Enhanced expression of epithelial sodium channels in the renal medulla of Dahl S rats

Author:

Amin Md. Shahrier1234,Reza Erona1234,El-Shahat Esraa1234,Wang Hong-Wei1234,Tesson Frédérique1234,Leenen Frans H.H.1234

Affiliation:

1. Hypertension Unit, University of Ottawa Heart Institute, Ottawa, ON K1Y 4W7, Canada.

2. Laboratory of Genetics of Cardiac Disease, University of Ottawa Heart Institute, Ottawa, ON K1Y 4W7, Canada.

3. Department of Cellular and Molecular Medicine, University of Ottawa, Ottawa, ON K1H 8M5, Canada.

4. Faculty of Health Sciences, University of Ottawa, Ottawa, ON K1H 8M5, Canada.

Abstract

Inner medullary collecting duct (IMCD) cells from salt-sensitive (S) Dahl rats transport twice as much Na+as cells from salt-resistant (R) rats, possibly related to dysregulation of the renal epithelial sodium channel (ENaC). The effect of a high-salt diet on ENaC expression in the inner medulla of S versus R rats has not yet been studied. Young, male S and R rats were placed on a regular-salt (0.3%) or high-salt (8%) diet for 2 or 4 weeks. mRNA and protein expression of ENaC subunits were studied by real-time PCR and immunoblotting. Intracellular distribution of the subunits in the IMCD was evaluated by immunohistochemistry. On regular salt, the abundance of the mRNA of β and γENaC was higher in the medulla of S rats than R rats. This was associated with a greater protein abundance of 90 kDa γENaC and higher immunoreactivity for both α and γ ENaC. High salt did not affect mRNA abundance in either strain and decreased apical staining of βENaC in IMCD of R rats. In contrast, high salt did not affect the higher apical localization of αENaC and increased the apical membrane staining for β and γENaC in the IMCD of S rats. Expression of ENaC subunits is enhanced in the medulla of S vs. R rats on regular salt, and further increased on high salt. The persistent high expression of αENaC and increase in apical localization of β and γENaC may contribute to greater retention of sodium in S rats on a high-salt diet.

Publisher

Canadian Science Publishing

Subject

Physiology (medical),Pharmacology,General Medicine,Physiology

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