Nitrendipine is a potent inhibitor of the Ca2+-activated K+ channel of human erythrocytes

J. Clive Ellory*, Kiaran Kirk, Steven J. Culliford, Gerard B. Nash, John Stuart

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

45 Citations (Scopus)

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 languageEnglish
Pages (from-to)219-221
Number of pages3
JournalFEBS Letters
Volume296
Issue number2
DOIs
Publication statusPublished - 20 Jan 1992
Externally publishedYes

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