Regulation of Cerebral Blood Flow After Traumatic Brain Injury

该建议的总体假设是，创伤性脑损伤导致脑血流量（CBF）调节障碍，从而在我们的头部损伤患者中产生一系列损伤，从直接缺血到对继发性损伤的易感性增加。在上一个资助期间，我们评估了一种管理策略，通过为大脑提供更高的灌注压力来防止缺血，这将补偿受伤大脑的压力自动调节能力受损。本研究表明，我们可以显著减少继发性损伤的发生，但高灌注压的其他后果（更多的成人呼吸窘迫综合征，可能加重脑水肿）抵消了减少缺血性损伤的有益作用。这项研究的结果强调了所提出的工作的重要性。本研究的总体目标是开发出识别继发性损伤风险最高的患者的方法，并开发出一种通过纠正导致受伤大脑对缺血性损伤敏感的潜在血管异常来预防继发性脑缺血的方法。第一个总体目标将通过研究头部受伤患者的脑血流调节来实现，并确定这些测试的异常是否预示着继发性损伤的更大风险（具体目标#1-2）。在研究结束时，我们计划确定可以在入院时进行的简单测试，以确定继发性损伤风险较大的患者，因此谁将从cbf靶向治疗中获益最多。第二个目标将通过研究分离血管中的肌原性反应与体内观察到的自我调节障碍之间的关系（Specific Aim #3），通过研究各种血管活性介质与体内观察到的CBF调节障碍之间的关系（Specific Aim #3），以及通过研究l -精氨酸对CBF和CBF调节的影响（Specific Aim #4）来实现。具体目标包括：1。开发监测重症监护病房CBF调节的实用方法：目的：探讨脑外伤后脑血流调节功能障碍的发生率和严重程度。3 .探讨脑外伤后脑血流调节功能受损的原因。研究l -精氨酸对脑外伤后局部或全身缺血（CBF<20 ml/100gm/min）患者脑血流动力学的影响：

The overall hypothesis of this proposal is that traumatic brain injury causes impairment of cerebral blood flow (CBF) regulation that produces a spectrum of injury in our head injured patients, ranging from frank ischemia to increased susceptibility to secondary insults. During the last grant period, we valuated a management strategy to prevent ischemia by providing the brain with a higher perfusion pressure that would compensate for the impaired ability of the injured brain to pressure autoregulate. This study demonstrated that we could significantly reduce the occurrence of secondary insults, but other consequences of the higher perfusion pressure (more adult respiratory distress syndrome, possibly worsened cerebral edema) offset the beneficial effects of reducing ischemic insults. The results of this study emphasize the importance of the proposed works. The overall goals of the proposed work are to develop methods for identifying those patients who are at greatest risk of secondary insults and to develop a way to prevent secondary cerebral ischemia by correcting the underlying vascular abnormalities that cause the injured brain to be sensitive to ischemic insults. The first overall goal will be achieved by studying CBF regulation in head injured patients and determining if abnormalities on these tests predict a greater risk of secondary insults (Specific Aims #1-2). At the end of the study, we plan to have identified simple tests that can be performed on admission to identify patients at greater risk from secondary insults and who therefore would benefit most from CBF-targeted therapy. The second goal will be achieved by studying the relationship of the myogenic response in isolated vessels to the impairment of autoregulation observed in vivo (Specific Aim #3), by studying the relationship of various vasoactive mediators to the impairment of CBF regulation observed in vivo (Specific Aim #3), and by studying the effect of L-arginine on CBF and on CBF regulation (Specific Aim #4). The specific aims include: 1. To develop practical methods for monitoring CBF regulation in the intensive care unit: 2. To study the incidence and severity of impairment of CBF regulation after TBI: 3. To study the cause of impairment of CBF regulation after TBI: 4. To study the effect of L-arginine on cerebral hemodynamics in patients with regional or global ischemia (CBF<20 ml/100gm/min) after TBI: