Androstenedione
From DrugPedia: A Wikipedia for Drug discovery
Androstenedione Pubchem(6128) (also known as 4-androstenedione) is a 19-carbon steroid hormone produced in the adrenal glands and the gonads as an intermediate step in the biochemical pathway that produces the androgen testosterone and the estrogens estrone and estradiol. A delta-4 C19 steroid that is produced not only in the TESTIS, but also in the OVARY and the ADRENAL CORTEX. Depending on the tissue type, androstenedione can serve as a precursor to TESTOSTERONE as well as ESTRONE and ESTRADIOL.
KEGG Pathway(C00280,D00051)
- Androgen and estrogen metabolism
- Prostate cancer
Drug Type: Small Molecule; Illicit; Experimental
| MMDB ID | PDB ID | Reference |
|---|---|---|
| 28531 | 1QYX | Shi R, Lin SXCofactor hydrogen bonding onto the protein main chain is conserved in the short chain dehydrogenase/reductase family and contributes to nicotinamide orientationJ. Biol. Chem. v279, p.16778-16785 |
| Physical Property | Value | Units | Temp (deg C) | Source |
|---|---|---|---|---|
| Melting Point | 158 | deg C | EXP | |
| log P (octanol-water) | 2.75 | (none) | EXP | |
| Water Solubility | 57.8 | mg/L | 25 | EXP |
| Vapor Pressure | 2.46E-06 | mm Hg | 25 | EST |
| Henry's Law Constant | 3.68E-08 | atm-m3/mole | 25 | EST |
| Atmospheric OH Rate Constant | 1.11E-10 | cm3/molecule-sec | 25 | EST |
Contents |
Synthesis
Androstenedione is the common precursor of male and female sex hormones. Some androstenedione is also secreted into the plasma, and may be converted in peripheral tissues to testosterone and estrogens.
Androstenedione originates either from the conversion of dehydroepiandrosterone or from 17-hydroxyprogesterone. Conversion of dehydroepiandrosterone to androstenedione requires 17,20 lyase. 17-hydroxyprogesterone, on the other hand, requires 17,20 lyase for its synthesis. Thus, both reactions that produce androstenedione directly or indirectly depend on 17,20 lyase.
Androstenedione is further converted to either testosterone or estrogen. Conversion of androstenedione to testosterone requires the enzyme 17β-hydroxysteroid dehydrogenase, while conversion of androstenedione to estrogen (e.g. estrone and estradiol requires the enzyme aromatase.
The production of adrenal androstenedione is governed by ACTH, whereas production of gonadal androstenedione is under control by gonadotropins. In premenopausal women, the adrenal glands and ovaries each produce about half of the total androstendione (about 3 mg/day). After menopause, androstenedione production is about halved, primarily due to the reduction of the steroid secreted by the ovary. Nevertheless, androstenedione is the principal steroid produced by the postmenopausal ovary.
Endocrine function
In females, androstenedione is released into the blood by theca cells. The function of this is to provide androstenedione substrate for estrogen production in granulosa cells, since these cells lack 17,20 lyase required for androstenedione. Similarly, theca cells lack the enzyme aromatase required to make estrogens themselves. Thus, theca cells and granulosa cells work together to form estrogen.<ref> Medical Physiology, Boron & Boulpaep, ISBN 1-4160-2328-3, Elsevier Saunders 2005. Updated edition. Page 1155 </ref>
Androstenedione as a supplement
History
Androstenedione was manufactured as a dietary supplement, often called andro (or andros) for short. Andro was in common use in Major League Baseball throughout the 1990s by record-breaking sluggers like Mark McGwire. The supplement is banned by the World Anti-Doping Agency, and hence from the Olympic Games.
On March 12, 2004, the Anabolic Steroid Control Act of 2004 was introduced into the United States Senate. It amended the Controlled Substance Act to place both anabolic steroids and prohormones on a list of controlled substances, making possession of the banned substances a federal crime. The law took effect on January 20, 2005. Surprisingly, andro was legally defined as an anabolic steroid, even though there is scant evidence that androstenedione itself is anabolic in nature.
On April 11, 2004, the United States Food and Drug Administration banned the sale of Andro, citing that the drug poses significant health risks commonly associated with steroids.
Androstenedione is currently banned by the US military.<ref>USAF Medical Service Home Page</ref>
Biological Effects
Androstenedione has been shown to increase serum testosterone levels over an eight-hour period in men when taken as a single oral dose of 300mg per day, but a 100mg dose had no significant effect on serum testosterone. However, serum levels of estradiol increased following both the 100mg and 300mg doses. The study also reported that the serum level of estrogens and testosterone produced varied widely between individuals.<ref>Leder, B., Longcope, C., Catlin, D., Ahrens, B. Shoenfeld, D., and Finkelstein, J.: "Oral Androstenedione Administration and Serum Testosterone Concentrations in Young Men", JAMA, 283(6):779-782</ref> A 2006 review paper summarized several studies which examined the effect of androstenedione on strength training. At dosages of 50mg or 100mg per day, andro had no effect on muscle strength or size, or on body fat levels. One study utilized a daily dosage of 300mg of androstenedione combined with several other supplements, and also found no increase in strength when compared to a control group that did not take the supplements. The review authors speculate that sufficiently high doses may indeed lead to increased muscle size and strength. However, due to the federal ban on androstenedione supplements, it is difficult to carry out new research on its positive and negative effects. The review authors conclude that individuals should not use androstenedione supplements due to the lack of evidence of beneficial effects, the wide variation in individual responses to the supplement, and the risk of unknown side effects.<ref> Brown, G., Vukovich, M., and King, D.:"Testosterone Prohormone Supplements", Medicine and Science in Sports and Exercise, 38(8):1451-1461.</ref>
Because androstenedione is converted in part to estrogens, persons taking this supplement may have estrogenic side-effects, although none of the studies cited above used a sufficiently high dosage to draw any conclusions.
References
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