Trestolone

Trestolone

Systematic (IUPAC) name
(7R,8R,9S,10R,13S,14S,17S)-17-Hydroxy-7,13-dimethyl-
Clinical data
Pregnancy cat.	?
Legal status	Unclassified
Identifiers
CAS number	3764-87-2 Y
ATC code	None
PubChem	CID 9838899
ChemSpider	21106398 Y
UNII	40P3287I94 Y
Synonyms	MENT; 7α-Methylnandrolone; 7α-methyl-19-nortestosterone; 17β-hydroxy-7α-methylestr-4-en-3-one
Chemical data
Formula	C19H28O2
Mol. mass	288.424
SMILES O=C2\C=C3\CC(C)[C@H]1[C@@H]4CCC(O)[C@@]4(C)CC[C@@H]1[C@H]3CC2
InChI InChI=1S/C19H28O2/c1-11-9-12-10-13(20)3-4-14(12)15-7-8-19(2)16(18(11)15)5-6-17(19)21/h10-11,14-18,21H,3-9H2,1-2H3/t11?,14-,15+,16-,17?,18+,19-/m0/s1 Y Key:YSGQGNQWBLYHPE-XOGXAEGHSA-N Y
Y (what is this?)  (verify)

Trestolone is a synthetic androgen as a potential candidate drug for use in hormonal male contraceptive methods. In males, regular administration of sufficient quantities of trestolone induces a state of temporary infertility.^{[citation needed]}

Trestolone is an experimental contraceptive treatment and is not yet available commercially. It is currently being evaluated for safety and effectiveness in scientific studies, supported by the Population Council.^{[citation needed]}

Mechanism of action

As a derivative of the anabolic steroid hormone nandrolone, trestolone's viability as a male contraceptive is twofold.

Inhibition of sperm production

Spermatozoa are produced in the testes of males in a process called spermatogenesis. In order to render a man infertile, a hormone-based male contraceptive method must stop spermatogenesis by interrupting the release of gonadotropins from the pituitary gland. Even in low concentrations, trestolone is a potent inhibitor of the release of the gonadotropin hormones, luteinizing hormone (LH) and follicle stimulating hormone (FSH).^{[citation needed]}

In order for spermatogenesis to occur in the testes, both FSH and the male hormone testosterone must be present. By inhibiting release of FSH, trestolone creates an endocrine environment in which conditions for spermatogenesis are not ideal. Manufacture of sperm is further impaired by the suppression of LH, which in turn drastically curtails the production of testosterone. Sufficient regular doses of trestolone cause severe oligozoospermia or azoospermia, and therefore infertility, in most male patients.^{[citation needed]}

Trestolone-induced sterility has been found to be quickly reversible upon discontinuation.^{[citation needed]}

Support of secondary sex characteristics

When LH release is inhibited, the amount of testosterone made in the testes declines dramatically. As a result of trestolone's gonadotropin-suppressing qualities, levels of serum testosterone fall sharply in patients. Testosterone is the primary hormone responsible for maintenance of male secondary sex characteristics.

Normally, inadequate testosterone levels cause undesirable effects, such as fatigue, loss of skeletal muscle mass, reduced libido, and weight gain. However, the androgenic and anabolic properties of trestolone largely ameliorate this problem. Essentially, trestolone replaces testosterone's role as the primary male hormone in the body.

External links

• MENT – project information from the Population Council