Sensory & Motor System Medicine, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Bone and Cartilage Regenerative Medicine, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Spine (Phila Pa 1976). 2018 May 15;43(10):E557-E564. doi: 10.1097/BRS.0000000000002427.
An experimental study to develop a mouse model of lumbar intervertebral disc degeneration (IDD).
The aim of this study was to develop a mouse lumbar IDD model using surgically induced instability and to compare the findings of this model to those in human IDD.
Previously, various kinds of inducers have been used to reproduce IDD in experimental animals; however, there is yet no standard mouse lumbar IDD model without direct injury to intervertebral disc.
A total number of 59 C57BL/6J male mice at 8 weeks old were used. Instability of lumbar spine was induced by surgical resection of posterior elements, including facet joints, supra- and interspinous ligaments. We then analyzed time course changes in radiographical (n = 17) and histological analyses (n = 42), and compared these findings with those in human IDD.
Radiographical analyses showed that the disc height began to decrease in the first 2 weeks after the surgery, and the decrease continued throughout 12 weeks. Bone spurs at the vertebral rims were observed in the late stage of 8 and 12 weeks after the surgery. Histological analyses showed that the disorder of the anterior anulus fibrosus (AF) was initially obvious, followed by posterior shift and degeneration of the nucleus pulposus (NP). Proteoglycan detected in inner layer of AF and periphery of NP was decreased after 8 weeks. Immunohistochemistry displayed the increase of type I and X collagen, and matrix metalloproteinase 13 in the anterior AF.
Surgical resection of posterior elements of mouse lumbar spine resulted in reproducible IDD. Because the present procedure does not employ direct injury to intervertebral disc and the radiological and histological findings are compatible with those in human IDD, it may contribute to further understanding of the native pathophysiology of IDD in future.
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开发腰椎间盘退变(IDD)小鼠模型的实验研究。
本研究旨在通过手术引起的不稳定性开发一种小鼠腰椎 IDD 模型,并将该模型的结果与人类 IDD 的结果进行比较。
以前,已经使用了各种诱导剂在实验动物中再现 IDD;然而,目前尚无不直接损伤椎间盘的标准小鼠腰椎 IDD 模型。
使用总共 59 只 8 周龄 C57BL/6J 雄性小鼠。通过切除后关节突关节、上下棘间韧带等后部元件来诱导脊柱不稳定。然后,我们分析了影像学(n=17)和组织学分析(n=42)的时间进程变化,并将这些结果与人类 IDD 进行了比较。
影像学分析显示,手术后 2 周内椎间盘高度开始下降,12 周内持续下降。手术后 8 周和 12 周后,可见椎缘骨赘。组织学分析显示,前纤维环(AF)的紊乱最初明显,随后是后移和髓核(NP)变性。术后 8 周,内层 AF 和 NP 周围的蛋白聚糖减少。免疫组织化学显示前 AF 中 I 型和 X 型胶原以及基质金属蛋白酶 13 的增加。
切除小鼠腰椎后部元件可导致可重复的 IDD。由于本程序不直接损伤椎间盘,并且影像学和组织学结果与人类 IDD 相符,因此它可能有助于未来进一步了解 IDD 的天然病理生理学。
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