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Discover Supplement-Drug Interactions

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Last Updated: 3 years ago

Possible Interaction: Dehydroepiandrosterone and Progesterone

Research Papers that Mention the Interaction

Pregnenolone, dehydroepiandrosterone , and their sulfate esters behave as sigma1 agonists, while progesterone is a potent antagonist.
Brain Research Reviews  •  2001  |  View Paper
Our group and others have noted that when women were placed on DHEA , baseline serum progesterone levels were markedly higher than those measured prior to DHEA supplementation [2].
Journal of Assisted Reproduction and Genetics  •  2015  |  View Paper
Progesterone levels on stimulation day 5 (ng/mL) (0.58 ± 0.29 vs. 1.54 ± 0.49; p < 0.0001); and on the day of hCG administration (0.75 ± 0.31 vs. 1.87 ± 0.49; p < 0.0001) were significantly higher during DHEA treatment.
Journal of Assisted Reproduction and Genetics  •  2014  |  View Paper
Progesterone levels on stimulation day 5 (0.58 ± 0.29 ng/ml vs. 1.54 ± 0.49 ng/ml; p < 0.0001) and on the … chorionic gonadotropin administration (0.75 ± 0.31 ng/ml vs. 1.87 ± 0.49 ng/ml; p < 0.0001) were significantly higher during DHEA ….
Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology  •  2011  |  View Paper
However, coincubation of progesterone with (+)pentazocine, pregnenolone, or DHEA reversed their potentiating effects.
Synapse  •  2004  |  View Paper
The increase of progesterone under DHEA supplementation in males should receive further attention.
Maturitas  •  2003  |  View Paper
The stimulation of prostaglandin F2 alpha production by the adrenal steroids was significantly reduced by the antiestrogen 4-hydroxytamoxifen at … actions on other systems) but was not affected by the antiandrogen 4-hydroxyflutamide at 10(-6) mol/L. Progesterone (… dehydroepiandrosterone (10(-6) mol/L) and … (10(-8) mol/L).
American journal of obstetrics and gynecology  •  1988  |  View Paper
The number of specific progesterone binding sites was increased 3.7-, 3.2-, and 2.0-fold by delta 5-diol, DHEA , and DHEAS, respectively.
Cancer research  •  1986  |  View Paper
At the same time, high concentrations (10(-5) M) of DHA and DHAS, but not 16 alpha-OH DHA, markedly suppressed progesterone production.
The Journal of clinical endocrinology and metabolism  •  1983  |  View Paper
In pregnant rats and following a 3‐week treatment with progesterone , 10 fold higher doses of DTG, (+)‐pentazocine and DHEA were required to elicit a selective potentiation of the NMDA response comparable to that obtained in control females.
British journal of pharmacology  •  1999  |  View Paper
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