The Animal Model Core will make available to investigators a broad range of mouse models of vascularinjury. These include (i) wire injury to the femoral or carotid arteries; (ii) low flow dependent model of thecarotid which retains endothelial integrity and (iii) a abdominal aortic aneurysm formation in response toangiotensin II infusion in hyperlipidemic mice. Additionally, the Core is well experienced in the quantitiativeand morphological analysis of atherosclerosis in diversified models of genetically prone mice.A second repertoire of models affords to assess other aspects of vascular function. Thus, continuoustelemetric monitoring of the diurnal variation in blood pressure is available in conscious mice. Additionally, amodel of free radical catalyzed injury to the carotid with subsequent carotid vascular occlusion is available topermit assessment of the response to a thrombogenic stimulus.The Animal Model Core is equipped for constant hemodynamic monitoring, urine collection in metaboliccages and blood sampling, cellular isolation and storage. Facilities exist for monitoring whole blood andplatelet aggregation.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Specialized Center (P50)
Project #
1P50HL083799-01
Application #
7140945
Study Section
Special Emphasis Panel (ZHL1-CSR-A (F1))
Project Start
2006-04-01
Project End
2011-03-31
Budget Start
2006-04-01
Budget End
2007-04-30
Support Year
1
Fiscal Year
2006
Total Cost
$154,748
Indirect Cost
Name
University of Pennsylvania
Department
Type
DUNS #
042250712
City
Philadelphia
State
PA
Country
United States
Zip Code
19104
Ferguson, Jane F; Xue, Chenyi; Gao, Yuanfeng et al. (2018) Tissue-Specific Differential Expression of Novel Genes and Long Intergenic Noncoding RNAs in Humans With Extreme Response to Evoked Endotoxemia. Circ Genom Precis Med 11:e001907
Tuteja, Sony; Wang, Lu; Dunbar, Richard L et al. (2017) Genetic coding variants in the niacin receptor, hydroxyl-carboxylic acid receptor 2, and response to niacin therapy. Pharmacogenet Genomics 27:285-293
Dunbar, Richard L; Goel, Harsh; Tuteja, Sony et al. (2017) Measuring niacin-associated skin toxicity (NASTy) stigmata along with symptoms to aid development of niacin mimetics. J Lipid Res 58:783-797
Ferguson, Jane F; Xue, Chenyi; Hu, Yu et al. (2016) Adipose tissue RNASeq reveals novel gene-nutrient interactions following n-3 PUFA supplementation and evoked inflammation in humans. J Nutr Biochem 30:126-32
Patel, Parth N; Shah, Rhia Y; Ferguson, Jane F et al. (2015) Human experimental endotoxemia in modeling the pathophysiology, genomics, and therapeutics of innate immunity in complex cardiometabolic diseases. Arterioscler Thromb Vasc Biol 35:525-34
Ferguson, Jane F; Shah, Rhia Y; Shah, Rachana et al. (2015) Activation of innate immunity modulates insulin sensitivity, glucose effectiveness and pancreatic ?-cell function in both African ancestry and European ancestry healthy humans. Metabolism 64:513-520
Ferguson, Jane F; Meyer, Nuala J; Qu, Liming et al. (2015) Integrative genomics identifies 7p11.2 as a novel locus for fever and clinical stress response in humans. Hum Mol Genet 24:1801-12
Ferguson, Jane F; Mulvey, Claire K; Patel, Parth N et al. (2014) Omega-3 PUFA supplementation and the response to evoked endotoxemia in healthy volunteers. Mol Nutr Food Res 58:601-13
Meyer, Nuala J; Ferguson, Jane F; Feng, Rui et al. (2014) A functional synonymous coding variant in the IL1RN gene is associated with survival in septic shock. Am J Respir Crit Care Med 190:656-64
Liu, Yichuan; Ferguson, Jane F; Xue, Chenyi et al. (2014) Tissue-specific RNA-Seq in human evoked inflammation identifies blood and adipose LincRNA signatures of cardiometabolic diseases. Arterioscler Thromb Vasc Biol 34:902-12

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