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Ovarian and Adrenal Contribution to Peripheral Androgens During the Menstrual Cycle
Abstract
In order to assess the ovarian and adrenal contribution to peripheral levels of testosterone (T), 5α-dihydrotestosterone (DHT), androstenedione (A), dehydroepiandrosterone (DHEA) and its sulfate (DHEA-S) in premenopausal women, six normally menstruating subjects were studied during two complete mentrual cycles. The first cycle served as control and dexamethasone was given during the second cycle. Plasma cortisol (F) was measured to assess the degree of adrenal suppression. Plasma progesterone (P), 17-hydroxyprogesterone (17-P) and estradiol-17β (E2) served as indirect indices of ovulation. The estimation of plasma LH located the midcycle peak and the data for all steroids were evaluated in relation to the LH peak. All cycles studied were apparently ovulatory, as judged by the plasma levels of P, 17-P and E2. Dexamethasone treatment had no detectable effect on the levels of these three steroids. Assuming that dexamethasone suppressed completely the adrenal cortex and had no detectable effect on ovarian steroidogenesis, the following conclusions were made: 1) the adrenal contribution to peripheral T, DHT, A, DHEA and DHEA-S is relatively constant within random fluctuations throughout the menstrual cycle; 2) the ovarian contribution of peripheral T, A and DHEA-S reaches maximum levels at midcycle, whereas ovarian contribution to peripheral DHT and DHEA does not seem to be influenced by the menstrual cycle; 3) the ovary and the adrenal cortex contribute equally to peripheral T, DHT and A, except for peripheral A at midcycle when the ovarian contribution is twice that of the adrenal; and 4) peripheral DHEA and DHEA-S originate predominantly from the adrenal cortex which contributes 80% of DHEA and greater than 90% of DHEA-S.
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In the citing paper
“In women, testosterone and A4 demonstrate cyclic changes in concentration during the course of the menstrual cycle due to the ovarian contribution, with levels peaking mid-cycle [283,284].”
From Human steroid biosynthesis, metabolism and excretion are differentially reflected by serum and urine steroid metabolomes: a comprehensive review (2019) · cites this paper as [284]
In the citing paper
“In ZR-75-1 cells, concentrations of DHT in the incubation medium similar to the plasma levels found in normal women (215-217) and breast cancer patients (Ref.218; 0.3-0.7 nm) are potent inhibitors of the mitogenic effect of E 2 and even inhibit growth in the absence of estrogens (208).”
From Endocrine and intracrine sources of androgens in women: inhibition of breast cancer and other roles of androgens and their precursor dehydroepiandrosterone (2003) · cites this paper as [216]
In the citing paper
“4-Dione also led to significant growth inhibition in ZR-75-1 cells, although the active concentrations (IC 50 , 15 nm) are in the upper range of the plasma concentrations (1-10 nm) found in women (215-218).”
From Endocrine and intracrine sources of androgens in women: inhibition of breast cancer and other roles of androgens and their precursor dehydroepiandrosterone (2003) · cites this paper as [216]
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Azziz, R., Carmina, E., Dewailly, D., Diamanti-Kandarakis, E., Escobar-Morreale, H. F., Futterweit, W., Janssen, O. E., Legro, R. S., Norman, R. J., Taylor, A. E., et al. (2009) · Fertility and Sterility · doi:10.1016/j.fertnstert.2008.06.035 · Cited by 2,132
Knochenhauer, E. S., Key, T. J., Kahsar-Miller, M., Waggoner, W., Boots, L. R., & Azziz, R. (1998) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem.83.9.5090 · Cited by 1,759
Asunción, M., Calvo, R. M., Millán, J. L. S., Sancho, J., Ávila, S., & Escobar-Morreale, H. F. (2000) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem.85.7.6682 · Cited by 1,328
Hirsutism: Implications, etiology, and management
Hatch, R., Rosenfield, R. L., Kim, M. H., & Tredway, D. R. (1981) · American Journal of Obstetrics and Gynecology · doi:10.1016/0002-9378(81)90746-8 · Cited by 1,013
Transdermal testosterone treatment in women with impaired sexual function after oophorectomy.
Shifren, J. L., Braunstein, G. D., Simon, J. A., Casson, P. R., Buster, J. E., Redmond, G. P., Burki, R. E., Ginsburg, E. S., Rosen, R. C., Leiblum, S. R., et al. (2000) · New England Journal of Medicine · doi:10.1056/nejm200009073431002 · Cited by 954
Metadata
- Authors
- ABRAHAM, G. E.
- Affiliations
- University of California, Los Angeles (US)
- Corresponding author
- ABRAHAM, GUY E.
- Venue
- The Journal of Clinical Endocrinology & Metabolism
- Publisher
- The Endocrine Society
- Published
- 1974-08
- Volume
- 39
- Issue
- 2
- Pages
- 340-346
- ISSN
- 0021-972X (ISSN-L)
- 1945-7197
- OpenAlex
- W2107541080
- Cited by
- 436
- References
- 0
- Citations by year
- 2026: 3 · 2025: 2 · 2024: 6 · 2023: 5 · 2022: 8 · 2021: 12 · 2020: 6 · 2019: 8 · 2018: 8 · 2017: 5 · 2016: 10 · 2015: 6 · 2014: 12 · 2013: 15 · 2012: 5
- FWCI
- 10.27
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- The Journal of Clinical Endocrinology & Metabolism (publishedVersion)
- PubMed (publishedVersion)
- Funders
- NIH Clinical Center
- Topics
- Health Sciences › Medicine › Reproductive Medicine › Ovarian function and disorders
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Adrenal Hormones and Disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Endocrinology › Estrogen and related hormone effects
- Keywords
- menstrual cycle, testosterone, dihydrotestosterone, androstenedione, dehydroepiandrosterone, DHEA sulfate, ovarian steroidogenesis, adrenal cortex, dexamethasone suppression, cortisol, luteinizing hormone, premenopausal women
- MeSH terms
- Adrenal Glands, Adult, Androgens, Androstenedione, Dehydroepiandrosterone, Dexamethasone, Estradiol, Female, Humans, Hydrocortisone, Hydroxyprogesterones, Menstruation, Ovary, Ovulation, Progesterone, Testosterone
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