Voluntary consumption of morphine in 15 inbred mouse strains
- PMID: 7871041
- DOI: 10.1007/BF02244932
Voluntary consumption of morphine in 15 inbred mouse strains
Abstract
To determine genetic differences in voluntary morphine consumption, 15 commonly used inbred strains of mice were given ad libitum two-bottle choice between saccharin alone or saccharin/morphine in one bottle and water in the other bottle. Subsequently, the saccharin was gradually reduced to zero, leaving only morphine. Independent groups of mice of the same strains were exposed to quinine in a parallel manner to control for the bitter alkaloid taste of morphine. Of the 15 strains, the C57BL/6J strain showed the highest consumption of morphine, both with or without saccharin and greatest consumption of morphine relative to quinine; it also showed only a slight decline in fluid consumption when morphine was added to the saccharin bottle. In marked contrast, the SWR/J strain showed the least consumption of morphine by the same criteria, followed closely by the AKR/J, CE/J, DBA/2J and SJL/J strains. The strain differences for all the morphine drinking measures exceeded an order of magnitude. Strain-specific voluntary morphine/saccharin consumption was not significantly correlated with saccharin consumption alone, but was highly correlated with morphine consumption alone. The results show that these behaviors are under an unusually large degree of genetic determination, and some of the largest strain differences remained essentially the same regardless of whether saccharin was present, or whether quinine was used as a control tastant.
Similar articles
-
Voluntary consumption of ethanol in 15 inbred mouse strains.Psychopharmacology (Berl). 1993;112(4):503-10. doi: 10.1007/BF02244901. Psychopharmacology (Berl). 1993. PMID: 7871064
-
Physical dependence induced by the voluntary consumption of morphine in inbred mice.Pharmacol Biochem Behav. 1990 Feb;35(2):311-5. doi: 10.1016/0091-3057(90)90161-a. Pharmacol Biochem Behav. 1990. PMID: 2320638
-
Fine mapping of a major QTL influencing morphine preference in C57BL/6 and DBA/2 mice using congenic strains.Neuropsychopharmacology. 2008 Nov;33(12):2801-9. doi: 10.1038/npp.2008.14. Epub 2008 Feb 20. Neuropsychopharmacology. 2008. PMID: 18288093
-
Contributions of taste factors and gender to opioid preference in C57BL and DBA mice.Psychopharmacology (Berl). 1988;95(2):237-44. doi: 10.1007/BF00174516. Psychopharmacology (Berl). 1988. PMID: 3137604
-
Chorda tympani responses in two inbred strains of mice with different taste preferences.Physiol Behav. 1999 Aug;67(2):287-97. doi: 10.1016/s0031-9384(99)00071-2. Physiol Behav. 1999. PMID: 10477061 Review.
Cited by
-
Behavioral effects of SGK1 knockout in VTA and dopamine neurons.Sci Rep. 2020 Sep 8;10(1):14751. doi: 10.1038/s41598-020-71681-9. Sci Rep. 2020. PMID: 32901079 Free PMC article.
-
Relative expression of mRNA for the somatostatin receptors in the caudate putamen of C57BL/6J and 129P3/J mice: strain and heroin effects.Brain Res. 2010 Jul 23;1345:206-12. doi: 10.1016/j.brainres.2010.05.025. Epub 2010 May 15. Brain Res. 2010. PMID: 20478275 Free PMC article.
-
Neuroimaging of opioid exposure: a review of preclinical animal models to inform addiction research.Psychopharmacology (Berl). 2023 Dec;240(12):2459-2482. doi: 10.1007/s00213-023-06477-6. Epub 2023 Oct 19. Psychopharmacology (Berl). 2023. PMID: 37857897 Review.
-
The role of endogenous dynorphin in ethanol-induced state-dependent CPP.Behav Brain Res. 2012 Feb 1;227(1):58-63. doi: 10.1016/j.bbr.2011.10.035. Epub 2011 Oct 29. Behav Brain Res. 2012. PMID: 22074899 Free PMC article.
-
The abundance of cis-acting loci leading to differential allele expression in F1 mice and their relationship to loci harboring genes affecting complex traits.BMC Genomics. 2016 Aug 11;17(1):620. doi: 10.1186/s12864-016-2922-9. BMC Genomics. 2016. PMID: 27515598 Free PMC article.
References
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Molecular Biology Databases