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  2. Pregnenolone - Wikipedia

    en.wikipedia.org/wiki/Pregnenolone

    Pregnenolone (P5), or pregn-5-en-3β-ol-20-one, is an endogenous steroid and precursor/metabolic intermediate in the biosynthesis of most of the steroid hormones, including the progestogens, androgens, estrogens, glucocorticoids, and mineralocorticoids. [1]

  3. Congenital adrenal hyperplasia due to 21-hydroxylase deficiency

    en.wikipedia.org/wiki/Congenital_adrenal...

    It catalyzes hydroxylation of 17α-hydroxyprogesterone (17OHP) to 11-deoxycortisol in the glucocorticoid pathway, which starts from pregnenolone and finishes with cortisol. It also catalyzes hydroxylation of progesterone to 11-deoxycorticosterone (DOC) in the mineralocorticoid pathway on its way from pregnenolone to aldosterone. [162]

  4. Congenital adrenal hyperplasia due to 3β-hydroxysteroid ...

    en.wikipedia.org/wiki/Congenital_adrenal...

    3β-HSD II mediates three parallel dehydrogenase/isomerase reactions in the adrenals that convert Δ 4 to Δ 5 steroids: pregnenolone to progesterone, 17α-hydroxypregnenolone to 17α-hydroxyprogesterone, and dehydroepiandrosterone (DHEA) to androstenedione. 3β-HSD II also mediates an alternate route of testosterone synthesis from androstenediol in the testes. 3β-HSD deficiency results in ...

  5. 3β-Hydroxysteroid dehydrogenase - Wikipedia

    en.wikipedia.org/wiki/3β-hydroxysteroid...

    3β-Hydroxysteroid dehydrogenase/Δ 5-4 isomerase (3β-HSD) (EC 1.1.1.145) is an enzyme that catalyzes the biosynthesis of the steroid progesterone from pregnenolone, 17α-hydroxyprogesterone from 17α-hydroxypregnenolone, and androstenedione from dehydroepiandrosterone (DHEA) in the adrenal gland.

  6. Congenital adrenal hyperplasia due to 17α-hydroxylase ...

    en.wikipedia.org/wiki/Congenital_adrenal...

    In these people the defect had the effect of an isolated impairment of sex steroid (e.g., DHEA in the adrenal, but also gonadal testosterone and estrogens) synthesis, whereas mineralocorticoid (e.g., aldosterone) and glucocorticoid (e.g., cortisol) levels remain normal. [citation needed]

  7. Aldosterone - Wikipedia

    en.wikipedia.org/wiki/Aldosterone

    Aldosterone is the primary of several endogenous members of the class of mineralocorticoids in humans. [citation needed] Deoxycorticosterone is another important member of this class. Aldosterone tends to promote Na + and water retention, and lower plasma K + concentration by the following mechanisms:

  8. List of steroid abbreviations - Wikipedia

    en.wikipedia.org/wiki/List_of_steroid_abbreviations

    Pregnenolone: P5 [2] or Preg [3] 3beta-hydroxy-5-pregnen-20-one 17α-Hydroxypregnenolone: 17-OHP5 [4] or 17P5 [5] 3beta,17-dihydroxy-5-pregnen-20-one Progesterone: P4 [6] or P [3] 4-pregnene-3,20-dione 17α-Hydroxyprogesterone: 17-OHP4 [4] or 17OHP [7] or 17P4 [5] 17α-hydroxy-4-pregnene-3,20-dione Allopregnanolone: ALLO 5α-pregnan-3α-ol-20 ...

  9. Congenital adrenal hyperplasia - Wikipedia

    en.wikipedia.org/wiki/Congenital_adrenal_hyperplasia

    Hyponatremia (due to hypoaldosteronism) - Aldosterone is the end product of the renin-angiotensin-aldosterone system that regulates blood pressure via blood pressure surveillance in the Kidney Juxtaglomerular apparatus. Aldosterone normally functions to increase sodium retention (which brings water as well) in exchange for potassium.

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