Ono Yuichi, Miyakoshi Naohisa, Kasukawa Yuji, Nagasawa Hiroyuki, Tsuchie Hiroyuki, Akagawa Manabu, Nagahata Itsuki, Yuasa Yusuke, Sato Chiaki, Shimada Yoichi
Department of Orthopedic Surgery, Akita University Graduate School of Medicine, Akita, Japan.
Osteoporos Sarcopenia. 2018 Dec;4(4):128-133. doi: 10.1016/j.afos.2018.11.085. Epub 2018 Dec 1.
Rheumatoid arthritis (RA) is characterized by chronic inflammation of the synovium, progressive erosion of the articular cartilage, and joint destruction. RA also causes secondary osteoporosis and muscle wasting. We investigated the effects of ibandronate (IBN), a bisphosphonate; eldecalcitol (ELD), an active vitamin D3 derivative; and combination treatment with both agents on secondary osteoporosis and muscle wasting using adjuvant-induced arthritis rats.
Arthritis was induced in 8-week-old male Lewis rats. Rats were randomized into 4 treatment groups and an untreated normal control group: IBN (subcutaneously, once every 2 weeks, 10 μg/kg), ELD (orally, once daily, 30 ng/kg/day), IBN + ELD, vehicle, and control. Paw thickness measurements were performed for evaluation of arthritis. The femur was scanned using dual-energy X-ray absorptiometry. Cross-sectional areas of left tibialis and anterior muscle fibers and the expression of MuRF1, atrogin-1, MyoD, and myogenin in the gastrocnemius muscle were measured to evaluate muscle wasting.
IBN and/or ELD increased bone mineral density (BMD) in the femur. In addition, there was an additive effect of combination treatment compared with single treatments for BMD. However, IBN and/or ELD did not inhibit muscle wasting in adjuvant-induced arthritis rats.
Combination treatment with IBN and ELD may be effective for secondary osteoporosis associated with RA. Other treatments are necessary for muscle wasting associated with RA. Studies in humans are needed to confirm these findings.
类风湿关节炎(RA)的特征为滑膜慢性炎症、关节软骨进行性侵蚀及关节破坏。RA还会导致继发性骨质疏松和肌肉萎缩。我们使用佐剂诱导的关节炎大鼠,研究了双膦酸盐伊班膦酸钠(IBN)、活性维生素D3衍生物 eldecalcitol(ELD)以及两者联合治疗对继发性骨质疏松和肌肉萎缩的影响。
对8周龄雄性Lewis大鼠诱导关节炎。将大鼠随机分为4个治疗组和1个未治疗的正常对照组:IBN(皮下注射,每2周1次,10μg/kg)、ELD(口服,每日1次,30ng/kg/天)、IBN + ELD、赋形剂组和对照组。测量爪厚度以评估关节炎。使用双能X线吸收法扫描股骨。测量左胫骨和股前肌纤维的横截面积以及腓肠肌中MuRF1、atrogin-1、MyoD和肌细胞生成素的表达,以评估肌肉萎缩。
IBN和/或ELD增加了股骨的骨矿物质密度(BMD)。此外,与单一治疗相比,联合治疗对BMD有相加作用。然而,IBN和/或ELD并未抑制佐剂诱导的关节炎大鼠的肌肉萎缩。
IBN和ELD联合治疗可能对RA相关的继发性骨质疏松有效。对于RA相关的肌肉萎缩,需要其他治疗方法。需要在人体进行研究以证实这些发现。