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Study Describes Molecules That Control Blood Pressure


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"What happens is that WNK4 normally inhibits WNK3, reducing salt resorption," Ellison said. "Mutant WNK4 blocks this effect, thereby generating more active WNK3, increasing salt transport and causing hypertension."

The WNK kinases are members of one of the largest protein families in the human body. There are 518 of them, coordinating a wide variety of biological functions. The WNK kinases, which were discovered in 2000, have been objects of research since a group led by Dr. Richard P. Lifton, who heads his own laboratory at Yale University, found a link between them and a rare inherited form of high blood pressure, called familial hyperkalemic hypertension.

Lifton had no immediate comment on the new report.

Text Continues Below



The new research is still at a basic level, Ellison said. "If we develop a new pharmaceutical approach to hypertension, that could be helpful," he added.

"I think what this report highlights is the importance of understanding the protein level of expression in every kind of cell," said Melanie Cobb, a professor of medical sciences and pharmacology at the University of Texas Southwestern Medical Center at Dallas, where the first WNK kinase was cloned.

"It certainly makes clear that they interact more among themselves than might be expected," Cobb said. "It highlights the complexity of interactions among the proteins, and the importance of understanding those interactions."

More information

A guide to lowering high blood pressure is offered by the U.S. National Heart, Lung, and Blood Institute.

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Copyright © 2007 ScoutNews, LLC. All rights reserved.
Last updated 11/2/2007

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From Healthscout's partner site on high blood pressure, HighBloodPressureConnection.com
Learn more about high blood pressure symptoms.
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SOURCES: David H. Ellison, M.D., professor, medicine, Oregon Health & Science University, Portland; Melanie Cobb, Ph.D., professor, medical sciences and pharmacology, University of Texas Southwestern Medical Center at Dallas; Nov. 1, 2007, Journal of Clinical Investigation


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