The kidney is the main organ involved in the long term regulation of total body potassium. Disorders of potassium balance occur frequently in patients who have hypertension, congestive heart failure, cirrhosis of the liver and renal dysfunction. Hypokalemia causes significant cardiovascular morbidity and mortality in patients treated with diuretics. Furthermore, abnormal regulation of K channels may play a role in the pathogenesis of hypertension. This laboratory is focused on the study of renal potassium channels. This work has let to the discovery of several novel K channel genes. One of these genes encode a cGMP-activated, K-selective channel (KCNA 10a) which is expressed in kidney, heart, muscle and blood vessels. KCNA10a has kinetic properties similar to those of the nitric oxide sensitive K channels detected in pulmonary artery smooth muscle cells. The work now proposed is an extension of the original proposal. The investigative team has recently succeeded in optimizing KCNA10a current expression in Xenopus oocytes and are now able to study its kinetic properties of the single channel level in detail. They will then determine if it is a hetero-multimeric protein and if its expression levels and/or kinetic properties are modulated by any of the live previously cloned a subunits. They will investigate the regulation of KCNA10a by cGMP and ask whether cGMP activates by binding to the cGMP-binding domain and/or via protein phosphorylation. Finally, a panel of high affinity polyclonal antibodies specific for the KCNA10a protein will be developed in order to examine its tissue distribution and membrane localization. The intent is that studies already carried out and those that are proposed in the current application will provide insight into the mechanisms by which K balance is maintained and should, therefore, have direct clinical applications. It is also hoped that the discovery of new molecular structures will expand the existing physiological framework of potassium homeostasis and will lead to the development of new therapeutic agents.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK048105-07
Application #
6380880
Study Section
Special Emphasis Panel (ZRG4-GRM (02))
Program Officer
Scherbenske, M James
Project Start
1994-04-01
Project End
2002-03-31
Budget Start
2001-04-01
Budget End
2002-03-31
Support Year
7
Fiscal Year
2001
Total Cost
$316,254
Indirect Cost
Name
Yale University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
082359691
City
New Haven
State
CT
Country
United States
Zip Code
06520
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Li, Guoyong; Xu, Jianchao; Wang, Peili et al. (2008) Catecholamines regulate the activity, secretion, and synthesis of renalase. Circulation 117:1277-82
Desir, Gary V (2008) Renalase deficiency in chronic kidney disease, and its contribution to hypertension and cardiovascular disease. Curr Opin Nephrol Hypertens 17:181-5
Li, Yanyan; Wang, Peili; Xu, Jianchao et al. (2007) Regulation of insulin secretion and GLUT4 trafficking by the calcium sensor synaptotagmin VII. Biochem Biophys Res Commun 362:658-64
Li, Yanyan; Wang, Peili; Xu, Jianchao et al. (2006) Voltage-gated potassium channel Kv1.3 regulates GLUT4 trafficking to the plasma membrane via a Ca2+-dependent mechanism. Am J Physiol Cell Physiol 290:C345-51
Hebert, Steven C; Desir, Gary; Giebisch, Gerhard et al. (2005) Molecular diversity and regulation of renal potassium channels. Physiol Rev 85:319-71
Xu, Jianchao; Li, Guoyong; Wang, Peili et al. (2005) Renalase is a novel, soluble monoamine oxidase that regulates cardiac function and blood pressure. J Clin Invest 115:1275-80
Xu, Jianchao; Wang, Peili; Li, Yanyan et al. (2004) The voltage-gated potassium channel Kv1.3 regulates peripheral insulin sensitivity. Proc Natl Acad Sci U S A 101:3112-7
Tian, Shulan; Liu, Weimin; Wu, Yanling et al. (2002) Regulation of the voltage-gated K+ channel KCNA10 by KCNA4B, a novel beta-subunit. Am J Physiol Renal Physiol 283:F142-9
Segal, Alan S; Hayslett, John P; Desir, Gary V (2002) On the natriuretic effect of verapamil: inhibition of ENaC and transepithelial sodium transport. Am J Physiol Renal Physiol 283:F765-70

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