Specificity of Classical and Putative Cl- Transport Inhibitors on Membrane Transport Pathways in Human Erythrocytes

The majority of anion transport inhibitors tend to be non-specific. This is problematic from a research point of view as caution is required when defining pathways purely based on pharmacology. Here we have tested a range of classical and putative Cl - transport inhibitors on three Cl - carrier syst...

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Veröffentlicht in:Cellular physiology and biochemistry 2003-01, Vol.13 (4), p.181-188
Hauptverfasser: Culliford, Steven, Ellory, Clive, Lang, Hans-Jochen, Englert, Heinrich, Staines, Hery, Wilkins, Robert
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Sprache:eng
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Zusammenfassung:The majority of anion transport inhibitors tend to be non-specific. This is problematic from a research point of view as caution is required when defining pathways purely based on pharmacology. Here we have tested a range of classical and putative Cl - transport inhibitors on three Cl - carrier systems (the KCl cotransporter (KCC), the NaK2Cl cotransporter (NKCC), and the Band 3 anion exchanger (AE)) found in human erythrocytes, using radiolabel tracer experiments. The study confirms the cross-reactivity of many anion transport inhibitors. However, two compounds, H25 and H156, were found to be both potent (IC 50 values < 0.1 mM) and specific (at least 1000-fold more effective against one carrier compared to the other two) inhibitors of NKCC and AE, respectively.
ISSN:1015-8987
1421-9778
DOI:10.1159/000072420