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Hyperbaric Oxygenation May Increase Lung Injury

Hyperbaric Oxygenation May Increase Lung Injury
高压氧可能会增加肺损伤
批准号:
7229973
负责人:
Michail Sitkovsky
金额:
$19.06万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2006
资助国家:
美国
项目状态:
已结题
起止时间:
2006-05-01 至 2008-04-30

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英文摘要
DESCRIPTION (provided by applicant): Hyperbaric Oxygen therapy (HBOT) is of interest to basic biomedical researchers and to practitioners of complementary and alternative medicine (CAM). HBOT is applied to a wide variety of diseases with symptoms caused by a lack of oxygen in the target tissues. It is not accepted as a treatment by the US medical community due to the lack of understanding of the underlying physiology and yet to be carefully evaluated potential dangers. Extensive pre-clinical studies are required to overcome the current bias towards HBOT and to determine its limitations. The central goal of this proposal is to understand the mechanisms of beneficial effects of HBOT and to identify its potential dangers. We recently established the critical role of the hypoxia-driven and A2A and A2B adenosine receptor (A2AR/A2BR)-mediated pathway in inhibition of overactive inflammatory cells and protection of normal tissues in hypoxic inflamed areas. We hypothesize that the elimination of this mechanism by oxygen during HBOT may explain the beneficial effects of HBOT in clearing infections by "de-inhibited" immunocytes. We are also concerned that the weakening of this protective mechanism by HBOT may lead to an unintended exacerbation of inflammatory tissue damage. We plan to test our hypothesis in studies of HBOT-treated wild type mice and of unique mice with total and tissue-specific deletion of A2AR and/or A2BR genes in different models of lung inflammation. Our specific aims #1 and 2 are to test whether HBOT exacerbates lung inflammation in studies of inhalative and intravenously induced models of lung injury in mice, while in Aim #3 we will test whether compensatory treatment with A2AR agonist will prevent the inflammatory lung injury exacerbation by HBOT in order to gain potential benefits of HBOT for other indications in CAM and other therapies.
期刊论文(4)
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DOI: 10.4049/jimmunol.1001567
发表时间: 2011-02-15
期刊: Journal of immunology (Baltimore, Md. : 1950)
影响因子: --
作者: [Belikoff BG, Hatfield S, Georgiev P, Ohta A, Lukashev D, Buras JA, Remick DG, Sitkovsky M]
通讯作者: Sitkovsky M
DOI: 10.1097/shk.0b013e3182085f12
发表时间: 2011-04
期刊: Shock (Augusta, Ga.)
影响因子: --
作者: [Belikoff B, Hatfield S, Sitkovsky M, Remick DG]
通讯作者: Remick DG
DOI: 10.1371/journal.pone.0000853
发表时间: 2007-09-05
期刊: PloS one
影响因子: 3.7
作者: [Thiel M, Caldwell CC, Kreth S, Kuboki S, Chen P, Smith P, Ohta A, Lentsch AB, Lukashev D, Sitkovsky MV]
通讯作者: Sitkovsky MV
[5,10,15,20-Tetra-kis(4-chloro-phen-yl)porphyrinato]bis-(tributyl-phosphine)cobalt(III) perchlorate.
[5,10,15,20-四-(4-氯-苯基)卟啉]双-(三丁基膦)钴(III)高氯酸盐。
DOI: 10.1107/s1600536809019163
发表时间: 2009
期刊: Acta crystallographica. Section E, Structure reports online
影响因子: --
作者: [Etemadi,Bijan, Kia,Reza, Asadi,Mozaffar, Mohammadi,Kh]
通讯作者: Mohammadi,Kh
Preventing the Hypoxia-Adenosinergic Inhibtion of Anti-HIV Immune Response
  • 批准号:
    8043237
  • 项目类别:
  • 资助金额:
    $28.45万
  • 财政年份:
    2010
  • 负责人:
    Michail Sitkovsky
  • 依托单位:
"Cancer Immunotherapy by Targeting A2 Adenosine Receptor"
  • 批准号:
    7100600
  • 项目类别:
  • 资助金额:
    $22.29万
  • 财政年份:
    2006
  • 负责人:
    Michail Sitkovsky
  • 依托单位:
"Cancer Immunotherapy by Targeting A2 Adenosine Receptor"
  • 批准号:
    7409103
  • 项目类别:
  • 资助金额:
    $21.65万
  • 财政年份:
    2006
  • 负责人:
    Michail Sitkovsky
  • 依托单位:
Cancer Immunotherapy by Targeting A2 Adenosine Receptor
  • 批准号:
    8464014
  • 项目类别:
  • 资助金额:
    $20.15万
  • 财政年份:
    2006
  • 负责人:
    Michail Sitkovsky
  • 依托单位:
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