Yazulla S, Schmidt J
Brain Res. 1977 Dec 9;138(1):45-57. doi: 10.1016/0006-8993(77)90783-1.
Pigeon retinae were analyzed for binding [125I]alpha-bungarotoxin (alphaBgt) by radioautographic and biochemical methods. Toxin binding, localized to the outer and inner plexiform layers (OPL and IPL), was inhibited by micromolar concentrations of native alphaBgt and D-tubocurarine and by 1 mM acetyl- and butyrylcholine in both synaptic layers. Nicotine, at comparable concentrations affected only the IPL. In vitro drug competition experiments showed that the pigeon retina contains two types of receptors for alphaBgt which differ in sensitivity to inhibition by nicotine by 4 orders of magnitued. The results suggest that: (1) the receptor for alphaBgt in the IPL is a nicotinic receptor, (2) the receptor for alphaBgt in the OPL may be involved in an unusual cholinergic system, and (3) ability to bind alphaBgt is not a sufficient criterion for identifying nicotinic-cholinergic receptors.
采用放射自显影和生化方法分析了鸽视网膜对[125I]α-银环蛇毒素(αBgt)的结合情况。毒素结合定位于外网状层和内网状层(OPL和IPL),在两个突触层中,微摩尔浓度的天然αBgt和筒箭毒碱以及1 mM乙酰胆碱和丁酰胆碱均可抑制这种结合。浓度相当的尼古丁仅影响IPL。体外药物竞争实验表明,鸽视网膜含有两种αBgt受体,它们对尼古丁抑制的敏感性相差4个数量级。结果表明:(1)IPL中的αBgt受体是烟碱型受体;(2)OPL中的αBgt受体可能参与一种不同寻常的胆碱能系统;(3)结合αBgt的能力不是鉴定烟碱型胆碱能受体的充分标准。