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Inhibition of adjuvant-induced arthritis by 16 alpha-fluoro-5-androsten-17-one.

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.
AuthorsArthur G Schwartz, Laura L Pashko
JournalMilitary medicine (Mil Med) Vol. 167 Issue 2 Suppl Pg. 60-3 (Feb 2002) ISSN: 0026-4075 [Print] England
PMID11873519 (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

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