The objectives of the proposed research are to develop additional support for the role of cyclic GMP in the vasodilation of isolated bovine intrapulmonary vessels and to use this system to reconstruct the physiological regulation of guanylate cyclase(GC). Several different classes of vasodilator agents, which potentially possess secondary actions, will be compared for the relationship between the degree of vascular relaxation and the magnitude of tissue level increases in cyclic GMP. These studies will be performed in isolated normal intra-pulmonary arteries and veins using phenylephrine for a contractile agent. The types of vasodilators to be studied include: acetylcholine or related endothelial cell dependent dilators, metabolites of oxygen, arachidonic acid(AA) and related non-prostanoid metabolites, and hydrazine derivatives including phenyl-hydrazine and hydralazine. These agents will be compared to the well characterized nitrogen oxide type vasodilators that are thought to act through cyclic GMP. The mechanism of vasodilator action will be probed by measurement of changes in cyclic nucleotide levels, the effects of some inhibitors of AA metabolism and determination of the endothelial cell dependence. Agents that directly activate purified GC will be compared for the maximal degree of enzyme activation and tissue level increases of cyclic GMP, and for responses to GC activation inhibitors. The mechanism of indirect activators of GC will be probed with additional inhibitors and by measurement of metabolites related to intra-cellular chemical redox pontential and hydroperoxide metabolism. Based on the results obtained, an attempt will be made to reconstruct the mechanism of the indirect activation of purified GC. Since the endothelial cell dependent activation of arterial smooth muscle GC by acetylcholine currently appears to be the best suited system for the study of the physiological regulation of GC, the mechanism of this process will be the primary focus of the proposal. In addition, these studies will contribute to the understanding of physiological and pharmacological mechanisms of vasodilation in the intra-pulmonary vessels.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Unknown (R23)
Project #
5R23HL031069-03
Application #
3448561
Study Section
Experimental Cardiovascular Sciences Study Section (ECS)
Project Start
1984-04-01
Project End
1987-03-31
Budget Start
1986-04-01
Budget End
1987-03-31
Support Year
3
Fiscal Year
1986
Total Cost
Indirect Cost
Name
New York Medical College
Department
Type
Schools of Medicine
DUNS #
City
Valhalla
State
NY
Country
United States
Zip Code
10595
Neo, Boon Hwa; Patel, Dhara; Kandhi, Sharath et al. (2013) Roles for cytosolic NADPH redox in regulating pulmonary artery relaxation by thiol oxidation-elicited subunit dimerization of protein kinase G1?. Am J Physiol Heart Circ Physiol 305:H330-43
Chettimada, Sukrutha; Rawat, Dhwajbahadur K; Dey, Nupur et al. (2012) Glc-6-PD and PKG contribute to hypoxia-induced decrease in smooth muscle cell contractile phenotype proteins in pulmonary artery. Am J Physiol Lung Cell Mol Physiol 303:L64-74
Wolin, Michael S (2012) Novel role for the regulation of mitochondrial fission by hypoxia inducible factor-1? in the control of smooth muscle remodeling and progression of pulmonary hypertension. Circ Res 110:1395-7
Gupte, Sachin A; Wolin, Michael S (2012) Relationships between vascular oxygen sensing mechanisms and hypertensive disease processes. Hypertension 60:269-75
Neo, Boon Hwa; Kandhi, Sharath; Wolin, Michael S (2011) Roles for redox mechanisms controlling protein kinase G in pulmonary and coronary artery responses to hypoxia. Am J Physiol Heart Circ Physiol 301:H2295-304
Wolin, Michael S (2011) Plasma glutathione peroxidase activity is potentially a key regulator of vascular disease-associated thrombosis. Circulation 123:1923-4
Suematsu, Nobuhiro; Ojaimi, Caroline; Recchia, Fabio A et al. (2010) Potential mechanisms of low-sodium diet-induced cardiac disease: superoxide-NO in the heart. Circ Res 106:593-600
Neo, Boon Hwa; Kandhi, Sharath; Wolin, Michael S (2010) Roles for soluble guanylate cyclase and a thiol oxidation-elicited subunit dimerization of protein kinase G in pulmonary artery relaxation to hydrogen peroxide. Am J Physiol Heart Circ Physiol 299:H1235-41
Wolin, Michael S; Gupte, Sachin A; Mingone, Christopher J et al. (2010) Redox regulation of responses to hypoxia and NO-cGMP signaling in pulmonary vascular pathophysiology. Ann N Y Acad Sci 1203:126-32
Ahmad, Mansoor; Kelly, Melissa R; Zhao, Xiangmin et al. (2010) Roles for Nox4 in the contractile response of bovine pulmonary arteries to hypoxia. Am J Physiol Heart Circ Physiol 298:H1879-88

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