| Literature DB >> 1733781 |
J C Ellory1, K Kirk, S J Culliford, G B Nash, J Stuart.
Abstract
Nitrendipine, a classical blocker of L-type Ca2+ channels, is shown to be a potent inhibitor of the Ca(2+)-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, nitrendipine inhibited K+(86Rb+) influx with an I50 of around 130 nM. Similar results were obtained for K+(86Rb+) efflux, and for K+(86Rb+) influx into cells suspended in a high-K+ medium.Entities:
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Year: 1992 PMID: 1733781 DOI: 10.1016/0014-5793(92)80383-r
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124