Angiotensin converting enzyme (ACE) is a carboxyl peptidase that converts the inactive precursor angiotensin I into angiotensin II. ACE is a key component of the renin-angiotensin system (RAS) and plays a very important role in the physiologic control of blood pressure and fluid balance. The physiologic actions of the RSA are more complex than simple blood pressure control, as evidenced by the phenotype of knockout mice that lack a functional renin-angiotensin system. During the first four years of this grant, this group has created and studied mice that lack ACE. These animals have very low systolic blood pressures, a variety of renal abnormalities, anemia, and reproductive abnormalities. This competitive application is to continue the study of these animals towards the goal of understanding the mechanisms by which the RAS influences normal and abnormal physiology. Specifically, the proposed experiments are designed to study 1) the role of the RAS in the fluid and hematological abnormalities present in ACE knockout mice, 2) the role of the RAS in the renal concentrating mechanism, and 3) the role of the local, tissue specific expression of ACE in regulating cardiovascular function.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK051445-08
Application #
6606138
Study Section
Cardiovascular and Renal Study Section (CVB)
Program Officer
Rasooly, Rebekah S
Project Start
1996-05-01
Project End
2005-07-31
Budget Start
2003-08-01
Budget End
2005-07-31
Support Year
8
Fiscal Year
2003
Total Cost
$352,810
Indirect Cost
Name
Emory University
Department
Pathology
Type
Schools of Medicine
DUNS #
066469933
City
Atlanta
State
GA
Country
United States
Zip Code
30322
Giani, Jorge F; Eriguchi, Masahiro; Bernstein, Ellen A et al. (2017) Renal tubular angiotensin converting enzyme isĀ responsible for nitro-L-arginine methyl esterĀ (L-NAME)-induced salt sensitivity. Kidney Int 91:856-867
Shen, Xiao Z; Ong, Frank S; Bernstein, Ellen A et al. (2012) Nontraditional roles of angiotensin-converting enzyme. Hypertension 59:763-8
Lin, Chentao; Datta, Vivekanand; Okwan-Duodu, Derick et al. (2011) Angiotensin-converting enzyme is required for normal myelopoiesis. FASEB J 25:1145-55
Gonzalez-Villalobos, Romer A; Billet, Sandrine; Kim, Catherine et al. (2011) Intrarenal angiotensin-converting enzyme induces hypertension in response to angiotensin I infusion. J Am Soc Nephrol 22:449-59
Li, Ping; Xiao, Hong D; Xu, Jianguo et al. (2010) Angiotensin-converting enzyme N-terminal inactivation alleviates bleomycin-induced lung injury. Am J Pathol 177:1113-21
Okwan-Duodu, Derick; Datta, Vivekanand; Shen, Xiao Z et al. (2010) Angiotensin-converting enzyme overexpression in mouse myelomonocytic cells augments resistance to Listeria and methicillin-resistant Staphylococcus aureus. J Biol Chem 285:39051-60
Silberman, Gad A; Fan, Tai-Hwang M; Liu, Hong et al. (2010) Uncoupled cardiac nitric oxide synthase mediates diastolic dysfunction. Circulation 121:519-28
Weiss, Daiana; Bernstein, Kenneth E; Fuchs, Sebastian et al. (2010) Vascular wall ACE is not required for atherogenesis in ApoE(-/-) mice. Atherosclerosis 209:352-8
Campbell, Duncan J; Xiao, Hong D; Fuchs, Sebastien et al. (2009) Genetic models provide unique insight into angiotensin and bradykinin peptides in the extravascular compartment of the heart in vivo. Clin Exp Pharmacol Physiol 36:547-53
Xiao, Hong D; Fuchs, Sebastien; Bernstein, Ellen A et al. (2008) Mice expressing ACE only in the heart show that increased cardiac angiotensin II is not associated with cardiac hypertrophy. Am J Physiol Heart Circ Physiol 294:H659-67

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