Abstract:
:A calcium-dependent potassium channel K(Ca) has been isolated in mouse motoneurons. With physiological concentrations of potassium across inside-out patches, a 100 pS K(Ca) channel was activated when the bath solution of Ca2+ was in excess of 1 microM. Introduction of the drug tedisamil, a blocker of repolarizing potassium channels in cardiac cells, at concentrations in the range 0.2-10 microM, caused a dose-dependent decrease in the mean open times for K(Ca). The drug action was consistent with open channel block of K(Ca) with an onward (blocking) rate constant of 6 x 10(7) M-1 s-1. Tedisamil, at concentrations of 1 microM and 5 microM, also blocked the K(Ca) channel when applied to outside-out patches with a similar potency as found with internal application. A large conductance K(Ca) channel in hippocampal neurons is also blocked by a number of putative Class III antiarrhythmic drugs, including tedisamil; thus, these agents may have utility in the characterization of the properties of K(Ca) channels in various cells.
journal_name
Neurosci Lettjournal_title
Neuroscience lettersauthors
McLarnon JG,Sawyer D,Michikawa M,Kim SUdoi
10.1016/0304-3940(92)90746-tkeywords:
subject
Has Abstractpub_date
1992-09-14 00:00:00pages
185-8issue
1-2eissn
0304-3940issn
1872-7972pii
0304-3940(92)90746-Tjournal_volume
144pub_type
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