Exercise training has been reported to be beneficial in preventing and/or treating coronary heart disease. However, the primary underlying mechanisms and the relative importance of training induced changes in the coronary vascular bed are not clear at this time. The major goal of the research outlined in this proposal is to provide a better understanding of the effects of exercise training on basic coronary function. Since the purpose of the coronary circulation is to transport nutrients and oxygen to the myocardial cells and to transport metabolites away from these cells, this grant focuses on the effects of training on coronary transport capacity. During the first year of this grant it was found that coronary transport capacity can be quantitated by measuring coronary blood flow reserve capacity and coronary capillary diffusion capacity. It was then found that exercise trained dogs have a large increase in coronary transport reserve in that blood flow and capillary diffusion capacities are both increased. The research outlined in this proposal will attain 5 specific aims that will determine the mechanisms responsible for and functional significance of this change: 1. Determine the mechanisms responsible for the exercise training induced increase in coronary transport reserve. 2. Determine the role of the sympathetic nervous system in the exercise training induced increase in coronary transport reserve. 3. Determine how the exercise training induced changes in the coronary vascular bed influence capillary transport during acute myocardial ischemia. 4. Determine the effects of exercise training on coronary transport reserve in minature swine. 5. Determine how the training induced increase in coronary transport reserve influences coronary transcapillary exchange and exchange capacity in conscious dogs. Transcapillary exchange will be measured with the multiple indicator diffusion technique. Coronary blood flow will be measured in conscious and anesthetized dogs with electromagnetic flow meters. Regional coronary blood flow and gross blood flow heterogeneity will be determined with the radiolabeled microsphere technique.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL036531-03
Application #
3351565
Study Section
Respiratory and Applied Physiology Study Section (RAP)
Project Start
1985-09-15
Project End
1990-03-31
Budget Start
1988-04-01
Budget End
1989-03-31
Support Year
3
Fiscal Year
1988
Total Cost
Indirect Cost
Name
University of Missouri-Columbia
Department
Type
Schools of Veterinary Medicine
DUNS #
112205955
City
Columbia
State
MO
Country
United States
Zip Code
65211
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Delp, M D; Laughlin, M H (1998) Regulation of skeletal muscle perfusion during exercise. Acta Physiol Scand 162:411-9
McAllister, R M (1998) Adaptations in control of blood flow with training: splanchnic and renal blood flows. Med Sci Sports Exerc 30:375-81
Jones, A W; Magliola, L; Waters, C B et al. (1998) Endothelin-1 activates phospholipases and channels at similar concentrations in porcine coronary arteries. Am J Physiol 274:C1583-91
Harris, P A; Lorenz, C H; Holburn, G E et al. (1997) Regional measurement of the Gd-DTPA tissue partition coefficient in canine myocardium. Magn Reson Med 38:541-5
McAllister, R M; Delp, M D; Laughlin, M H (1997) A review of effects of hypothyroidism on vascular transport in skeletal muscle during exercise. Can J Appl Physiol 22:1-10
McAllister, R M; Reiter, B L; Amann, J F et al. (1997) Skeletal muscle biochemical adaptations to exercise training in miniature swine. J Appl Physiol 82:1862-8
Laughlin, M H; McAllister, R M; Jasperse, J L et al. (1996) Endothelium-medicated control of the coronary circulation. Exercise training-induced vascular adaptations. Sports Med 22:228-50
Huxley, V H; Williams, D A (1996) Basal and adenosine-mediated protein flux from isolated coronary arterioles. Am J Physiol 271:H1099-108
McAllister, R M; Kimani, J K; Webster, J L et al. (1996) Effects of exercise training on responses of peripheral and visceral arteries in swine. J Appl Physiol 80:216-25

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