Zieglgänsberger W, French E D, Mercuri N, Pelayo F, Williams J T
Life Sci. 1982;31(20-21):2343-6. doi: 10.1016/0024-3205(82)90152-7.
Experiments were performed in rat spinal cord cells in vivo and on hippocampal pyramidal cells in vitro. These investigations suggest that acute and chronic treatment renders the neurons subsensitive to opiate alkaloids without altering their sensitivity to opioid peptides. The experiments performed in the dorsal horn of the spinal cord provide evidence that in this structure mu- and delta-receptors may also be localized on the same cell. The evidence for the existence of distinct types of opiate receptors as originally proposed by (1) and suggested by the differing pattern of opiate and opioid peptide activity in various assay systems has been substantiated by investigations involving the selective development of tolerance and the protection of a particular receptor subtype by chemical manipulation. Furthermore, they have been characterized by the use of low concentrations of radiolabelled agonists and antagonists and through the ability of GTP to influence differentially their binding to the opiate receptor (for refs. see: 2). Recently autoradiographic techniques were able to provide direct evidence by mu- and delta-receptors in the mammalian brain (3; 4; 5; 6; and cits. therein). The presence of multiple opiate receptors located on the same cell is suggested by the present study.
实验在大鼠脊髓细胞体内以及海马锥体细胞体外进行。这些研究表明,急性和慢性治疗使神经元对阿片生物碱不敏感,而不改变其对阿片肽的敏感性。在脊髓背角进行的实验提供了证据,表明在该结构中μ受体和δ受体也可能定位于同一细胞。最初由(1)提出并由各种检测系统中阿片和阿片肽活性的不同模式所暗示的不同类型阿片受体存在的证据,已通过涉及耐受性的选择性发展以及通过化学操作对特定受体亚型的保护的研究得到证实。此外,它们已通过使用低浓度放射性标记激动剂和拮抗剂以及通过GTP对其与阿片受体结合的差异影响能力来表征(参考文献见:2)。最近,放射自显影技术能够提供哺乳动物脑中μ受体和δ受体的直接证据(3;4;5;6;以及其中的参考文献)。本研究表明同一细胞上存在多种阿片受体。