Buckley N J, Burnstock G
Brain Res. 1986 Jun 4;375(1):83-91. doi: 10.1016/0006-8993(86)90961-3.
A novel antimuscarinic agent, pirenzepine, has been proposed to distinguish at least two subtypes of muscarinic receptor. M1 receptors have been designated as those displaying a high affinity for pirenzepine. Both functional and binding studies have revealed a prevalence of M1 receptors in sympathetic ganglia while autonomic effector tissues have only low densities of M1 receptors. In the present study, in vitro autoradiographic procedures have been used to localize specifically high affinity binding sites for pirenzepine (M1 receptors) in sections of guinea-pig ileum, rat superior cervical ganglion and rat submaxillary gland. The overall localization of muscarinic receptors was also studied using the non-selective antagonist, [3H]N-methylscopolamine. The highest densities of M1 receptors were found in superior cervical ganglion, sympathetic nerve bundles, myenteric ganglia and mucous secreting cells of the submaxillary gland, while lower densities were found in smooth muscle and serous secreting cells of the submaxillary gland. No area found to possess muscarinic receptors was devoid of M1 receptors.
一种新型抗毒蕈碱剂哌仑西平已被提出用于区分至少两种毒蕈碱受体亚型。M1受体被定义为对哌仑西平具有高亲和力的受体。功能研究和结合研究均表明,交感神经节中M1受体占优势,而自主效应器组织中M1受体密度较低。在本研究中,体外放射自显影程序已被用于在豚鼠回肠、大鼠颈上神经节和大鼠颌下腺切片中特异性定位哌仑西平(M1受体)的高亲和力结合位点。还使用非选择性拮抗剂[3H]N-甲基东莨菪碱研究了毒蕈碱受体的总体定位。在颈上神经节、交感神经束、肌间神经节和颌下腺的粘液分泌细胞中发现M1受体密度最高,而在颌下腺的平滑肌和浆液分泌细胞中发现密度较低。未发现拥有毒蕈碱受体的区域缺乏M1受体。