Literature DB >> 15555492

Gonadal hormones provide the biological basis for sex differences in behavioral responses to cocaine.

Eugene D Festa1, Vanya Quinones-Jenab.   

Abstract

Both clinical and rodent studies show sexually dimorphic patterns in the behavioral response to cocaine in all phases of the addiction process (induction, maintenance, and relapse). Clinical and rodent studies also indicate that hormonal fluctuations during the menstrual/estrous cycle modulate cocaine-induced subjective effects in women and locomotor activity in female rats. Evidence suggests that gonadal hormones underlie these observed differences and could be the biological basis of sex-specific differences in cocaine addiction. To study the effects of gonadal hormones on cocaine-induced activity, two approaches have been used. First, studies have examined the role of endogenous hormones through gonadectomy (GDX) and side-by-side comparisons with intact rats. Second, the individual contributions of testosterone, progesterone, and estrogen have been determined by hormone replacement in GDX rats. In this review, we discuss gonadal hormones as the biological basis for the behavioral responses to cocaine, and the clinical implications of these findings.

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Year:  2004        PMID: 15555492     DOI: 10.1016/j.yhbeh.2004.04.009

Source DB:  PubMed          Journal:  Horm Behav        ISSN: 0018-506X            Impact factor:   3.587


  54 in total

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5.  Low doses of cocaine decrease, and high doses increase, anxiety-like behavior and brain progestogen levels among intact rats.

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Journal:  Horm Behav       Date:  2010-02-19       Impact factor: 3.587

6.  Effects of RU 486 and tamoxifen on cocaine-induced behavioral and endocrinologic activations in male and female Fischer rats.

Authors:  Hui-Bing Katie Wu; Tipyamol Niyomchai; Eugene Festa; AnaChristina E Minerly; Karen Weierstall; Deirtra Hunter; Weilun Sun; Jan Weiner; Shirzad Jenab; Vanya Quinones-Jenab
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Journal:  Nicotine Tob Res       Date:  2015-04       Impact factor: 4.244

9.  Cocaine is pharmacologically active in the nonhuman primate fetal brain.

Authors:  Helene Benveniste; Joanna S Fowler; William D Rooney; Bruce A Scharf; W Walter Backus; Igor Izrailtyan; Gitte M Knudsen; Steen G Hasselbalch; Nora D Volkow
Journal:  Proc Natl Acad Sci U S A       Date:  2010-01-04       Impact factor: 11.205

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Journal:  Behav Neurosci       Date:  2015-12-14       Impact factor: 1.912

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