Mitochondrial Mechanisms of Hydrogen Sulfide Induced Suspended Animation

硫化氢诱导悬浮动画的线粒体机制

• 批准号: 7665145
• 负责人: SHANNON MARIE BAILEY
• 金额: $ 35.8万
• 依托单位: UNIVERSITY OF ALABAMA AT BIRMINGHAM
• 依托单位国家: 美国
• 财政年份: 2008
• 资助国家: 美国
• 起止时间: 2008-08-01 至 2012-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7665145
• 关键词: Active Sites; Acute; Air; Animals; Area; Bicarbonates; Blood; Blood Pressure; Blood flow; Blood specimen; Body Temperature; Breathing; Calcium; Cardiovascular Diseases; Cardiovascular Pathology; Cardiovascular system; Chemistry; Cleaved cell; Consumption; Critical Care; Cytochromes; Data; Disease Progression; Drops; Exposure to; Garlic; Glutathione Disulfide; Heart; Hepatocyte; Hibernation; Human; Hydrogen Sulfide; Hypertension; Intervention; Investigation; Ischemia; Kinetics; Knowledge; Laboratories; Lead; Learning; Liver; Liver Mitochondria; Lung; Mammals; Measurement; Measures; Membrane Potentials; Metabolic; Metabolism; Mitochondria; Modeling; Molecular; Morbidity - disease rate; Operative Surgical Procedures; Organ; Organ Transplantation; Oxidation-Reduction; Oxygen; Patients; Permeability; Physiological; Physiology; Production; Recovery; Reperfusion Injury; Reperfusion Therapy; Respiration; Rodent; Rodent Model; Signal Transduction; Signaling Molecule; Site; Stroke; Sulfhydryl Compounds; Sulfides; Swelling; Technology; Testing; Therapeutic Uses; Time; Tissues; Translating; Trauma; Vascular blood supply; Whole Blood; absorption; animation; body system; disulfide bond; falls; human disease; improved; mortality; new therapeutic target; novel; oxidation; polysulfide; prevent; research study; response; sensor; tool; uptake

DESCRIPTION (provided by applicant): The study of natural molecular and cellular adaptations to extreme environmental conditions could result in new therapeutic targets and interventions to treat and prevent numerous human diseases. For example, cardiovascular pathologies resulting from low blood flow and limited O2 supply, such as ischemia/reperfusion damage and stroke, can be studied using animal hibernation models. In hibernating animals, blood flow is globally and reversibly reduced to all organ systems, but ischemia/ reperfusion insults are absent as the reduced vascular supply is matched by global reduction in metabolism. Recent experiments have demonstrated that mammals that do not normally hibernate can be induced to enter a fully reversible hibernation-like state by exposure to air containing low levels of hydrogen sulfide (H2S) in a phenomenon called H2S-induced suspended animation. Rapid induction and controlled reversal of a hibernation-like state in humans would be immediately applicable for critical care, trauma management, organ transplantation, and general surgical procedures. Moreover, H2S, which is known to inhibit mitochondrial respiration, has recently gained recognition as an endogenously produced cell signaling molecule capable of reducing hypertension and cardiovascular disease progression, suggesting therapeutic uses for H2S as well. However, physiological systemic and cellular concentrations of H2S and those that lead to H2S-induced suspended animation are currently unknown, and very little is understood about the altered physiological responses or targeted systemic and mitochondrial responses during H2S-induced suspended animation. With a novel polarographic hydrogen sulfide sensor (PHSS) developed in our laboratory, we make real time H2S measurements under physiological conditions, allowing us to make unique contributions to the understanding of the H2S-induced suspended animation state. In a collaborative effort, we propose to define the H2S-induced suspended animation state and recovery, to characterize blood H2S chemistry, and to investigate mitochondrial responses to H2S. This will allow us to test the mechanistic hypothesis that H2S-induced suspended animation in non-hibernating rodents occurs when inhaled H2S causes an increased concentration of dissolved H2S in whole blood that results in reversible and protected suppression of mitochondrial respiration in tissues. Learning the mechanisms of H2S-induced suspended animation will allow us to test the ability of pharmacologic interventions to mimic conditions of the hibernator in non-hibernating mammalian species. A more detailed investigation and definition of the H2S-induced suspended animation model will uncover novel targets that may improve the morbidity and mortality of numerous patients with acute or even long term cardiovascular pathologies. PUBLIIC HEALTH RELEVANCE: Cardiovascular pathologies resulting from low blood flow and limited oxygen supply, such as ischemia/reperfusion damage and stroke, can be studied using animal hibernation models. Recent experiments have demonstrated that mammals that do not normally hibernate can be induced to enter a fully reversible hibernation-like state by exposure to air containing low levels of hydrogen sulfide (H2S) in a phenomenon called H2S-induced suspended animation. A more detailed definition of the H2S-induced suspended animation model, including physiological responses, blood H2S chemistry and mitochondrial mechanisms, as described in this proposal, will enable this model to be translated to humans as we uncover novel targets that may improve the morbidity and mortality of numerous patients with acute or even long term cardiovascular pathologies.

