Biomechanics of Pediatric Head Injury

描述（由申请人提供）：创伤性脑损伤是儿童死亡的最常见原因，但儿科头部损伤的病因和治疗仍存在争议。在此之前，我们建立了一个跨学科的研究范式，使用急性动物实验，生物力学组织测试，回顾性临床研究，拟人化的“娃娃”研究，和计算模拟。我们的数据表明，儿童确实有不同于成人的损伤机制，需要针对年龄的损伤预防策略和治疗。在这次竞争性更新中，我们建立在我们已经建立的基础上，既加深了我们对基本损伤机制的理解，又增强了我们研究结果的临床相关性。我们将补充我们目前的平台与新的准备-生存研究，猪的行为结果，脑血流量（CBF）的措施，损伤后呼吸功能不全，和损伤治疗研究-以加强研究结果从实验室到临床环境的翻译。我们的总体假设是，未成熟大脑的快速旋转没有影响，通过机械和生化信号产生脑损伤，导致持续的功能和组织学异常。我们将比较单次和多次头部损伤后的长期结果，以确定损伤间隔是否调节损伤严重程度，以及补充叶酸是否减少轴突损伤（目标1）。我们将使用人类计算模型将我们的动物研究扩展到周期性振动运动，以估计谐波放大对损伤风险的贡献（目标2）。使用动物实验和计算机模型，我们将识别与CBF快速区域性减少相关的脑应变和与脑自动调节丧失相关的脑干变形（目的3）。我们将通过改变旋转方向来调节局部变形，并使用高渗盐水调节内皮反应，以验证急性机械和生化信号传导途径。在头部损伤后呼吸功能不全的仔猪中（目的4），我们假设100% FiO 2复苏导致自由基释放介导的神经病理学恶化，我们将比较室内空气和100% FiO 2以及有和没有自由基清除剂的结果，以验证功能。拟议的研究解决了我们的长期目标，阐明儿童创伤性脑损伤的损伤机制和潜在的治疗策略。

DESCRIPTION (provided by applicant): Traumatic brain injury is the most common cause of death in childhood, yet etiology and treatment of pediatric head injuries remain controversial. Previously, we established an interdisciplinary research paradigm using acute animal experiments, biomechanical tissue tests, retrospective clinical studies, anthropomorphic "doll" studies, and computational simulations. Our data show that children do indeed have injury mechanisms that are distinct from the adult, and require age-specific injury prevention strategies and treatments. In this competitive renewal, we build on the foundation we have established, both to deepen our understanding of basic injury mechanisms and to enhance the clinical relevance of our findings. We will supplement our current platforms with novel preparations - survival studies, porcine behavioral outcomes, cerebral blood flow (CBF) measures, post-injury respiratory insufficiency, and injury treatment studies - to enhance translation of research findings from the laboratory to the clinical setting. Our overall hypothesis is that rapid rotations of the immature brain without impact produce brain injury via both mechanical and biochemical signals, resulting in sustained functional and histological abnormalities. We will compare long-term outcomes after single and multiple head injuries to determine if injury interval modulates injury severity and if axonal injury is reduced with folate supplementation (Aim 1). We will use human computational models to extend our animal studies to cyclic shaking motions to estimate contribution of harmonic amplification to injury risk (Aim 2). Using animal experiments and computer models, we will identify cerebral strains associated with rapid regional decreases in CBF and brainstem deformations associated with loss of cerebral autoregulation (Aim 3). We will modulate regional deformations by altering rotation direction, and endothelial response with hypertonic saline to validate acute mechanical and biochemical signaling pathways. In piglets with respiratory insufficiency after head injury (Aim 4), we hypothesize that resuscitation with 100% FiO2 results in exacerbated neuropathology mediated by free radical release, and we will compare outcomes with room air and 100% FiO2, as well as with and without free radical scavengers to verify functionality. The proposed studies address our long-term goal of elucidating injury mechanisms and potential treatment strategies for traumatic brain injuries in children.