Role of the C-Terminal Part of the Extracellular Domain of the α-ENaC in Activation by Sulfonylurea Glibenclamide

Role of the C-Terminal Part of the Extracellular Domain of the α-ENaC in Activation by... The epithelial sodium channel (ENaC) is regulated by hormones and by other intracellular or extracellular factors. It is activated by the sulfonylurea drug glibenclamide. The activator effect of glibenclamide is fast and reversible and was observed in Xenopus oocytes coexpressing the α subunit from human, Xenopus, or guinea pig (but not rat) with βγ-rat ENaC subunits. The mechanism of this effect is not yet well understood. We hypothesize that the extracellular loop of ENaC plays a major role in this activation. Mutants and chimeras of α subunits harboring different parts of the rat and guinea pig α-subunit extracellular loops were generated and coexpressed with βγ-rat subunits in Xenopus oocytes. The effect of glibenclamide on ENaC activity was measured using two-electrode voltage-clamp technique. The α-rat ENaC chimera containing the C-terminal part of the extracellular loop of the α-guinea pig ENaC was significantly stimulated by glibenclamide (1.26-fold), whereas the rat-α combination was not activated by this sulfonylurea. Mutagenesis of specific residues on the rat α subunit did not generate channels sensitive to glibenclamide, suggesting that the overall structure of the extracellular loop is required for activation of the channel by this drug. These results support the hypothesis of the existence of a role played by the last 100 amino acids of the extracellular loop and confirm that the ENaC behaves as a ligand-gated channel similar to several other members of the ENaC/degenerin family. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png The Journal of Membrane Biology Springer Journals

Role of the C-Terminal Part of the Extracellular Domain of the α-ENaC in Activation by Sulfonylurea Glibenclamide

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Publisher
Springer-Verlag
Copyright
Copyright © 2009 by Springer Science+Business Media, LLC
Subject
Life Sciences; Human Physiology ; Biochemistry, general
ISSN
0022-2631
eISSN
1432-1424
D.O.I.
10.1007/s00232-009-9193-1
Publisher site
See Article on Publisher Site

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