Department of Orthopedics, Shanghai Tenth People's Hospital, Tongji University School of Medicine. No.301 Yanchang Middle Road, Shanghai 200072, China; Department of Orthopedics, Shanghai East Hospital, Tongji University School of Medicine, China. No. 150 Jimo Road, Shanghai 200120, China.
Department of Orthopedics, Shanghai East Hospital, Tongji University School of Medicine, China. No. 150 Jimo Road, Shanghai 200120, China.
Injury. 2021 Aug;52(8):2084-2094. doi: 10.1016/j.injury.2021.05.034. Epub 2021 May 27.
The purpose of this study was to construct a rat caudal vertebral body fracture model and to analyze the association and histological characteristics of vertebral body fracture with endplate injury and adjacent intervertebral disc degeneration.
This study included 144 clean-grade male Sprague-Dawley rats, which were randomly divided into a control, middle vertebral body injury (MI), and endplate injury (EI) groups. A vertebral body fracture with or without endplate injury was developed by either drilling a hole in the middle of a rat caudal vertebral body to create a fracture with an intact endplate or drilling a hole in the vertebral body near the intervertebral disc to create a vertebral body fracture with endplate injury. The histological differences in the adjacent intervertebral discs of vertebral body fractures with or without endplate injury were detected using imaging, non-specific histological staining, immunohistochemistry and TUNEL assay.
Imaging results revealed that the EI group showed a significant decrease in intervertebral space height and intervertebral disc T2 signal over time. Non-specific histological staining revealed that in the EI group, the intervertebral disc was degenerative. Immunohistochemistry indicated that Aggrecan and Collagen-II were decreased and inflammatory factors were increased in the EI group. The TUNEL detection found that apoptosis was significantly increased in the EI group as compared with the MI and control groups.
In rat caudal vertebral body fractures, a fracture with endplate injury is more likely to induce or accelerate degeneration of adjacent intervertebral discs.
本研究旨在构建大鼠尾椎椎体骨折模型,并分析椎体骨折与终板损伤和邻近椎间盘退变的相关性和组织学特征。
本研究纳入 144 只清洁级雄性 Sprague-Dawley 大鼠,随机分为对照组、中椎体损伤(MI)组和终板损伤(EI)组。通过在大鼠尾椎中部钻孔形成完整终板的骨折或在椎间盘附近钻孔形成终板损伤的骨折来建立伴有或不伴有终板损伤的椎体骨折。通过影像学、非特异性组织学染色、免疫组织化学和 TUNEL 检测,检测伴有或不伴有终板损伤的椎体骨折相邻椎间盘的组织学差异。
影像学结果显示,EI 组的椎间高度和椎间盘 T2 信号随时间推移显著降低。非特异性组织学染色显示,EI 组椎间盘退行性变。免疫组织化学显示,EI 组聚集蛋白聚糖和 Collagen-II 减少,炎症因子增加。TUNEL 检测发现,与 MI 和对照组相比,EI 组的细胞凋亡明显增加。
在大鼠尾椎椎体骨折中,伴有终板损伤的骨折更易诱发或加速邻近椎间盘的退变。