The Program Project Grant integrates molecular and physiological approaches to examine regulation of cerebral blood vessels under physiological and pathophysiological conditions. The program represents an interactive and productive group of investigators with complimentary areas of expertise who are committed to studies of cerebral circulation. The Program has several themes: First, molecular and functional studies are proposed to examine the role of endothelium and nitric oxide in regulation of cerebral vascular function and structure. Second, state-of-the-art molecular approaches are used throughout the program, with strong emphasis on gene transfer and genetically-engineered mice. Third, a major goal is to understand cerebral vascular pathophysiology and risk factors for stroke. Studies are proposed to examine mechanisms by which chronic hypertension, byperhomo-cysteinemia, and inflammatory stimuli alter cerebral vessels. The Program has several strengths; First, the investigators have a long history of interactive studies of cerebral vessels under physiological and pathophysiological conditions. Second, strong new investigators with key expertise have been integrated into the program. Preliminary data indicate feasibility of new approaches which are proposed. Third, the investigators are leaders in physiological studies of cerebral vascular endothelium, nitric oxide, and potassium channels. They also are leaders in studies of cerebral vascular dysfunction and structural changes during pathophysiological conditions, including chronic hypertension and hyper-homocysteinemia. Fourth, the investigators use diverse, sophisticated physiological approaches in their studies. Molecular approaches now have been incorporated to facilitate novel insight into cerebral vascular structure and function. The program consists of four projects supported by three core facilities: Administration, Transgenic Animal Core, and a Vector Core. This integrated, multidiscriplinary approach is intended to facilitate rapid progress, and more penetrating insight, in understanding mechanisms that affect cerebral blood vessels.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Program Projects (P01)
Project #
5P01NS024621-12
Application #
2668985
Study Section
Neurological Disorders Program Project Review A Committee (NSPA)
Program Officer
Jacobs, Tom P
Project Start
1987-04-01
Project End
2002-02-28
Budget Start
1998-03-01
Budget End
1999-02-28
Support Year
12
Fiscal Year
1998
Total Cost
Indirect Cost
Name
University of Iowa
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
041294109
City
Iowa City
State
IA
Country
United States
Zip Code
52242
Ketsawatsomkron, Pimonrat; Keen, Henry L; Davis, Deborah R et al. (2016) Protective Role for Tissue Inhibitor of Metalloproteinase-4, a Novel Peroxisome Proliferator-Activated Receptor-? Target Gene, in Smooth Muscle in Deoxycorticosterone Acetate-Salt Hypertension. Hypertension 67:214-22
Dayal, Sanjana; Gu, Sean X; Hutchins, Ryan D et al. (2015) Deficiency of superoxide dismutase impairs protein C activation and enhances susceptibility to experimental thrombosis. Arterioscler Thromb Vasc Biol 35:1798-804
Rodionov, Roman N; Jarzebska, Natalia; Weiss, Norbert et al. (2014) AGXT2: a promiscuous aminotransferase. Trends Pharmacol Sci 35:575-82
De Silva, T Michael; Modrick, Mary L; Ketsawatsomkron, Pimonrat et al. (2014) Role of peroxisome proliferator-activated receptor-? in vascular muscle in the cerebral circulation. Hypertension 64:1088-93
Chrissobolis, Sophocles; Drummond, Grant R; Faraci, Frank M et al. (2014) Chronic aldosterone administration causes Nox2-mediated increases in reactive oxygen species production and endothelial dysfunction in the cerebral circulation. J Hypertens 32:1815-21
Chu, Yi; Lund, Donald D; Weiss, Robert M et al. (2013) Pioglitazone attenuates valvular calcification induced by hypercholesterolemia. Arterioscler Thromb Vasc Biol 33:523-32
Klykov, Corinne M; Lentz, Steven R (2013) Trends in clinical laboratory homocysteine testing from 1997 to 2010: the impact of evidence on clinical practice at a single institution. Clin Chem Lab Med 51:671-5
Dayal, Sanjana; Wilson, Katina M; Motto, David G et al. (2013) Hydrogen peroxide promotes aging-related platelet hyperactivation and thrombosis. Circulation 127:1308-16
Miller, Jordan D; Chu, Yi; Castaneda, Lauren E et al. (2013) Vascular function during prolonged progression and regression of atherosclerosis in mice. Arterioscler Thromb Vasc Biol 33:459-65
Pelham, Christopher J; Keen, Henry L; Lentz, Steven R et al. (2013) Dominant negative PPAR? promotes atherosclerosis, vascular dysfunction, and hypertension through distinct effects in endothelium and vascular muscle. Am J Physiol Regul Integr Comp Physiol 304:R690-701

Showing the most recent 10 out of 432 publications