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一种由腰段脊髓硬膜外压迫诱导的慢性脊髓空洞症大鼠模型。

A rat model of chronic syringomyelia induced by epidural compression of the lumbar spinal cord.

作者信息

Lee Ji Yeoun, Kim Shin Won, Kim Saet Pyoul, Kim Hyeonjin, Cheon Jung-Eun, Kim Seung-Ki, Paek Sun Ha, Pang Dachling, Wang Kyu-Chang

机构信息

Departments of 1 Anatomy and.

Neural Development and Anomaly Laboratory, Seoul National University College of Medicine.

出版信息

J Neurosurg Spine. 2017 Oct;27(4):458-467. doi: 10.3171/2016.9.SPINE16188. Epub 2017 Feb 17.

Abstract

OBJECTIVE There has been no established animal model of syringomyelia associated with lumbosacral spinal lipoma. The research on the pathophysiology of syringomyelia has been focused on Chiari malformation, trauma, and inflammation. To understand the pathophysiology of syringomyelia associated with occult spinal dysraphism, a novel animal model of syringomyelia induced by chronic mechanical compression of the lumbar spinal cord was created. METHODS The model was made by epidural injection of highly concentrated paste-like kaolin solution through windows created by partial laminectomy of L-1 and L-5 vertebrae. Behavioral outcome in terms of motor (Basso-Beattie-Bresnahan score) and urinary function was assessed serially for 12 weeks. Magnetic resonance images were obtained in some animals to confirm the formation of a syrinx and to monitor changes in its size. Immunohistochemical studies, including analysis for glial fibrillary acidic protein, NeuN, CC1, ED-1, and caspase-3, were done. RESULTS By 12 weeks after the epidural compression procedure, syringomyelia formation was confirmed in 85% of the rats (34 of 40) on histology and/or MRI. The syrinx cavities were found rostral to the epidural compression. Motor deficit of varying degrees was seen immediately after the procedure in 28% of the rats (11 of 40). In 13 rats (33%), lower urinary tract dysfunction was seen. Motor deficit improved by 5 weeks after the procedure, whereas urinary dysfunction mostly improved by 2 weeks. Five rats (13%, 5 of 40) died 1 month postoperatively or later, and 3 of the 5 had developed urinary tract infection. At 12 weeks after the operation, IHC showed no inflammatory process, demyelination, or accelerated apoptosis in the spinal cords surrounding the syrinx cavities, similar to sham-operated animals. CONCLUSIONS A novel experimental model for syringomyelia by epidural compression of the lumbar spinal cord has been created. The authors hope that it will serve as an important research tool to elucidate the pathogenesis of this type of syringomyelia, as well as the CSF hydrodynamics of the lumbar spinal cord.

摘要

目的

目前尚无成熟的与腰骶部脊髓脂肪瘤相关的脊髓空洞症动物模型。脊髓空洞症病理生理学的研究主要集中在Chiari畸形、创伤和炎症方面。为了解与隐匿性脊柱裂相关的脊髓空洞症的病理生理学,创建了一种通过慢性机械压迫腰段脊髓诱导脊髓空洞症的新型动物模型。方法:通过L-1和L-5椎板部分切除所形成的窗口,硬膜外注射高浓度膏状高岭土溶液制作模型。连续12周评估运动(Basso-Beattie-Bresnahan评分)和泌尿功能方面的行为结果。对部分动物进行磁共振成像,以确认脊髓空洞的形成并监测其大小变化。进行免疫组织化学研究,包括对胶质纤维酸性蛋白、NeuN、CC1、ED-1和半胱天冬酶-3的分析。结果:硬膜外压迫术后12周,组织学和/或MRI证实85%的大鼠(40只中的34只)形成了脊髓空洞症。脊髓空洞腔位于硬膜外压迫的头侧。术后立即有28%的大鼠(40只中的11只)出现不同程度的运动功能障碍。13只大鼠(33%)出现下尿路功能障碍。术后5周运动功能障碍有所改善,而泌尿功能障碍大多在2周后改善。5只大鼠(13%,40只中的5只)在术后1个月或更晚死亡,其中5只中有3只发生了尿路感染。术后12周,免疫组化显示脊髓空洞腔周围的脊髓中无炎症过程、脱髓鞘或加速凋亡,与假手术动物相似。结论:创建了一种通过硬膜外压迫腰段脊髓诱导脊髓空洞症的新型实验模型。作者希望它将成为阐明此类脊髓空洞症发病机制以及腰段脊髓脑脊液动力学的重要研究工具。

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