Impact of Sex and Gonadal Hormones on Cocaine and Food Reinforcement Paradigms - PubMed (original) (raw)
Impact of Sex and Gonadal Hormones on Cocaine and Food Reinforcement Paradigms
Kerry A Kerstetter et al. J Addict Res Ther. 2011.
Abstract
Men and women express sexually dimorphic patterns of cocaine abuse, such that women progress faster from initially trying cocaine to becoming dependent upon the drug and display a greater incidence of relapse. Sex differences in response to cocaine are also seen in the laboratory in both humans and animal models. In this review, animal models of cocaine abuse that have reported sex differences in appetitive reinforcement are discussed. In both human and animal studies, sex differences in the subjective and behavioral effects of cocaine are often related to the female reproductive cycle and ovarian hormones. As a comparison, food reinforcement studies have shown the opposite profile of sex differences and the impact of sex steroids on food intake and response rate. In contrast, limited attention has been given to "choice" models in rodents of either sex, however, our recent studies have indicated a role of sex and estrogen in cocaine choice over food with intact females, and OVX females treated with estrogen, choosing cocaine significantly more than males. Interestingly, estrous cycle phase does not seem to impact cocaine choice as it does response rate in single-reinforcer studies, suggesting that genomic rather than neurosteroid effects of estrogen modulate sex differences in this model. Future studies should more fully explore the impact of sex hormones on concurrent reinforcement and discrete choice models of addiction.
Figures
Figure 1
Estrogen mediation of high female choice for cocaine over food reinforcement. Males and females (intact or ovariectomized, OVX) are trained to press separate levers for cocaine IV and food reinforcement on alternating sessions under a FR1 schedule of reinforcement (with 20 s time-out) and then are examined for cocaine choice during discrete trials with 25 trials per session [see for details]. (A). Females have higher cocaine choice than do males at 0.4 and 1.0 mg/kg IV cocaine reinforcement; cocaine dose increased cocaine choice in both sexes. (B). OVX abolishes and estrogen replacement (5 μg per day; EB) restores high cocaine (1.0 mg/kg, i.v) choice in females. (C). Estrous cycle stage is not associated with changes in cocaine choice in females. *p < 0.05 versus (intact) females.
References
- Westermeyer J, Kopka S, Nugent S. Course and severity of substance abuse among patients with comorbid major depression. Am J Addict. 1997;6:284–292. - PubMed
- McCance-Katz EF, Carroll KM, Rounsaville BJ. Gender differences in treatment-seeking cocaine abusers--implications for treatment and prognosis. Am J Addict. 1999;8:300–311. - PubMed
- Kosten TA, Gawin FH, Kosten TR, Rounsaville BJ. Gender differences in cocaine use and treatment response. J Subst Abuse Treat. 1993;10:63–66. - PubMed
- ong CJ, Badger GJ, Sigmon SC, Higgins ST. Examining possible gender differences among cocaine-dependent outpatients. Exp Clin Psychopharmacol. 2002;10:316–323. - PubMed
- Back SE, Brady KT, Jackson JL, Salstrom S, Zinzow H. Gender differences in stress reactivity among cocaine-dependent individuals. Psychopharmacology (Berl) 2005;180:169–176. - PubMed
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