NITROXIDES AS PROTECTORS AGAINST OXIDATIVE STRESS

氮氧化物作为氧化应激的保护剂

基本信息

  • 批准号:
    3752336
  • 负责人:
  • 金额:
    --
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
  • 资助国家:
    美国
  • 起止时间:
  • 项目状态:
    未结题

项目摘要

Nitroxides which have been used as EPR spin labels have been shown to exhibit superoxide dismutase (SOD) activity and are quite effective agents in protecting cells against a wide variety of oxidative stresses including hydrogen peroxide, superoxide, organic hydroperoxides, redox-cycling chemotherapy drugs, and ionizing radiation. We have demonstrated that Tempol protects both cells in vitro and mice against ionizing radiation. Thus, the nitroxides represent a new class of radiation protectors that may have widespread use in protecting humans against radiation. Preliminary studies using a rodent tumor model have shown that Tempol does not protect tumor tissue. The mechanism of this finding may involve differential metabolic reduction properties of normal versus tumor. Additionally, work has begun to identify the most efficient nitroxide for protection purposes. We are currently evaluating approximately 75 nitroxides in a structure-activity relationship study. These nitroxides were kindly given to us from Dr. Hideg of Hungary, an international expert on nitroxide synthesis. We are presently screening the compounds in vitro and when appropriate candidates are identified in vivo testing will begin. Preliminary studies have identified at least 3 agents which provide more in vitro radioprotection than Tempol (the nitroxide used for all the studies noted above). Unexpectedly, we have also identified a novel non- toxic radiation sensitizer in this screen and further work is being conducted to determine the mechanism for this interesting finding. Since these agents readily penetrate cell membranes, they may be of use in other areas of medical research such as ischemia/reperfusion injury studies. Furthermore, these studies have opened the possibility of inter-relating the biochemistry and metabolism of nitroxides to endogenously produced endothelial relaxation factor, nitric oxide.
用作EPR自旋标签的氮氧化物已被证明具有

项目成果

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A RUSSO其他文献

A RUSSO的其他文献

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{{ truncateString('A RUSSO', 18)}}的其他基金

INTRACELLULAR MODULATION OF SPECIFIC INTRACELLULAR PROTEINS
特定细胞内蛋白质的细胞内调节
  • 批准号:
    2464488
  • 财政年份:
  • 资助金额:
    --
  • 项目类别:
INTRACELLULAR MODULATION OF SPECIFIC INTRACELLULAR PROTEINS
特定细胞内蛋白质的细胞内调节
  • 批准号:
    3752415
  • 财政年份:
  • 资助金额:
    --
  • 项目类别:
DEVELOPMENT OF SUPEROXIDE DISMUTASE MIMICS
超氧化物歧化酶模拟物的开发
  • 批准号:
    3774576
  • 财政年份:
  • 资助金额:
    --
  • 项目类别:
RELATIONSHIP OF CELLULAR REDOX STATE AND THERMOTOLERANCE
细胞氧化还原态与耐热性的关系
  • 批准号:
    3939515
  • 财政年份:
  • 资助金额:
    --
  • 项目类别:
RELATIONSHIP OF CELLULAR REDOX STATE AND THERMOTOLERANCE
细胞氧化还原态与耐热性的关系
  • 批准号:
    3963241
  • 财政年份:
  • 资助金额:
    --
  • 项目类别:
MECHANISMS OF RADIOPROTECTION
辐射防护机制
  • 批准号:
    4692120
  • 财政年份:
  • 资助金额:
    --
  • 项目类别:
PHOTOTHERAPY OF INTRACAVITARY SPACES
腔内空间的光疗
  • 批准号:
    3916586
  • 财政年份:
  • 资助金额:
    --
  • 项目类别:
MOLECULAR BIOLOGY--TISSUE CULTURE CORE FACILITY
分子生物学--组织培养核心设施
  • 批准号:
    3854423
  • 财政年份:
  • 资助金额:
    --
  • 项目类别:
MOLECULAR BIOLOGY--TISSUE CULTURE CORE FACILITY
分子生物学--组织培养核心设施
  • 批准号:
    3896917
  • 财政年份:
  • 资助金额:
    --
  • 项目类别:
REDIRECTION OF REDOX PROTEINS TO THE NUCLEUS OF EUKARYOTIC CELLS
氧化还原蛋白重定向至真核细胞的细胞核
  • 批准号:
    3752414
  • 财政年份:
  • 资助金额:
    --
  • 项目类别:
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