This a new program project on the central theme of imaging regional myocardial and pulmonary transport, and functions and on the relationship of these functions to local, regional flows. These will be studied under normal conditions in order to gain understanding of the several-fold range of normal regional flows in heart and lung, and in ischemia or occlusion an during reperfusion. The five projects include continuations or offshoots of four well-developed research programs and a new one on myocardial stunning. In addition to standard physiological methods, the projects exploit the use of non-invasive methods, positron emission tomography (PET), single photon emission completed tomography (SPECT) and nuclear magnetic resonance (NMR). The projects concern: (1) Cardiac Metabolism/Flow (Bassingthwaighte): Assessment of the influence of local metabolism of lipids and O2 on regional flows in the normal heart with its 5-fold range of local flows, and the perturbation of the relationship in abnormal vasomotor states. (2) Pulmonary Blood and Gas Flow (Robertson): Quantitation and evaluation of the anatomic and physiologic determinants of the heterogeneity of pulmonary blood and gas flow as they relate to overall pulmonary gas exchange. (3) Cardiac Energetics/Lipids/Mechanics (Wesbey): Determination of the role of regional myocardial high energy phosphates and lipids in the recovery of regional mechanical function following transient ischemia (""""""""stunning""""""""). (4) Lung Ischemia (Modell): Mechanisms of lung injury during pulmonary artery obstruction. (5) Cardiac Ischemia (Caldwell): Determination of the relationship between regional lipid metabolism in hypoxia and ischemia, as measured by PET and SPECT, and the recovery of regional function. These five projects are served by core programs on imaging (radiopharmaceutical synthesis, imaging by positron emission and single photon emission computed tomography), and analysis (of data on regional tissue tracer content as a function of time), an animal physiology laboratory, and administration. The program brings together investigators from Cardiology, Respiratory Disease, Radiology, Radiation Oncology, Pathology, Anesthesiology, and Bioengineering, sharing a common set of goals and approaches to gaining fundamental understanding of regional flows, metabolism, and function in the heart and lung in the normal state and during ischemia and reperfusion.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Program Projects (P01)
Project #
5P01HL038736-04
Application #
3098623
Study Section
Heart, Lung, and Blood Research Review Committee A (HLBA)
Project Start
1987-09-30
Project End
1992-09-29
Budget Start
1990-09-30
Budget End
1991-09-29
Support Year
4
Fiscal Year
1990
Total Cost
Indirect Cost
Name
University of Washington
Department
Type
Schools of Medicine
DUNS #
135646524
City
Seattle
State
WA
Country
United States
Zip Code
98195
Beyer Jr, Richard P; Bassingthwaighte, James B; Deussen, Andreas J (2002) A computational model of oxygen transport from red blood cells to mitochondria. Comput Methods Programs Biomed 67:39-54
Graham, M M; Peterson, L M; Muzi, M et al. (1998) 1-[Carbon-11]-glucose radiation dosimetry and distribution in human imaging studies. J Nucl Med 39:1805-10
Graham, M M; Peterson, L M; Link, J M et al. (1997) Fluorine-18-fluoromisonidazole radiation dosimetry in imaging studies. J Nucl Med 38:1631-6
Deussen, A; Bassingthwaighte, J B (1996) Modeling [15O]oxygen tracer data for estimating oxygen consumption. Am J Physiol 270:H1115-30
Stapleton, D D; Moffett, T C; Baskin, D G et al. (1995) Autoradiographic assessment of blood flow heterogeneity in the hamster heart. Microcirculation 2:277-82
Caldwell, J H; Revenaugh, J R; Martin, G V et al. (1995) Comparison of fluorine-18-fluorodeoxyglucose and tritiated fluoromisonidazole uptake during low-flow ischemia. J Nucl Med 36:1633-8
Caldwell, J H; Martin, G V; Raymond, G M et al. (1994) Regional myocardial flow and capillary permeability-surface area products are nearly proportional. Am J Physiol 267:H654-66
Kroll, K; Martin, G V (1994) Steady-state catecholamine stimulation does not increase cytosolic adenosine in canine hearts. Am J Physiol 266:H503-10
King, R B; Deussen, A; Raymond, G M et al. (1993) A vascular transport operator. Am J Physiol 265:H2196-208
Martin, G V; Biskupiak, J E; Caldwell, J H et al. (1993) Characterization of iodovinylmisonidazole as a marker for myocardial hypoxia. J Nucl Med 34:918-24

Showing the most recent 10 out of 23 publications