Department of Internal Medicine III, University Hospital of Jena, Jena, Germany.
Inflamm Res. 2010 Sep;59(9):731-41. doi: 10.1007/s00011-010-0184-6. Epub 2010 Mar 20.
To investigate the influence of a combined therapy consisting of dexamethasone and osteoprotegerin (OPG) on bone alterations and disease activity in antigen-induced arthritis (AIA) in the rat.
AIA rats received dexamethasone (0.25 mg kg(-1) day(-1), i.p.), OPG (2.5 mg kg(-1) day(-1), i.p.), or a combination of both at regular intervals for 21 consecutive days. At the end of the treatment, bone structure was analyzed by histomorphometry. Primary spongiosa was measured using linear scanning.
AIA led to significant periarticular and axial bone loss. Dexamethasone monotherapy substantially suppressed joint swelling without inhibiting bone loss of the secondary spongiosa, whereas OPG monotherapy showed no anti-inflammatory effect. Despite reduction of bone resorption, OPG did not inhibit AIA-induced bone loss. In contrast, the combination of dexamethasone and OPG not only produced an anti-inflammatory effect, but also resulted in inhibition of periarticular and axial bone loss. OPG increased trabecular number of the primary spongiosa whilst combination therapy led to an increase in both trabecular number and trabecular width.
The principle of combining a glucocorticoid together with inhibition of the receptor activator of NF-kappaB ligand (RANKL) may be an effective bone-saving therapy in rheumatoid arthritis.
研究地塞米松和骨保护素(OPG)联合治疗对大鼠诱导性关节炎(AIA)中骨改变和疾病活动的影响。
AIA 大鼠每隔一天接受地塞米松(0.25mg/kg,腹腔注射)、OPG(2.5mg/kg,腹腔注射)或两者的组合治疗 21 天。在治疗结束时,通过组织形态计量学分析骨结构。使用线性扫描测量初级松质骨。
AIA 导致明显的关节周围和轴向骨丢失。地塞米松单药治疗显著抑制关节肿胀,但不能抑制次级松质骨的骨丢失,而 OPG 单药治疗则没有抗炎作用。尽管减少了骨吸收,但 OPG 并没有抑制 AIA 引起的骨丢失。相比之下,地塞米松和 OPG 的联合治疗不仅产生了抗炎作用,而且还抑制了关节周围和轴向的骨丢失。OPG 增加了初级松质骨的小梁数量,而联合治疗则导致小梁数量和宽度都增加。
将糖皮质激素与核因子 κB 受体激活剂配体(RANKL)抑制剂联合使用的原则可能是类风湿关节炎中一种有效的保骨治疗方法。