Etiocholanedione Explained

Etiocholanedione, also known as 5β-androstanedione or as etiocholane-3,17-dione, is a naturally occurring etiocholane (5β-androstane) steroid and an endogenous metabolite of androgens like testosterone, dihydrotestosterone, dehydroepiandrosterone (DHEA), and androstenedione.[1] It is the C5 epimer of androstanedione (5α-androstanedione). Although devoid of androgenic activity like other 5β-reduced steroids, etiocholanedione has some biological activity of its own.[2] [3] The compound has been found to possess potent haematopoietic effects in a variety of models. In addition, it has been found to promote weight loss in animals and in a double-blind, placebo-controlled clinical study in humans conducted in 1993.[4] These effects are said to be similar to those of DHEA.[5] Unlike DHEA however, etiocholanedione cannot be metabolized further into steroid hormones like androgens and estrogens.

External links

Notes and References

  1. Web site: Human Metabolome Database: Showing metabocard for Etiocholanedione (HMDB0003769). hmdb.ca. 2018-07-13.
  2. Bradlow HL, Murphy J, Byrne JJ . Immunological properties of dehydroepiandrosterone, its conjugates, and metabolites . Ann. N. Y. Acad. Sci. . 876 . 91–101 . June 1999 . 1 . 10415598 . 10.1111/j.1749-6632.1999.tb07627.x . 1999NYASA.876...91B . 46148045 .
  3. Book: Douglas McKeag. James L. Moeller. ACSM's Primary Care Sports Medicine. 2007. Lippincott Williams & Wilkins. 978-0-7817-7028-6. 616–.
  4. Book: James M. Rippe. Lifestyle Medicine, Second Edition. 15 March 2013. CRC Press. 978-1-4398-4544-8. 559–.
  5. Clore JN . Dehydroepiandrosterone and body fat . Obes. Res. . 3 . 613S–616S . November 1995 . Suppl 4 . 8697065 . 10.1002/j.1550-8528.1995.tb00234.x . free .