Institut National de la Santé et de la Recherche Médicale U583, Institute for Neurosciences of Montpellier, Montpellier, France.
J Neurosurg Spine. 2010 Jan;12(1):106-13. doi: 10.3171/2009.7.SPINE0989.
Neuroprotective and repair strategies in spinal cord injuries (SCIs) have been so far largely unsuccessful. One of the prerequisites is the use of appropriate preclinical models to decipher pathophysiological mechanisms; another is the identification of optimal time windows for therapeutic interventions. The authors undertook this study to characterize early motor, sensory, autonomic, and histological outcomes after balloon compression of the spinal cord at the T8-9 level in adult rats.
A total of 91 rats were used in this study. Spinal cord balloon compression was performed at T8-9 in adult rats by inflation of a 2 Fr Fogarty catheter into the epidural space. The authors first characterized early motor, sensory, and autonomic outcomes of 2 volumes of compression (10 and 15 microl) using behavioral tests and then examined histological outcomes in the spinal cord using Luxol fast blue staining. To further substantiate the characterization of the epidural balloon-compression model, they used a noncompetitive N-methyl-D-aspartate antagonist, GK11, and demonstrated the involvement of excitotoxicity in this model.
Proportional and reproducible functional impairment resulted from compression caused by balloon inflation with either 10 or 15 microl of water and corresponded to the extent of the lesion. Indeed, during the early phase following SCI (1 week postinjury), recovery of locomotor function and bladder control correlated with the volume of inflation, whereas outcomes with respect to sensory function and reflexes were independent of compression severity. Treatment with GK11 significantly improved motor function in all groups of rats 1 week after injury and bladder voiding in the 10-microl injured rats compared to the 15-microl injured rats.
The results of this study demonstrate that spinal balloon-compression injury in the rat is a well-characterized, reproducible, and predictable model to analyze early events following SCI.
迄今为止,脊髓损伤(SCI)的神经保护和修复策略在很大程度上尚未成功。其中一个前提是使用适当的临床前模型来解析病理生理机制;另一个是确定治疗干预的最佳时间窗。作者进行了这项研究,以描述成年大鼠 T8-9 脊髓球囊压迫后早期运动、感觉、自主和组织学结果。
本研究共使用了 91 只大鼠。通过将 2 Fr Fogarty 导管充气到硬膜外腔,在成年大鼠的 T8-9 处进行脊髓球囊压迫。作者首先使用行为测试来描述 2 种压缩体积(10 和 15 微升)的早期运动、感觉和自主功能结果,然后使用 Luxol 快速蓝染色检查脊髓的组织学结果。为了进一步证实硬膜外球囊压迫模型的特征,作者使用了非竞争性 N-甲基-D-天冬氨酸拮抗剂 GK11,并证明了兴奋性毒性在该模型中的作用。
球囊充气引起的压迫导致了比例和可重复的功能障碍,这与损伤的程度相对应。事实上,在 SCI 后的早期阶段(损伤后 1 周),运动功能和膀胱控制的恢复与充气量有关,而感觉功能和反射的结果与压缩严重程度无关。与 15 微升损伤组相比,GK11 治疗在损伤后 1 周时显著改善了所有大鼠的运动功能和 10 微升损伤大鼠的膀胱排空功能。
本研究的结果表明,大鼠脊髓球囊压迫损伤是一种经过充分验证的、可重复的、可预测的模型,可用于分析 SCI 后的早期事件。