Matsuo Atsushi, Shuto Toshihide, Hirata Go, Satoh Hideshi, Matsumoto Yoshihiro, Zhao Hongpu, Iwamoto Yukihide
Department of Orthopaedic Surgery, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
J Rheumatol. 2003 Jun;30(6):1280-90.
Incadronate is a third-generation bisphosphonate that suppresses bone resorption and is used to treat skeletal disorders and prevent bone loss in pathological conditions. We evaluated its therapeutic potential and antiinflammatory effects in established adjuvant induced arthritis (AIA), a rat model of rheumatoid arthritis (RA).
Rats were administered incadronate subcutaneously at a dose of either 0.1 or 1.0 mg/kg/day, or 0.1 or 1.0 mg/kg/week, while a positive control group received phosphate buffered saline alone from Day 14 (after the onset of arthritis) to Day 42. The destruction of bone and cartilage and the antiinflammatory effects of incadronate in rats with established AIA were assessed during treatment, with reference to the arthritis index, hind paw volume, and radiological and histological examinations. To establish whether incadronate affects the migration of inflammatory cells, a chemotaxis assay was carried out using macrophage-like RAW 264.7 cells. Results. In vivo, incadronate suppressed the clinical manifestations of AIA in a dose-dependent manner. In vitro, the various concentrations of incadronate suppressed the migration of macrophages, but the viability and adhesion of these cells were not suppressed.
Incadronate not only inhibits bone destruction but also reduces cartilage degeneration and joint inflammation in rats with established AIA. The mechanism underlying these antiinflammatory actions of incadronate may be attributable to the inhibition of macrophage migration to the site of inflammation. Bisphosphonates might be effective in preventing the progressive joint destruction and inflammation seen in patients with RA.
因卡膦酸盐是一种第三代双膦酸盐,可抑制骨吸收,用于治疗骨骼疾病并预防病理状态下的骨质流失。我们评估了其在佐剂诱导性关节炎(AIA)(一种类风湿性关节炎(RA)大鼠模型)中的治疗潜力和抗炎作用。
大鼠皮下注射因卡膦酸盐,剂量为0.1或1.0毫克/千克/天,或0.1或1.0毫克/千克/周,而阳性对照组从第14天(关节炎发作后)至第42天仅接受磷酸盐缓冲盐水。在治疗期间,参照关节炎指数、后爪体积以及放射学和组织学检查,评估因卡膦酸盐对已患AIA大鼠的骨和软骨破坏以及抗炎作用。为确定因卡膦酸盐是否影响炎性细胞的迁移,使用巨噬细胞样RAW 264.7细胞进行趋化试验。结果:在体内,因卡膦酸盐以剂量依赖方式抑制AIA的临床表现。在体外,不同浓度的因卡膦酸盐抑制巨噬细胞的迁移,但这些细胞的活力和黏附未受抑制。
因卡膦酸盐不仅抑制骨破坏,还可减轻已患AIA大鼠的软骨退变和关节炎症。因卡膦酸盐这些抗炎作用的潜在机制可能归因于抑制巨噬细胞向炎症部位的迁移。双膦酸盐可能对预防RA患者出现的进行性关节破坏和炎症有效。