The proposed studies are directed to the understanding of the mechanisms underlying heterogeneity of vascular responses, which under normal conditions provides for optimal integration of the functions of the vascular system, whereas in pathological states it can cause vasospasm or hypertensive disorders. We will continue the ongoing studies on isolated arteries and veins taken from different vascular beds. The proposed research will analyze three aspects of endothelium-dependent responsiveness. In a first part, we will attempt to identify the reasons for the heterogeneous behavior of different arteries and large veins under normal conditions. We will determine whether the heterogeneity is due to the endothelium of the smooth muscle. We will examine in particular the possibilities that the endothelial cells generate several vasoactive factors, and that the sensitivity of vascular smooth muscle to endothelium-derived relaxing and contracting factors varies. To examine the role of the endothelium in releasing relaxing and contracting factors, we will compare preparations with and without endothelium, bio-assay the vasoactive properties of solutions exposed to endothelial cells, measure the release of metabolities of arachidonic aid and the production of ammonia. To study responses of vascular smooth muscle, we will measure changes in isometric tension, cell membrane potential and production of cyclic nucleotides. In a second part, we will examine how physiological factors can affect endothelium-dependent responses chronically; the variables to be studied are chronic alterations in blood flow, adrenergic innervation, sex hormones or changes in dietary lipids. In the final part of the proposal, we will study the endothelium- dependent responsiveness of segments of coronary arteries of the pig which have been exposed to a previous injury after which the endothelium has regenerated. The consequences of altered lipid intake on the ability of that endothelium to induce changes in contractility of vascular smooth muscle will be tested also. Among the stimuli causing vascular responses in this model special attention will be paid to aggregating platelets, since these may play a key role in coronary vasospasm.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL031183-07
Application #
3342212
Study Section
Experimental Cardiovascular Sciences Study Section (ECS)
Project Start
1989-07-01
Project End
1992-06-30
Budget Start
1990-07-01
Budget End
1991-06-30
Support Year
7
Fiscal Year
1990
Total Cost
Indirect Cost
Name
Baylor College of Medicine
Department
Type
Schools of Medicine
DUNS #
074615394
City
Houston
State
TX
Country
United States
Zip Code
77030
Miller, V M; Vanhoutte, P M (2000) Prostaglandins but not nitric oxide are endothelium-derived relaxing factors in the trout aorta. Acta Pharmacol Sin 21:871-6
Zellers, T M; Wu, Y Q; McCormick, J et al. (2000) Prostacyclin-induced relaxations of small porcine pulmonary arteries are enhanced by the basal release of endothelium-derived nitric oxide through an effect on cyclic GMP-inhibited-cyclic AMP phosphodiesterase. Acta Pharmacol Sin 21:131-8
Durante, W; Kroll, M H; Orloff, G J et al. (1996) Regulation of interleukin-1-beta-stimulated inducible nitric oxide synthase expression in cultured vascular smooth muscle cells by hemostatic proteins. Biochem Pharmacol 51:847-53
Joly, G A; Schini, V B; Hughes, H et al. (1995) Potentiation of the hyporeactivity induced by in vivo endothelial injury in the rat carotid artery by chronic treatment with fish oil. Br J Pharmacol 115:255-60
Schini-Kerth, V B; Fisslthaler, B; Andersen, T T et al. (1995) Thrombin prevents the expression of inducible nitric oxide synthase in vascular smooth muscle cells by a proteolytically-activated thrombin receptor. Thromb Haemost 74:980-6
Shimokawa, H; Takeshita, A (1995) Endothelium-dependent regulation of the cardiovascular system. Intern Med 34:939-46
Scott-Burden, T; Vanhoutte, P M (1994) Regulation of smooth muscle cell growth by endothelium-derived factors. Tex Heart Inst J 21:91-7
Durante, W; Schini, V B; Kroll, M H et al. (1994) Platelets inhibit the induction of nitric oxide synthesis by interleukin-1 beta in vascular smooth muscle cells. Blood 83:1831-8
Scott-Burden, T; Elizondo, E; Ge, T et al. (1994) Simultaneous activation of adenylyl cyclase and protein kinase C induces production of nitric oxide by vascular smooth muscle cells. Mol Pharmacol 46:274-82
Schini, V B; Catovsky, S; Schray-Utz, B et al. (1994) Insulin-like growth factor I inhibits induction of nitric oxide synthase in vascular smooth muscle cells. Circ Res 74:24-32

Showing the most recent 10 out of 128 publications