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首页> 外文期刊>Journal of Neuroscience Methods >Technical aspects of an impact acceleration traumatic brain injury rat model with potential suitability for both microdialysis and P(ti)O(2) monitoring.
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Technical aspects of an impact acceleration traumatic brain injury rat model with potential suitability for both microdialysis and P(ti)O(2) monitoring.

机译:具有潜在适用性的微透析和P(ti)O(2)监测的冲击加速创伤性脑损伤大鼠模型的技术方面。

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摘要

This report describes technical adaptations of a traumatic brain injury (TBI) model-largely inspired by Marmarou-in order to monitor microdialysis data and P(ti)O(2) (brain tissue oxygen) before, during and after injury. We particularly focalize on our model requirements which allows us to re-create some drastic pathological characteristics experienced by severely head-injured patients: impact on a closed skull, no ventilation immediately after impact, presence of diffuse axonal injuries and secondary brain insults from systemic origin... We notably give priority to minimize anaesthesia duration in order to tend to banish any neuroprotection. Our new model will henceforth allow a better understanding of neurochemical and biochemical alterations resulting from traumatic brain injury, using microdialysis and P(ti)O(2) techniques already monitored in our Intensive Care Unit. Studies on efficiency and therapeutic window of neuroprotective pharmacological molecules are now conceivable to ameliorate severe head-injury treatment.
机译:本报告介绍了创伤性脑损伤(TBI)模型的技术改编,该模型在很大程度上受Marmarou的启发,目的是监测伤前,伤中和伤后的微透析数据和P(ti)O(2)(脑组织氧)。我们特别关注模型要求,这使我们能够重新创建一些头部严重受伤的患者所经历的剧烈病理特征:对闭合颅骨的撞击,撞击后立即无通气,弥漫性轴索损伤的存在以及系统性起源的继发性脑损伤……我们尤其优先考虑尽量减少麻醉时间,以消除任何神经保护作用。此后,我们的新模型将使用我们的重症监护病房中已监测的微透析和P(ti)O(2)技术,使人们更好地了解由颅脑外伤引起的神经化学和生化改变。现在可以考虑对神经保护药理学分子的功效和治疗范围进行研究,以改善严重的颅脑损伤治疗。

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