5-alpha reductase
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| steroid-5-alpha-reductase, alpha polypeptide 1
| |
| Identifiers | |
| Symbol(s) | SRD5A1 |
| Entrez | 6715 |
| OMIM | 184753 |
| RefSeq | NM_001047 |
| UniProt | P18405 |
| Other data | |
| EC number | 1.3.99.5 |
| Locus | Chr. 5 p15 |
| steroid-5-alpha-reductase, alpha polypeptide 2
| |
| Identifiers | |
| Symbol(s) | SRD5A2 |
| Entrez | 6716 |
| OMIM | 607306 |
| RefSeq | NM_000348 |
| UniProt | P31213 |
| Other data | |
| EC number | 1.3.99.5 |
| Locus | Chr. 2 p23 |
5-alpha reductase is an enzyme (EC 1.3.99.5) that converts testosterone, the male sex hormone, into dihydrotestosterone. There are two isoenzymes, steroid 5-alpha reductase 1 and 2 (SRD5A1 and SRD5A2). The second isoenzyme is deficient in 5-alpha-reductase deficiency which leads to a form of intersexualism.
Inhibition of 5-alpha reductase results in decreased produciton of DHT, increased levels of testosterone and possibly increased levels of estradiol. Gynecomastia is a possible side effect of 5-alpha reductase inhibition.
[edit] Genetics
SRD5A1 is located on chromosome 5p15, while SRD5A2 is located on 2p23.
[edit] Pharmacology
Finasteride inhibits the function of only one of the isoenzymes (type 1), while dutasteride inhibits both forms. These drugs are used in benign prostatic hyperplasia, prostate cancer and baldness (finasteride).
[edit] External
- Mendelian Inheritance in Man (OMIM) 184753 (SRD5A1) and Mendelian Inheritance in Man (OMIM) 607306 (SRD5A2)
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