Heart failure is a clinical problem of great magnitude in which the complex mechanisms, natural history and therapeutic options remain largely unexplored. It is now apparent that the syndrome represents an interaction of disturbed myocardial function with altered peripheral vascular function. The relative role of the heart and the periphery in influencing the progressive course of this disease process is still unclear. This Program Project is aimed at exploring potentially important myocardial factors and neurohumoral influences on the peripheral vasculature that may play a critical role in the progression of heart failure in experimental models and in man. Myocardial factors to be studied include: (1) genetic disease of the myocardium in the turkey; (2) myocardial necrosis in the dog; (3) myocardial toxins in the turkey; (4) myocardial ischemia in the dog; (5) myocardial infarcts in the rat; (6) pressure overload in the rat; and (7) ischemic and non-ischemic myocardial dysfunction in man. Neurohumoral and peripheral vascular studies will include: (1) pre-synaptic and post-synaptic Alpha-adrenoreceptor function; (2) beta-adrenoreceptor function and down-regulation; (3) renin-angiotensin stimulation and blockade; (4) vasopressin-induced vasoconstruction; (5) vascular impedance measurements; (6) regional blood flow measurements; (7) atrial natriuretic peptide measurements; and (8) measurement of sympathetic nerve traffic. The seven projects and four cores that constitute the Program are heavily dependent on certain methodology including nuclear magnetic resonance spectroscopy, measurement of plasma and tissue catecholamines, assessment of adrenoreceptor sensitivity and density, microsphere measurement of blood flow distribution and exercise as a stress to the myocardium and peripheral vasculature. The strength to be gained from the Program Project concept is the sharing of ideas, experimental methods, blood samples and tissue, and biometric and administrative support that a joint effort will facilitate.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Program Projects (P01)
Project #
5P01HL032427-05
Application #
3098298
Study Section
Heart, Lung, and Blood Research Review Committee A (HLBA)
Project Start
1986-09-30
Project End
1991-09-29
Budget Start
1990-09-30
Budget End
1991-09-29
Support Year
5
Fiscal Year
1990
Total Cost
Indirect Cost
Name
University of Minnesota Twin Cities
Department
Type
Schools of Medicine
DUNS #
168559177
City
Minneapolis
State
MN
Country
United States
Zip Code
55455
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Bank, A J; Lee, P C; Kubo, S H (2000) Endothelial dysfunction in patients with heart failure: relationship to disease severity. J Card Fail 6:29-36
Traverse, J H; Melchert, P; Pierpont, G L et al. (1999) Regulation of myocardial blood flow by oxygen consumption is maintained in the failing heart during exercise. Circ Res 84:401-8
Goldsmith, S R (1999) Angiotensin II and sympathoactivation in heart failure. J Card Fail 5:139-45
Traverse, J H; Kinn, J W; Klassen, C et al. (1998) Nitric oxide inhibition impairs blood flow during exercise in hearts with a collateral-dependent myocardial region. J Am Coll Cardiol 31:67-74
Bank, A J; Shammas, R A; Mullen, K et al. (1998) Effects of short-term forearm exercise training on resistance vessel endothelial function in normal subjects and patients with heart failure. J Card Fail 4:193-201
Bank, A J; Kaiser, D R (1998) Smooth muscle relaxation: effects on arterial compliance, distensibility, elastic modulus, and pulse wave velocity. Hypertension 32:356-9
Goldsmith, S R; Garr, M; McLaurin, M (1998) Regulation of regional norepinephrine spillover in heart failure: the effect of angiotensin II and beta-adrenergic agonists in the forearm circulation. J Card Fail 4:305-10
Ishibashi, Y; Duncker, D J; Zhang, J et al. (1998) ATP-sensitive K+ channels, adenosine, and nitric oxide-mediated mechanisms account for coronary vasodilation during exercise. Circ Res 82:346-59
Wei, H; Merkle, H; Xu, Y et al. (1997) Detection of 13C-labeled metabolites in the in vivo canine heart by B1 insensitive heteronuclear coherent polarization transfer and comparison of signal enhancement with NOE. Magn Reson Med 37:327-30

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