Related Experiment Videos
Intracrinology and the skin
F Labrie1, V Luu-The, C Labrie
1Oncology and Molecular Endocrinology Research Center, Laval University Medical Center (CHUL), Québec City, Canada. fernand.labrie@crchul.ulaval.ca
Hormone Research
|October 12, 2001
Summary
Dehydroepiandrosterone (DHEA) is converted to dihydrotestosterone (DHT) in the skin, stimulating sebaceous glands. This conversion is primarily androgenic in the skin but estrogenic in the vagina.
Area of Science:
- Endocrinology
- Dermatology
- Biochemistry
Background:
- The skin contains androgen-sensitive components that convert dehydroepiandrosterone (DHEA) into dihydrotestosterone (DHT).
- Adrenal DHEA production decreases with age, impacting skin steroidogenesis, especially in post-menopausal women.
- DHEA's effects in the skin are predominantly androgenic, as evidenced by antiandrogen blocking of sebaceous gland stimulation.
Purpose of the Study:
- To elucidate the specific enzymes and pathways involved in DHEA conversion to active androgens in human skin.
- To investigate the differential effects of DHEA in various tissues, including skin, vagina, and endometrium.
Main Methods:
- RNase protection assays and immunocytochemistry were used to identify steroidogenic enzymes in human skin.
- In vivo and in vitro studies using animal models and human tissues were conducted to assess DHEA's effects.
Main Results:
- Human skin expresses type 1 3beta-hydroxysteroid dehydrogenase (3beta-HSD) converting DHEA to androstenedione, and type 5 17beta-HSD converting androstenedione to testosterone.
- Type 1 5alpha-reductase is responsible for converting testosterone to DHT in the skin.
- DHEA exhibits estrogenic effects in the vagina but does not affect the endometrial epithelium in experimental animals and post-menopausal women.
Conclusions:
- The skin possesses a complete enzymatic system for converting DHEA into potent androgens like DHT.
- DHEA's tissue-specific actions (androgenic in skin, estrogenic in vagina) highlight its complex role in hormone physiology.
- DHEA's lack of endometrial effects suggests its safety for hormone replacement therapy without necessitating progestins.