IMPACT OF HYDROGEN SULFIDE ON OUTCOME OF CARDIAC ARREST AND CARDIOPULMONARY RESUS

硫化氢对心脏骤停和心肺复苏结果的影响

基本信息

  • 批准号:
    8055816
  • 负责人:
  • 金额:
    $ 43.33万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    2010
  • 资助国家:
    美国
  • 起止时间:
    2010-04-05 至 2015-03-31
  • 项目状态:
    已结题

项目摘要

DESCRIPTION (provided by applicant): Sudden cardiac arrest (CA) is one of the leading causes of death worldwide. Despite advances in cardiopulmonary resuscitation (CPR) methods, 60-80% of these arrests result in immediate death, and of the remaining, only about 5 percent are successfully resuscitated to the extent that they are returned to productive lives. Innovative approach is needed to improve the outcome of cardiac arrest and CPR. Hydrogen sulfide is a colorless gas with a characteristic rotten-egg odor found in various natural and industrial sources. Recent studies suggested that H2S is endogenously produced and exerts a host of biological effects on various targets, resulting in responses that range from cytotoxic to cytoprotective effects. It has been reported that administration of an H2S donor (Na2S) attenuates myocardial ischemia-reperfusion (IR) injury in rodents and pig. In studies presented in the Preliminary Studies section, we observed that administration of Na2S at the time of CPR markedly improved myocardial and neurological function and survival 24h after CA/CPR in mice. The robust protective effect of Na2S was associated with attenuated oxidative stress, neuronal death, and enhanced NO signal. Of note, the protective effects of Na2S were abolished by NOS3 deficiency. Importantly, administration of Na2S prevented CA/CPR-induced development of marked cerebral edema 24h after CA/CPR as demonstrated by diffusion-weighted MRI in live mice. The overall goal of this proposal is to elucidate the role of H2S and develop novel therapeutic strategies to improve outcomes of CA/CPR complicated with post-cardiac arrest syndrome. Specifically, we propose: (Aim 1) To characterize time-dependent evolution of neurological and myocardial dysfunction and systemic inflammation in a mouse model of CA/CPR with optimized post-cardiac arrest care, (Aim 2) To define the impact of hydrogen sulfide on the evolution of neurological and myocardial dysfunction after CA/CPR, (Aim 3) To define the role of NOS for the protective effects of H2S on outcome of CA/CPR, and (Aim 4) To elucidate the molecular signaling mechanisms responsible for the protective effects of hydrogen sulfide in cultured neurons, endothelial cells, and cardiomyocytes. We anticipate that proposed studies will illuminate the unique protective effects of sulfide-based approach to CA/CPR using our innovative in vivo model of murine cardiac arrest and CPR. PUBLIC HEALTH RELEVANCE: Sudden cardiac arrest (CA) is one of the leading causes of death worldwide. Despite advances in cardiopulmonary resuscitation (CPR) methods, 60-80% of these arrests result in immediate death, and of the remaining, only about 5 percent are successfully resuscitated to the extent that they are returned to productive lives. Innovative approach is needed to improve the outcome of cardiac arrest and CPR. The overall goal of this proposal is to elucidate the role of H2S and develop novel therapeutic strategies to improve outcomes of CA/CPR complicated with post-cardiac arrest syndrome. We anticipate that proposed studies will illuminate the unique protective effects of sulfide-based approach to CA/CPR using our innovative in vivo model of murine cardiac arrest and CPR.
描述(由申请人提供):心脏骤停(CA)是全球主要死亡原因之一。尽管心肺复苏(CPR)方法取得了进展,但这些骤停中有60-80%导致立即死亡,而在其余的人中,只有约5%成功复苏,恢复了生产性生活。需要创新的方法来改善心脏骤停和CPR的结果。 硫化氢是一种无色气体,具有典型的臭鸡蛋气味,存在于各种天然和工业来源中。最近的研究表明,H2S是内源性产生的,并对各种靶点产生许多生物学效应,导致从细胞毒性到细胞保护作用的反应。据报道,施用H2S供体(Na 2S)减轻啮齿动物和猪的心肌缺血-再灌注(IR)损伤。在“初步研究”部分中介绍的研究中,我们观察到在CPR时给予Na 2S显著改善了小鼠CA/CPR后24小时的心肌和神经功能以及存活率。Na 2S的强大保护作用与减弱的氧化应激、神经元死亡和增强的NO信号有关。值得注意的是,Na 2S的保护作用被NOS 3缺乏所消除。重要的是,如通过活体小鼠中的扩散加权MRI所证明的,施用Na 2S防止CA/CPR后24小时CA/CPR诱导的显著脑水肿的发展。 本提案的总体目标是阐明H2S的作用,并开发新的治疗策略,以改善CA/CPR并发心脏骤停后综合征的结局。具体而言,我们建议:(目的1)在具有优化的心脏骤停后护理的CA/CPR小鼠模型中表征神经和心肌功能障碍以及全身炎症的时间依赖性演变,(目的2)确定硫化氢对CA/CPR后神经和心肌功能障碍演变的影响,(目的3)确定NOS在H2S对CA/CPR结果的保护作用中的作用,目的4)阐明硫化氢对培养的神经细胞、内皮细胞和心肌细胞的保护作用的分子信号机制。 我们预计,拟议的研究将阐明独特的保护作用的硫化物为基础的方法CA/CPR使用我们的创新的小鼠心脏骤停和CPR的体内模型。 公共卫生相关性:心脏骤停(CA)是全球主要死亡原因之一。尽管心肺复苏(CPR)方法取得了进展,但这些骤停中有60-80%导致立即死亡,而在其余的人中,只有约5%成功复苏,恢复了生产性生活。需要创新的方法来改善心脏骤停和CPR的结果。本提案的总体目标是阐明H2S的作用,并开发新的治疗策略,以改善CA/CPR并发心脏骤停后综合征的结局。我们预计,拟议的研究将阐明独特的保护作用的硫化物为基础的方法CA/CPR使用我们的创新的小鼠心脏骤停和CPR的体内模型。

