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(Hypertension. 2004;43:413.)
© 2004 American Heart Association, Inc.

Scientific Contribution

Apamin-Sensitive K⁺ Currents Mediate Arachidonic Acid-Induced Relaxations of Rabbit Aorta

From the Department of Pharmacology and Toxicology, Medical College of Wisconsin, Milwaukee.

Correspondence to Kathryn M. Gauthier, PhD, Department of Pharmacology and Toxicology, Medical College of Wisconsin, 8701 Watertown Plank Rd, Milwaukee, WI 53226. kgauth{at}mcw.edu

Arachidonic acid induces an endothelium-dependent relaxation of the rabbit aorta that is blocked by lipoxygenase inhibitors. The cellular vasodilatory mechanisms activated by arachidonic acid metabolites remain undefined. In rabbit thoracic aortic rings pretreated with indomethacin (10 µmol/L) and contracted with phenylephrine, arachidonic acid (0.1 to 100 µmol/L) induced concentration-dependent relaxations. Maximal relaxations averaged 45±3% and were inhibited by increasing extracellular K⁺ (30 mmol/L, 15±5%; P<0.001) or incubation with apamin (100 nmol/L, 26±7%; P<0.05) but not incubation with charybdotoxin (100 nmol/L, 41±5%). In aortic strips with an intact endothelium that were treated with phenylephrine, arachidonic acid (10 µmol/L) increased the membrane potential from -28.7±1.3 to -37.8±3.0 mV (P<0.01). Preincubation with apamin did not alter basal membrane potential but inhibited arachidonic acid-induced hyperpolarization (-31.5±1.5 mV). Incubation of rabbit aortic segments with apamin or charybdotoxin did not alter [¹⁴C]arachidonic acid metabolism. Whole-cell outward K⁺ currents from isolated rabbit aortic smooth muscle cells averaged 43.0±4.8 pA/pF at 60 mV and were significantly decreased to 35.7±4.2 pA/pF by apamin (P<0.001). Subsequent addition of charybdotoxin further decreased maximal currents to 14.4±2.3 pA/pF. Addition of 11,12,15-trihydroxyeicosatrienoic acid increased the outward whole-cell K⁺ current. In inside-out patches of aortic smooth muscle, apamin inhibited the calcium activation (100 to 300 nmol/L; P<0.001) of a small-conductance K⁺ channel (24 pS). These results suggest that arachidonic acid induces endothelium-dependent hyperpolarization and relaxation of rabbit aorta through activation of smooth muscle, apamin-sensitive K⁺ currents.

Key Words: lipoxygenase • endothelium-derived factors • potassium channels • hyperpolarization • membranes

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