Recombinant human interleukin-11 does not modify biochemical parameters of bone remodeling and bone mineral density in adult ovariectomized rats

被引:14
作者
Verhaeghe, J
Van Herck, E
van Bree, R
Bouillon, R
Dequeker, J
Keith, JC
机构
[1] Katholieke Univ Leuven, Dept Obstet & Gynecol, B-3001 Louvain, Belgium
[2] Katholieke Univ Leuven, Lab Expt Geneeskunde Endocrinol, B-3001 Louvain, Belgium
[3] Katholieke Univ Leuven, Arthrit & Metab Bone Dis Res Unit, B-3001 Louvain, Belgium
[4] Genet Inst Inc, Dept Preclin Res & Dev, Andover, MA USA
关键词
D O I
10.1089/jir.1998.18.49
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Interleukin (IL)-11 stimulates osteoclast formation and inhibits osteoblast function in vitro and has been implicated in estrogen deficiency-induced bone loss. Herein we report the in vivo effect of recombinant human IL-11 (rHU-IL-11), administered s.c. in doses between 10 and 200 mu g/kg/day for 6 weeks into 6-month-old rats after ovariectomy, There was no difference between vehicle-treated and rHu-IL-11 treated rats in the ovariectomy-induced increase in the urinary excretion of pyridinoline and deoxypyridinoline. Neither was there a significant effect of rHu-IL-11 on the plasma concentrations of osteocalcin and on bone mineral density (BMD) measured at a metaphyseal area of the distal femur after 6 weeks. At all dosages tested, rHu-IL-11 increased the femoral diaphyseal area. In conclusion, IL-11 has no deleterious in vivo effect on biochemical parameters of bone remodeling and BMD in estrogen-deficient rats.
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收藏
页码:49 / 53
页数:5
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