Genetic variation in heroin-induced changes in behaviour: Effects of B6 strain dose on conditioned reward and locomotor sensitization in 129-B6 hybrid mice

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Abstract

Substantial interindividual variability exists in the propensity to develop opiate addiction. Genetic variation in opiate reward may contribute to this variability. A large body of evidence indicates genetic variation in mice for several effects of opiate drugs. The present study examined heroin-induced place conditioning and locomotor sensitization in the two strains of mice employed most frequently in the generation of transgenic animals, C57BL/6J (B6) and 129X1/sVJ (129), as well as in groups of B6-129 hybrid mice, differing in their amount of B6 genetic background. Four pairings of 100 μg/kg of heroin elicited robust place conditioning and locomotor sensitization in B6 controls and in N10 congenic B6-129 hybrid mice. In comparison, the identical treatment produced no locomotor sensitization and induced place aversion in 129 controls. No heroin-induced changes in the behaviour of N3 congenic B6-129 hybrid mice or F5-8 non-congenic B6-129 hybrid mice were observed. The expression of place conditioning was not facilitated in any group by the administration of a heroin-priming injection prior to testing. These data indicate that genetic variation exists in mice for the rewarding and locomotor-sensitizing effects of heroin and that the capacity of heroin to induce conditioned reward and locomotor sensitization can be modulated in a B6 strain dose-dependent manner in B6-129 hybrid mice. Thus, strain differences in heroin responsiveness should be considered when examining transgenic lines on B6-129 backgrounds for opiate-induced changes in behaviour that may be relevant for addiction. Copyright © Blackwell Munksgaard 2004.

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Szumlinski, K. K., Lominac, K. D., Frys, K. A., & Middaugh, L. D. (2005). Genetic variation in heroin-induced changes in behaviour: Effects of B6 strain dose on conditioned reward and locomotor sensitization in 129-B6 hybrid mice. Genes, Brain and Behavior, 4(5), 324–336. https://doi.org/10.1111/j.1601-183X.2004.00111.x

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