描述（由申请人提供）：对极端环境条件的自然分子和细胞适应性的研究可能会产生新的治疗靶点和干预措施，以治疗和预防许多人类疾病。例如，可以使用动物冬眠模型来研究由低血流量和有限的O2供应引起的心血管病理，例如缺血/再灌注损伤和中风。在冬眠动物中，所有器官系统的血流量全面且可逆地减少，但不存在缺血/再灌注损伤，因为减少的血管供应与代谢的全面减少相匹配。最近的实验表明，通常不冬眠的哺乳动物可以通过暴露于含有低水平硫化氢（H2S）的空气中进入完全可逆的冬眠状态，这种现象称为H2S诱导假死。人类冬眠样状态的快速诱导和受控逆转将立即适用于重症监护、创伤管理、器官移植和普通外科手术。此外，已知抑制线粒体呼吸的H2S最近被认为是能够降低高血压和心血管疾病进展的内源性产生的细胞信号传导分子，这也表明H2S的治疗用途。然而，H2S的生理系统和细胞浓度以及导致H2S诱导假死的浓度目前尚不清楚，并且对H2S诱导假死期间改变的生理反应或靶向系统和线粒体反应知之甚少。利用本实验室研制的一种新型极谱硫化氢传感器（PHSS），我们在生理条件下进行了真实的H2S测量，为理解H2S诱导的假死状态做出了独特的贡献。在一个合作的努力，我们建议定义硫化氢引起的假死状态和恢复，表征血液硫化氢化学，并调查线粒体对硫化氢的反应。这将使我们能够测试的机制假设，即H2S诱导假死在非冬眠啮齿动物发生时，吸入H2S导致全血中溶解的H2S浓度增加，导致可逆的和保护性的抑制组织中的线粒体呼吸。了解H2S诱导假死的机制将使我们能够测试药物干预的能力，以模拟非冬眠哺乳动物物种中冬眠动物的条件。更详细的调查和定义的硫化氢诱导假死模型将发现新的目标，可能会改善许多患者的发病率和死亡率与急性甚至长期心血管病变。公众健康相关性：由低血流量和有限的氧气供应导致的心血管病理学，如缺血/再灌注损伤和中风，可以使用动物冬眠模型进行研究。最近的实验表明，通常不冬眠的哺乳动物可以通过暴露于含有低水平硫化氢（H2S）的空气中进入完全可逆的冬眠状态，这种现象称为H2S诱导假死。H2S诱导假死模型的更详细定义，包括生理反应，血液H2S化学和线粒体机制，如本提案所述，将使该模型能够转化为人类，因为我们发现了可能改善许多急性甚至长期心血管疾病患者发病率和死亡率的新靶点。