In order to investigate the effects of SKF96365 (SKF), which is a non-selective cationic channel blocker, on K
+ channel currents, we recorded currents through ATP sensitive K
+ (I
KATP), voltage-gated K
+ (I
Kv) and Ca
2+ activated K
+ channels (I
BK) in the absence and presence of SKF in single small intestinal myocytes of mice with patch-clamp techniques. SKF (10
µM) reversibly abolished I
KATP that was induced by cromakalim (10
µM), which is a selective ATP sensitive K
+ channel opener. These inhibitory effects were induced in a concentration-dependent and voltage-independent manner. The 50% inhibitory concentration (IC
50) was 0.85
µM, which was obviously lower than that reported for the muscarinic cationic current. In addition, SKF (1
µM ≈ the IC
50 value in I
KATP suppression) reversibly inhibited the I
Kv that was induced by repetitive depolarizing pulses from −80 to 20 mV. However, the extent of the inhibitory effects was only ~30%. In contrast, SKF (1
µM) had no significant effects on spontaneous transient I
BK and caffeine-induced I
BK. These results indicated that SKF inhibited ATP sensitive K
+ channels and voltage-gated K
+ channels, with the ATP sensitive K
+ channels being more sensitive than the voltage-gated K
+ channels. These inhibitory effects on K
+ channels should be considered when SKF is used as a cationic channel blocker.
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