A forskolin and verapamil sensitive K+ current in human tracheal cells.

Abstract:

:A voltage-dependent K+ current has been revealed in whole-cell recordings carried out on immortalized cells obtained from the human tracheal epithelium. At positive membrane potentials the current shows a time dependent inactivation which is accelerated by increasing the depolarizing step. Forskolin, a direct activator of adenylyl cyclase, and verapamil, a Ca2+ channel blocker, induce the K+ current to inactivate more rapidly. Control experiments show that the action of these two compounds is not mediated by cyclic AMP and Ca2+. The application of 1,9-dideoxyforskolin, an analogue which does not stimulate adenylate cyclase, inhibits the current in the same way as forskolin; on the contrary, the dibutyryl analogue of cyclic AMP is ineffective. Furthermore, eliminating extracellular Ca2+ does not affect K+ current kinetics. Tetraethylammonium is an effective blocker of this current with an IC50 of 0.3 mM.

authors

Galietta LJ,Rasola A,Barone V,Gruenert DC,Romeo G

doi

10.1016/0006-291x(91)91692-6

subject

Has Abstract

pub_date

1991-09-30 00:00:00

pages

1155-60

issue

3

eissn

0006-291X

issn

1090-2104

pii

0006-291X(91)91692-6

journal_volume

179

pub_type

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