Pelchen-Matthews A, Dolly J O
Department of Biochemistry, Imperial College of Science and Technology, London, U.K.
Brain Res. 1988 Feb 16;441(1-2):127-38. doi: 10.1016/0006-8993(88)91390-x.
High-affinity acceptors for 125I-beta-bungarotoxin have been identified on rat brain cryostat sections and mapped quantitatively using 3H-sensitive sheet film autoradiography. A unique distribution of acceptors has thus been observed; the toxin sites are particularly enriched in grey matter areas and synaptic regions, consistent with the pharmacological action of beta-bungarotoxin. As the binding was abolished by dendrotoxin, a related polypeptide known to inhibit fast-activating K+ conductances, the occurrence of beta-bungarotoxin acceptors may indicate the location of certain voltage-sensitive K+ channels. The overall distribution is, however, distinct from that of any other ion channel described.
在大鼠脑低温切片上已鉴定出125I-β-银环蛇毒素的高亲和力受体,并使用对3H敏感的片膜放射自显影法定量绘制了图谱。由此观察到受体的独特分布;毒素位点在灰质区域和突触区域特别丰富,这与β-银环蛇毒素的药理作用一致。由于树突毒素可消除这种结合,树突毒素是一种已知可抑制快速激活钾离子电导的相关多肽,因此β-银环蛇毒素受体的存在可能表明某些电压敏感性钾离子通道的位置。然而,其总体分布与所描述的任何其他离子通道的分布都不同。