Effect of trimebutine on voltage‐activated calcium current in rabbit ileal smooth muscle cells

Open Access
Publisher Website
Google Scholar
Abstract
1 The effect of trimebutine on the voltage-dependent inward Ca2+ current was investigated by the whole-cell voltage-clamp technique in single smooth muscle cells from rabbit ileum. 2 Trimebutine (3–100 μm) reduced the Ca2+ current in a concentration-dependent manner. The inhibitory effect on the Ca2+ current was also dependent on the holding potential. The Ca2+ current after a low holding potential was inhibited to a greater extent than that after a high membrane potential: the IC50 values were 7 μm and 36 μm at holding potentials of −40 mV and −60 mV, respectively. The Ca2+ current elicited from a holding potential of −80 mV could not be reduced by as much as 50% of the control by trimebutine at concentrations as high as 100 μm. 3 Trimebutine (30 μm) shifted the voltage-dependent inactivation curve for the Ca2+ current by 18 mV in the negative direction. The affinity of the drug for Ca2+ channels was calculated to be 36 times higher in the inactivated state than in the closed-available state. 4 Blockade of the Ca2+ current by trimebutine, unlike verapamil, was not use-dependent. 5 The results suggest that trimebutine inhibits the voltage-dependent inward Ca2+ current through a preferential binding to Ca2+ channels in the inactivated state in the smooth muscle cell from rabbit ileum. The inhibitory effect of trimebutine on gastrointestinal motility is discussed in the light of the present findings.