This core has two functions and serves all four Projects: 1. Central Facility: This section of the Core is for maintenance, record keeping, and procurement of animals for the four projects. The Core will maintain all surgical records. The personnel associated with the Core will perform ordering, shipping and handling of the rats and transgenic mice. Personnel employed by the Biologic Resources Laboratory (BRL) will be responsible for feeding, watering, and cage cleaning (per diem costs included in budget, see Table 1). Any post-operative complications resulting from the animal surgeries will be addressed by consultation of Core personnel with the veterinary staff at the BRL. Data obtained from the physiological and echocardiographic measurements of the animals will be analyzed and summarized by the Core personnel and presented to the individual project principal investigators. 2. Animal Model and Cardiac Analysis Facility: This section of the core will provide surgical models of transverse aortic banding (pressure overload), aorta-cava fistula (volume overload), and coronary artery ligation (myocardial infarction) in rats, and transverse aortic banding in mice. Core personnel will also instrument rats and mice for measurements of left ventricular hemodynamics using a Millar pressure/volume catheter. Pressure/volume curves will be constructed under baseline conditions and subsequent to inotropic challenges with beta- and alpha-adrenergic agonists. The Core will also perform 2-dimensional and M-mode echocardiography and Doppler aortic and pulmonary flows on mice and rats, before and after surgery, to demonstrate changes with cardiac remodeling and confirm any changes in contractile performance of the heart as assessed by pressure/volume measurements.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Program Projects (P01)
Project #
5P01HL062426-10
Application #
7924061
Study Section
Heart, Lung, and Blood Initial Review Group (HLBP)
Project Start
Project End
Budget Start
2009-06-01
Budget End
2010-05-31
Support Year
10
Fiscal Year
2009
Total Cost
$514,131
Indirect Cost
Name
University of Illinois at Chicago
Department
Type
DUNS #
098987217
City
Chicago
State
IL
Country
United States
Zip Code
60612
Dvornikov, Alexey V; de Tombe, Pieter P; Xu, Xiaolei (2018) Phenotyping cardiomyopathy in adult zebrafish. Prog Biophys Mol Biol 138:116-125
Le, Long V; Mohindra, Priya; Fang, Qizhi et al. (2018) Injectable hyaluronic acid based microrods provide local micromechanical and biochemical cues to attenuate cardiac fibrosis after myocardial infarction. Biomaterials 169:11-21
Mkrtschjan, Michael A; Gaikwad, Snehal B; Kappenman, Kevin J et al. (2018) Lipid signaling affects primary fibroblast collective migration and anchorage in response to stiffness and microtopography. J Cell Physiol 233:3672-3683
Yan, Jiajie; Thomson, Justin K; Zhao, Weiwei et al. (2018) Role of Stress Kinase JNK in Binge Alcohol-Evoked Atrial Arrhythmia. J Am Coll Cardiol 71:1459-1470
Bohlooli Ghashghaee, Nazanin; Li, King-Lun; Solaro, R John et al. (2018) Role of the C-terminus mobile domain of cardiac troponin I in the regulation of thin filament activation in skinned papillary muscle strips. Arch Biochem Biophys 648:27-35
Yan, Jiajie; Zhao, Weiwei; Thomson, Justin K et al. (2018) Stress Signaling JNK2 Crosstalk With CaMKII Underlies Enhanced Atrial Arrhythmogenesis. Circ Res 122:821-835
Ait Mou, Younss; Lacampagne, Alain; Irving, Thomas et al. (2018) Altered myofilament structure and function in dogs with Duchenne muscular dystrophy cardiomyopathy. J Mol Cell Cardiol 114:345-353
Ferrantini, Cecilia; Coppini, Raffaele; Pioner, Josè Manuel et al. (2017) Pathogenesis of Hypertrophic Cardiomyopathy is Mutation Rather Than Disease Specific: A Comparison of the Cardiac Troponin T E163R and R92Q Mouse Models. J Am Heart Assoc 6:
Alves, Marco L; Warren, Chad M; Simon, Jillian N et al. (2017) Early sensitization of myofilaments to Ca2+ prevents genetically linked dilated cardiomyopathy in mice. Cardiovasc Res 113:915-925
Zak, Taylor J; Koshman, Yevgenia E; Samarel, Allen M et al. (2017) Regulation of Focal Adhesion Kinase through a Direct Interaction with an Endogenous Inhibitor. Biochemistry 56:4722-4731

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