Mice required for the 4 projects of this PPG will be bred and maintained by the Animal Core. The Core will arrange the purchase and transfer of breeder pairs for 5 developed strains: eNOS, nNOS, EC-SOD, NAD(P)H oxidase-p47/phox subunit, and D5-R. Colonies to support adult male mice of 8-14 weeks will be developed from the initial breeders. Heterozygous (+/-) mice will be bred to provide both homozygous (+/+) wild type and homozygous (-/-) deleted mice in the same litter, to maximize the genetic background of the control groups. The Core has in place a detailed plan that specifies the number of mice required to generated sufficient study animals. The Core will maintain a database of pertinent information that correlates to the ear tag identification number of each mouse. The Core will collect blood from weaning mice for genotyping, which will be performed fin the Molecular Core. The systolic blood pressure of each animal will be measured before and during placement of subcutaneous mini-pumps. Mini-pumps will contain either vehicle or angiotensin II (Ang II). 24 hour urine will be collected and analyzed for 8-isoprostane, lipid peroxidation, nitric oxide metabolites, and creatinine. The Core will also measure the conscious mean arterial blood pressure directly by radio telemetry in a subset of each single-gene deleted strain, before and during mini-pumps placement. The Core will provide technical support for each project in all areas relating to animals and analysis.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Program Projects (P01)
Project #
5P01HL068686-02
Application #
6656541
Study Section
Heart, Lung, and Blood Initial Review Group (HLBP)
Project Start
2002-09-01
Project End
2003-08-31
Budget Start
2002-09-01
Budget End
2003-08-31
Support Year
2
Fiscal Year
2002
Total Cost
$335,964
Indirect Cost
Name
Georgetown University
Department
Type
DUNS #
049515844
City
Washington
State
DC
Country
United States
Zip Code
20057
Li, Lingli; Lai, En Yin; Luo, Zaiming et al. (2018) High Salt Enhances Reactive Oxygen Species and Angiotensin II Contractions of Glomerular Afferent Arterioles From Mice With Reduced Renal Mass. Hypertension 72:1208-1216
Schmidt, Marcel Oliver; Garman, Khalid Ammar; Lee, Yong Gu et al. (2018) The Role of Fibroblast Growth Factor-Binding Protein 1 in Skin Carcinogenesis and Inflammation. J Invest Dermatol 138:179-188
Tassi, Elena; Lai, En Yin; Li, Lingli et al. (2018) Blood Pressure Control by a Secreted FGFBP1 (Fibroblast Growth Factor-Binding Protein). Hypertension 71:160-167
Tassi, Elena; Garman, Khalid A; Schmidt, Marcel O et al. (2018) Fibroblast Growth Factor Binding Protein 3 (FGFBP3) impacts carbohydrate and lipid metabolism. Sci Rep 8:15973
Wang, Xiaoyan; Villar, Van Anthony; Tiu, Andrew et al. (2018) Dopamine D2 receptor upregulates leptin and IL-6 in adipocytes. J Lipid Res 59:607-614
Asico, Laureano D; Cuevas, Santiago; Ma, Xiaobo et al. (2018) Nephron segment-specific gene expression using AAV vectors. Biochem Biophys Res Commun 497:19-24
Yang, Jian; Jose, Pedro A; Zeng, Chunyu (2017) Gastrointestinal-Renal Axis: Role in the Regulation of Blood Pressure. J Am Heart Assoc 6:
Zhao, L; Gao, Y; Cao, X et al. (2017) High-salt diet induces outward remodelling of efferent arterioles in mice with reduced renal mass. Acta Physiol (Oxf) 219:652-659
Tiu, Andrew C; Bishop, Michael D; Asico, Laureano D et al. (2017) Primary Pediatric Hypertension: Current Understanding and Emerging Concepts. Curr Hypertens Rep 19:70
Li, Lingli; Lai, En Yin; Luo, Zaiming et al. (2017) Superoxide and hydrogen peroxide counterregulate myogenic contractions in renal afferent arterioles from a mouse model of chronic kidney disease. Kidney Int 92:625-633

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