创伤性脊髓损伤猪 72 小时镇静模型

IF 1.9 Q3 CLINICAL NEUROLOGY
Mathias Møller Thygesen , Seyar Entezari , Nanna Houlind , Teresa Haugaard Nielsen , Nicholas Østergaard Olsen , Tim Damgaard Nielsen , Mathias Skov , Joel Borgstedt-Bendixen , Alp Tankisi , Mads Rasmussen , Halldór Bjarki Einarsson , Peter Agger , Dariusz Orlowski , Stig Eric Dyrskog , Line Thorup , Michael Pedersen , Mikkel Mylius Rasmussen
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引用次数: 0

摘要

引言人们越来越关注预防创伤性脊髓损伤(TSCI)后的继发性损伤,特别是通过改善脊髓灌注和免疫调节。这些治疗策略需要对人类创伤性脊髓损伤急性期的疾病进展建立可转化和可控的动物模型。研究问题是否有可能建立一个 72 小时镇静的不完全胸椎创伤性脊髓损伤猪模型,从而在创伤性脊髓损伤的整个亚急性阶段可控地使用连续性、侵入性和非侵入性方法?所有动物均接受椎板切除术,TSCI组动物则接受体重下降损伤。结果 在所有动物中,我们都成功地维持了 72 小时的镇静,且没有影响重要的生理指标。基于核磁共振成像的纤维束成像显示,所有 TSCI 动物的脊髓神经元的完整性都受到破坏,而组织学检查显示脊柱横切面没有完全损伤。值得注意的是,一些动物的头颅和尾部显示出继发性缺血组织的迹象。讨论与结论这项研究成功地建立了不完全TSCI猪模型,该模型在72小时内生理状态稳定。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A 72-h sedated porcine model of traumatic spinal cord injury

Introduction

There is an increasing focus on the prevention of secondary injuries following traumatic spinal cord injury (TSCI), especially through improvement of spinal cord perfusion and immunological modulation. Such therapeutic strategies require translational and controlled animal models of disease progression of the acute phases of human TSCI.

Research question

Is it possible to establish a 72-h sedated porcine model of incomplete thoracic TSCI, enabling controlled use of continuous, invasive, and non-invasive modalities during the entire sub-acute phase of TSCI?

Material and methods

A sham-controlled trial was conducted to establish the model, and 10 animals were assigned to either sham or TSCI. All animals underwent a laminectomy, and animals in the TSCI group were subjected to a weight-drop injury. Animals were then kept sedated for 72 h. The amount of injury was assessed by ex-vivo measures MRI-based fiber tractography, histology and immunohistochemistry.

Results

In all animals, we were successful in maintaining sedation for 72 h without comprising vital physiological parameters. The MRI-based fiber tractography showed that all TSCI animals revealed a break in the integrity of spinal neurons, whereas histology demonstrated no transversal sections of the spine with complete injury. Notably, some animals displayed signs of secondary ischemic tissue in the cranial and caudal sections.

Discussion and conclusions

This study succeeded in producing a porcine model of incomplete TSCI, which was physiologically stable up to 72 h. We believe that this TSCI model will constitute a potential translational model to study the pathophysiology secondary to TSCI in humans.

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来源期刊
Brain & spine
Brain & spine Surgery
CiteScore
1.10
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