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Epithelial Sodium Channel Alpha Subunit (αENaC) Is Associated with Inverse Salt Sensitivity of Blood Pressure

  • Peng Xu
    ,
  • Anastasia V. Sudarikova
    ,
  • ,
  • John J. Gildea
    ,
  • Mahabuba Akhter
    ,
  • Robert M. Carey
*Corresponding author for this work
  • University of Virginia
    ,
  • Medical University of South Carolina
    ,
  • RAS - Institute of Cytology
    ,
  • ,
  • Augusta University
    ,
  • George Washington University
Scholary Output:
Contribution to journal
Article
Peer-review

Open access

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well

Abstract

Salt sensitivity of blood pressure (BP) refers to an increase in BP following an increase in dietary salt, which is associated with increased incidence of cardiovascular disease and early death. However, decreased sodium intake also increases mortality and morbidity. Inverse salt sensitivity (ISS), defined as a paradoxical increase in BP on a low-salt diet, about 11% of the population, may be the cause of this phenomenon. The epithelial sodium channel (ENaC) is a major regulator of sodium reabsorption in the kidney. In this study, human renal tubular epithelial cells (hRTC) were cultured from the urine of phenotyped salt study participants. αENaC expression was significantly lower in ISS than salt resistant (SR) hRTC, while ENaC-like channel activity was dramatically increased by trypsin treatment in ISS cells analyzed by patch clamp. αENaC expression was also decreased under high-salt treatment and increased by aldosterone treatment in ISS cells. Moreover, the αENaC variant, rs4764586, was more prevalent in ISS. In summary, αENaC may be associated with ISS hypertension on low salt. These findings may contribute to understanding the mechanisms of ISS and low salt effect on morbidity and mortality.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Article number

981

Journal (Volume, Issue Number)

Biomedicines (Volume 10, Issue 5)

Publication milestones

  • Published - 05/2022

Publication status

Published - 05/2022

Publication IDs

  • Scopus: 85129610722

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5
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1

Funding Details

Funding: These studies were funded by P01HL074940 and R00 DK105160, R01HL148114, R01DK119652, 2-R01-HL-128189, Dialysis Clinic Inc Reserve Fund, the APS Research Career Enhancement, and Lazaro J Madel awards.
FundersFunding numbers
Dialysis Clinic Inc Reserve Fund C-4153
-
APS
-