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  2. Androgen backdoor pathway - Wikipedia

    en.wikipedia.org/wiki/Androgen_backdoor_pathway

    The term "backdoor pathway" was coined by Auchus in 2004 [25] and was described as 5α-reduction of 17α-hydroxyprogesterone (17OHP) which is a first step in a pathway that ultimately leads to the production of dihydrotestosterone (DHT). and defined as a route to DHT that: (1) bypasses conventional intermediates androstenedione (A4) and T; (2 ...

  3. Dihydrotestosterone - Wikipedia

    en.wikipedia.org/wiki/Dihydrotestosterone

    Dihydrotestosterone (DHT, 5α-dihydrotestosterone, 5α-DHT, androstanolone or stanolone) is an endogenous androgen sex steroid and hormone primarily involved in the growth and repair of the prostate and the penis, as well as the production of sebum and body hair composition.

  4. File:Androgen backdoor pathway.svg - Wikipedia

    en.wikipedia.org/wiki/File:Androgen_backdoor...

    Download QR code; In other projects ... The androgen backdoor pathway (red arrows) embedded in the known pathways that lead to 5α-dihydrotestosterone synthesis.

  5. 5α-Pregnan-17α-ol-3,20-dione - Wikipedia

    en.wikipedia.org/wiki/5α-Pregnan-17α-ol-3,20-dione

    The androgen backdoor pathway (red arrows) roundabout testosterone embedded in within conventional androgen synthesis that lead to 5α-dihydrotestosterone through testosterone. [ 7 ] [ 8 ] [ 9 ] 5α-Pregnan-17α-ol-3,20-dione (17-OH-DHP) is a progestogen , i.e., it binds to the progesterone receptors .

  6. Androgen - Wikipedia

    en.wikipedia.org/wiki/Androgen

    Dihydrotestosterone increased the number of BrdU cells, while flutamide inhibited these cells. Moreover, estrogens had no effect. This research demonstrates how androgens can increase AHN. [19] Researchers also examined how mild exercise affected androgen synthesis which in turn causes AHN activation of N-methyl-D-aspartate (NMDA) receptors.

  7. 17β-Hydroxysteroid dehydrogenase - Wikipedia

    en.wikipedia.org/wiki/17β-hydroxysteroid...

    Also involved into a backdoor pathway from 17α-hydroxyprogesterone to dihydrotestosterone by 3α-reduction of a metabolic intermediary, 17α-hydroxydihydroprogesterone, into another intermediary, 17α-hydroxyallopregnanolone. [21] May be involved in the pathophysiology of PCOS Tooltip polycystic ovary syndrome. [12]

  8. 5α-Reductase inhibitor - Wikipedia

    en.wikipedia.org/wiki/5α-reductase_inhibitor

    5α-Reductase inhibitors (5-ARIs), also known as dihydrotestosterone (DHT) blockers, are a class of medications with antiandrogenic effects which are used primarily in the treatment of enlarged prostate and scalp hair loss. They are also sometimes used to treat excess hair growth in women and as a component of hormone therapy for transgender ...

  9. Androgen receptor - Wikipedia

    en.wikipedia.org/wiki/Androgen_receptor

    The AR plays a role in regulating female sexual, somatic, and behavioral functions. Experimental data using AR knockout female mice, provides evidence that the promotion of cardiac growth, kidney hypertrophy, cortical bone growth and regulation of trabecular bone structure is a result of DNA-binding-dependent actions of the AR in females.