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• W2004146784 abstract "To examine the effect of vasopressin on the sarcolemmal ATP-sensitive K (KATP) channel, cell-attached, inside-out and open-cell-attached methods of patch clamp techniques were used in isolated guinea pig ventricular myocytes. Suppressing both glycolytic and oxidative ATP production attained KATP channel activation. In the cell-attached mode, vasopressin inhibited KATP channels in a concentration-dependent manner with an IC50 of 15.1 ±1.8 nmol/L. In the inside-out configuration, vasopressin failed to block KATP channels. In the cell-attached mode, manning compound (1 μmol/L), a V1 receptor-selective antagonist, blocked the inhibitory action of vasopressin, although OPC-31260 (1 μmol/L), a V2 receptor-selective antagonist could not affect the action of vasopressin. In addition, vasopressin lost its inhibitory action on KATP channels when the channel was activated by pinacidil, a K channel opener and in the open-cell-attached mode effected by streptolysin-O. Thus, the inhibitory action of vasopressin KATP channels may occur via V1 receptor related mechanism. (Circ J 2002; 66: 277 - 282)" @default.
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• W2004146784 date "2002-01-01" @default.
• W2004146784 modified "2023-10-16" @default.
• W2004146784 title "Vasopressin Inhibits Sarcolemmal ATP-Sensitive K+ Channels via V1 Receptors Activation in the Guinea Pig Heart." @default.
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• W2004146784 doi "https://doi.org/10.1253/circj.66.277" @default.
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