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  2. Pharmacokinetics of progesterone - Wikipedia

    en.wikipedia.org/wiki/Pharmacokinetics_of...

    Progesterone is used as part of hormone replacement therapy in people who have low progesterone levels, and for other reasons. For purposes of comparison with normal physiological circumstances, luteal phase levels of progesterone are 4 to 30 ng/mL, while follicular phase levels of progesterone are 0.02 to 0.9 ng/mL, menopausal levels are 0.03 to 0.3 ng/mL, and levels of progesterone in men ...

  3. Pharmacodynamics of progesterone - Wikipedia

    en.wikipedia.org/wiki/Pharmacodynamics_of...

    Progesterone is a progestogen, or an agonist of the nuclear progesterone receptors (PRs), the PR-A, PR-B, and PR-C. [1] In one study, progesterone showed EC 50 Tooltip half-maximal effective concentration values of 7.7 nM for the human PR-A and 8.0 nM for the human PR-B. [5] In addition to the PRs, progesterone is an agonist of the membrane progesterone receptors (mPRs), including the mPRα ...

  4. Progesterone - Wikipedia

    en.wikipedia.org/wiki/Progesterone

    [125] [126] [44] In addition, progesterone can be hydroxylated in the liver by other cytochrome P450 enzymes which are not steroid-specific. [127] 6β-Hydroxylation, which is catalyzed mainly by CYP3A4, is the major transformation, and is responsible for approximately 70% of cytochrome P450-mediated progesterone metabolism. [127]

  5. Progestogen - Wikipedia

    en.wikipedia.org/wiki/Progestogen

    Progesterone is the major progestogen produced by the corpus luteum of the ovary in all mammalian species. Luteal cells possess the necessary enzymes to convert cholesterol to pregnenolone, which is subsequently converted into progesterone. Progesterone is highest in the diestrus phase of the estrous cycle.

  6. Progesterone (medication) - Wikipedia

    en.wikipedia.org/wiki/Progesterone_(medication)

    It opposes the effects of estrogens in various parts of the body like the uterus and also blocks the effects of the hormone aldosterone. [20] [29] In addition, progesterone has neurosteroid effects in the brain. [20] Progesterone was first isolated in pure form in 1934. [30] [31] It first became available as a medication later that year.

  7. Membrane progesterone receptor - Wikipedia

    en.wikipedia.org/wiki/Membrane_progesterone_receptor

    The mPRs mediate important physiological functions in male and female reproductive tracts, liver, neuroendocrine tissues, and the immune system as well as in breast and ovarian cancer. The mPRs appear to be involved in the neuroprotective and antigonadotropic effects of progesterone and allopregnanolone.

  8. Progestogen (medication) - Wikipedia

    en.wikipedia.org/wiki/Progestogen_(medication)

    A progestogen, also referred to as a progestagen, gestagen, or gestogen, is a type of medication which produces effects similar to those of the natural female sex hormone progesterone in the body. [1] A progestin is a synthetic progestogen. [1] Progestogens are used most commonly in hormonal birth control and menopausal hormone therapy. [1]

  9. Etonogestrel - Wikipedia

    en.wikipedia.org/wiki/Etonogestrel

    Etonogestrel is a progestin, or a synthetic progestogen, and hence is an agonist of the progesterone receptor, the biological target of progestogens like progesterone. [16] It works by stopping ovulation , thickening the mucus around the opening of the cervix , and altering the lining of the uterus . [ 17 ]