Crofton K M, Reiter L W, Mailman R B
Toxicol Lett. 1987 Feb;35(2-3):183-90. doi: 10.1016/0378-4274(87)90205-0.
Radioligand binding displacement studies were conducted to determine the effects of Type I and II pyrethroids on [3H]flunitrazepam (FLU), [3H]muscimol (MUS), and [35S]t-butylbicyclophosphorothionate (TBPS) binding. Competition experiments with [3H]FLU and [3H]MUS indicate a lack of competition for binding by the pyrethroids. Type I pyrethroids failed to compete for the binding of [35S]TBPS at concentrations as high as 50 microM. Type II pyrethroids inhibited [35S]TBPS binding to rat brain synaptosomes with Ki values ranging from 5-10 microM. The data presented here suggest that the interaction of Type II pyrethroids with the gamma-aminobutyric acid (GABA) receptor-ionophore complex is restricted to a site near the TBPS/picrotoxinin binding site.
进行放射性配体结合置换研究以确定 I 型和 II 型拟除虫菊酯对 [3H]氟硝西泮(FLU)、[3H]蝇蕈醇(MUS)和 [35S]叔丁基双环磷硫酯(TBPS)结合的影响。用 [3H]FLU 和 [3H]MUS 进行的竞争实验表明拟除虫菊酯缺乏结合竞争。I 型拟除虫菊酯在高达 50 μM 的浓度下未能竞争 [35S]TBPS 的结合。II 型拟除虫菊酯抑制 [35S]TBPS 与大鼠脑突触体的结合,其 Ki 值范围为 5 - 10 μM。此处呈现的数据表明,II 型拟除虫菊酯与γ-氨基丁酸(GABA)受体-离子载体复合物的相互作用仅限于 TBPS/印防己毒素结合位点附近的一个位点。