. They showed lesser sensitivity to acute EtOH hypothermia and longer duration loss of righting reflex than HS. HDID-1 and control HS lines did not differ in sensitivity on 2 measures of intoxication, the balance beam and the accelerating rotarod. None of the acute response results could be explained by differences in EtOH metabolism. HDID-2 differed from HS on some, but not all, of the above responses. Conclusions: These results show that some EtOH responses share common genetic control with reaching high BECs after DID, a finding consistent with other data regarding genetic contributions to EtOH responses.

Original languageEnglish (US)
Pages (from-to)1162-1170
Number of pages9
JournalAlcoholism: Clinical and Experimental Research
Volume36
Issue number7
DOIs
StatePublished - Jul 2012
Externally publishedYes

Keywords

  • Activity
  • Ataxia
  • Genetic correlation
  • High Drinking in the Dark Mice
  • Hypothermia
  • Loss of righting reflex
  • Selected mouse lines

ASJC Scopus subject areas

  • Medicine (miscellaneous)
  • Toxicology
  • Psychiatry and Mental health

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