ijmm
www.spandidos-publications.com
Home  | About  | Contact
Spandidos Logo
Advanced Search
Login  | Register


congress_banner

main_table_top_image
   Current Issue Early Online Archive Manuscript Submission About Editor and Editorial Academy Sitemap
Oral treatment with HE3286 ameliorates disease in rodent models of rheumatoid arthritis

Authors:
Dominick L. Auci, Katia Mangano, Daniel Destiche, Steven K. White, Yujin Huang, David Boyle, James Frincke, Christopher L. Reading, Ferdinando Nicoletti

Affiliations:
HollisEden Pharmaceuticals, 4435 Eastgate Mall, San Diego, CA, USA

Doi:
10.3892/ijmm_00000385

Pages:
625-633

Abstract:

HE3286 (17α-ethynyl-5-androstene-3β, 7β, 17β-triol) is an orally bio-available synthetic derivative of naturally occurring androstene-3β, 7β, 17β-triol. Our present data show that oral treatment with HE3286, favourably influenced the course of arthritis in the rat model of adjuvant-induced arthritis (reduced cumulative disease scores and paw edema), and in the mouse model of collagen antibody-induced arthritis (reduced clinical paw scores). Importantly, HE3286 was not immune suppressive in human mixed lymphocyte reaction or in animals challenged with Coxsackie B3 virus. HE3286 is currently in phase I/II clinical trials in rheumatoid arthritis and ulcerative colitis and these findings further strengthen the possibility that HE3286 may represent an effective anti-inflammatory agent useful for treating chronic inflammation with a more attractive safety profile than glucocorticoids or cyclooxygenase inhibitors.

International Journal of Molecular Medicine

April 2010
Volume 25 Number 4


Viewing options: Sign up for eToc alerts

Share this article:



main_table_bottom_image