Journal article
Novelty-induced locomotion is positively associated with cocaine ingestion in adolescent rats; anxiety is correlated in adults
Pharmacology, biochemistry and behavior, Vol.91(3), pp.398-408
2009
DOI: 10.1016/j.pbb.2008.08.019
PMCID: PMC2715835
PMID: 18790706
Abstract
The present studies assessed the roles of sex, age, novelty-seeking and plus-maze behavior on cocaine drinking in rats. Cocaine/saccharin solution was available in three daily, 5-hour sessions then a saccharin-only solution was also available in following sessions. In the one-bottle drinking phase, early and late adolescent males, post-natal day 28 (PN28) and PN42, consumed more cocaine/saccharin solution than young adults (PN65), but females did not exhibit significant age differences. Adolescents of both sexes consumed more cocaine/saccharin than adults during choice drinking. Saccharin availability in the two-bottle trials decreased cocaine/saccharin consumption in PN28 and PN65 rats. After a drug-free period, cocaine-stimulated locomotion was lower in cocaine/saccharin drinking than saccharin-only males, indicating tolerance. We tested the hypothesis that individual differences in pre-screened behavioral traits would correlate with cocaine/saccharin consumption in PN28 and PN65 male rats. High locomotor responses to novelty were associated with greater cocaine/saccharin drinking in adults in one-bottle sessions. In the subsequent choice drinking phase, correlations were age-specific. Adolescents with high novelty-induced locomotion and adults that spent less time on open arms of the elevated plus-maze drank more cocaine/saccharin. Thus, behavioral phenotypes correlated with individual differences in cocaine/saccharin consumption in an age-related manner.
Details
- Title: Subtitle
- Novelty-induced locomotion is positively associated with cocaine ingestion in adolescent rats; anxiety is correlated in adults
- Creators
- Q. David WALKER - Department of Pharmacology and Cancer Biology, Duke University Medical Center, Durham, NC 27710, United StatesNicole L SCHRAMM-SAPYTA - Department of Pharmacology and Cancer Biology, Duke University Medical Center, Durham, NC 27710, United StatesJoseph M CASTER - Department of Pharmacology and Cancer Biology, Duke University Medical Center, Durham, NC 27710, United StatesSamuel T WALLER - Department of Pharmacology and Cancer Biology, Duke University Medical Center, Durham, NC 27710, United StatesMatthew P BROOKS - Department of Pharmacology and Cancer Biology, Duke University Medical Center, Durham, NC 27710, United StatesCynthia M KUHN - Department of Pharmacology and Cancer Biology, Duke University Medical Center, Durham, NC 27710, United States
- Resource Type
- Journal article
- Publication Details
- Pharmacology, biochemistry and behavior, Vol.91(3), pp.398-408
- DOI
- 10.1016/j.pbb.2008.08.019
- PMID
- 18790706
- PMCID
- PMC2715835
- NLM abbreviation
- Pharmacol Biochem Behav
- ISSN
- 0091-3057
- eISSN
- 1873-5177
- Publisher
- Elsevier; Kidlington
- Language
- English
- Date published
- 2009
- Academic Unit
- Radiation Oncology
- Record Identifier
- 9984046910302771
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