The Role of the Mitochondrion in the Metabolic Stress Response to Burn Trauma

线粒体在烧伤代谢应激反应中的作用

• 批准号: 10275153
• 负责人: Craig Porter
• 金额: $ 38.5万
• 依托单位: ARKANSAS CHILDREN'S HOSPITAL RES INST
• 依托单位国家: 美国
• 财政年份: 2021
• 资助国家: 美国
• 起止时间: 2021-09-01 至 2026-06-30
• 项目状态: 未结题
• 来源: https://reporter.nih.gov/project-details/10275153
• 关键词: Adipose tissue; Animal Model; Antioxidants; Award; Bioenergetics; Blood Circulation; Blood specimen; Burn Trauma; Burn injury; Carrier Proteins; Clinical; Critical Illness; Data; Deuterium Oxide; Development; Dose; Energy Metabolism; Goals; Homeostasis; Insulin Resistance; Isotope Labeling; Knowledge; Measurement; Measures; Mediator of activation protein; Membrane Potentials; Metabolic; Metabolic dysfunction; Metabolic stress; Metabolism; Mitochondria; Mitochondrial DNA; Mitochondrial Proteins; Modeling; Morbidity - disease rate; Muscular Atrophy; Patients; Protons; Quality of life; Reactive Oxygen Species; Recovery; Research; Research Personnel; Respiratory physiology; Rodent Model; Role; Skeletal Muscle; Stress; Superoxides; Survivors; Temperature; Testing; Tissue Sample; Tissues; Trauma; United States; biological adaptation to stress; in vivo; innovation; insight; lipid metabolism; novel; oxidation; pre-clinical; programs; protein degradation; response; restoration; severe burns; systemic inflammatory response

PROJECT SUMMARY The main objective of this Maximizing Investigators' Research Award (MIRA) is to provide new mechanistic insight regarding the metabolic stress response to burn trauma. Specifically, the overarching goal of this research program is to elucidate the role of the mitochondrion in burn-induced hypermetabolism and metabolic dysfunction. Burns are a leading cause of non-fatal trauma in the United States. Today, even the most severe burns are survivable. However, burn survivors endure a protracted recovery, where restoration of function and quality of life are not readily achieved. Accordingly, there is a pressing need for new strategies that reduce morbidity and hasten the recovery of burn survivors. Recent data have implicated mitochondria as mediators of the metabolic stress response to burn trauma. Indeed, altered bioenergetics are thought underlay the hypermetabolic response to burns, and may contribute to burn-induced insulin resistance, altered lipid metabolism and muscle wasting. Further, mitochondrial stress appears to impact cellular homeostasis post burn through the formation of oxygen radicals, and may contribute to the systemic inflammatory response to burns by releasing fragments of mitochondrial DNA (mtDNA) into the circulation. This MIRA will support the development of innovative rodent models of isotopically labeled adipose tissue and skeletal muscle. These models will be leveraged to trace the turnover, redistribution and oxidation of specific substrates in response to burn injury. By combining these novel models with deuterium oxide dosing in vivo, we will generate important data regarding synthesis rates of key mitochondrial proteins in multiple tissues in response to burn trauma. By dovetailing measurements of substrate flux and mitochondrial carrier protein turnover with direct measures of mitochondrial respiratory function, proton leak, membrane potential and superoxide formation, we will elucidate the mechanistic basis of altered bioenergetics and metabolism in response to burn injury. In addition, the utility of ambient temperature, protonophores and mitochondrial targeted antioxidants as strategies to restore bioenergetics and metabolic function post burn will also rigorously tested. Furthermore, blood and tissue samples collected from burn patients will be used to validate preclinical data and to probe the role of mtDNA in the systemic inflammatory response to burn injury. By bettering our mechanistic understanding of the metabolic stress response to burns this research program will contribute new knowledge that may be leveraged to lessen the suffering and promote the recovery of burn survivors. Moreover, since hypermetabolism is present in other forms critical illness, the new information generated by this research program may have broader scientific and clinical impact.

项目摘要 这个最大化研究者研究奖（MIRA）的主要目标是提供新的 关于烧伤创伤的代谢应激反应的机制性见解。具体而言， 这项研究计划的目的是阐明在烧伤诱导的神经元的作用， 高代谢和代谢功能障碍。烧伤是美国非致命性创伤的主要原因 States.今天，即使是最严重的烧伤也是可以存活的。然而，烧伤幸存者忍受着长期的 恢复，其中功能和生活质量的恢复不容易实现。因此，有一个 迫切需要新的战略，以减少发病率和加速恢复烧伤幸存者。 最近的数据表明，线粒体是烧伤后代谢应激反应的介质。 事实上，生物能量学的改变被认为是烧伤后高代谢反应的原因， 导致烧伤引起的胰岛素抵抗、脂质代谢改变和肌肉萎缩。此外，本发明还 线粒体应激似乎通过氧的形成影响烧伤后的细胞内稳态 自由基，并可能有助于全身炎症反应烧伤释放碎片 线粒体DNA（mtDNA）进入血液循环。 该MIRA将支持同位素标记脂肪的创新啮齿动物模型的开发， 组织和骨骼肌。这些模型将被用来跟踪营业额，再分配和 烧伤后特定底物的氧化。通过将这些新颖的模型与 氧化氘剂量在体内，我们将产生重要的数据，关于合成率的关键 线粒体蛋白在多种组织中的表达。通过对以下各项的测量结果进行跟踪， 底物通量和线粒体载体蛋白周转与线粒体呼吸的直接措施 功能，质子漏，膜电位和超氧化物的形成，我们将阐明的机制 烧伤后生物能量学和代谢改变的基础。此外，环境的效用 温度，质子载体和线粒体靶向抗氧化剂作为恢复的策略 烧伤后的生物能量学和代谢功能也将受到严格的测试。此外，血液和组织 从烧伤患者中采集的样本将用于验证临床前数据， 线粒体DNA在烧伤全身炎症反应中的作用 通过改善我们对烧伤后代谢应激反应的机械理解， 该计划将提供新的知识，可以利用这些知识来减轻痛苦，促进 烧伤幸存者的康复此外，由于高代谢存在于其他形式的危重病中， 本研究项目产生的新信息可能具有更广泛的科学和临床影响。