Coronary vascular function after hemorrhagic hypotension in dogs

• Published in: Circulatory shock Vol. 41; no. 2; p. 119
• Main Authors: Parker, J L, Shelton, J A, Defily, D V, Gute, D, Laughlin, M H, Adams, H R
• Format: Journal Article
• Language: English
• Published: United States 01-10-1993
• Subjects: Acetylcholine - pharmacology; Animals; Coronary Circulation - physiology; Coronary Vessels - drug effects; Coronary Vessels - physiopathology; Dinoprost - pharmacology; Disease Models, Animal; Dogs; Hemorrhage - physiopathology; Hypotension - physiopathology; In Vitro Techniques; Male; Muscle, Smooth, Vascular - physiopathology; Nitric Oxide - secretion; Nitroprusside - pharmacology; Potassium - pharmacology; Regional Blood Flow; Shock, Hemorrhagic - physiopathology; Vasoconstriction - drug effects; Vasoconstriction - physiology; Vasodilation - drug effects
• ISSN: 0092-6213

This study tested the hypothesis that hemorrhagic hypotension alters intrinsic contraction-relaxation mechanisms of coronary arteries. Coronary vascular smooth muscle (VSM) was evaluated ex vivo using left circumflex coronary artery preparations isolated from beagle dogs 4 hr after sham hemorrhage (controls) or maintained hemorrhagic hypovolemia. Hemorrhaged dogs exhibited systemic hypotension (mean arterial pressure approximately 65 mm Hg), tachycardia, and tachypnea during the 4 hr in vivo phase of the study, accompanied by 30-50% reductions in left ventricular myocardial blood flows (P < 0.05). Coronary arteries isolated from these dogs were stretched to the asymptote of their length-contractile tension relationship; no significant differences were observed in length-active tension or length-passive tension relations between hemorrhage and control arteries. Similarly, neither the maximal responses nor the EC50 values for isometric contractions produced by prostaglandin F2 alpha (PGF2 alpha) (10(-8) to 3 x 10(-5) M) or depolarizing concentrations of K+ (10-100 mM) were altered by hemorrhage (P > 0.05). Vasodilator responses to the cyclic guanosine monophosphate (GMP)-dependent VSM relaxant nitroprusside (10(-4) M) also were not prevented by the hemorrhage protocol. In contrast, coronary VSM relaxation induced by the endothelium-dependent vasodilator acetylcholine (10(-9)-10(-5) M) was significantly decreased by 25-50% in K(+)- and PGF2 alpha-precontracted coronary arteries from the hemorrhaged dogs (P < 0.01). We conclude that receptor (PGF2 alpha)-dependent and membrane depolarization (K+)-dependent contractile mechanisms remained operational in coronary arteries during hemorrhagic hypotension, as did basal cyclic GMP-dependent VSM relaxation mechanisms. However, diminution of acetylcholine-induced relaxation of coronary VSM suggests impaired endothelium-dependent vasodilation in the coronary vasculature during acute (4 hr) hemorrhagic hypotension.