Akiyama Tomoyuki, Mori Satoshi, Mashiba Tasuku, Miyamoto Kensaku, Komatsubara Satoshi, Cao Yongping, Manabe Takeshi, Norimatsu Hiromichi, Dobashi Hiroaki, Tokuda Michiaki
Department of Orthopedic Surgery, Faculty of Medicine, Kagawa University, 1750-1 Ikenobe, Miki-cho, Kagawa 761-0793, Japan.
J Bone Miner Metab. 2005;23(4):295-301. doi: 10.1007/s00774-004-0602-3.
Destruction of articular cartilage and subchondral bone loss in the affected joints of rat adjuvant arthritis have never been quantified histologically. This study aimed to evaluate the effect of incadronate disodium on joint destruction and periarticular bone loss, using histomorphometric measurements. Seven-week-old female Lewis rats were injected with 0.1 mg of heat-killed Mycobacterium butyricum into the tail base. Immediately after sensitization, vehicle, or incadronate at 10 or 100 microg/kg per day, was administered subcutaneously, three times per week. Hind-paw volume was measured weekly and the animals were killed at 2, 4, 6, and 10 weeks after sensitization. After taking X-rays, decalcified sagittal sections of the ankle joint were prepared and stained with toluidine blue and tartarate-resistant acid phosphatase. Articular cartilage destruction and subchondral bone loss were evaluated histomorphometrically. At 2 weeks after sensitization, no radiographic or histologic changes were observed. However, at 4 weeks, severe articular cartilage destruction and subchondral bone loss were found in the arthritic control group, while these changes were inhibited dose-dependently by incadronate treatment. At 6 and 10 weeks, both the destructive changes and the bone loss had further progressed, and they were not inhibited by incadronate treatment. Incadronate dose-dependently inhibited articular cartilage destruction and subchondral bone loss at 4 weeks after sensitization in this adjuvant arthritis model. However, the suppressive effects of incadronate did not continue until 6 and 10 weeks.
大鼠佐剂性关节炎受累关节的关节软骨破坏和软骨下骨丢失从未进行过组织学定量分析。本研究旨在通过组织形态计量学测量评估因卡膦酸二钠对关节破坏和关节周围骨质丢失的影响。7周龄雌性Lewis大鼠尾基部注射0.1mg热灭活丁酸分枝杆菌。致敏后立即皮下给予溶媒或每天10或100μg/kg的因卡膦酸,每周3次。每周测量后足体积,致敏后2、4、6和10周处死动物。拍摄X线片后,制备踝关节脱钙矢状切片,用甲苯胺蓝和抗酒石酸酸性磷酸酶染色。组织形态计量学评估关节软骨破坏和软骨下骨丢失。致敏后2周,未观察到放射学或组织学变化。然而,在4周时,关节炎对照组出现严重的关节软骨破坏和软骨下骨丢失,而因卡膦酸治疗剂量依赖性地抑制了这些变化。在6周和10周时,破坏变化和骨质丢失均进一步进展,因卡膦酸治疗未抑制这些变化。在该佐剂性关节炎模型中,因卡膦酸在致敏后4周剂量依赖性地抑制关节软骨破坏和软骨下骨丢失。然而,因卡膦酸的抑制作用在6周和10周时未持续。