Role of M1, M3, and M5 muscarinic acetylcholine receptors in cholinergic dilation of small arteries studied with gene-targeted mice

被引:54
|
作者
Gericke, Adrian [1 ]
Sniatecki, Jan J. [1 ]
Mayer, Veronique G. A. [1 ]
Goloborodko, Evgeny [1 ]
Patzak, Andreas [2 ]
Wess, Juergen [3 ]
Pfeiffer, Norbert [1 ]
机构
[1] Johannes Gutenberg Univ Mainz, Univ Med Ctr, Dept Ophthalmol, D-55131 Mainz, Germany
[2] Charite, Inst Vegetat Physiol, D-13353 Berlin, Germany
[3] NIDDK, Mol Signaling Sect, Bioorgan Chem Lab, NIH, Bethesda, MD USA
关键词
muscarinic receptors; vasodilation; genetically altered mice; SUBTYPES MEDIATING VASODILATION; IN-VIVO CHARACTERIZATION; MESENTERIC VASCULAR BED; BLOOD-FLOW; PHARMACOLOGICAL CHARACTERIZATION; KNOCKOUT MICE; RELAXATION; M3; ENDOTHELIUM; CONTRACTION;
D O I
10.1152/ajpheart.00982.2010
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Gericke A, Sniatecki JJ, Mayer VG, Goloborodko E, Patzak A, Wess J, Pfeiffer N. Role of M-1, M-3, and M-5 muscarinic acetylcholine receptors in cholinergic dilation of small arteries studied with gene-targeted mice. Ant J Physiol Heart Circ Physiol 300: H1602-H1608, 2011. First published February 18, 2011; doi:10.1152/ajpheart.00982.2010.-Acetylcholine regulates perfusion of numerous organs via changes in local blood flow involving muscarinic receptor-induced release of vasorelaxing agents from the endothelium. The purpose of the present study was to determine the role of M-1, M-3, and M-5 muscarinic acetylcholine receptors in vasodilation of small arteries using gene-targeted mice deficient in either of the three receptor subtypes (MIR-/-, M3R(-/-), or M5R(-/-) mice, respectively). Muscarinic receptor gene expression was determined in murine cutaneous, skeletal muscle, and renal interlobar arteries using real-time PCR. Moreover, respective arteries from M1R(-/-) M3R(-/-), M5R(-/-), and wild-type mice were isolated, cannulated with micropipettes, and pressurized. Luminal diameter was measured using video microscopy. mRNA for all five muscarinic receptor subtypes was detected in all three vascular preparations from wild-type mice. However, M-3 receptor mRNA was found to be most abundant. Acetylcholine produced dose-dependent dilation in all three vascular preparations from M1R(-/-), M5R(-/-), and wild-type mice. In contrast, cholinergic dilation was virtually abolished in arteries from M3R(-/-) mice. Deletion of either M-1, M-3, or M-5 receptor genes did not affect responses to nonmuscarinic vasodilators, such as substance P and nitroprusside. These findings provide the first direct evidence that M-3 receptors mediate cholinergic vasodilation in cutaneous, skeletal muscle, and renal interlobar arteries. in contrast, neither M-1 nor M-5 receptors appear to be involved in cholinergic responses of the three vascular preparations tested.
引用
收藏
页码:H1602 / H1608
页数:7
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