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Vascular Biology |
From the Department of Internal Medicine and Pharmacology (K.G.L., D.W.N., F.M.F.), University of Iowa, Roy J. and Lucille A. Carver School of Medicine and the Veterans Administration Medical Center (K.G.L., D.W.N.), Iowa City, IA; and the Laboratory of Bioorganic Chemistry (J.W., Y.C.), National Institute of Diabetes and Digestive and Kidney Diseases, Bethesda, MD.
Correspondence to Kathryn G. Lamping, PhD, Medical Services (111), Veterans Affairs Medical Center, 601 Highway 6 W, Iowa City, IA 52246. E-mail kathryn-lamping{at}uiowa.edu
Objective Determining the role of specific muscarinic (M) receptor subtypes mediating responses to acetylcholine (ACh) has been limited by the specificity of pharmacological agents. Deletion of the gene for M5 receptors abolished response to ACh in cerebral blood vessels but did not affect dilation of coronary arteries. The goal of this study was to determine the M receptors mediating responses to ACh in coronary circulation using mice deficient in M2 or M3 receptors (M2/, M3/, respectively).
Methods and Results Coronary arteries from respective wild-type, M2/, or M3/ mice were isolated, cannulated, and pressurized. Diameter was measured with video microscopy. After preconstriction with U46619, ACh produced dose-dependent dilation of coronary arteries that was similar in wild-type and M2/ mice. In contrast, dilation of coronary arteries from M3/ mice to ACh was reduced by
80% compared with wild type. The residual response to ACh was atropine insensitive. Relaxation of coronary arteries to other stimuli was similar in M2/ and M3/ mice. Similar results were obtained in aorta rings.
Conclusion These findings provide the first direct evidence that relaxation to ACh in coronary circulation is mediated predominantly by activation of M3 receptors.
This study examined the M receptor subtype (M2 versus M3 receptors) involved in the response of coronary circulation to ACh using mice deficient in the genes for M2 and M3 receptors. M3 receptor activation and not M2 receptors primarily mediates responses to ACh in the coronary circulation.
Key Words: acetylcholine muscarinic receptors genetically altered mice
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