The Journal of Neuroscience, November 15, 2001, 21(22):9077-9081
Mouse Strain Differences in Opiate Reward Learning Are Explained
by Differences in Anxiety, Not Reward or Learning
Colleen L.
Dockstader and
Derek
van der Kooy
Department of Anatomy and Cell Biology, University of Toronto,
Toronto, Ontario, M5S 1A8 Canada
Gene-targeting techniques to produce null mutations provide a
powerful method for evaluating the contribution of particular candidate
genes involved in motivation. The embryonic stem cell lines in
which homologous recombination is undertaken are derived from 129 mice,
but because of the impoverished performance of 129 mice on a number of
behavioral tasks, mice chimeric for the mutation are often bred with a
C57BL/6 mouse strain. Thus, an examination of both parental strains is
important in the study of the knock-out mice. Although the C57BL/6
behavioral phenotype is well documented, details of the 129 phenotype
have not been the focus of study until recently. We investigated
opiate motivation in both 129/SvJ and C57BL/6J mouse strains to
determine whether, and under what circumstances, the 129/SvJ mouse
exhibited motivated behavior toward opiates. 129/SvJ mice required both
drug and contextual cues to demonstrate morphine conditioned place
preferences on test day, whereas C57BL/6J mice required only contextual
cues to express opiate place conditioning. Pentobarbital and diazepam but not saline, cocaine, or naloxone could substitute for morphine on
test day in 129/SvJ mice, demonstrating that morphine indeed has
rewarding motivational valence in the 129/SvJ mouse strain. This
critical, interoceptive cue in 129/SvJ mice on test day may be the
anxiolytic properties of the effective drugs. Therefore, some deficits
observed in 129 mice and mice harboring this genetic background may be
attributed to high levels of anxiety during the retrieval period rather
than to sensory, learning, or motivational deficits.
Key words:
129/SvJ; C57BL6/J; strain differences; knock-out mice; anxiety; opiates
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