Effects of dissociated glucocorticoids on OPG and RANKL in osteoblastic cells

被引:117
作者
Humphrey, E. L.
Williams, J. H. H.
Davie, M. W. J.
Marshall, M. J. [1 ]
机构
[1] Robert Jones & Agnes Hunt Orthopaed Hosp, Charles Salt Ctr, Oswestry SY10 7AG, Shrops, England
[2] Univ Coll Chester, Chester Ctr Stress Res, Chester CH1 4BJ, Cheshire, England
关键词
dissociated glucocorticoids; OPG; RANKL; deflazacort; osteoblast;
D O I
10.1016/j.bone.2005.10.004
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Glucocorticoids are effective anti-inflammatory and immunosuppressive agents, but their use is often associated with debilitating side effects such as glucocorticoid-induced osteoporosis. Newly developed glucocorticoid analogues such as the so-called dissociated glucocorticoids are potent immunosuppressants and have the potential for fewer side effects. The effects of these new analogues on osteoprotegerin (OPG) and receptor activator of NF-kappa B ligand (RANKL) in osteoblastic cells have not been studied. OPG and RANKL are osteoblast-derived proteins pivotal to the regulation of bone mass. RANKL stimulates bone resorption by increasing osteoclast differentiation, activation and survival. OPG is the decoy receptor for RANKL and thus inhibits bone resorption. Here, we show that dexamethasone, prednisolone, deflazacort and the dissociated glucocorticoids, RU24858, RU40066, RU24782, AL438-F1 and ZK216348 significantly inhibit OPG production in two human osteoblastic cell lines (MG63 and hFOB). The potency for OPG inhibition was ligand and cell-type specific. In both cell types, dexamethasone and prednisolone were the most potent ligands inhibiting OPG production with IC(50)s of similar to 0.1 nM and 10 nM respectively. In MG63 cells, deflazacort and the RU compounds were the next most potent ligands followed by AL438-F1 and ZK216348. In hFOB cells, however, the RU compounds were the least potent ligands with an IC50 74 times higher than in MG63 cells. In contrast, the level of maximum inhibition or effectiveness of OPG inhibition did not vary between cell types but did vary according to the ligand. Dexamethasone, prednisolone, deflazacort and the RU compounds all inhibited OPG production by a maximum of similar to 70-80%, whereas AL438-F1 and ZK 216348 inhibited OPG production by a maximum of only 40-50% at 1 mu M. All of the dissociated glucocorticoids and deflazacort were poor stimulators of RANKL gene expression stimulating by only similar to 1-3-fold compared to 7-fold by prednisolone. These data demonstrate that deflazacort and the dissociated glucocorticoids are weak stimulators of the RANKL:OPG ratio compared to prednisolone. Therefore, these compounds have the potential to cause less bone loss than that seen with prednisolone, though this was not investigated here. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:652 / 661
页数:10
相关论文
共 49 条
  • [1] Adachi J D, 1998, J Am Med Womens Assoc (1972), V53, P25
  • [2] Glucocorticoid-regulated transcription factors
    Adcock, IM
    [J]. PULMONARY PHARMACOLOGY & THERAPEUTICS, 2001, 14 (03) : 211 - 219
  • [3] Comparison of the pharmacodynamic effects of deflazacort and prednisolone in healthy subjects
    Babadjanova, G
    Allolio, B
    Vollmer, M
    Reincke, M
    Schulte, HM
    [J]. EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 1996, 51 (01) : 53 - 57
  • [4] TRANSCRIPTIONAL CONTROL BY NUCLEAR RECEPTORS
    BEATO, M
    [J]. FASEB JOURNAL, 1991, 5 (07) : 2044 - 2051
  • [5] Crystal structure of the glucocorticoid receptor ligand binding domain reveals a novel mode of receptor dimerization and coactivator recognition
    Bledsoe, RK
    Montana, VG
    Stanley, TB
    Delves, CJ
    Apolito, CJ
    McKee, DD
    Consler, TG
    Parks, DJ
    Stewart, EL
    Willson, TM
    Lambert, MH
    Moore, JT
    Pearce, KH
    Xu, HE
    [J]. CELL, 2002, 110 (01) : 93 - 105
  • [6] Secondary osteoporosis: Underlying disease and the risk for glucocorticoid-induced osteoporosis
    Boling, EP
    [J]. CLINICAL THERAPEUTICS, 2004, 26 (01) : 1 - 14
  • [7] GLUCOCORTICOID THERAPY FOR IMMUNE-MEDIATED DISEASES - BASIC AND CLINICAL CORRELATES
    BOUMPAS, DT
    CHROUSOS, GP
    WILDER, RL
    CUPPS, TR
    BALOW, JE
    [J]. ANNALS OF INTERNAL MEDICINE, 1993, 119 (12) : 1198 - 1208
  • [8] Buckbinder Leonard, 2002, Current Drug Targets - Inflammation and Allergy, V1, P127, DOI 10.2174/1568010023344751
  • [9] Receptor activator for nuclear factor kappaB ligand and osteoprotegerin: regulators of bone physiology and immune responses/potential therapeutic agents and biochemical markers
    Buckley, KA
    Fraser, WD
    [J]. ANNALS OF CLINICAL BIOCHEMISTRY, 2002, 39 : 551 - 556
  • [10] Structure/activity elements of the multifunctional protein, GMEB-1 - Characterization of domains relevant for the modulation of glucocorticoid receptor transactivation properties
    Chen, J
    Kaul, S
    Simons, SS
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (24) : 22053 - 22062