Abstract |
The adrenal steroid dehydroepiandrosterone ( DHEA) produces cancer-preventive, antiatherosclerotic, antidiabetic, immunomodulating, and anti-inflammatory effects in laboratory animals. The clinical use of DHEA is limited by its androgenicity. We have developed a synthetic congener of DHEA called fluasterone that, in animal tests, lacks the androgenicity, estrogenicity, and peroxisome-proliferating effects of DHEA but retains the cancer-preventive, antidiabetic, and anti-inflammatory efficacy. This report discusses how fluasterone ameliorates the development of joint inflammation in an adjuvant-arthritis model in Lewis rats.
|
Authors | Arthur G Schwartz, Laura L Pashko |
Journal | Military medicine
(Mil Med)
Vol. 167
Issue 2 Suppl
Pg. 60-3
(Feb 2002)
ISSN: 0026-4075 [Print] England |
PMID | 11873519
(Publication Type: Journal Article)
|
Chemical References |
- Antineoplastic Agents
- Dehydroepiandrosterone
- 5-androstene-16-fluoro-17-one
|
Topics |
- Animals
- Antineoplastic Agents
(pharmacology)
- Arthritis, Experimental
(drug therapy)
- Dehydroepiandrosterone
(analogs & derivatives, pharmacology)
- Female
- Rats
- Rats, Inbred Lew
|