Kamikawa Y, Uchida K, Shimo Y
Gastroenterology. 1985 Mar;88(3):706-16. doi: 10.1016/0016-5085(85)90141-6.
Pharmacologic characteristics of muscarinic receptors in the muscularis mucosae of the guinea pig esophagus were examined in vitro and compared with those of the longitudinal muscle of the guinea pig ileum. All cholinomimetics tested produced a sustained contraction of the muscularis mucosae, in a concentration-dependent manner, which was associated with a small biphasic change in membrane potential, initially a hyperpolarization followed by a depolarization. The contractile response was hardly modified by verapamil, but was depressed by calcium removal from the bathing medium. Both atropine and pirenzepine antagonized the contractile response in a competitive manner, with higher pA2 values than those in the ileum. These results indicate that the muscarinic receptors of the muscularis mucosae of the guinea pig esophagus mainly link with calcium ion channels which are independent of changes in membrane potential and that their subtype populations are probably pharmacologically distinct from those in the ileal longitudinal muscle.
在体外研究了豚鼠食管黏膜肌层毒蕈碱受体的药理学特性,并与豚鼠回肠纵肌的药理学特性进行了比较。所有受试拟胆碱药均以浓度依赖性方式使黏膜肌层产生持续性收缩,这与膜电位的小幅双相变化有关,最初是超极化,随后是去极化。维拉帕米对收缩反应几乎没有影响,但从浴液中去除钙会抑制收缩反应。阿托品和哌仑西平均以竞争性方式拮抗收缩反应,其pA2值高于回肠中的pA2值。这些结果表明,豚鼠食管黏膜肌层的毒蕈碱受体主要与钙离子通道相连,这些通道与膜电位变化无关,并且它们的亚型群体在药理学上可能与回肠纵肌中的不同。