Abstract
Epithelial chloride channels can be blocked by various inhibitors, which show considerable differences in their molecular structure. In the present patch-clamp study, we compared different blockers of one type of epithelial Cl− channel with respect to their inhibitory potency. We applied the blockers to excised inside-out-or outside-out-oriented membrane patches of cultured HT29 colon carcinoma and respiratory epithelial cells (REC) containing the outwardly rectifying intermediate-conductance (ICOR) chloride channel. Four types of inhibitory compounds were tested: stilbene disulphonate derivatives, indanyloxyacetic acid, amidine, and arylaminobenzoates. The concentrations for half-maximal inhibition (IC50) for the different channel blockers were (μmol/l): 4-acetamido-4′-isothiocyanato-stilbene-2,2′-disulphonic acid 100; 4,4′-diisothiocyanato-stilbene-2,2′-disulphonic acid 80; indanyloxyacetic acid 9; 4,4′-dinitrostilbene-2, 2′-disulphonic acid 8; amidine 8 and 5-nitro-2-(3-phenylpropylamino)-benzoate (NPPB) 0.9. All compounds, when applied to the cytosolic side of the channel, induced a flicker-type block of the ICOR Cl− channel at lower concentrations and a complete channel inhibition at higher concentrations. The inhibitory potency of NPPB was much higher when it was added to the external surface of the channel in outside-out-oriented membrane patches. At 1 μmol/l the inhibition was complete. All blocker effects were fully reversible. The probe with the highest affinity (NPPB) and a closely related compound 5-nitro-2-(3-phenylethylamino)-benzoate (NPFB) were used to construct macromolecular probes by linking these blockers to aminopolyethyleneglycol (PEG) or aminoethyl-O-dextran (5 kDa). These macromolecular NPPB and NPEB derivatives inhibited the ICOR Cl− channels only from the outside but had no effect on the cytosolic side. In the case of PEG-NPPB an IC50 of 30 nmol/l was determined in outside-out patches. The data indicate that the interaction site for arylaminobenzoates is accessible from the outer aspects of the Cl− channel facing the extracellular medium. Furthermore, these data show that the macromolecular probes of arylaminobenzoates have affinities to the Cl− channel very similar to those of the respective parent compounds.
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Tilmann, M., Kunzelmann, K., Fröbe, U. et al. Different types of blockers of the intermediate-conductance outwardly rectifying chloride channel in epithelia. Pflügers Arch 418, 556–563 (1991). https://doi.org/10.1007/BF00370571
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DOI: https://doi.org/10.1007/BF00370571