Abstract
Nitrendipine, a classical blocker of L-type Ca2+ channels, is shown to be a potent inhibitor of the Ca2+-activated K+ channel of human erythrocytes. In erythrocytes suspended in a solution with physiological Na+ and K+ concentrations and in which the channel was activated using the Ca2+ ionophore ionomycin, nitrendipene inhibited K+(80Rb+) influx with an I50 of around 130 nM. Similar results were obtained for K+(80Rb+) efflux, and for K+(80Rb+) influx into cells suspended in a high-K+ medium.
Original language | English |
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Pages (from-to) | 219-221 |
Number of pages | 3 |
Journal | FEBS Letters |
Volume | 296 |
Issue number | 2 |
DOIs | |
Publication status | Published - 20 Jan 1992 |
Externally published | Yes |