Wu B Q, Yang L, Kao C Y, Levinson S R, Yotsu-Yamashita M, Yasumoto T
Department of Pharmacology, State University of New York, Downstate Medical Center, Brooklyn 11203-2098, USA.
Toxicon. 1996 Apr;34(4):407-16. doi: 10.1016/0041-0101(95)00168-9.
Tetrodotoxin was oxidized to a hydrated aldehyde, 11-oxo-tetrodotoxin, which shares the specificity of tetrodotoxin for the Na+ channel of the isolated voltage-clamped frog skeletal muscle fiber, but is four to five times more potent. It binds to the solubilized Na+ channel of eel electroplax with a similarly higher potency, because of an equilibrium dissociation constant about 0.25, and a dissociation rate constant 2.4 times slower than those for tetrodotoxin. 11-Oxo-tetrodotoxin can be reduced to regenerate a tetrodotoxin, which is chemically and biologically indistinguishable from the original tetrodotoxin. By reducing with tritiated sodium borohydride, a 3H marker can be inserted regiospecifically to yield 11-[3H]-tetrodotoxin. Because it has a defined specific activity of > 2.5 Ci/mmole, and a 3H marker which does not exchange with solvent proton, 11-[3H]-tetrodotoxin is an ideal tracer for tetrodotoxin. It may enable studies of problems which require higher signals and/or better stability of the marker than those obtainable from currently available tracer Na(+)-channel ligands.
河豚毒素被氧化为一种水合醛,即11-氧代河豚毒素,它与河豚毒素对分离的电压钳制青蛙骨骼肌纤维的钠离子通道具有相同的特异性,但效力要强4至5倍。它以类似的更高效力与鳗鱼电板的可溶钠离子通道结合,其平衡解离常数约为0.25,解离速率常数比河豚毒素慢2.4倍。11-氧代河豚毒素可以被还原以再生河豚毒素,再生后的河豚毒素在化学和生物学上与原始河豚毒素无法区分。通过用氚化硼氢化钠还原,可以区域特异性地插入一个3H标记,得到11-[3H]-河豚毒素。由于其具有大于2.5居里/毫摩尔的确定比活度,以及不与溶剂质子交换的3H标记,11-[3H]-河豚毒素是河豚毒素的理想示踪剂。它可能使我们能够研究一些问题,这些问题需要比目前可用的示踪剂钠离子通道配体获得更高的信号和/或更好的标记稳定性。