Bénavidès J, Begassat F, Phan T, Tur C, Uzan A, Renault C, Dubroeucq M C, Guérémy C, Le Fur G
Life Sci. 1984 Sep 17;35(12):1249-56. doi: 10.1016/0024-3205(84)90095-x.
[3H]PK 11195 binding to peripheral type benzodiazepine binding sites in kidney membranes is inhibited by the histidine blocking agent diethylpyrocarbonate. This reagent irreversibly decreases the Bmax for [3H]PK 11195 without affecting the affinity. By contrast binding of [3H]RO5-4864 is not affected by diethylpyrocarbonate treatment. However RO5-4864 can protect in a concentration dependent manner the [3H]PK 11195 binding site from diethylpyrocarbonate whereas clonazepam and RO15-1788 are not active. These results suggest that PK 11195 and RO5-4864 interact with different conformational states of the receptors that RO5-4864. This is in agreement with our previous hypothesis that PK 11195 is an antagonist and RO5-4864 an agonist at the "peripheral type" benzodiazepine receptors.
[3H]PK 11195与肾膜中周边型苯二氮䓬结合位点的结合受到组氨酸阻断剂焦碳酸二乙酯的抑制。该试剂不可逆地降低了[3H]PK 11195的最大结合容量(Bmax),而不影响亲和力。相比之下,[3H]RO5 - 4864的结合不受焦碳酸二乙酯处理的影响。然而,RO5 - 4864可以以浓度依赖的方式保护[3H]PK 11195结合位点免受焦碳酸二乙酯的影响,而氯硝西泮和RO15 - 1788则无此活性。这些结果表明,PK 11195和RO5 - 4864与受体的不同构象状态相互作用,RO5 - 4864也是如此。这与我们之前的假设一致,即PK 11195是“周边型”苯二氮䓬受体的拮抗剂,而RO5 - 4864是激动剂。