| Literature DB >> 17762186 |
Ingolf Bernhardt1, Erwin Weiss, Hannah C Robinson, Robert Wilkins, Poul Bennekou.
Abstract
Residual K(+) fluxes in red blood cells can be stimulated in conditions of low ionic strength. Previous studies have identified both the non-selective, voltage-dependent cation (NSVDC) channel and the K(+)(Na(+))/H(+) exchanger as candidate pathways mediating this effect, although it is possible that these pathways represent different modes of operation of a single system. In the present study the effects of HOE642, recently characterised as an inhibitor of the K(+)(Na(+))/H(+) exchanger, on NSVDC has been determined to clarify this question. Radioisotope flux measurements and conductance determinations showed that HOE642 exerted differential effects on the NSVDC channel and the K(+)(Na(+))/H(+) exchanger, confirming that the salt loss observed in low ionic strength solutions represents contributions from at least two independent ion transport pathways. The findings are discussed in the context of red blood cell apoptosis (eryptosis) and disease. Copyright (c) 2007 S. Karger AG, Basel.Entities:
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Year: 2007 PMID: 17762186 DOI: 10.1159/000107543
Source DB: PubMed Journal: Cell Physiol Biochem ISSN: 1015-8987