Excitotoxicity in Circulatory Arrest ? Brain Injury

循环骤停中的兴奋性毒性？

• 批准号: 8029596
• 负责人: WILLIAM Anthony BAUMGARTNER
• 金额: $ 99.91万
• 依托单位: JOHNS HOPKINS UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2009
• 资助国家: 美国
• 起止时间: 2009-03-01 至 2013-02-28
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8029596
• 关键词: Animal Model; Animals; Anoxic Encephalopathy; Anticonvulsants; Apoptosis; Asses; Attenuated; Basal Ganglia; Behavioral; Biological Markers; Brain; Brain Injuries; Brain Ischemia; Calpain; Canis familiaris; Cardiac Surgery procedures; Cardiology; Cardiopulmonary Bypass; Cerebellum; Cerebrospinal Fluid; Cessation of life; Clinical; Clinical Medicine; Collaborations; Congenital Heart Defects; Core Facility; Development; Diagnosis; Disease; Encephalopathies; Faculty; Florida; Funding; Gene Expression; Gene Proteins; Genes; Genome; Genomics; Glutamates; Goals; Harvest; Health; Hippocampus (Brain); Hour; Human; Immunoblot Analysis; Impairment; Injury; Institutes; Institution; International; Intervention; Laboratories; Link; Measurable; Mediator of activation protein; Medical; Messenger RNA; Microarray Analysis; Modeling; Molecular; Necrosis; Neurocognitive; Neurologic; Neurologic Deficit; Neuronal Injury; Neurons; Neuroprotective Agents; Oligonucleotide Microarrays; Parietal Lobe; Pathogenesis; Pathologic; Pathology; Pathway interactions; Patients; Pattern; Pharmaceutical Preparations; Planning Techniques; Play; Proteins; Proteolysis; Proteomics; Protocols documentation; Regulation; Repair Complex; Research Personnel; Research Project Grants; Role; Running; Seizures; Series; Serum; Severities; Spectrin; Stroke; Techniques; Therapeutic; Thoracic aorta; Time; Translational Research; Translations; Traumatic Brain Injury; United States National Institutes of Health; Universities; Valproic Acid; Work; base; brain tissue; caspase-3; choreoathetosis; clinical practice; clinically relevant; design; dicesium N-succinimidyl 3-(undecahydrododecaboranyldithio)propionate; effective therapy; excitotoxicity; experience; insight; interdisciplinary approach; mRNA Expression; multidisciplinary; neuronal patterning; neuroprotection; novel; novel therapeutics; outcome forecast; preconditioning; prevent; prognostic

DESCRIPTION (provided by applicant): The technique of hypothermic circulatory arrest (HCA) is an established neuroprotective strategy allowing complex repairs of the thoracic aorta and congenital cardiac malformations. Despite its utility in clinical medicine, HCA is not without significant neurological sequelae which include intellectual and neuropsychomotor impairment, seizures, choreoathetosis, delayed development and stroke. Under continuous NIH support since 1992 our laboratory has completed an important body of work in which we have investigated the mechanisms of neurologic injury in a clinically relevant model of cardiopulmonary bypass (CPB) and HCA. In our canine model, which replicates clinical experience during cardiac surgical procedures, dogs subjected to two hours of HCA at 180C sustain a consistent neurologic deficit and histological pattern of selective neuronal death. The recent sequencing of the complete canine genome and the development of canine oligonucleotide microarrays has given us a unique opportunity to examine the molecular mechanisms of neurologic injury following HCA (both for prolonged and brief durations) as well as with standard cardiopulmonary bypass (CPB). Our current proposal focuses on the following objectives: 1.) To delineate, using microarray analysis, the underlying genomic regulation responsible for excitotoxic neuronal injury caused by 1 and 2 hours of HCA and standard CBP without HCA 2.) To identify neuroprotective changes in gene expression that result from a novel therapeutic strategy (Valproic acid) and 3.) To investigate gene-products (proteins) present in the cerebral spinal fluid (CSF) and serum for identification of brain and/or neuronal specific protein biomarkers for diagnosis and prognosis in HCA and CPB. To help us accomplish these goals, we have enlisted the help of an outstanding multidisciplinary group of investigators from the Johns Hopkins Medical Institutions (JHMI) Microarray Core Facility, Division of Cardiology, Department of Pathology and the University of Florida/Banyan Biomarkers; in addition to our previous collaboration with neuroscientists at the Kennedy Krieger Institute. We are confident that we have assembled a team with broad expertise to help us as we pursue these exciting new directions in our work. Multidisciplinary translational research is the cornerstone to reducing neurologic injury in patients undergoing hypothermic circulatory arrest. By applying an integrated approach of genomics and proteomics to our canine model of HCA, we hope to uncover new insights in the mechanisms of brain injury, how pharmacologic intervention attenuates that injury, and how we can clearly identify the injury, even when subtle on exam. PUBLIC HEALTH RELEVANCE Brain injury resulting from various causes is a significant international health concern. In this project, we focus on brain injury that occurs commonly in cardiac surgery (with both short and prolonged application of hypothermic circulatory arrest, HCA, and standard cardiopulmonary bypass, CPB, without HCA) in order to elucidate its mechanisms, develop biomarkers for diagnosis and prognosis, and discover effective therapies. Clearly, the translation of this work to clinical practice can have benefits not only for those patients with neurologic complications from HCA but also for patients undergoing routine cardiac surgical procedures and for those suffering brain injury from a number of factors, such as, stroke, traumatic brain injury or anoxic brain injury.

