Development of a Novel Rat Intervertebral Disc Degeneration Model by Surgical Multifidus Resection–Induced Instability

医学 H&E染色 病理 免疫组织化学 椎间盘 免疫印迹 病态的 组织学 腰椎 逆转录聚合酶链式反应 解剖 基因表达 生物 生物化学 基因
作者
Daocheng Zhu,Zhimin Miao,Mingwei Dong,Jiahao Lin,Yihan Wang,Naifeng Tian,Peng Luo,Yan Lin,Yaosen Wu,Mochuan Chen
出处
期刊:World Neurosurgery [Elsevier]
卷期号:165: e357-e364 被引量:2
标识
DOI:10.1016/j.wneu.2022.06.051
摘要

This study aimed to investigate whether surgical resection of multifidus in rats could generate a reliable model of intervertebral disc degeneration (IVDD).Instability of the lumbar spine in Sprague-Dawley rats was induced by multifidus resection. Longissimus changes were examined by hematoxylin and eosin staining and immunohistochemistry. Specific protein and mRNA changes in the nucleus pulposus (NP) were quantified by Western blot and reverse transcription-polymerase chain reaction. Bone alterations were assessed using X-ray imaging, and disc changes were evaluated by hematoxylin and eosin staining, immunofluorescence, and immunohistochemistry.Fat infiltration and increased tumor necrosis factor-α expression in the longissimus were detected following surgery. Reverse transcription-polymerase chain reaction and Western blot results demonstrated that the inflammation and catabolism in the NP were increased after the surgical intervention. Moreover, X-ray imaging showed that the disc height had decreased and bone spurs had formed at the vertebral rims. Histological analyses further revealed degeneration of the annulus fibrosus, endplate, and NP. Furthermore, in contrast to the sham group, the collagen II expression was reduced, while matrix metalloproteinase-13 was increased in the surgery group.Surgical resection of the multifidus in rats resulted in a reproducible IVDD model. Because the present procedure does not impart direct injury to the intervertebral disc, it can better imitate the pathological states in humans. Therefore, our rat multifidus resection model might help us further understand the intrinsic pathophysiology of IVDD.
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