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DESCRIPTION (provided by applicant): The biology of nitric oxide (NO) is 1 of the most prolific fields in biomedical science and has impacted our understanding of both basic physiology and disease etiology. NO is a unique endogenous signaling agent since its chemistry is the single most important determinant of its biological function. Research efforts in this field have primarily focused on NO and related oxidized species; however, recent attention has been devoted to the reduced species nitroxyl (HNO). Comparative studies have demonstrated that the chemistry and thus the biological responses to NO and HNO donors are often discrete. Our long-term goal is to utilize this diversity in conjunction with a thorough understanding of the chemical biology of nitrogen oxides to provide disease treatments. The relevance of HNO to endogenous signaling is still a matter of debate, in part due to a poor understanding of its basic chemistry and to limited techniques to define its role in biology. Further, due to rapid self-consumption, HNO must be produced in situ. The most common donor is a nitrogen oxide salt, Na2N2O3, which has proven to be invaluable in the initiation of the study of the unique chemical properties and pharmacological effects of HNO. However, therapeutic exploitation of HNO will only be possible with development of donors with adaptable backbones to complement those that already exist for NO. The specific aims of this proposal are 1) to design, synthesize and characterize novel HNO donors based on organic backbones; 2) to utilize this donor library and existing HNO donors to elucidate fundamental aspects of the chemical biology of HNO; and 3) to identify specific biological targets. Completion of these aims will expand our understanding of the chemistry of HNO and its roles in biology and may have direct implications for the treatment of heart failure, myocardial infarct and stroke. Additionally, new biological targets, such as zinc fingers and non-heme iron centers, are likely to be revealed, which may suggest other therapeutic interventions.
期刊论文(12)
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DOI: 10.1016/j.freeradbiomed.2015.06.002
发表时间: 2015-10
期刊: Free radical biology & medicine
影响因子: 7.4
作者: [Thomas DD, Heinecke JL, Ridnour LA, Cheng RY, Kesarwala AH, Switzer CH, McVicar DW, Roberts DD, Glynn S, Fukuto JM, Wink DA, Miranda KM]
通讯作者: Miranda KM
DOI: 10.1016/j.cbi.2016.06.009
发表时间: 2016-08-25
期刊: Chemico-biological interactions
影响因子: 5.1
作者: [Longhi-Balbinot DT, Rossaneis AC, Pinho-Ribeiro FA, Bertozzi MM, Cunha FQ, Alves-Filho JC, Cunha TM, Peron JP, Miranda KM, Casagrande R, Verri WA Jr]
通讯作者: Verri WA Jr
DOI: 10.1016/j.neuropharm.2013.03.009
发表时间: 2013-08
期刊: Neuropharmacology
影响因子: 4.7
作者: [Zarpelon AC, Souza GR, Cunha TM, Schivo IR, Marchesi M, Casagrande R, Pinge-Filho P, Cunha FQ, Ferreira SH, Miranda KM, Verri WA Jr]
通讯作者: Verri WA Jr
DOI: 10.1021/ja106552p
发表时间: 2010-11-24
期刊: Journal of the American Chemical Society
影响因子: 15
作者: [Andrei D, Salmon DJ, Donzelli S, Wahab A, Klose JR, Citro ML, Saavedra JE, Wink DA, Miranda KM, Keefer LK]
通讯作者: Keefer LK
6
    MARC Biomedical Research and Training Program at the University of Arizona
    • 批准号:
      10629764
    • 项目类别:
    • 资助金额:
      $26.62万
    • 财政年份:
      2023
    • 负责人:
      Katrina M. Miranda
    • 依托单位:
    Assessment of the Chemical Biology of HNO via New Donors
    • 批准号:
      7252062
    • 项目类别:
    • 资助金额:
      $22.52万
    • 财政年份:
      2006
    • 负责人:
      Katrina M. Miranda
    • 依托单位:
    Assessment of the Chemical Biology of HNO via New Donors
    • 批准号:
      7465393
    • 项目类别:
    • 资助金额:
      $22.51万
    • 财政年份:
      2006
    • 负责人:
      Katrina M. Miranda
    • 依托单位:
    Assessment of the Chemical Biology of HNO via New Donors
    • 批准号:
      7644826
    • 项目类别:
    • 资助金额:
      $22.5万
    • 财政年份:
      2006
    • 负责人:
      Katrina M. Miranda
    • 依托单位: