Literature DB >> 3659083

Mice genetically selected for differences in open-field activity after ethanol.

J C Crabbe1, E R Young, C M Deutsch, B R Tam, A Kosobud.   

Abstract

Starting from a population of genetically heterogeneous mice, selective breeding is being used to develop lines differing in sensitivity to ethanol-induced open-field activity. Mice are tested twice for 4 min in an open field. The first test is between min 2-6 after injection of saline. Twenty-four hr later, a similar test is performed after injection of ethanol (1.5 g/kg). Two independent FAST lines are being selected for ethanol-induced increases in activity, and two independent SLOW lines are being selected for ethanol-induced decreases. After four generations of selection, the lines have diverged significantly. These lines should be useful for exploring the neuropharmacological basis for the activating and rewarding properties of ethanol.

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Year:  1987        PMID: 3659083     DOI: 10.1016/0091-3057(87)90371-6

Source DB:  PubMed          Journal:  Pharmacol Biochem Behav        ISSN: 0091-3057            Impact factor:   3.533


  25 in total

1.  Response to selection for ethanol-induced locomotor activation: genetic analyses and selection response characterization.

Authors:  T J Phillips; S Burkhart-Kasch; E S Terdal; J C Crabbe
Journal:  Psychopharmacology (Berl)       Date:  1991       Impact factor: 4.530

2.  Identification of an acute ethanol response quantitative trait locus on mouse chromosome 2.

Authors:  K Demarest; J McCaughran; E Mahjubi; L Cipp; R Hitzemann
Journal:  J Neurosci       Date:  1999-01-15       Impact factor: 6.167

3.  Naloxone does not attenuate the locomotor effects of ethanol in FAST, SLOW, or two heterogeneous stocks of mice.

Authors:  Sarah E Holstein; Raúl Pastor; Paul J Meyer; Tamara J Phillips
Journal:  Psychopharmacology (Berl)       Date:  2005-10-19       Impact factor: 4.530

Review 4.  Selected mouse lines, alcohol and behavior.

Authors:  T J Phillips; D J Feller; J C Crabbe
Journal:  Experientia       Date:  1989-09-15

5.  Intracranial self-stimulation in FAST and SLOW mice: effects of alcohol and cocaine.

Authors:  Eric W Fish; J Elliott Robinson; Michael C Krouse; Clyde W Hodge; Cheryl Reed; Tamara J Phillips; C J Malanga
Journal:  Psychopharmacology (Berl)       Date:  2011-10-07       Impact factor: 4.530

6.  Locomotor responses to benzodiazepines, barbiturates and ethanol in diazepam-sensitive (DS) and -resistant (DR) mice.

Authors:  T J Phillips; E J Gallaher
Journal:  Psychopharmacology (Berl)       Date:  1992       Impact factor: 4.530

Review 7.  Influence of the endogenous opioid system on high alcohol consumption and genetic predisposition to alcoholism.

Authors:  C Gianoulakis
Journal:  J Psychiatry Neurosci       Date:  2001-09       Impact factor: 6.186

8.  Dopamine antagonist effects on locomotor activity in naive and ethanol-treated FAST and SLOW selected lines of mice.

Authors:  E H Shen; J C Crabbe; T J Phillips
Journal:  Psychopharmacology (Berl)       Date:  1995-03       Impact factor: 4.530

Review 9.  Behavioral genetic contributions to the study of addiction-related amphetamine effects.

Authors:  Tamara J Phillips; Helen M Kamens; Jeanna M Wheeler
Journal:  Neurosci Biobehav Rev       Date:  2007-11-29       Impact factor: 8.989

10.  Relationship between ethanol's acute locomotor effects and ethanol self-administration in male Long-Evans rats.

Authors:  Ann M Chappell; Jeff L Weiner
Journal:  Alcohol Clin Exp Res       Date:  2008-09-25       Impact factor: 3.455

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