Heterogeneity of glyceryl trinitrate response in isolated bovine coronary arteries

• Published in: European journal of pharmacology Vol. 318; no. 1; pp. 65 - 71
• Main Authors: De la Lande, Ivan S, Stafford, Irene, Horowitz, John D
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 27-12-1996
• Subjects: 15-Hydroxy-11 alpha,9 alpha-(epoxymethano)prosta-5,13-dienoic Acid; Animals; bovine; Bradykinin - pharmacology; Cattle; Coronary artery; Coronary Vessels - drug effects; Coronary Vessels - physiology; Glyceryl trinitrate; In Vitro Techniques; Isoprenaline; Isoproterenol - pharmacology; Muscle Contraction - drug effects; Muscle Relaxation - drug effects; Muscle, Smooth, Vascular - drug effects; Muscle, Smooth, Vascular - physiology; Nitroglycerin - pharmacology; Nitroprusside - pharmacology; Penicillamine - analogs & derivatives; Penicillamine - pharmacology; Prostaglandin Endoperoxides, Synthetic - pharmacology; S-Nitroso- N-acetylpenicillamine; Sodium nitroprusside; Thromboxane A2 - analogs & derivatives; Thromboxane A2 - pharmacology; Vascular heterogeneity; Vasoconstrictor Agents - pharmacology; Vasodilator Agents - pharmacology; Sodium nitroprusside; Isoprenaline; Vascular heterogeneity; S-Nitroso- N-acetylpenicillamine; Coronary artery; Glyceryl trinitrate
• ISSN: 0014-2999; 1879-0712
• DOI: 10.1016/S0014-2999(96)00762-5

Factors determining heterogeneity of response to glyceryl trinitrate in coronary microvessels have been extensively documented in recent years, but determinants of heterogeneity between conduit and large resistance vessels are poorly understood. The current study has characterised heterogeneity to glyceryl trinitrate and other vasodilators in bovine isolated proximal (4.5 mm i.d.) and distal (0.5 mm i.d.) segments of left anterior descending artery. Compared with proximal segments, distal segments were less responsive to glyceryl trinitrate and sodium nitroprusside, equi-responsive to
S-nitroso-
N-acetylpenicillamine, and more responsive to isoprenaline. Heterogeneity to glyceryl trinitrate was unaffected by the presence of the thiols (cysteine or
N-acetylcysteine, 100 μM). The results are interpreted as evidence that heterogeneity of vascular responsiveness to glyceryl trinitrate reflects impairment in the small artery of the cellular events which precede activation of the cyclic GMP pathway. An implication is that the impairment is not a consequence of limited thiol availability, and in this respect the cellular mechanism of heterogeneity differs from those proposed for the coronary microvasculature.