Betz H
Neurosci Lett. 1982 Nov 30;33(2):153-8. doi: 10.1016/0304-3940(82)90243-9.
The frog alkaloid histrionicotoxin inhibits neuromuscular transmission in a non-competitive fashion and is thought to bind to the ion channel region of the nicotinic acetylcholine receptor (nAChR) of skeletal muscle and fish electric organ. Here, the use of histrionicotoxin as a probe for the putative nAChR of the chick visual system was investigated. Histrionicotoxin inhibited the binding of [125I]alpha-bungarotoxin to synaptic membranes of optic lobe or of retina in a competitive manner (Ki = 6 +/- 3 microM). However, the number of displaceable membrane binding sites for the physiologically active derivative [3H]perhydrohistrionicotoxin was 20-100-fold higher than of [125I]alpha-bungarotoxin binding sites. Also, the binding of [3H]perhydrohistrionicotoxin to the membranes could be displaced by local anaesthetics and phencyclidine, but was insensitive to nicotinic-cholinergic ligands or to alpha-bungarotoxin. It is concluded that histrionicotoxins are not specific ligands for nAChR in the chick CNS.
青蛙生物碱组氨毒素以非竞争性方式抑制神经肌肉传递,据认为它可与骨骼肌和鱼类电器官的烟碱型乙酰胆碱受体(nAChR)的离子通道区域结合。在此,研究了将组氨毒素用作雏鸡视觉系统假定nAChR的探针的用途。组氨毒素以竞争性方式抑制[125I]α-银环蛇毒素与视叶或视网膜突触膜的结合(Ki = 6±3 microM)。然而,生理活性衍生物[3H]全氢组氨毒素的可置换膜结合位点数量比[125I]α-银环蛇毒素结合位点高20至100倍。此外,[3H]全氢组氨毒素与膜的结合可被局部麻醉剂和苯环己哌啶取代,但对烟碱型胆碱能配体或α-银环蛇毒素不敏感。得出的结论是,组氨毒素不是雏鸡中枢神经系统中nAChR的特异性配体。