描述（由申请人提供）：低温停循环（HCA）技术是一种既定的神经保护策略，可用于胸主动脉和先天性心脏畸形的复杂修复。尽管HCA在临床医学中具有实用性，但它并非没有显著的神经系统后遗症，包括智力和神经精神障碍、癫痫发作、舞蹈手足徐动症、发育延迟和中风。自1992年以来，在NIH的持续支持下，我们的实验室完成了一项重要的工作，在这项工作中，我们研究了心肺转流（CPB）和HCA临床相关模型中神经损伤的机制。在我们的犬模型中，该模型复制了心脏外科手术期间的临床经验，在180 ℃下接受两小时HCA的犬维持了一致的神经功能缺损和选择性神经元死亡的组织学模式。最近的犬全基因组测序和犬寡核苷酸微阵列的发展给了我们一个独特的机会，以检查HCA后神经损伤的分子机制（无论是长期和短暂的持续时间），以及与标准的心肺转流（CPB）。我们当前的提案重点关注以下目标：1.）使用微阵列分析，描绘负责由1和2小时的HCA和不含HCA 2的标准CBP引起的兴奋性毒性神经元损伤的潜在基因组调控。确定由新的治疗策略（丙戊酸）引起的基因表达的神经保护性变化，3.）研究脑脊液（CSF）和血清中存在的基因产物（蛋白质），以鉴定用于HCA和CPB诊断和预后的脑和/或神经元特异性蛋白质生物标志物。为了帮助我们实现这些目标，我们已经从约翰霍普金斯医疗机构（JHMI）微阵列核心设施，心脏病科，病理学系和佛罗里达大学/Banyan生物标志物的优秀多学科研究小组中获得了帮助;除了我们之前与肯尼迪克里格研究所的神经科学家的合作之外。我们相信，我们已经组建了一个具有广泛专业知识的团队，帮助我们在工作中追求这些令人兴奋的新方向。多学科转化研究是减少低温停循环患者神经损伤的基石。通过将基因组学和蛋白质组学的综合方法应用于我们的HCA犬模型，我们希望揭示脑损伤机制的新见解、药物干预如何减轻这种损伤，以及我们如何清楚地识别损伤，即使在检查中很微妙。公共卫生相关性各种原因导致的脑损伤是一个重大的国际卫生问题。在这个项目中，我们专注于心脏手术中常见的脑损伤（短期和长期应用低温停循环，HCA和标准心肺转流，CPB，无HCA），以阐明其机制，开发诊断和预后的生物标志物，并发现有效的治疗方法。显然，将这项工作转化为临床实践不仅对患有HCA神经系统并发症的患者有益，而且对接受常规心脏外科手术的患者以及因多种因素（如中风、创伤性脑损伤或缺氧性脑损伤）而遭受脑损伤的患者也有益。