Document Detail


Sex differences in selecting between food and cocaine reinforcement are mediated by estrogen.
MedLine Citation:
PMID:  22871910     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Cocaine-dependent women, relative to their male counterparts, report shorter cocaine-free periods and report transiting faster from first use to entering treatment for addiction. Similarly, preclinical studies indicate that female rats, particularly those in the estrus phase of their reproductive cycle, show increased operant responding for cocaine under a wide variety of schedules. Making maladaptive choices is a component of drug dependence, and concurrent reinforcement schedules that examine cocaine choice offers an animal model of the conditions of human drug use; therefore, the examination of sex differences in decision-making may be critical to understanding why women display a more severe profile of cocaine addiction than men. Accordingly, we assessed sex and estrous cycle differences in choice between food (45 mg grain pellets) and intravenous cocaine (0.4 or 1.0 mg/kg per infusion) reinforcement in male, female (freely cycling), and ovariectomized (OVX) females treated with either estrogen benzoate (EB; 5 μg per day) or vehicle. At both cocaine doses, intact female rats choose cocaine over food significantly more than male rats. However, the estrous cycle did not impact the level of cocaine choice in intact females. Nevertheless, OVX females treated with vehicle exhibited a substantially lower cocaine choice compared with those receiving daily EB or to intact females. These results demonstrate that intact females have a greater preference for cocaine over food compared with males. Furthermore, this higher preference is estrogen-dependent, but does not vary across the female reproductive cycle, suggesting that ovarian hormones regulate cocaine choice. The present findings indicate that there is a biological predisposition for females to forgo food reinforcement to obtain cocaine reinforcement, which may substantially contribute to women experiencing a more severe profile of cocaine addiction than men.
Authors:
Kerry A Kerstetter; Maya A Ballis; Stevie Duffin-Lutgen; Amanda E Carr; Alexandra M Behrens; Tod E Kippin
Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't     Date:  2012-08-08
Journal Detail:
Title:  Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology     Volume:  37     ISSN:  1740-634X     ISO Abbreviation:  Neuropsychopharmacology     Publication Date:  2012 Nov 
Date Detail:
Created Date:  2012-10-16     Completed Date:  2013-03-22     Revised Date:  2013-11-06    
Medline Journal Info:
Nlm Unique ID:  8904907     Medline TA:  Neuropsychopharmacology     Country:  England    
Other Details:
Languages:  eng     Pagination:  2605-14     Citation Subset:  IM    
Affiliation:
Department of Psychological and Brain Sciences, University of California, Santa Barbara, CA 98101, USA. kerry.kerstetter@seattlechildrens.org
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Analysis of Variance
Animals
Choice Behavior / drug effects,  physiology
Cocaine / pharmacology*
Conditioning, Operant / drug effects*
Data Interpretation, Statistical
Estrogens / pharmacology,  physiology*
Estrous Cycle / physiology
Female
Food*
Male
Ovariectomy
Rats
Rats, Sprague-Dawley
Reinforcement (Psychology)*
Sex Characteristics
Grant Support
ID/Acronym/Agency:
DA027115/DA/NIDA NIH HHS; DA027525/DA/NIDA NIH HHS
Chemical
Reg. No./Substance:
0/Estrogens; 50-36-2/Cocaine
Comments/Corrections

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  A fMRI Study of Prefrontal Cortical Function in Subcortical Ischemic Vascular Cognitive Impairment.
Next Document:  Seizure susceptibility and epileptogenesis in a rat model of epilepsy and depression co-morbidity.