The Japanese Journal of Pharmacology | |
M2 and M3 Muscarinic Receptors Couple, Respectively, With Activation of Nonselective Cationic Channels and Potassium Channels in Intestinal Smooth Muscle Cells | |
Hidenori Ohashi1  Takahisa Nakayama1  Toshihiro Unno1  Seiichi Komori1  | |
[1] Laboratory of Pharmacology, Department of Veterinary Science, Faculty of Agriculture, Gifu University | |
关键词: Carbachol; Muscarinic receptor; Smooth muscle; Ca2+-activated K+ current; Nonselective cationic current; | |
DOI : 10.1254/jjp.76.213 | |
学科分类:药理学 | |
来源: Nihon Yakuri Gakkai Henshuubu / Japanese Pharmacological Society | |
【 摘 要 】
References(24)Cited-By(20)Smooth muscle cells of guinea pig ileum express both M2 and M3 subtypes of muscarinic receptors. Under voltage clamp, activation of the muscarinic receptors with carbachol (CCh) induces Ca2+-activated K+ current (IK-Ca) and nonselective cationic current (Icat). Receptor subtypes mediating the current responses were characterized by using pirenzepine, AF-DX116, 4-DAMP and atropine, which have different profiles of the affinity constants for muscarinic receptor subtypes. The muscarinic antagonists inhibited either CCh-evoked IK-Ca or Icat with different potencies. Their relative potencies for IK-Ca and Icat inhibition resembled the relative affinity constants for M3 and M2 subtypes, respectively. Thus, the IK-Ca is mediated via the M3 subtype and the Icat via the M2 subtype.
【 授权许可】
Unknown
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