The characteristics of the cromakalim-induced membrane current were examine
d in single tracheal myocytes of the guinea-pig under voltage-clamp conditi
ons. When K+ concentrations in the pipette and bathing solutions were simil
ar to 140 mM, cromakalim activated a membrane current (I-crom) which was in
ward at -60 mV and reversed at -2 mV. I-crom was blocked by 10 mu M glibenc
lamide and potentiated when the ATP concentration in the pipette solution w
as decreased. The K-d and Hill coefficient of glibenclamide for I-crom bloc
k were 200 nM and 1.05, respectively. Application of the tyrosine kinase in
hibitors, genistein and alpha-cyano-3-ethoxy-4-hydroxy-5-phenylthiomethylci
nnamamid (ST638), reduced I-crom in a concentration-dependent manner. Daidz
ein, which does not inhibit tyrosine kinase, was about 10 times less effect
ive than genistein. Herbimycin A had no effect on I-crom. Internal applicat
ion of these inhibitors from the pipette did not affect I-crom. In conclusi
on, cromakalim is a potent activator of the ATP-sensitive K+ channel (K-ATP
channel) in guinea-pig tracheal myocytes. The inhibition of I-crom by geni
stein and ST638 may be due to the direct block of the channel from outside.
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