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Vol. 280, Issue 2, 1001-1007, 1997
Biomedical Research Center (T.Ö., T.V., L.L.,
K.K., I.P., R.H., R.S.), Leiras Oy, Turku, Finland, and
Department of
Anatomy and Biocenter (K.V.), University of Oulu, Oulu, Finland
The effects of slow-release calcium clodronate on rat adjuvant
arthritis were investigated using two different dosing schedules. In
prophylactic treatment, calcium clodronate was given on the same day as
the adjuvant injection, and in therapeutic treatment, calcium
clodronate administration was delayed until the animals had active
disease, to day 14 postadjuvant. Calcium clodronate was given as single
i.m. injections into the thigh muscles. Arthritis index, histopathology
of hindpaw, quantitative histomorphometry, bone mineral density and
serum osteocalcin, alkaline phosphatase and calcium were studied.
Calcium clodronate given therapeutically decreased the severity of paw
swelling slightly more than prophylactic treatment, a result seen as
lower scores of arthritis index. Histopathological evaluation of
hindpaws showed that calcium clodronate protected against
inflammation-induced bone loss and reactive bone formation in the
hindpaw, but not against inflammatory changes involving articular
cartilage. Quantitative histomorphometric analysis of the distal femur
indicated that trabecular bone area was decreased by 86% in arthritic
rats compared with normal untreated controls. Both the prophylactic and
the therapeutic treatment with calcium clodronate prevented this
osteopenia (P < .001). Bone mineral density measured by computed
tomography was also significantly reduced in distal femoral metaphysis
in adjuvant arthritic rats, but restoration to virtually normal values
occurred with calcium clodronate (P < .001). In both dosing
schedules, we observed a suppression of arthritis, which was associated
with a decrease in paw swelling and an inhibition of the severe
osteopenia in the distal femoral metaphysis. The long duration of
action after a single injection of calcium clodronate indicates that
the insoluble salt remains at the injection site and is released slowly
into the bloodstream.