Effects of Potassium Channel Blockers on Resting Tone in Isolated Coronary Arteries

• Published in: Journal of cardiovascular pharmacology Vol. 27; no. 5; pp. 636 - 642
• Main Author: O'Rourke, Stephen T
• Format: Journal Article
• Language: English
• Published: Philadelphia, PA Lippincott-Raven Publishers 01-05-1996; Hagerstown, MD Lippincott
• Subjects: 4-Aminopyridine - pharmacology; Animals; Biological and medical sciences; Cardiovascular system; Coronary Vessels - drug effects; Coronary Vessels - physiology; Dose-Response Relationship, Drug; Glyburide - pharmacology; In Vitro Techniques; Medical sciences; Miscellaneous; Pharmacology. Drug treatments; Potassium Channel Blockers; Swine; Tetraethylammonium Compounds - pharmacology; Coronary artery; Smooth muscle; Potassium channel blocker; In vitro; Biological activity; Pig; Vertebrata; Mammalia; Animal; Blood vessel; Artiodactyla; Ungulata; Muscular tonus
• ISSN: 0160-2446; 1533-4023
• DOI: 10.1097/00005344-199605000-00004

The effects of several potassium channel blockers on resting vasomotor tone were studied in porcine isolated coronary arteries. Coronary artery rings were suspended in organ baths for isometric tension recording. The nonselective potassium channel blockers tetraethylammonium (TEA 10-3 × 10 M) and 4-aminopyridine (4-AP 10-10 M) caused concentration-dependent contractions that were similar in rings with and without endothelium. The concentration-response curves to TEA and 4-AP were unaffected by treatment with phentolamine (3 × 10 M), propranolol (10 M), or atropine (10 M). Diltiazem (10 M) almost abolished the contractions evoked by TEA and 4-AP. Charybdotoxin (10-10 M) and apamin (10-10 M), selective blockers of large and small calcium-activated potassium channels, respectively, and glyburide (10-10 M), a selective blocker of ATP-sensitive potassium channels, caused little or no contraction in rings with or without endothelium. Therefore, in isolated coronary arteries, TEA and 4-AP caused contractions that were independent of the release of vasoactive mediators from the endothelium or perivascular nerves. These effects are not mediated by ATP-sensitive potassium channels or by large and small conductance calcium-activated potassium channels. The data are consistent with an effect of TEA and 4-AP on resting membrane potassium conductance in coronary arteries, resulting in contractions that are sensitive to inhibition by diltiazem. This pattern of responsiveness of isolated coronary arteries to potassium channel blockers differs from that observed in vessels from other vascular beds.