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 |
|---|---|
| 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 |
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