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Regulation of Glucose Transport in the Ischemic Heart

Regulation of Glucose Transport in the Ischemic Heart
缺血心脏中葡萄糖转运的调节
批准号:
7388163
负责人:
LAWRENCE H YOUNG
金额:
$34.88万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2000
资助国家:
美国
项目状态:
已结题
起止时间:
2000-09-30 至 2009-07-31

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中文摘要
翻译
描述(由申请人提供):这项研究的总体目标是确定心肌缺血期间葡萄糖转运的细胞和分子机制。葡萄糖代谢在维持缺血心脏的功能和存活方面起着关键作用,并由葡萄糖转运蛋白GLUT4和GLUT1介导。AMP激活的蛋白激酶(AMPK)是一种由能量应激激活的丝氨酸-苏氨酸蛋白激酶,在心脏和许多组织中是一条重要的细胞内信号通路,调节着主要的代谢途径、基因转录和线粒体的生物发生。这项研究将进一步阐明AMPK在介导缺血葡萄糖摄取中起关键作用,以及AMPK缺乏导致缺血和再灌注期间心肌损伤和细胞凋亡增加的假说。本研究的目的将是:1)确定GLUT4转位到细胞表面的新机制;2)确定AMPK在缺血心脏中激活的分子机制;3)确定AMPK通路在心脏缺血/再灌注过程中是否具有心脏保护作用。目前提案中概述的实验利用了新的细胞、分子和遗传学方法,试图更好地了解缺血心脏中葡萄糖运输的调节。与冠状动脉疾病相关的心肌缺血是美国人群发病率和死亡率的主要原因。这项拟议研究的最终目标是开发新的方法来保护心脏免受缺血损伤,这将补充现有的治疗和程序。这些新的治疗方法可能会改善生活质量,防止心脏死亡,并对美国民众的健康有重大好处。
英文摘要
DESCRIPTION (provided by applicant): The overall goal of this research is to determine the cellular and molecular mechanisms regulating glucose transport during myocardial ischemia. Glucose metabolism has a key role in maintaining the function and viability in the ischemic heart and is mediated by the glucose transport proteins GLUT4 and GLUT1. The AMP-activated protein kinase (AMPK) is a serine-threonine protein kinase which is activated by energetic stress and is emerging as an important intracellular signaling pathway in the heart and many tissues, modulating the major metabolic pathways, gene transcription, and mitochondrial biogenesis. This research will further address the hypothesis that AMPK has a critical role in mediating ischemic glucose uptake and that AMPK deficiency leads to increased myocardial injury and apoptosis during ischemia and reperfusion. The aims of the proposed research will be i) to determine novel mechanisms mediating GLUT4 translocation to the cell surface in the ischemic heart, ii) to determine the molecular mechanisms responsible for AMPK activation in the ischemic heart and iii) to determine whether the AMPK pathway has a cardioprotective action during ischemia/reperfusion in the heart. The experiments outlined in the current proposal utilize novel cellular, molecular and genetic approaches in an attempt to better understand the regulation of glucose transport in the ischemic heart. Myocardial ischemia associated with coronary artery disease is the major cause of morbidity and mortality in the U.S. population. The ultimate goal of the proposed research is to develop novel approaches to protecting the heart against ischemic injury which will complement existing therapies and procedures. Such novel therapies may improve the quality of life and prevent cardiac death and have significant health benefit for the U.S. population.
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  • 项目类别:
  • 资助金额:
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  • 财政年份:
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  • 负责人:
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  • 依托单位:
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  • 项目类别:
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  • 财政年份:
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  • 批准号:
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  • 项目类别:
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  • 财政年份:
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海外基金