Mechanisms of glucocorticoid-induced osteoporosis

被引:123
作者
Canalis, E
机构
[1] St Francis Hosp & Med Ctr, Dept Res, Hartford, CT 06105 USA
[2] Univ Connecticut, Sch Med, Farmington, CT USA
关键词
D O I
10.1097/00002281-200307000-00013
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Glucocorticoids modify osteoblastic cell differentiation, number, and function. Glucocorticoids stimulate osteoclastogenesis and increase the expression of receptor activator of Nuclear factor-kappaB ligand and colony-stimulating factor-1, and decrease the expression of osteoprotegerin. However, the most significant effect of glucocorticoids in bone is an inhibition of bone formation. This inhibition is caused by a decrease in the number of osteoblasts secondary to a shift in the differentiation of mesenchymal cells away from the osteoblastic lineage, and an increase in the death of mature osteoblasts. Glucocorticoids decrease the function of the remaining osteoblasts directly and indirectly through the inhibition of insulin-like growth factor I expression. The stimulation of bone resorption is likely responsible for the initial bone loss after glucocorticoid exposure. Eventually, the inhibition of bone formation will cause a decrease in bone remodeling and a continued increased risk of fractures. (C) 2003 Lippincott Williams Wilkins.
引用
收藏
页码:454 / 457
页数:4
相关论文
共 36 条
[1]   Cortisol inhibits hepatocyte growth factor/scatter factor expression and induces c-met transcripts in osteoblasts [J].
Blanquaert, F ;
Pereira, RC ;
Canalis, E .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2000, 278 (03) :E509-E515
[2]   Human 11 beta-hydroxysteroid dehydrogenase: Studies on the stably transfected isoforms and localization of the type 2 isozyme within renal tissue [J].
Bujalska, O ;
Shimojo, M ;
Howie, A ;
Stewart, PM .
STEROIDS, 1997, 62 (01) :77-82
[3]   Mechanisms of glucocorticoid action in bone: Implications to glucocorticoid-induced osteoporosis [J].
Canalis, E .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1996, 81 (10) :3441-3447
[4]   11β-hydroxysteroid dehydrogenase, an amplifier of glucocorticoid action in osteoblasts [J].
Canalis, E ;
Delany, AM .
JOURNAL OF BONE AND MINERAL RESEARCH, 2002, 17 (06) :987-990
[5]   INSULIN-LIKE GROWTH FACTOR-I MEDIATES SELECTIVE ANABOLIC EFFECTS OF PARATHYROID-HORMONE IN BONE CULTURES [J].
CANALIS, E ;
CENTRELLA, M ;
BURCH, W ;
MCCARTHY, TL .
JOURNAL OF CLINICAL INVESTIGATION, 1989, 83 (01) :60-65
[6]   Comparison of trabecular bone microarchitecture and remodeling in glucocorticoid-induced and postmenopausal osteoporosis [J].
Carbonare, LD ;
Arlot, ME ;
Chavassieux, PM ;
Roux, JP ;
Portero, NR ;
Meunier, PJ .
JOURNAL OF BONE AND MINERAL RESEARCH, 2001, 16 (01) :97-103
[7]   Estrogen deficiency induces bone loss by enhancing T-cell production of TNF-α [J].
Cenci, S ;
Weitzmann, MN ;
Roggia, C ;
Namba, N ;
Novack, D ;
Woodring, J ;
Pacifici, R .
JOURNAL OF CLINICAL INVESTIGATION, 2000, 106 (10) :1229-1237
[8]   Osteoblastic 11β-hydroxysteroid dehydrogenase type 1 activity increases with age and glucocorticoid exposure [J].
Cooper, MS ;
Rabbitt, EH ;
Goddard, PE ;
Bartlett, WA ;
Hewison, M ;
Stewart, PM .
JOURNAL OF BONE AND MINERAL RESEARCH, 2002, 17 (06) :979-986
[9]   Expression and functional consequences of 11-β-hydroxysteroid dehydrogenase activity in human bone [J].
Cooper, MS ;
Walker, EA ;
Bland, R ;
Fraser, WD ;
Hewison, M ;
Stewart, PM .
BONE, 2000, 27 (03) :375-381
[10]   CORTISOL DOWN-REGULATES OSTEOBLAST ALPHA-1(I) PROCOLLAGEN MESSENGER-RNA BY TRANSCRIPTIONAL AND POSTTRANSCRIPTIONAL MECHANISMS [J].
DELANY, AM ;
GABBITAS, BY ;
CANALIS, E .
JOURNAL OF CELLULAR BIOCHEMISTRY, 1995, 57 (03) :488-494