Instituto de Medicina Molecular, Faculdade de Medicina, Universidade de Lisboa, Lisbon, Portugal.
Research Unit of Medical Imaging, Physics and Technology, Faculty of Medicine, University of Oulu, Oulu, Finland.
Rheumatology (Oxford). 2018 Aug 1;57(8):1461-1471. doi: 10.1093/rheumatology/kex258.
The main goal of this work was to analyse how treatment intervention with tofacitinib prevents the early disturbances of bone structure and mechanics in the rat model of adjuvant-induced arthritis. This is the first study to access the impact of tofacitinib on the skeletal bone effects of inflammation.
Fifty Wistar rats with adjuvant-induced arthritis were randomly housed in experimental groups, as follows: non-arthritic healthy group (n = 20); arthritic non-treated group (n = 20); and 10 animals undergoing tofacitinib treatment. Rats were monitored during 22 days after disease induction for the inflammatory score, ankle perimeter and body weight. Healthy non-arthritic rats were used as controls for comparison. After 22 days of disease progression, rats were killed and bone samples collected for histology, micro-CT, three-point bending and nanoindentation analysis. Blood samples were also collected for quantification of bone turnover markers and systemic cytokines.
At the tissue level, measured by nanoindentation, tofacitinib increased bone cortical and trabecular hardness. However, micro-CT and three-point bending tests revealed that tofacitinib did not reverse the effects of arthritis on the cortical and trabecular bone structure and on mechanical properties.
Possible reasons for these observations might be related to the mechanism of action of tofacitinib, which leads to direct interactions with bone metabolism, and/or to the kinetics of its bone effects, which might need longer exposure.
本研究的主要目的是分析托法替尼治疗如何预防佐剂诱导关节炎大鼠模型中骨结构和力学的早期紊乱。这是第一项评估托法替尼对炎症骨骼影响的研究。
将 50 只佐剂诱导关节炎大鼠随机分为实验组,如下:非关节炎健康组(n=20);关节炎未治疗组(n=20);和 10 只接受托法替尼治疗的动物。在疾病诱导后 22 天内监测大鼠的炎症评分、踝关节周长和体重。健康非关节炎大鼠作为对照组进行比较。疾病进展 22 天后,处死大鼠并采集骨样本进行组织学、微 CT、三点弯曲和纳米压痕分析。还收集血液样本以定量测定骨转换标志物和全身细胞因子。
通过纳米压痕测量,在组织水平上,托法替尼增加了皮质骨和小梁骨的硬度。然而,微 CT 和三点弯曲测试表明,托法替尼并未逆转关节炎对皮质骨和小梁骨结构以及机械性能的影响。
这些观察结果的可能原因与托法替尼的作用机制有关,它直接与骨代谢相互作用,和/或与它的骨骼作用动力学有关,这可能需要更长的暴露时间。