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Vol. 291, Issue 3, 1380-1386, December 1999
Departments of Bone and Cartilage Biology (A.M.B., S.M.B., R.A.D.,
B.A.S., D.J.R., G.B.S., S.J.H., M.G.) and Immunopharmacology (D.E.G.),
SmithKline Beecham Pharmaceuticals, King of Prussia,
Pennsylvania
Idoxifene, a selective estrogen receptor modulator, was evaluated in
male and female rats with adjuvant-induced arthritis (AA). AA was
induced in Lewis rats with Mycobacterium butyricum in
paraffin oil injected into the base of the tail, and the animals were
treated with idoxifene prophylactically (days 0-21) or therapeutically (days 10-21). Efficacy was determined by measurements of paw
inflammation, bone mineral content, and bone mineral density (BMD) with
dual X-ray absorptiometry and by histological evaluation. Serum
interleukin-6 levels were measured as a marker of the anti-inflammatory
effects of the compound. Estrogen was included for comparison and was administered at 5 mg/kg, three times a week s.c. Prophylactic treatment
of male AA rats with idoxifene at 10, 3, and 1 mg/kg and estrogen at 5 mg/kg significantly inhibited paw inflammation. There was improved
joint integrity measured by BMD and reduced serum interleukin-6 levels
in animals treated with 10 mg/kg/day idoxifene. Idoxifene and estrogen
were as effective for AA in female Lewis rats as in male rats,
significantly inhibiting paw inflammation and improving BMD.
Histological evaluation of the tibiotarsal joints of female rats
treated with 10 mg/kg showed protection of bone, cartilage, and soft
tissue. Therapeutic treatment with either idoxifene or estrogen
(starting on day 10 of disease) of male and female Lewis rats also was
effective in reducing paw inflammation in these animals, although the
effect was much less than that observed with the prophylactic dosing protocol.
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