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The role of estradiol and progesterone in modulating the subjective effects of stimulants in humans

Authors :
Suzette M. Evans
Source :
Experimental and Clinical Psychopharmacology. 15:418-426
Publication Year :
2007
Publisher :
American Psychological Association (APA), 2007.

Abstract

Although stimulant abuse is a growing problem among women, few studies have focused on factors that may be implicated in potential sex differences. Numerous preclinical studies have indicated that female rodents are more sensitive than male rodents to the behavioral effects of stimulants and that the hormone estradiol is involved in these sex differences. In humans, the subjective response to stimulants is greater in the follicular phase (characterized by moderate estradiol levels and minimal progesterone levels) than in the luteal phase (characterized by elevated estradiol levels and elevated progesterone levels). Differences between men and women emerge only when men are compared with women in the luteal phase; the subjective response to stimulants is similar in men and women in the follicular phase. In contrast to rodents, there is minimal evidence that estradiol enhances the subjective response to stimulants in humans. Rather, the hormone progesterone has been shown to attenuate the subjective response to stimulants, particularly in women. Recent preclinical data confirm that progesterone reduces the behavioral response to stimulants. In summary, there is converging evidence from studies in humans that (a) men and women do differ in their subjective response to stimulants; (b) these sex differences are evident when women are in the luteal phase, when progesterone levels are elevated; and (c) progesterone administration attenuates the subjective response to stimulants. Therefore, the menstrual cycle should be addressed in mixed-gender studies. Moreover, the modulatory effects of progesterone on reducing the positive effects of cocaine may have some clinical utility in treating stimulant abusers.

Details

ISSN :
19362293 and 10641297
Volume :
15
Database :
OpenAIRE
Journal :
Experimental and Clinical Psychopharmacology
Accession number :
edsair.doi.dedup.....f03a9c612019658805ef823946b57b56
Full Text :
https://doi.org/10.1037/1064-1297.15.5.418