Kurtel H, Yegen B C, Dedeoglu A, Ulusoy N B, Oktay S
Department of Pharmacology, Mamara University, School of Medicine, Istanbul, Turkey.
Arch Int Pharmacodyn Ther. 1990 Nov-Dec;308:39-46.
The antagonism of acetylcholine-induced contractions of guinea-pig gallbladder and ileum smooth muscle strips via various antagonists has been investigated in order to find out the muscarinic receptor subtype(s) of gallbladder smooth muscle. Atropine, pirenzepine, 4-DAMP and AF-DX 116 were used as nonselective, M1-selective, M1- and smooth muscle M3-selective and cardiac M2-selective muscarinic antagonists, respectively. All the muscarinic antagonists examined displaced the concentration-response curves to the right parallelly in a concentration-dependent manner without affecting the maximum response in both tissues. Schild analysis of data was consistent with competitive antagonism. pA2 values of the antagonists were as follows: a) gallbladder: atropine: 8.43; pirenzepine: 7.81; 4-DAMP: 8.10; AF-DX 116: 6.71; b) ileum: atropine: 9.62; pirenzepine: 6.94; 4-DAMP: 9.41; AF-DX 116: 6.55. It may be concluded that the muscarinic receptors of the guinea-pig gallbladder, which mediate acetylcholine-induced contractions, are not of the cardiac M2-subtype and may be distinguished from ileal smooth muscle M3-receptors because 4-DAMP has a 20.4 times greater affinity for ileal smooth muscle muscarinic receptors.
为了找出豚鼠胆囊平滑肌的毒蕈碱受体亚型,研究了通过各种拮抗剂对乙酰胆碱诱导的豚鼠胆囊和回肠平滑肌条收缩的拮抗作用。阿托品、哌仑西平、4-二甲基氨基吡啶(4-DAMP)和AF-DX 116分别用作非选择性、M1选择性、M1和M3平滑肌选择性以及心脏M2选择性毒蕈碱拮抗剂。所有检测的毒蕈碱拮抗剂均以浓度依赖性方式使浓度-反应曲线平行右移,且不影响两种组织中的最大反应。对数据进行的Schild分析与竞争性拮抗作用一致。拮抗剂的pA2值如下:a)胆囊:阿托品:8.43;哌仑西平:7.81;4-DAMP:8.10;AF-DX 116:6.71;b)回肠:阿托品:9.62;哌仑西平:6.94;4-DAMP:9.41;AF-DX 116:6.55。可以得出结论,介导乙酰胆碱诱导收缩的豚鼠胆囊毒蕈碱受体不是心脏M2亚型,并且可能与回肠平滑肌M3受体不同,因为4-DAMP对回肠平滑肌毒蕈碱受体的亲和力高20.4倍。