项目成果

期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)

数据更新时间:{{ journalArticles.updateTime }}

{{ item.title }}
{{ item.translation_title }}
  • DOI:
    {{ item.doi }}
  • 发表时间:
    {{ item.publish_year }}
  • 期刊:
  • 影响因子:
    {{ item.factor }}
  • 作者:
    {{ item.authors }}
  • 通讯作者:
    {{ item.author }}

数据更新时间:{{ journalArticles.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ monograph.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ sciAawards.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ conferencePapers.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ patent.updateTime }}

FUMITO ICHINOSE其他文献

FUMITO ICHINOSE的其他文献

{{ item.title }}
{{ item.translation_title }}
  • DOI:
    {{ item.doi }}
  • 发表时间:
    {{ item.publish_year }}
  • 期刊:
  • 影响因子:
    {{ item.factor }}
  • 作者:
    {{ item.authors }}
  • 通讯作者:
    {{ item.author }}

{{ truncateString('FUMITO ICHINOSE', 18)}}的其他基金

Role of Sedation in the Post-Cardiac Arrest Neurological Recovery
镇静在心脏骤停后神经恢复中的作用
  • 批准号:
    10735115
  • 财政年份:
    2023
  • 资助金额:
    $ 43.33万
  • 项目类别:
Role of sulfide catabolism in ischemic brain injury
硫化物分解代谢在缺血性脑损伤中的作用
  • 批准号:
    10378758
  • 财政年份:
    2019
  • 资助金额:
    $ 43.33万
  • 项目类别:
Role of sulfide catabolism in ischemic brain injury
硫化物分解代谢在缺血性脑损伤中的作用
  • 批准号:
    10588192
  • 财政年份:
    2019
  • 资助金额:
    $ 43.33万
  • 项目类别:
IMPACT OF HYDROGEN SULFIDE ON OUTCOME OF CARDIAC ARREST AND CARDIOPULMONARY RESUS
硫化氢对心脏骤停和心肺复苏结果的影响
  • 批准号:
    8236893
  • 财政年份:
    2010
  • 资助金额:
    $ 43.33万
  • 项目类别:
IMPACT OF HYDROGEN SULFIDE ON OUTCOME OF CARDIAC ARREST AND CARDIOPULMONARY RESUS
硫化氢对心脏骤停和心肺复苏结果的影响
  • 批准号:
    8463026
  • 财政年份:
    2010
  • 资助金额:
    $ 43.33万
  • 项目类别:
IMPACT OF HYDROGEN SULFIDE ON OUTCOME OF CARDIAC ARREST AND CARDIOPULMONARY RESUS
硫化氢对心脏骤停和心肺复苏结果的影响
  • 批准号:
    8645697
  • 财政年份:
    2010
  • 资助金额:
    $ 43.33万
  • 项目类别:
IMPACT OF HYDROGEN SULFIDE ON OUTCOME OF CARDIAC ARREST AND CARDIOPULMONARY RESUS
硫化氢对心脏骤停和心肺复苏结果的影响
  • 批准号:
    7862033
  • 财政年份:
    2010
  • 资助金额:
    $ 43.33万
  • 项目类别:
Impact of nitric oxide synthase on myocardial dysfunction of sepsis
一氧化氮合酶对脓毒症心肌功能障碍的影响
  • 批准号:
    7618495
  • 财政年份:
    2007
  • 资助金额:
    $ 43.33万
  • 项目类别:
Impact of nitric oxide synthase on myocardial dysfunction of sepsis
一氧化氮合酶对脓毒症心肌功能障碍的影响
  • 批准号:
    7186477
  • 财政年份:
    2007
  • 资助金额:
    $ 43.33万
  • 项目类别:
Impact of nitric oxide synthase on myocardial dysfunction of sepsis
一氧化氮合酶对脓毒症心肌功能障碍的影响
  • 批准号:
    7418618
  • 财政年份:
    2007
  • 资助金额:
    $ 43.33万
  • 项目类别:

