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A New Model of Traumatic Axonal Injury to Determine the Effects of Strain and Displacement Rates

机译:一种创伤性轴突损伤的新模型,以确定应变和位移率的影响

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Traumatic brain injury (TBI) continues to be a major health problem, with over 500,000 cases per year with a societal cost of approximately $85 billion in the US. Motor vehicle accidents are the leading cause of such injuries. In many cases of TBI widespread disruption of the axons occurs through a process known as diffuse axonal injury (DAI) or traumatic axonal injury (TAI). In the current study, an in vivo TAI model was developed using spinal nerve roots of adult rats. This model was used to determine functional and structural responses of axons to various strains and displacement rates. Fifty-six L5 dorsal nerve roots were each subjected to a predetermined strain range (<10%, 10-20% and >20%) at a specified displacement rate (0.01 mm/sec and 15 mm/sec) only once. Image analysis was used to determine actual strains on the roots during the pull. Neurophysiologic recordings were performed on the nerve root before and after stretch to determine functional changes in response to stretch, including conduction velocity (CV) and area of the evoked compound action potential (CAP). Structural changes including vascular injury, axotomy, and impaired axoplasmic transport (IAT) were evaluated using hematoxylin and eosin, Palmgren silver impregnation and β-APP staining techniques, respectively. Results showed that CV and the area of the CAP decreased as strain and displacement rate increased. Also, threshold strains for complete nerve conduction loss were 16% and 9% at 0.01 mm/sec and 15 mm/sec rate, respectively. These threshold values indicate the rate dependency of functional injury and indicate that axons tolerate slow loading rates better than higher loading rates. Histological studies revealed increased spacing, tearing of axons, IAT and occurrence of hemorrhage to be strain and displacement rate dependent. Linear relationships existed between the increasing strain and the occurrence rate of axonal injury as evidenced by multiple indicators (IAT, hemorrhage, torn fibers or primary axotomy) at both rates. In conclusion, the results from this study indicate that the severity of both functional and structural injury increased with increases in strain and displacement rate.
机译:创伤性脑损伤(TBI)仍然是一个重大的健康问题,每年有超过500,000例,美国的社会成本约为8.5亿美元。机动车事故是这种伤害的主要原因。在许多情况下,通过称为弥漫性轴突损伤(DAI)或创伤性轴突损伤(TAI)的过程发生轴突的普遍破坏轴突。在目前的研究中,使用成年大鼠的脊神经根部开发了一个体内泰模型。该模型用于确定轴突对各种菌株和位移率的功能和结构响应。每次以特定的位移率(0.01mm / sec和15mm / sec)以预定的应变范围(<10%,10-20%和> 20%)的预定应变范围(<10%,10-20%和> 20%)。图像分析用于在拉动期间确定根部的实际菌株。神经生理记录是之前对神经根进行和拉伸后,以确定响应于拉伸的功能变化,包括传导速度(CV)和诱发复合动作电位(CAP)的面积。使用血管基和曙红银浸渍和β-APP染色技术评估包括血管损伤,腋窝和受损的轴质转运(IAT)的结构变化。结果表明,随着应变和位移率的增加,CV和帽区域降低。此外,完全神经传导损失的阈值菌株分别为0.01mm / sec和15mm / sec速率为16%和9%。这些阈值表明功能损伤的速率依赖性,并表明轴突可以优于更高的加载速率而容忍慢的加载率。组织学研究表明,轴突的间距增加,颅骨,出血的发生,依赖于菌株和置换率。随着多种指标(IAT,出血,撕裂纤维或原发性轴突)在轴突损伤的增加和轴突损伤的发生率之间存在线性关系。总之,该研究的结果表明,功能性和结构损伤的严重程度随着应变和排量率的增加而增加。

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