The myocardium is a continually working aerobic organ. Consequently it is essential for normal myocardial function, that continual supply of oxygen is maintained to ensure a proper balance between myocardial oxygen demands and myocardial oxygen supply. Thus, oxygen balance must be maintained during a variety of physiologic stresses, e.g., exercise, excitement, to prevent myocardial ischemia and dysfunction. Oxygen balance is intimately dependent on myocardial blood flow, which is determined by physical (inertia, viscosity, pressure contraction) and reactive (resistance, capacitance) components of the coronary circulation. Although there has been extensive definition of these parameters, for the entire coronary circulation as a single compartment, there have been a paucity of studies dealing with potential compartmental hierarchies of the reactive components as """"""""fine tuning"""""""" mechanisms responsible for modulation of myocardial perfusion. The overall goal of the proposal is to define these reactive components of the coronary system and the potential functional hierarchy of the components. To accomplish these goals, I used a computer-controlled system which compensates for cardiac motion to enable microvascular pressure and diameter measurements in the beating heart. This computer controlled device can move a micropipette in three dimensions in concert with a moving microvessel on a beating heart. Furthermore, using stroboscopic illumination (1 flash per heart cycle) microvessels are always in focus and """"""""appear"""""""" stationary. With this approach in the beating heart, there is little trauma to the coronary system and I can obtain continuous measurements of coronary microvascular pressures and diameters. The specific goals are to answer the following questions: (1) What is the distribution of resistance in the coronary circulation of the left ventricle? (2) What are the changes in the distribution of resistance in the left ventricular coronary circulation during autoregulation? (3) What are the effects of neural stimulation or norepinephrine infusion on the distribution of resistance in the coronary circulation of the left ventricle?

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
7R01HL032788-02
Application #
3344253
Study Section
Cardiovascular Study Section (CVA)
Project Start
1987-02-01
Project End
1989-01-31
Budget Start
1987-02-01
Budget End
1988-01-31
Support Year
2
Fiscal Year
1987
Total Cost
Indirect Cost
Name
University of Iowa
Department
Type
Schools of Medicine
DUNS #
041294109
City
Iowa City
State
IA
Country
United States
Zip Code
52242
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Yin, Liya; Ohanyan, Vahagn; Pung, Yuh Fen et al. (2012) Induction of vascular progenitor cells from endothelial cells stimulates coronary collateral growth. Circ Res 110:241-52
Pung, Yuh Fen; Rocic, Petra; Murphy, Michael P et al. (2012) Resolution of mitochondrial oxidative stress rescues coronary collateral growth in Zucker obese fatty rats. Arterioscler Thromb Vasc Biol 32:325-34
Belmadani, Souad; Matrougui, Khalid; Kolz, Chris et al. (2009) Amplification of coronary arteriogenic capacity of multipotent stromal cells by epidermal growth factor. Arterioscler Thromb Vasc Biol 29:802-8
Yun, June; Rocic, Petra; Pung, Yuh Fen et al. (2009) Redox-dependent mechanisms in coronary collateral growth: the ""redox window"" hypothesis. Antioxid Redox Signal 11:1961-74

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