Gotti C, Spagnoli D, Omini C, Clementi F
Neurosci Lett. 1985 Jun 24;57(3):227-31. doi: 10.1016/0304-3940(85)90495-1.
alpha-Bungarotoxin (alpha-Bgtx) demonstrates a specific and saturable binding to rat superior cervical ganglion, yet it does not block ganglionic response mediated by nicotinic receptors in the guinea pig vas deferens-hypogastric nerve preparation. P15 toxin, a probe for ganglionic nicotinic receptor, prevents the binding of alpha-Bgtx to rat ganglia, and alpha-Bgtx prevents the ganglioplegic action of hexamethonium. Hexamethonium does not block the binding of alpha-Bgtx and P15 to rat ganglia. It is concluded that alpha-Bgtx and P15 bind to ganglionic nicotinic receptor at a common site which is different from that of cholinergic agonists and antagonists.
α-银环蛇毒素(α-Bgtx)对大鼠颈上神经节表现出特异性且可饱和的结合,但在豚鼠输精管-腹下神经制备中,它并不阻断由烟碱受体介导的神经节反应。P15毒素是一种神经节烟碱受体探针,可阻止α-Bgtx与大鼠神经节的结合,而α-Bgtx可阻止六甲铵的神经节阻断作用。六甲铵并不阻断α-Bgtx和P15与大鼠神经节的结合。得出的结论是,α-Bgtx和P15在一个与胆碱能激动剂和拮抗剂不同的共同位点结合神经节烟碱受体。