Effects of H-7, U-73122, and GDPβS on M1 receptor-mediated inhibition of the KATP current. The COS7 cells were cotransfected with cDNAs of Kir6.2, SUR2A, and the M1 receptor. The KATP current was activated by the perfusion of 100 μM pinacidil (started at ↑). (A) The effect of H-7 on M1 receptor-mediated inhibition. The applications of 1 μM ACh, 100 μM H-7, and 10 μM glibenclamide are indicated by the bars above the recording. (B) The effect of 1 μM U-73122. (C) A COS7 cell was dialyzed with the pipette solution containing 1 mM GDPβS. (D) Summary of the magnitudes of 1 μM ACh-induced maximal inhibition of the KATP current in control, H-7-, U-73122-, and GDPβS-treated cells. The numerals in parentheses indicate numbers of experiments. **, P < 0.01 vs. control.