Li Zhi, Wan Pu, Liu Xuemiao, Jiang Guichun, Li Jie, Chen Dapeng, Zhang Weiguo, Tian Kang
Department of Joint and Sports Medicine, First Affiliated Hospital of Dalian Medical University, Dalian, Liaoning, 116011, China.
Clinical Skills Training Center, Liaoning Cancer Hospital & Institute, Shenyang, Liaoning, 110042, China.
BMC Musculoskelet Disord. 2025 Oct 6;26(1):918. doi: 10.1186/s12891-025-09194-7.
Cam morphology is associated with acetabular cartilage lesions and early-onset osteoarthritis in patients with femoroacetabular impingement syndrome. Here, we propose a novel iterative rabbit model of cam morphology to characterize the pathophysiology of femoroacetabular impingement-related cartilage lesions.
We described a repeatable method for establishing a New Zealand white rabbit model of cam morphology by interfering with the epiphyseal tubercle and evaluated the histological outcomes of acetabular cartilage lesions. Cam morphology and subchondral bone were evaluated by micro-CT scanning. The expression of anabolic and catabolic biomarkers of acetabular cartilage was investigated via western blotting and immunohistochemical staining. Chondrocyte apoptosis was detected via TUNEL staining. Kinematics of the hip joint in the sagittal plane were evaluated by a passive optical motion capture system.
There were remarkable pathological similarities between this model and human diseases. The cam morphology rabbit model exhibited early cartilage degeneration and subsequent phenotypes of hip osteoarthritis, and this pathological process is not affected by surgical trauma. Hip motion in the cam morphology models resembled that in the healthy controls, and had only a slightly lower joint angle at all phases of the half-bounding gait cycle. This model preserved the natural and predictable movement pattern.
This rabbit model of cam morphology replicates the disease phenotype and allows for scientifically sound evaluation of disease mechanisms. It can be employed to study human cam-type femoroacetabular impingement syndrome.
凸轮形态与股骨髋臼撞击综合征患者的髋臼软骨损伤和早发性骨关节炎相关。在此,我们提出一种新型的凸轮形态迭代兔模型,以表征股骨髋臼撞击相关软骨损伤的病理生理学。
我们描述了一种通过干扰骨骺结节建立新西兰白兔凸轮形态模型的可重复方法,并评估髋臼软骨损伤的组织学结果。通过微型计算机断层扫描评估凸轮形态和软骨下骨。通过蛋白质印迹和免疫组织化学染色研究髋臼软骨合成代谢和分解代谢生物标志物的表达。通过TUNEL染色检测软骨细胞凋亡。通过被动光学运动捕捉系统评估髋关节在矢状面的运动学。
该模型与人类疾病存在显著的病理相似性。凸轮形态兔模型表现出早期软骨退变及随后的髋骨关节炎表型,且该病理过程不受手术创伤影响。凸轮形态模型中的髋关节运动与健康对照相似,在半边界步态周期的所有阶段关节角度仅略低。该模型保留了自然且可预测的运动模式。
这种凸轮形态兔模型复制了疾病表型,并允许对疾病机制进行科学合理的评估。它可用于研究人类凸轮型股骨髋臼撞击综合征。