Funds are requested to purchase a VisualSonics Vevo 2100 research ultrasound imaging system for the Cardiovascular Phenotype Core at the University of Iowa. The Core was founded in 2002 with NIH funds. In the time since, the Core has provided about 20,000 imaging studies in mice and rats, and has introduced a number of novel methods for assessment of organ structure and function in vivo. In 2010, a Vevo 2100 system was purchased with NIH funds. Usage of that instrument has exceeded projections by > 50%; reaching 3113 studies in 2013. Recruitment of new NIH-funded faculty, whose research depends on animals housed in a pathogen-free barrier facility, will increase demands on the existing Vevo 2100 system beyond its capacity. Accommodation of new Users, along with existing Users, will incur significant hardship, expense, and compromise of experimental design unless an additional Vevo 2100 system is purchased. This request coincides with the launch of a new paradigm-shifting initiative by the University of Iowa Carver College of Medicine (UICCOM). The requested instrument will be housed and operated in the new Pappajohn Biomedical Discovery Building, which will open in June, 2014, at a cost of $147M. Two whole floors of that building will be devoted to research imaging, managed by the Iowa Institute for Biomedical Imaging (IIBI). Commensurate with this new vision, IIBI will provide state of the art space and infrastructure for the requested instrument without financial encumbrance. UICCOM will fund the instrument's service contract. The Cardiovascular Research Center will provide funds for faculty and technical personnel to operate the instrument. Together, the institution will provide $213,350 per year for operation of the requested instrument alone, in addition to space and infrastructure. The requested instrument will support the research of NIH-funded investigators in the fields of hypertension, vascular disease, cardiac arrhythmia, cardiomyopathy, and valvular heart disease. The Core will build on its track record of innovation and productivity, and on its history of training new imaging scientists.

Agency
National Institute of Health (NIH)
Institute
Office of The Director, National Institutes of Health (OD)
Type
Biomedical Research Support Shared Instrumentation Grants (S10)
Project #
1S10OD019941-01
Application #
8824742
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Horska, Alena
Project Start
2015-03-01
Project End
2016-02-29
Budget Start
2015-03-01
Budget End
2016-02-29
Support Year
1
Fiscal Year
2015
Total Cost
Indirect Cost
Name
University of Iowa
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
062761671
City
Iowa City
State
IA
Country
United States
Zip Code
52246
Sandgren, Jeremy A; Deng, Guorui; Linggonegoro, Danny W et al. (2018) Arginine vasopressin infusion is sufficient to model clinical features of preeclampsia in mice. JCI Insight 3:
Yu, Yang; Wei, Shun-Guang; Weiss, Robert M et al. (2018) Angiotensin II Type 1a Receptors in the Subfornical Organ Modulate Neuroinflammation in the Hypothalamic Paraventricular Nucleus in Heart Failure Rats. Neuroscience 381:46-58
Yu, Yang; Wei, Shun-Guang; Weiss, Robert M et al. (2017) TNF-? receptor 1 knockdown in the subfornical organ ameliorates sympathetic excitation and cardiac hemodynamics in heart failure rats. Am J Physiol Heart Circ Physiol 313:H744-H756
Vikram, Ajit; Lewarchik, Christopher M; Yoon, Jin-Young et al. (2017) Sirtuin 1 regulates cardiac electrical activity by deacetylating the cardiac sodium channel. Nat Med 23:361-367
Spitler, Kathryn M; Ponce, Jessica M; Oudit, Gavin Y et al. (2017) Cardiac Med1 deletion promotes early lethality, cardiac remodeling, and transcriptional reprogramming. Am J Physiol Heart Circ Physiol 312:H768-H780
Hall, Duane D; Ponce, Jessica M; Chen, Biyi et al. (2017) Ectopic expression of Cdk8 induces eccentric hypertrophy and heart failure. JCI Insight 2:
Chu, Yi; Lund, Donald D; Doshi, Hardik et al. (2016) Fibrotic Aortic Valve Stenosis in Hypercholesterolemic/Hypertensive Mice. Arterioscler Thromb Vasc Biol 36:466-74
Yu, Yang; Wei, Shun-Guang; Zhang, Zhi-Hua et al. (2016) ERK1/2 MAPK signaling in hypothalamic paraventricular nucleus contributes to sympathetic excitation in rats with heart failure after myocardial infarction. Am J Physiol Heart Circ Physiol 310:H732-9
Wei, Shun-Guang; Yu, Yang; Weiss, Robert M et al. (2016) Inhibition of Brain Mitogen-Activated Protein Kinase Signaling Reduces Central Endoplasmic Reticulum Stress and Inflammation and Sympathetic Nerve Activity in Heart Failure Rats. Hypertension 67:229-36
Wei, Shun-Guang; Yu, Yang; Weiss, Robert M et al. (2016) Endoplasmic reticulum stress increases brain MAPK signaling, inflammation and renin-angiotensin system activity and sympathetic nerve activity in heart failure. Am J Physiol Heart Circ Physiol 311:H871-H880

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