Awad M, Gavish M
Rappaport Family Institute for Research in the Medical Sciences, Haifa, Israel.
Life Sci. 1988;43(2):167-75. doi: 10.1016/0024-3205(88)90294-9.
The present study demonstrates a differential effect of various detergent treatments on [3H]Ro 5-4864 and [3H]PK 11195 binding to peripheral benzodiazepine binding sites (PBS). Triton X-100 (0.0125%) caused a decrease of about 70% in [3H]Ro 5-4864 binding to membranes from various peripheral tissues of rat, but had only a negligible effect on [3H]PK 11195 binding. A similar effect of Triton X-100 was observed on guinea pig and rabbit kidney membranes. The decrease in [3H]Ro 5-4864 binding after treatment with Triton X-100 was apparently due to a decrease in the density of PBS, since the affinity remained unaltered. The detergents 3-[(3-cholamidopropyl)-dimethylammonio]-1-propane sulfonate (CHAPS), Tween 20, deoxycholic acid, or digitonin (0.0125%) caused only a minor change in [3H]Ro 5-4864 and [3H]PK 11195 binding to rat kidney membranes; but when concentrations were substantially increased (0.1%), all detergents caused a decrease of at least 50% in [3H]Ro 5-4864 binding, while [3H]PK 11195 binding to rat kidney membranes remained unaffected by the first three detergents, with only a minor decrease (15%) after treatment with digitonin. These results may further support the assumption that Ro 5-4864 and PK 11195 are agonist and antagonist, respectively, of PBS and interact with two different conformations or domains in the peripheral-type benzodiazepine binding site molecule.
本研究表明,各种去污剂处理对[3H]Ro 5-4864和[3H]PK 11195与外周苯二氮䓬结合位点(PBS)的结合具有不同的影响。Triton X-100(0.0125%)使[3H]Ro 5-4864与大鼠各种外周组织膜的结合减少约70%,但对[3H]PK 11195的结合影响可忽略不计。在豚鼠和兔肾膜上也观察到了Triton X-100的类似作用。用Triton X-100处理后[3H]Ro 5-4864结合的减少显然是由于PBS密度的降低,因为亲和力保持不变。去污剂3-[(3-胆酰胺丙基)-二甲基铵]-1-丙烷磺酸盐(CHAPS)、吐温20、脱氧胆酸或洋地黄皂苷(0.0125%)对[3H]Ro 5-4864和[3H]PK 11195与大鼠肾膜的结合仅引起微小变化;但当浓度大幅增加(0.1%)时,所有去污剂均使[3H]Ro 5-4864的结合减少至少50%,而[3H]PK 11195与大鼠肾膜的结合在前三种去污剂处理后不受影响,仅在洋地黄皂苷处理后有轻微降低(15%)。这些结果可能进一步支持以下假设,即Ro 5-4864和PK 11195分别是PBS的激动剂和拮抗剂,并与外周型苯二氮䓬结合位点分子中的两种不同构象或结构域相互作用。