Tawaratsumida Hiroki, Iuchi Tomohiro, Masuda Yusuke, Ide Takayuki, Maesako Shingo, Miyazaki Takasuke, Ijuin Toshiro, Maeda Shingo, Taniguchi Noboru
Department of Orthopaedic Surgery, Graduate School of Medical and Dental Sciences, Kagoshima University, Kagoshima, Kagoshima 890-8520, Japan.
Department of Orthopaedic Surgery, Graduate School of Medical and Dental Sciences, Kagoshima University, Kagoshima, Kagoshima 890-8520, Japan; Department of Medical Joint Materials, Graduate School of Medical and Dental Sciences, Kagoshima University, Kagoshima, Kagoshima 890-8520, Japan.
Osteoarthritis Cartilage. 2025 Jan;33(1):101-115. doi: 10.1016/j.joca.2024.08.005. Epub 2024 Aug 15.
To evaluate the humeral head bone volume of patients with cuff tear arthropathy (CTA) and examine the therapeutic effect of zoledronate in a rat modified model of CTA (mCTA).
The bone mass in patients with CTA was measured using Hounsfield units from CT images. The mCTA was induced by transecting the rotator cuff, biceps brachii tendon, and superior half of the joint capsule in adult rat shoulders. A single subcutaneous injection of zoledronate was followed by bone histomorphometry and immunohistochemistry of the humeral head, as well as the Murine Shoulder Arthritis Score (MSAS) assessment.
The humeral head bone volume was decreased in patients with CTA. In the mCTA model, M1 macrophages were increased in the synovium and were decreased by zoledronate treatment. The increased expressions of TNF-α, IL-1β and IL-6 in mCTA synovium and articular cartilage were suppressed in the zoledronate-treated mCTA group. The expression of catabolic enzymes in the articular cartilage and MSAS showed similar results. The zoledronate-treated mCTA group showed a decreased subchondral bone collapse with a decreased RANKL/OPG expression ratio and a suppressed number of osteoclasts compared with the control mCTA group. The enhanced expressions of HMGB1 and S100A9 in the mCTA shoulders were eliminated in the zoledronate-treated mCTA group.
The humeral head subchondral bone was decreased in patients with CTA. In the mCTA model, the collapse and osteoarthritic changes were prevented by zoledronate administration. Zoledronate seemed to suppress the number of M1 macrophages in the synovium and osteoclasts in the subchondral bone.
评估肩袖撕裂性关节病(CTA)患者的肱骨头骨体积,并研究唑来膦酸在大鼠改良CTA模型(mCTA)中的治疗效果。
利用CT图像的亨氏单位测量CTA患者的骨量。通过切断成年大鼠肩部的肩袖、肱二头肌肌腱和关节囊上半部分诱导建立mCTA模型。单次皮下注射唑来膦酸后,对肱骨头进行骨组织形态计量学和免疫组织化学分析,以及小鼠肩关节炎评分(MSAS)评估。
CTA患者的肱骨头骨体积减少。在mCTA模型中,滑膜中M1巨噬细胞增加,唑来膦酸治疗可使其减少。唑来膦酸治疗的mCTA组抑制了mCTA滑膜和关节软骨中TNF-α、IL-1β和IL-6表达的增加。关节软骨中分解代谢酶的表达和MSAS显示出相似的结果。与对照mCTA组相比,唑来膦酸治疗的mCTA组软骨下骨塌陷减少,RANKL/OPG表达比值降低,破骨细胞数量受到抑制。唑来膦酸治疗的mCTA组消除了mCTA肩部HMGB1和S100A9表达的增强。
CTA患者的肱骨头软骨下骨减少。在mCTA模型中,唑来膦酸给药可预防塌陷和骨关节炎变化。唑来膦酸似乎可抑制滑膜中M1巨噬细胞的数量和软骨下骨中破骨细胞的数量。