相似海外基金

Quantification of Neurovasculature Changes in a Post-Hemorrhagic Stroke Animal-Model
出血性中风后动物模型中神经血管变化的量化
  • 批准号:
    495434
  • 财政年份:
    2023
  • 资助金额:
    $ 43.33万
  • 项目类别:
Small animal model for evaluating the impacts of cleft lip repairing scar on craniofacial growth and development
评价唇裂修复疤痕对颅面生长发育影响的小动物模型
  • 批准号:
    10642519
  • 财政年份:
    2023
  • 资助金额:
    $ 43.33万
  • 项目类别:
Bioactive Injectable Cell Scaffold for Meniscus Injury Repair in a Large Animal Model
用于大型动物模型半月板损伤修复的生物活性可注射细胞支架
  • 批准号:
    10586596
  • 财政年份:
    2023
  • 资助金额:
    $ 43.33万
  • 项目类别:
A Comparison of Treatment Strategies for Recovery of Swallow and Swallow-Respiratory Coupling Following a Prolonged Liquid Diet in a Young Animal Model
幼年动物模型中长期流质饮食后吞咽恢复和吞咽呼吸耦合治疗策略的比较
  • 批准号:
    10590479
  • 财政年份:
    2023
  • 资助金额:
    $ 43.33万
  • 项目类别:
Diurnal grass rats as a novel animal model of seasonal affective disorder
昼夜草鼠作为季节性情感障碍的新型动物模型
  • 批准号:
    23K06011
  • 财政年份:
    2023
  • 资助金额:
    $ 43.33万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Longitudinal Ocular Changes in Naturally Occurring Glaucoma Animal Model
自然发生的青光眼动物模型的纵向眼部变化
  • 批准号:
    10682117
  • 财政年份:
    2023
  • 资助金额:
    $ 43.33万
  • 项目类别:
A whole animal model for investigation of ingested nanoplastic mixtures and effects on genomic integrity and health
用于研究摄入的纳米塑料混合物及其对基因组完整性和健康影响的整体动物模型
  • 批准号:
    10708517
  • 财政年份:
    2023
  • 资助金额:
    $ 43.33万
  • 项目类别:
A Novel Large Animal Model for Studying the Developmental Potential and Function of LGR5 Stem Cells in Vivo and in Vitro
用于研究 LGR5 干细胞体内外发育潜力和功能的新型大型动物模型
  • 批准号:
    10575566
  • 财政年份:
    2023
  • 资助金额:
    $ 43.33万
  • 项目类别:
Elucidating the pathogenesis of a novel animal model mimicking chronic entrapment neuropathy
阐明模拟慢性卡压性神经病的新型动物模型的发病机制
  • 批准号:
    23K15696
  • 财政年份:
    2023
  • 资助金额:
    $ 43.33万
  • 项目类别:
    Grant-in-Aid for Early-Career Scientists
The effect of anti-oxidant on swallowing function in an animal model of dysphagia
抗氧化剂对吞咽困难动物模型吞咽功能的影响
  • 批准号:
    23K15867
  • 财政年份:
    2023
  • 资助金额:
    $ 43.33万
  • 项目类别:
    Grant-in-Aid for Early-Career Scientists
{{ showInfoDetail.title }}

作者:{{ showInfoDetail.author }}

知道了