Emergency Department, First Affiliated Hospital of Gannan Medical University, Ganzhou, 341000, China.
Department of Orthopedics, First Affiliated Hospital of Gannan Medical University, Ganzhou, 341000, China.
J Orthop Surg Res. 2021 Jan 4;16(1):5. doi: 10.1186/s13018-020-02124-4.
This study was undertaken to establish a rat bipedal walking model of cervical kyphosis (CK) associated with chronic forward flexed neck and assess the effects of chronic forward flexed neck on endplate chondrocytes.
Forty-eight 1-month-old Sprague-Dawley rats were randomly divided into 3 groups: forward flexed neck group (n = 16), bipedal group (n = 16), and normal group (n = 16). Cervical curves were analyzed on a lateral cervical spine X-ray using Harrison's posterior tangent method before the experiment and at 2-week intervals for a 6-week period. Histologic changes in cartilaginous endplate chondrocytes were observed using hematoxylin and eosin (H&E) staining, transmission electron microscopy (TEM), and terminal deoxyribonucleotidyl transferase (TdT)-mediated dUTP nick-end labeling.
Radiographic findings suggested a significantly decreased cervical physiological curvature in the forward flexed neck group over the 6-week follow-up; normal cervical curves were maintained in other groups. The average cervical curvature (C2-C7) was - 7.6 ± 0.9° in the forward flexed neck group before the experiment, - 3.9 ± 0.8° at 2 weeks post-experiment, 10.7 ± 1.0° at 4 weeks post-experiment, and 20.5 ± 2.1° at the last follow-up post-experiment. Histologically, results of H&E staining unveiled that cartilaginous endplate chondrocytes were arranged in an irregular fashion, with the decreased number at the observation period; the incidence of apoptotic cells in the forward flexed neck group was noticeably higher at the 6-week follow-up than that in other groups.
CK developed as the result of chronic forward flexed neck. Histologic changes suggested that chondrocyte apoptosis may play a critical role in the development of cervical kyphotic deformity associated with chronic forward flexed neck.
本研究旨在建立一种与慢性前屈性颈部相关的颈椎后凸(CK)大鼠双足行走模型,并评估慢性前屈性颈部对终板软骨细胞的影响。
48 只 1 月龄 Sprague-Dawley 大鼠随机分为三组:前屈性颈部组(n = 16)、双足组(n = 16)和正常组(n = 16)。实验前和实验后 6 周内每 2 周通过 Harrison 后切线法对颈椎侧位 X 线片进行颈椎曲度分析。采用苏木精-伊红(H&E)染色、透射电镜(TEM)和末端脱氧核苷酸转移酶(TdT)介导的 dUTP 缺口末端标记法观察软骨终板软骨细胞的组织学变化。
影像学结果提示,前屈性颈部组在 6 周随访过程中颈椎生理曲度明显降低;其他组维持正常颈椎曲线。前屈性颈部组实验前平均颈椎曲率(C2-C7)为-7.6 ± 0.9°,实验后 2 周为-3.9 ± 0.8°,4 周为 10.7 ± 1.0°,末次随访时为 20.5 ± 2.1°。H&E 染色结果显示,软骨终板软骨细胞排列不规则,观察期内数量减少;前屈性颈部组在 6 周随访时凋亡细胞的发生率明显高于其他组。
慢性前屈性颈部导致 CK 发生。组织学变化表明,软骨细胞凋亡可能在慢性前屈性颈部相关颈椎后凸畸形的发展中起关键作用。