Project Grant R01DK140219

Award Date 8/7/24
Completion Date 6/30/29
Dollars Obligated $467K
Federal Grant Program
93.847
Assistance Type
Project Grant
Place of Performance
Richmond, VA 23219, USA
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This Project Grant award from the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), under the Diabetes, Digestive, and Kidney Diseases Extramural Research program (CFDA 93.847), will support research to investigate the role of EPAC signaling in regulating sodium reabsorption and its impact on hypertension. The $678,566 award will be used to determine how EPAC isoforms 1 and 2 regulate sodium transport in the proximal tubule and collecting duct of the kidney, and to test...
This Project Grant award from the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), under the Diabetes, Digestive, and Kidney Diseases Extramural Research program (CFDA 93.847), provides $115,500.00 to Wayne State University to conduct research on the regulation of the sodium-potassium-chloride cotransporter (NKCC2) in the thick ascending limb of the kidney. The research aims to discover additional E3-ubiquitin ligases that mediate NKCC2 ubiquitination and their role in...
This federal Project Grant award from the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), under the Diabetes, Digestive, and Kidney Diseases Extramural Research program (CFDA 93.847), is focused on advancing therapies for chronic kidney disease (CKD) through blockade of the sphingosine 1-phosphate (S1P) signaling pathway. The $616,104 award to Virginia Polytechnic Institute & State University (Virginia Tech) aims to: 1) improve the oral availability of SPHK2...
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This $467,473 Project Grant award from the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) under the Diabetes, Digestive, and Kidney Diseases Extramural Research program (CFDA 93.847) will fund research by Virginia Commonwealth University to investigate the role of the acid ceramidase-sphingosine-1-phosphate (AC-S1P) pathway in the kidneys and its impact on salt-sensitive hypertension.

The key objectives are to: 1) Determine if activation of the AC-S1P pathway in the renal medulla promotes sodium excretion and mitigates salt-sensitive hypertension, 2) Evaluate if deficiency in the AC-S1P pathway contributes to the development of salt-sensitive hypertension in a preclinical model, and 3) Examine the mechanisms by which the transcription factor AP2A regulates AC expression in the renal medulla and how this is impaired in salt-sensitive hypertension. The research aims to uncover novel molecular mechanisms underlying renal sodium handling and salt-sensitive hypertension, which could lead to new therapeutic approaches.

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