Effects of prostaglandin E2 on bone in mice in vivo

被引:24
作者
Gao, Qi [1 ]
Xu, Manshan [1 ]
Alander, Cynthia B. [1 ]
Choudhary, Shilpa [1 ]
Pilbeam, Carol C. [1 ]
Raisz, Lawrence G. [1 ]
机构
[1] Univ Connecticut, Ctr Hlth, New England Musculoskeletal Inst, Farmington, CT 06030 USA
关键词
Prostaglandin E-2; Gene expression; Bone histomorphometry; Bone formation; Bone resorption; Anabolic effect; RECEPTOR AGONISTS; CORTICAL BONE; EP2; RECEPTOR; PGE(2); RATS; FEMALE; PTH;
D O I
10.1016/j.prostaglandins.2009.03.003
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
We have examined the effects of varying doses, schedules and routes of administration of prostaglandin E-2 (PGE(2)) on bone in mice. Male C57BL/6 mice treated with a high dose of PGE(2) (6mg/kg/d) showed decreased trabecular bone volume (BV/TV) by 14 d, indicating increased bone resorption. However, there was also stimulation of bone formation at 14 d after 3 d treatment with PGE(2), since mineral apposition rate (MAR) and bone formation rate (BFR/BS) were increased. In CD-1 male and female mice, PGE(2) (3 mg/kg, 2/wk for 4 wk) increased MAR by 50% and BFR/BS by 100%, but there was no significant change in BV/TV. Tibial mRNA showed an increase in BMP-2 and RUNX-2 expression with PGE(2). Additional experiments using a higher dose or longer exposure did not increase bone mass. We conclude that exposure to high doses of PGE(2) in mice may be anabolic but is balanced by catabolic effects. Studies of PGE(2) in combination with an inhibitor of resorption could lead to development of a true anabolic model and permit assessment of the roles of specific PGE(2) receptors and signal transduction pathways. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:20 / 25
页数:6
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