Coronary heart disease is the number one cause of death in western societies. A rapid and noninvasive method of early detection would be important for the timely institution of therapy. Several noninvasive methods have been applied. NMR imaging is a promising, new noninvasive technique that has several possible advantages over other existing methods, i.e. electrocardiographic and radionuclide. Combined with functionally specific contrast agents, NMR imaging has the potential to enable the early detection of abnormalities in myocardial perfusion and of damaged myocardium. These agents affect the contrast of water proton T1, or T2, differently in different tissues, between normal and diseased states, and between intracellular, interstitial and vascular compartments thus effecting functional enhancement of contrast in images obtained by NMR. The central aim of this proposal is to develop clinically applicable paramagnetic contrast agents for NMR imaging of damaged myocardium and of regional myocardial perfusion. The research will be focused around the development of two agents, one that would be preferentially retained in the myocardium in proportion to perfusion, and another that would highlight infarcted heart tissue. In our search for these two agents a systematic approach will be followed based on the anticipated chemical, transport and magnetic properties of certain complexes of paramagnetic metals, in particular of gadolinium. Guided by the optimization of these properties, synthesis of new ligands for gadolinium will be carried out within several, carefully selected families of organic compounds. These will include nonhydrolyzable derivatives of polyphosphates and lipophilic fatty acid and phospholipid derivatives. The magnetic and transport properties of the most promising agents will be tested in vitro and in animal heart tissue. To ensure lack of clinical hazard, detailed toxicology studies will also be performed. Ultimately, the most promising agents will be evaluated using NMR imaging in dog models.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL033200-02
Application #
3344806
Study Section
Diagnostic Radiology Study Section (RNM)
Project Start
1985-07-01
Project End
1988-06-30
Budget Start
1986-07-01
Budget End
1987-06-30
Support Year
2
Fiscal Year
1986
Total Cost
Indirect Cost
Name
University of Alabama Birmingham
Department
Type
School of Medicine & Dentistry
DUNS #
004514360
City
Birmingham
State
AL
Country
United States
Zip Code
35294
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Prince, L S; Miller, S K; Pohost, G M et al. (1992) The longitudinal relaxation time (T1) of the intracellular 23Na NMR signal in the isolated perfused rat heart during hypoxia and reoxygenation. Magn Reson Med 23:376-82
Lotan, C S; Miller, S K; Cranney, G B et al. (1992) The effect of postinfarction intramyocardial hemorrhage on transverse relaxation time. Magn Reson Med 23:346-55
Lotan, C S; Miller, S K; Pohost, G M et al. (1992) Amiloride in ouabain-induced acidification, inotropy and arrhythmia: 23Na & 31P NMR in perfused hearts. J Mol Cell Cardiol 24:243-57
Miller, S K; Chu, W J; Pohost, G M et al. (1991) Improvement of spectral resolution in shift-reagent-aided 23Na NMR spectroscopy in the isolated perfused rat heart system. Magn Reson Med 20:184-95
Kim, S K; Pohost, G M; Elgavish, G A (1991) Fatty-acyl iminopolycarboxylates: lipophilic bifunctional contrast agents for NMR imaging. Magn Reson Med 22:57-67
Lotan, C S; Miller, S K; Bouchard, A et al. (1990) Detection of intramyocardial hemorrhage using high-field proton (1H) nuclear magnetic resonance imaging. Cathet Cardiovasc Diagn 20:205-11