Increased oxygen free radical and nitric oxide (NO) generation has been hypothesized to be a central mechanism of the injury which occurs on reperfusion of ischemic tissues. Questions and controversy remain, however, regarding the role of this radical generation in the processes of myocardial stunning and infarction and how best to intervene to prevent radical generation and subsequent injury. Within the present grant, EPR techniques were developed and applied to measure the process of oxygen radical and NO generation in the isolated heart. New instrumentation enabling in-vivo EPR spectroscopy and imaging of free radicals in whole beating hearts at L-band (1-2 GHz) was also developed. In this renewal application, we propose studies to determine the role of oxygen radical and NO generation in the process of myocardial stunning and infarction, extending these observations from isolated buffer perfused to blood perfused hearts, and then to the setting of in-vivo regional ischemia as occurs with acute occlusion of a coronary artery. Direct and spin trapping EPR studies at X-band, as well as in vivo EPR studies at L-band will be performed to measure, quantitate, and characterize oxygen radical and NO generation in isolated hearts and in- vivo animal models of myocardial stunning and infarction. The importance and inter-relationship of the cellular mechanisms of this radical generation will be determined in order to develop optimal therapeutic approaches to prevent radical generation and radical mediated injury. Radical generation will be correlated with alterations in contractile function, high energy phosphates, and the metabolic state of the heart. Cell death will be measured by enzyme release, and histology. In-vivo EPR spectroscopy and imaging will be applied to measure and spatially map myocardial oxygenation, radical metabolism, NO formation, and cell death during ischemia and reflow. These experiments will provide new insight into the fundamental nature and mechanisms of oxygen free radical and nitric oxide generation in the postischemic heart and their role in myocardial stunning and infarction.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL038324-12
Application #
2901092
Study Section
Biophysical Chemistry Study Section (BBCB)
Project Start
1987-04-01
Project End
2002-03-31
Budget Start
1999-04-01
Budget End
2000-03-31
Support Year
12
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Johns Hopkins University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
045911138
City
Baltimore
State
MD
Country
United States
Zip Code
21218
Liu, Xiaoping; El-Mahdy, Mohamed A; Boslett, James et al. (2017) Cytoglobin regulates blood pressure and vascular tone through nitric oxide metabolism in the vascular wall. Nat Commun 8:14807
Velayutham, Murugesan; Hemann, Craig F; Cardounel, Arturo J et al. (2016) Sulfite Oxidase Activity of Cytochrome c: Role of Hydrogen Peroxide. Biochem Biophys Rep 5:96-104
Xie, Lin; Talukder, M A Hassan; Sun, Jian et al. (2015) Liposomal tetrahydrobiopterin preserves eNOS coupling in the post-ischemic heart conferring in vivo cardioprotection. J Mol Cell Cardiol 86:14-22
Long 3rd, Victor P; Bonilla, Ingrid M; Vargas-Pinto, Pedro et al. (2015) Heart failure duration progressively modulates the arrhythmia substrate through structural and electrical remodeling. Life Sci 123:61-71
Reyes, Levy A; Boslett, James; Varadharaj, Saradhadevi et al. (2015) Depletion of NADP(H) due to CD38 activation triggers endothelial dysfunction in the postischemic heart. Proc Natl Acad Sci U S A 112:11648-53
Joddar, Binata; Firstenberg, Michael S; Reen, Rashmeet K et al. (2015) Arterial levels of oxygen stimulate intimal hyperplasia in human saphenous veins via a ROS-dependent mechanism. PLoS One 10:e0120301
Moldovan, Nicanor I; Anghelina, Mirela; Varadharaj, Saradhadevi et al. (2014) Reoxygenation-derived toxic reactive oxygen/nitrogen species modulate the contribution of bone marrow progenitor cells to remodeling after myocardial infarction. J Am Heart Assoc 3:e000471
De Pascali, Francesco; Hemann, Craig; Samons, Kindra et al. (2014) Hypoxia and reoxygenation induce endothelial nitric oxide synthase uncoupling in endothelial cells through tetrahydrobiopterin depletion and S-glutathionylation. Biochemistry 53:3679-88
Chen, Yeong-Renn; Zweier, Jay L (2014) Cardiac mitochondria and reactive oxygen species generation. Circ Res 114:524-37
Tong, Jianjing; Zweier, Joseph R; Huskey, Rachael L et al. (2014) Effect of temperature, pH and heme ligands on the reduction of Cygb(Fe(3+)) by ascorbate. Arch Biochem Biophys 554:1-5

Showing the most recent 10 out of 74 publications