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. Author manuscript; available in PMC: 2010 Aug 31.
Published in final edited form as: Anesthesiology. 2009 May;110(5):986–995. doi: 10.1097/ALN.0b013e31819dadc7

Fig. 6.

Fig. 6

Whole cell adenosine triphosphate–sensitive K+ (KATP) currents are not affected by specific openers of mito K-ATP channel openers. (A) Whole cell recording from HEK293 cell expressing Kir6.2 and SUR1. Plotted is the mean holding current at −20 mV every 15 s. The SUR1-specific K+ channel opener diazoxide (Dz) is applied as indicated by the solid bars and concentration-dependently potentiated the whole cell current. (B) Current–voltage relations demonstrating the lack of effect of the cardiac K+ channel opener pinacidil (Pin, 0.1 mm) on Kir6.2/SUR1 currents in HEK293 cells. (C) Mean effects of the various K+ channel openers on Kir6.2/SUR1 currents. (D) Diazoxide at 10 μm increases the plasma KATP current independently of its potential effect on mitochondrial KATP channels, as demonstrated by the lack of effect of the mitochondrial KATP channel inhibitor 5-hydroxy-decanoic acid (5-HD) on the diazoxide activation of the whole cell current. Numbers (n) are given above the bars. *P < 0.05.