Molecular Imaging of the Lung Using Hyperpolarized Carbon-13 Compounds

使用超极化碳 13 化合物对肺部进行分子成像

基本信息

  • 批准号:
    8692014
  • 负责人:
  • 金额:
    $ 39.2万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    2012
  • 资助国家:
    美国
  • 起止时间:
    2012-09-25 至 2017-06-30
  • 项目状态:
    已结题

项目摘要

DESCRIPTION (provided by applicant): Once considered a metabolically passive organ responsible only for gas exchange, the lung has been shown to perform a variety of critical roles in maintaining body homeostasis in the last few decades. Studies show that some of these homeostatic processes are compromised in lung disease and the lung itself may be damaged by exposure to the products of its regulation and deactivation pathways. While advances in imaging methods have enabled new approaches for structural and functional characterization of pulmonary disorders and their role in gas exchange, imaging methods capable of providing information about the molecular and cellular pathways of these metabolic processes that maintain homeostasis are less understood and developed. This proposal seeks to develop agents specific to three of the more rapid and better-characterized metabolic roles of the lung. Specifically, these include the regulation of glycolytc intermediates, amino acid levels, and vasoactive amines in both the lung tissue and the blood plasma. Significant evidence exists that each metabolic role is modified in obstructive disease, or in conditions that lead to or exacerbate the disease. The work is aided by the development of general techniques to produce and study hyperpolarized 13C probes using high-sensitivity NMR and imaging, and recent results which show how the hyperpolarized state may be maintained for a longer period than was previously thought possible. Furthermore, the targets chosen here are well suited to hyperpolarized 13C technology because they are among the most rapid molecular events that take place within the organ. The central hypotheses of this proposal are that 1) hyperpolarized probes, beyond those in use for studying ventilation and gas exchange, will provide a sensitive probe of the ability of the lung to achieve homeostasis, 2) derived metrics are detectably dependent on disease state relevant to human obstructive disease, and 3) these probes are extensible to imaging applications. In addressing these hypotheses we propose the following specific aims: 1) Development and testing of molecular probes for studying glycolysis, amino acid synthesis, metabolism of inflammatory cells, and non-metabolitzed agents for tissue perfusion measurement, 2) Testing the applicability of each of the aforementioned probes in the isolated, perfused rat lung, 3) Studying the primary importance of redox states in healthy diseased lung, and 4) Performing a series of metabolic studies in rat and pig models of lung disease. Many pulmonary disorders and in particular COPD are characterized by dysfunctional whole-body energy metabolism, which may in part result from the lung's failure to maintain homeostasis of glycolytic intermediates. We believe that the development of hyperpolarized agents targeted to lung molecular activity and accomplishment of the above specific aims will address the shortcomings of existing techniques for studying lung homeostatic functions and their associations with disease state.
描述(由申请人提供):曾经被认为是一个仅负责气体交换的代谢被动器官,在过去的几十年里,肺已被证明在维持身体稳态方面发挥着各种关键作用。研究表明,这些稳态过程中的一些在肺部疾病中受到损害,并且肺部本身可能因暴露于其调节和失活途径的产物而受损。虽然成像方法的进步为肺部疾病的结构和功能特征及其在气体交换中的作用提供了新的方法,但能够提供这些维持体内平衡的代谢过程的分子和细胞途径的信息的成像方法却很少被了解和开发。

项目成果

期刊论文数量(3)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Tidal changes on CT and progression of ARDS.
  • DOI:
    10.1136/thoraxjnl-2016-209833
  • 发表时间:
    2017-11
  • 期刊:
  • 影响因子:
    10
  • 作者:
    Cereda M;Xin Y;Hamedani H;Bellani G;Kadlecek S;Clapp J;Guerra L;Meeder N;Rajaei J;Tustison NJ;Gee JC;Kavanagh BP;Rizi RR
  • 通讯作者:
    Rizi RR
Visualizing the Propagation of Acute Lung Injury.
可视化急性肺损伤的传播。
  • DOI:
    10.1097/aln.0000000000000916
  • 发表时间:
    2016-01
  • 期刊:
  • 影响因子:
    8.8
  • 作者:
    Cereda M;Xin Y;Meeder N;Zeng J;Jiang Y;Hamedani H;Profka H;Kadlecek S;Clapp J;Deshpande CG;Wu J;Gee JC;Kavanagh BP;Rizi RR
  • 通讯作者:
    Rizi RR
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RAHIM R RIZI其他文献

RAHIM R RIZI的其他文献

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{{ truncateString('RAHIM R RIZI', 18)}}的其他基金

Imaging the functional response of the lung to bronchoscopic lung volume reduction
成像肺对支气管镜肺减容的功能反应
  • 批准号:
    10528137
  • 财政年份:
    2022
  • 资助金额:
    $ 39.2万
  • 项目类别:
Imaging the functional response of the lung to bronchoscopic lung volume reduction
成像肺对支气管镜肺减容的功能反应
  • 批准号:
    10680458
  • 财政年份:
    2022
  • 资助金额:
    $ 39.2万
  • 项目类别:
Predicting the onset of chronic rejection in lung transplant recipients using hyperpolarized 129Xe imaging
使用超极化 129Xe 成像预测肺移植受者慢性排斥反应的发生
  • 批准号:
    10192820
  • 财政年份:
    2020
  • 资助金额:
    $ 39.2万
  • 项目类别:
The sixth international workshop on metabolic imaging
第六届代谢影像国际研讨会
  • 批准号:
    10063645
  • 财政年份:
    2020
  • 资助金额:
    $ 39.2万
  • 项目类别:
Predicting the onset of chronic rejection in lung transplant recipients using hyperpolarized 129Xe imaging
使用超极化 129Xe 成像预测肺移植受者慢性排斥反应的发生
  • 批准号:
    10407561
  • 财政年份:
    2020
  • 资助金额:
    $ 39.2万
  • 项目类别:
Improving lung transplant outcomes through the use of imaging in a DBD rat model
通过在 DBD 大鼠模型中使用成像来改善肺移植结果
  • 批准号:
    9764471
  • 财政年份:
    2018
  • 资助金额:
    $ 39.2万
  • 项目类别:
Improving lung transplant outcomes through the use of imaging in a DBD rat model
通过在 DBD 大鼠模型中使用成像来改善肺移植结果
  • 批准号:
    10198021
  • 财政年份:
    2018
  • 资助金额:
    $ 39.2万
  • 项目类别:
Prediction and assessment of COPD lung volume reduction outcomes with polarized MRI
使用偏振 MRI 预测和评估 COPD 肺减容结果
  • 批准号:
    9228404
  • 财政年份:
    2016
  • 资助金额:
    $ 39.2万
  • 项目类别:
Prediction and assessment of COPD lung volume reduction outcomes with polarized MRI
使用偏振 MRI 预测和评估 COPD 肺减容结果
  • 批准号:
    9051246
  • 财政年份:
    2016
  • 资助金额:
    $ 39.2万
  • 项目类别:
Imaging-based characterization of the COPDGene cohort
COPDGene 队列的基于成像的表征
  • 批准号:
    9127347
  • 财政年份:
    2015
  • 资助金额:
    $ 39.2万
  • 项目类别:
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