Journal
NEUROPSYCHOPHARMACOLOGY
Volume 25, Issue 6, Pages 881-891Publisher
NATURE PUBLISHING GROUP
DOI: 10.1016/S0893-133X(01)00301-3
Keywords
estrogen; tamoxifen; stress; HPA axis; glucocarticoids
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Funding
- NIMH NIH HHS [MH00427] Funding Source: Medline
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Previous studies have found that female rats are less sensitive than males to hypothalamic-pituitary-adrenal axis feedback inhibition by exogenous glucocorticoid administration. To determine whether estrogen contributes to this sex difference, we examined the effects of the estrogen antagonists tamoxifen and C1628 on the ACTH and corticosterone responses to restraint stress. C1628 increased both the ACTH and corticosterone response to restraint stress, and tamoxifen increased the ACTH response to restraint. Using overiectomized female rats, we also examined the effects of seven days of estradiol and/or progesterone replacement. Low dose estradiol decreased the ACTH but not the corticosterone response to restraint stress while progesterone had no effect on ACTH or corticosterone responses. The combination of estradiol and progesterone also decreased the ACTH response to stress, and the magnitude of the effect did not differ from that found with estradiol treatment alone. These data suggest that in the physiological range estradiol is an important inhibitory factor in the hypothalamic-pituitary-adrenal stress response of females. [Neuropsychopharmacology 25:881-891] (C) 2001 American College of Neuropsychopharmacology. Published by Elsevier Science Inc. All rights reserved.
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