Physical activity represents one of the most potent physiological stimuli for angiogenesis (capillary proliferation) in muscle and arteriogenesis (enlargement of existing vessels) of collateral arteries that can benefit patients with peripheral arterial insufficiency. Our previous work, using a claudicate rat model produced by femoral artery occlusion, has shown that these adaptations improve muscle performance and increase collateral-dependent blood flow, the latter due to structural enlargement of collateral vessels. We now propose experiments to determine the mechanisms involved in collateral vessel expansion and microvascular proliferation, and the modulation of these processes by exercise and angiogenic growth factors. Unique approaches will evaluate: a) collateral vessel function and vasoreactivity in vitro, b) vascular signals contributing to collateral vessel arteriogenesis, and c) mechanisms controlling collateral blood flow increases in vivo. We will determine how vascular occlusion modifies affected collateral vessels to promote receptivity to arteriogenic stimuli, and how the dysfunction of collateral vessels is improved with exercise training and exogenous VEGF delivery. Adult rats are exercised by treadmill running. We will assess the means by which endothelial signaling of NO, alters regulation of VEGF and its receptors (VEGFR-1 and VEGFR-2), and the angiopoietins (Ang1 and Ang2, and their receptor Tie2) is modified to stimulate arteriogenesis in collateral vessels in vivo, using real-time rtPCR. NO, VEGF, Ang1, Ang2, and collateral flow demands will be experimentally managed to establish their interactions in controlling arteriogenesis and collateral blood flow increases following femoral artery occlusion. Collateral blood flow is determined during treadmill running in vivo. Further, we will evaluate the control of capillary proliferation induced by exercise and the functional impact of its absence in otherwise trained muscle. The outcome of these novel, physiologically relevant studies will enhance our understanding of vascular remodeling induced by physical activity and its applicability to managing patients with peripheral arterial insufficiency.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL037387-17
Application #
6751173
Study Section
Respiratory and Applied Physiology Study Section (RAP)
Program Officer
Ershow, Abby
Project Start
1986-12-01
Project End
2006-05-31
Budget Start
2004-06-01
Budget End
2006-05-31
Support Year
17
Fiscal Year
2004
Total Cost
$362,500
Indirect Cost
Name
University of Missouri-Columbia
Department
Veterinary Sciences
Type
Schools of Veterinary Medicine
DUNS #
153890272
City
Columbia
State
MO
Country
United States
Zip Code
65211
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Colleran, Patrick N; Li, Zeyi; Yang, Hsiao T et al. (2010) Vasoresponsiveness of collateral vessels in the rat hindlimb: influence of training. J Physiol 588:1293-307
Taylor, Jessica C; Yang, H T; Laughlin, M Harold et al. (2008) Alpha-adrenergic and neuropeptide Y Y1 receptor control of collateral circuit conductance: influence of exercise training. J Physiol 586:5983-98
Yang, H T; Prior, B M; Lloyd, P G et al. (2008) Training-induced vascular adaptations to ischemic muscle. J Physiol Pharmacol 59 Suppl 7:57-70
Taylor, Jessica C; Li, Zeyi; Yang, H T et al. (2008) Alpha-adrenergic inhibition increases collateral circuit conductance in rats following acute occlusion of the femoral artery. J Physiol 586:1649-67