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OHSU discovers molecular channel that regulates blood pressure

Breakthrough could lead to ‘new and better blood pressure medications’
Human epithelial sodium channel model
Using a cryo-electron microscope, researchers at OHSU generated a three-dimensional model of the human epithelial sodium channel. The channel is critical in controlling blood pressure, among other functions in the body. (OHSU)

New research for the first time reveals the three-dimensional structure of a membrane channel that’s critical in controlling blood pressure.

Sigrid Noreng
Sigrid Noreng
Isabelle Baconguis Ph.D. (2018)
Isabelle Baconguis, Ph.D.

The findings, published today in the open-access journal eLife,  represent the first time the human epithelial sodium channel has been shown so precisely since it was first isolated and described through expression cloning in 1993, said senior author Isabelle Baconguis, Ph.D., assistant professor in the OHSU Vollum Institute. Lead author Sigrid Noreng, a graduate student in the Baconguis lab, added that the discovery provides a starting point for the development of better treatments for a range of diseases associated with the channel.

“It’s definitely going to move the field forward,” Baconguis agreed.

The channel enables sodium ions to be absorbed into tissues throughout the body, including the kidney. As such, it is a crucial aspect of human health by regulating sodium balance, blood volume and blood pressure.

Richard Posert
Richard Posert

“We wouldn’t have been able to leave the ocean without it,” quipped co-author Richard Posert, a graduate student in Baconguis’ lab.

Dysfunction of the epithelial sodium channel, or ENaC, can lead to severe forms of hypertension such as Liddle syndrome or neonatal salt-wasting disorder. The discovery answers fundamental biophysical questions about the specific architecture of the channel, which ultimately could lead to the development of medications to improve the treatment of diseases such as severe hypertension, heart failure and nephrotic syndrome.

“This is the first visual representation of a protein that is connected to many diseases,” Baconguis said. “As soon as you perturb this membrane protein, everything downstream becomes disrupted as well.”

Noreng noted the discovery may be especially helpful in developing targeted medications to control high blood pressure.

“There are no good medications that target this protein specifically,” Noreng said. “Discovering the structure of this channel will be very important toward the development of new and better blood pressure medications.”

The researchers made the discovery through the use of a cryo-electron microscope housed in OHSU’s Robertson Life Sciences Building. Cryo-EM technology is part of a newly designated national center intended to widen the use of a technique that is revolutionizing structural biology. The technique enables scientists to visualize biological molecules at an atomic scale and to see them in their natural state.

Craig Yoshioka Ph.D. (2018)
Craig Yoshioka, Ph.D.
Arpita Bharadwaj
Arpita Bharadwaj

In addition to Noreng, Baconguis and Posert, co-authors included Arpita Bharadwaj, a senior research associate in the lab, and Craig Yoshioka, Ph.D., research assistant professor of biomedical engineering in the OHSU School of Medicine.

The work was supported by National Institutes of Health grant NIH Director’s Early Independence Award DP5OD017871.

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