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Mitochondrial Dysfunction in Pediatric Head Injury

Mitochondrial Dysfunction in Pediatric Head Injury
小儿头部损伤中的线粒体功能障碍
批准号:
7122130
负责人:
COURTNEY L ROBERTSON
金额:
$16.85万
依托单位国家:
美国
项目类别:
财政年份:
2002
资助国家:
美国
项目状态:
已结题
起止时间:
2002-09-30 至 2008-07-31

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DESCRIPTION (provided by applicant): Following traumatic brain injury (TBI), the immature rat brain experiences many secondary insults that lead to delayed cell death. Although considerable evidence indicates that mitochondria are primary mediators of ischemic and excitotoxic neural cell death and survival, relatively little is known regarding mitochondrial involvement in adult TBI, and nothing has been reported for models of pediatric TBI. Limited studies of the immature rat brain have demonstrated vulnerability to many known mediators of mitochondrial injury, including elevated intracellular calcium and oxidative stress. Mitochondrial alterations can also trigger the cascade of caspase activities that mediate apoptosis, a process of programmed cell death that appears particularly important in TBI. The working hypothesis for the proposed study is that the response of brain mitochondria to metabolic acidosis, elevated calcium, oxidative stress, and pro-apoptotic proteins plays an integral role in the neurochemical, histologic, and neurologic outcome following pediatric TBI. We will test the following mechanistic hypotheses using a clinically relevant model of pediatric TBI: 1) Mitochondrial injury early after TBI increases the sensitivity of mitochondria to cellular factors that promote apoptotic or necrotic cell death cascades. 2) Cerebral lactic acidosis after TBI promotes cytochrome c release, mediated by mitochondrial swelling due to activation of the membrane permeability transition. 3) Oxidative stress following TBI contributes to mitochondrial dysfunction, cell death and neurologic injury. This study will help define the molecular mechanisms by which mitochondria are injured after TBI in immature animals. This may identify novel targets for neuroprotection following TBI in infants and children. This proposal is intended to provide for the research experience and career development of the applicant, specifically involving the mechanisms of, and therapeutic strategies for, the treatment of acute brain injury. The Departments of Anesthesiology and Pediatrics, and the Brain Injury and Neuroprotection Research Group at the University of Maryland will provide a rich environment for the study of experimental brain injury, and have a strong commitment to fostering meaningful and contemporary research in this field.
期刊论文(5)
专著(0)
科研奖励(0)
会议论文
Synthes Award for Resident Research on Brain and Craniofacial Injury: normoxic ventilatory resuscitation after controlled cortical impact reduces peroxynitrite-mediated protein nitration in the hippocampus.
脑和颅面损伤住院医师研究综合奖:受控皮质冲击后的常氧通气复苏可减少海马体中过氧亚硝酸盐介导的蛋白质硝化。
DOI: --
发表时间: 2005
期刊: Clinical neurosurgery.
影响因子: --
作者: [Ahn,EdwardS, Robertson,CourtneyL, Vereczki,Viktoria, Hoffman,GloriaE, Fiskum,Gary]
通讯作者: Fiskum,Gary
40th National Neurotrauma Society (NNS) Annual Symposium 2023 - Celebrating the Landmarks of Neurotrauma
  • 批准号:
    10753817
  • 项目类别:
  • 资助金额:
    $2.15万
  • 财政年份:
    2023
  • 负责人:
    COURTNEY L ROBERTSON
  • 依托单位:
Role of 20-HETE in Pediatric Traumatic Brain Injury
  • 批准号:
    9233784
  • 项目类别:
  • 资助金额:
    $35.44万
  • 财政年份:
    2016
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  • 依托单位:
Role of 20-HETE in Pediatric Traumatic Brain Injury
  • 批准号:
    9883849
  • 项目类别:
  • 资助金额:
    $35.44万
  • 财政年份:
    2016
  • 负责人:
    COURTNEY L ROBERTSON
  • 依托单位:
Mitochondrial Dysfunction in Pediatric Head Injury
  • 批准号:
    6666677
  • 项目类别:
  • 资助金额:
    $16.85万
  • 财政年份:
    2002
  • 负责人:
    COURTNEY L ROBERTSON
  • 依托单位:
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