Brown G B, Tieszen S C, Daly J W, Warnick J E, Albuquerque E X
Cell Mol Neurobiol. 1981 Mar;1(1):19-40. doi: 10.1007/BF00736037.
Batrachotoxinin-A 20-alpha-benzoate (BTX-B), an analog of the potent depolarizing agent batrachotoxin (BTX), was prepared by selective esterification of naturally occurring batrachotoxin-A with benzoic acid. BTX-B depolarized rat phrenic nerve-diaphragm preparations with a time course and concentration dependence virtually indistinguishable from that of BTX. A specific, saturable component of equilibrium binding of [3H]BTX-B to mouse cerebral cortex homogenates was measured, described by an equilibrium dissociation constant of 0.7 microM and a maximum number of binding sites of 90 pmol per gram of tissue (wet weight). Specific binding is inhibited by BTX and other BTX analogs, veratridine, and grayanotoxin but is unaffected by tetrodotoxin and cevine. Under conditions of this assay, neither crude Leiurus quinquestriatus scorpion venom nor purified sea anemone toxin have any effect of specific binding. The data support the conclusion that BTX-B interacts with a recognition site associated with voltage sensitive sodium channels which is identical to the recognition site for BTX.
蟾毒素 A 20-α-苯甲酸酯(BTX-B)是强效去极化剂蟾毒素(BTX)的类似物,通过天然存在的蟾毒素 A 与苯甲酸的选择性酯化反应制备而成。BTX-B 使大鼠膈神经-膈肌标本去极化,其时程和浓度依赖性与 BTX 几乎无法区分。测定了 [3H]BTX-B 与小鼠大脑皮质匀浆平衡结合的一个特异性、可饱和成分,其平衡解离常数为 0.7 μM,每克组织(湿重)的最大结合位点数为 90 pmol。特异性结合受到 BTX 和其他 BTX 类似物、藜芦碱和灰藓毒素的抑制,但不受河豚毒素和瑟文的影响。在该测定条件下,粗制的以色列金蝎毒液和纯化的海葵毒素对特异性结合均无任何影响。这些数据支持以下结论:BTX-B 与一个与电压敏感性钠通道相关的识别位点相互作用,该识别位点与 BTX 的识别位点相同。