Effect of Selective Inhibition of Potassium Channels on Vasorelaxing Response to Cromakalim, Nitroglycerin and Nitric Oxide of Canine Coronary Arteries

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Abstract

A comparative study was performed on the sensitivity of in‐vitro vasorelaxation by nitroglycerin and cromakalim to block glibenclamide, a blocker of ATP‐sensitive potassium channels, and iberiotoxin, a selective inhibitor of large‐conductance calcium‐activated potassium channels. In isolated canine coronary arteries preconstricted with 25 μM prostaglandin F, nitroglycerin (0.005–1.8 μM) and cromakalim (0.15–9.6 μM) produced dose‐dependent vasodilations. Glibenclamide (30 μM) had no significant effect on relaxation of the dose‐response curve to nitroglycerin and almost completely abolished the relaxation by cromakalim, a known opener of ATP‐sensitive potassium channels. Iberiotoxin (90 nM) decreased the maximal response to nitroglycerin and had no effect on the vasodilation induced by cromakalim. The effect of iberiotoxin on the vasorelaxing action of nitric oxide, the active metabolite of nitroglycerin, was also examined. In a low potassium chloride (14.4–20.4 mM) medium, as a contractile stimulus, iberiotoxin inhibited relaxations by exogenous nitric oxide (100–200 nM). Enhancement of potassium concentrations to 35.4–40.4 mM significantly decreased relaxation by nitric oxide and under these conditions the inhibitory action of iberiotoxin disappeared. The present study demonstrated that in canine coronary arteries, the functional role of two potassium channels can be separated by pharmacological means. Nitroglycerin‐induced vasorelaxation may be mediated, at least in part, by its enzymatic breakdown product, nitric oxide that activates large‐conductance calcium‐activated potassium channels. 1995 Royal Pharmaceutical Society of Great Britain

Original languageEnglish
Pages (from-to)921-925
Number of pages5
JournalJournal of Pharmacy and Pharmacology
Volume47
Issue number11
DOIs
Publication statusPublished - Nov 1995

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ASJC Scopus subject areas

  • Pharmacology
  • Pharmaceutical Science

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