Abstract
A number of compounds of widely differing chemical structure have been developed in an attempt to alter the open probability of what has become known as the adenosine triphosphate-sensitive potassium channel (KATP channel). They include channel openers (such as pinacidil, aprikalim, nicorandil, bimakalim, cromakalim and its active enantiomer levcromakalim) and channel blockers such as glibenclamide, tolbutamide and 5-hydroxydecanoate. They all are able to override the actions of an array of biochemical regulators of channel activity including ATP (an inhibitor of channel opening), adenosine diphosphate, adenosine, fatty acids, lactate, pyruvate and pH (for detailed reviews on the nature of the KATP channel and its biological and pharmacological control see (1–6)
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Hearse, D.J. (1995). Activation of ATP-Sensitive Potassium Channels: A Novel Pharmacological Approach to Myocardial Protection?. In: Yellon, D.M., Gross, G.J. (eds) Myocardial Protection and the KATP Channel. Developments in Cardiovascular Medicine, vol 179. Springer, Boston, MA. https://doi.org/10.1007/978-1-4613-0453-1_3
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