(verbatim from application) The overall goals of the proposal (IRPG#3) are to explore the molecular mechanisms of hormonal regulation of ROMK channels and to define the role of ROMK channels in forming apical K + channels in the thick ascending limb (TAL). ROMK channels share the key biophysical properties with the native small-conductance ATP-sensitive K+ channel (SKatp) in the TAL and collecting duct. However, mechanisms by which SKstp is regulated in the TAL are not completely understood since the density of the SKatp is low. This difficulty can now be overcome since preliminary results have demonstrated that in the mouse TAL the density of the apical K channels is significantly increased by either adding forskolin or removal of extracellular Ca2+. Thus, the first goal of Specific Aim 1 is to study the biophysical properties of the apical K+ channels in the mouse TAL. The information will be important for further studying the role of ROMK channels in forming the apical K+ channels when the ROMK‑knockout mice are available. The second goal is to explore the hypothesis that interaction between the vasopressin receptor and the Ca2+-sensing receptor (CaR)-mediated action plays a key role in determining the activity of the apical K+ channels in the mouse TAL. The goal of Specific Aim 2 is to examine the role of kinase anchoring proteins in mediating the effect of PKA and PKC in modulating ROMK channel function and phosphorylation. The goal of Specific Aim 3 is to investigate the mechanism by which PGE2 regulates the apical K+ channels in the TAL. The effect of PGE2 has relevance to Bartter's Syndrome where hyperprostaglandinemia is prominent and inhibition of prostaglandin production reverses partially the physiological consequences of impaired TAL function.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK054983-03
Application #
6635131
Study Section
Special Emphasis Panel (ZRG1-GRM (02))
Program Officer
Ketchum, Christian J
Project Start
2001-03-01
Project End
2005-01-31
Budget Start
2003-03-01
Budget End
2004-01-31
Support Year
3
Fiscal Year
2003
Total Cost
$246,488
Indirect Cost
Name
New York Medical College
Department
Pharmacology
Type
Schools of Medicine
DUNS #
041907486
City
Valhalla
State
NY
Country
United States
Zip Code
10595
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Pandey, Varunkumar; Garcia, Victor; Gilani, Ankit et al. (2017) The Blood Pressure-Lowering Effect of 20-HETE Blockade in Cyp4a14(-/-) Mice Is Associated with Natriuresis. J Pharmacol Exp Ther 363:412-418
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