Hydrogen sulfide attenuates heart failure through Nrf2-mediated signaling

硫化氢通过 Nrf2 介导的信号传导减轻心力衰竭

• 批准号: 8197419
• 负责人: John Winter Calvert
• 金额: $ 38.36万
• 依托单位: EMORY UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2010
• 资助国家: 美国
• 起止时间: 2010-01-04 至 2014-11-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8197419
• 关键词: Acute; Address; Affect; Antioxidants; Apoptosis; Attenuated; Biogenesis; Biological Models; Cardiac; Cardiovascular Diseases; Cardiovascular system; Caring; Cystathionine; Developed Countries; Development; Enzymes; Experimental Models; Foundations; Functional disorder; Health; Healthcare; Heart; Heart Hypertrophy; Heart failure; Histone Deacetylase; Homeostasis; Hydrogen Sulfide; Hypertrophy; In Vitro; Incidence; Injury; Ischemia; Lyase; Mediating; Mitochondria; Modeling; Mus; Myocardial Infarction; Myocardial Ischemia; Myocardium; Nuclear; Oxidative Stress; Pharmacotherapy; Physiological; Play; Prevalence; Regulation; Reperfusion Injury; Reperfusion Therapy; Role; Signal Transduction; Signaling Molecule; Staging; System; Testing; Therapeutic; Thioredoxin; United States; Up-Regulation; Work; clinically relevant; cost; design; heme oxygenase-1; hemodynamics; improved; in vitro Model; in vivo; in vivo Model; meetings; mitochondrial dysfunction; novel; nuclear respiratory factor; pressure; protective effect; protein complex; protein expression; public health relevance; therapy design; transcription factor

DESCRIPTION (provided by applicant): Heart failure is the inability of the heart to meet hemodynamic demands and represents the end stage of various forms of cardiovascular disease. In industrialized nations, heart failure represents a major health problem that has been increasing in prevalence and incidence. It is estimated that 5.7 million people in the United States have heart failure resulting in about $37.2 billion being spent a year to cover associated health care related costs. Therefore, drug therapy designed to coincide with the standard means of care are needed to decrease the extent of injury leading to the development of heart failure. Recently, hydrogen sulfide (H2S) has been shown to be cardioprotective in various in vitro and in vivo models of cardiac injury. Although the physiological and cardioprotective effects of H2S in acute models of ischemia- reperfusion injury have previously been documented, the signaling mechanisms that mediate these effects have not been fully studied. Moreover, the signaling mechanisms that have been attributed to H2S have predominantly been studied in in vitro model systems, with very few studies actually exploring the protective effects in in vivo systems. Additionally, the cardioprotective effects of H2S in the setting of heart failure have not been investigated. For this reason, the studies proposed in this application are extremely important and timely. The overall aim of this proposal is to evaluate the signaling mechanisms responsible for the observed cardioprotective effects of H2S therapy in the setting of heart failure. To this end, the transcription factor, Nrf2, has been identified as a possible regulator of these cardioprotective effects. Therefore, the central hypothesis for the proposed studies is that H2S up-regulates endogenous antioxidants, alleviates mitochondrial dysfunction, and reduces hypertrophy in a Nrf2-dependent manner. To test this hypothesis, 3 Specific Aims have been proposed. Specific Aim 1 will evaluate the role of Nrf2 signaling in mediating the antioxidant effects of H2S. Specific Aim 2 will investigate if H2S suppresses apoptosis and cardiac hypertrophy via Nrf2/Trx1- dependent signaling. Specific Aim 3 will investigate if H2S induces mitochondrial biogenesis via Nrf2- dependent signaling. The proposed studies will significantly advance our current understanding of the mechanisms responsible for the development of heart failure and will answer important questions regarding the signaling mechanism responsible for the cardioprotective effects of H2S in the setting of heart failure. Additionally, information gained from these studies will provide the foundation for the development of H2S therapy for the treatment of heart failure. PUBLIC HEALTH RELEVANCE: Despite numerous advances in health care, cardiovascular disease remains the number one killer in the United States and heart failure, as a direct result of cardiovascular disease, affects nearly 5.3 million people in the United States resulting in about $34.8 billion being spent a year to cover associated health care related costs. The proposed studies will evaluate the efficacy of a hydrogen sulfide releasing compound in clinically relevant and highly translational experimental model systems of heart failure. The proposed studies will significantly advance our current understanding of the mechanisms responsible for the development of heart failure and will answer important questions regarding the signaling mechanism responsible for the cardioprotective effects of hydrogen sulfide in the setting of heart failure.

描述(申请人提供)：心力衰竭是心脏不能满足血液动力学需求，代表各种形式的心血管疾病的终末期。在工业化国家，心力衰竭是一个主要的健康问题，其患病率和发病率一直在上升。据估计，美国有570万人患有心力衰竭，导致每年花费约372亿美元来支付相关的医疗保健费用。因此，需要设计与标准护理手段相一致的药物治疗，以减少导致心力衰竭发展的损伤程度。最近，在各种体外和体内心脏损伤模型中，硫化氢(H_2S)被证明具有心脏保护作用。虽然H_2S在急性缺血再灌注损伤模型中的生理和心脏保护作用已有报道，但介导这些作用的信号机制尚未完全研究。此外，被归因于硫化氢的信号机制主要是在体外模型系统中研究的，很少有研究实际探索在体内系统中的保护作用。此外，在心力衰竭的背景下，硫化氢的心脏保护作用还没有被研究。因此，本申请中提出的研究是极其重要和及时的。这项建议的总体目标是评估在心力衰竭背景下观察到的硫化氢治疗的心脏保护作用的信号机制。为此，转录因子Nrf2已被确定为这些心脏保护作用的可能调节因子。因此，提出的研究的中心假设是，硫化氢上调内源性抗氧化剂，减轻线粒体功能障碍，并以Nrf2依赖的方式减少肥大。为了验证这一假设，我们提出了3个具体目标。具体目标1将评估Nrf2信号在介导硫化氢抗氧化作用中的作用。特异性目标2将研究硫化氢是否通过Nrf2/Trx1依赖的信号抑制细胞凋亡和心肌肥大。具体目标3将研究硫化氢是否通过Nrf2依赖的信号诱导线粒体生物发生。建议的研究将极大地促进我们目前对心力衰竭发生机制的理解，并将回答有关在心力衰竭背景下硫化氢对心脏保护作用的信号机制的重要问题。此外，从这些研究中获得的信息将为开发治疗心力衰竭的硫化氢疗法提供基础。 与公共健康相关：尽管在医疗保健方面取得了许多进展，但心血管疾病仍然是美国的头号杀手，心力衰竭作为心血管疾病的直接结果，影响着美国近530万人，导致每年花费约348亿美元来支付相关的医疗保健费用。拟议的研究将评估一种硫化氢释放化合物在临床相关和高度平移的心力衰竭实验模型系统中的有效性。这些拟议的研究将极大地促进我们目前对心力衰竭发生机制的理解，并将回答有关硫化氢在心力衰竭环境中对心脏保护作用的信号机制的重要问题。