Johnson M D, Wang J K, Morgan J I, Spector S
J Pharmacol Exp Ther. 1986 Sep;238(3):855-9.
Peripheral-type benzodiazepine (BZD) binding sites undergo a rapid and pronounced downregulation after exposure to these compounds in vitro. Friend erythroleukemia cells were incubated with micromolar concentrations of BZD after which they were washed thoroughly and the binding of the specific peripheral-type BZD radioligand [3H]Ro5-4864 was determined. Exposure to the peripheral-type BZD Ro7-3351 decreased the number of [3H]Ro5-4864 binding sites from 324 to 41 fmol/10(6) cells with no change in affinity. Downregulation appears to require active cellular processes because it is blocked when exposure to BZD is at 4 degrees C rather than at 37 degrees C. Furthermore, whereas [3H]Ro5-4864 binding is decreased substantially in membrane preparations made from downregulated cells, it is not altered when membrane preparations from control cells are exposed to BZD. The time course of downregulation is quite rapid, as it occurs within minutes. In contrast, the return of sites requires days and there is a close relationship between return of sites and growth of new cells. The ability of BZDs to downregulate correlates more closely with affinity for the peripheral-type site than with biological activity. The ability to undergo downregulation is characteristic of receptors and its occurrence suggests that peripheral-type BZD binding sites are functional receptors.
外周型苯二氮䓬(BZD)结合位点在体外暴露于这些化合物后会经历快速且显著的下调。将弗氏红白血病细胞与微摩尔浓度的BZD一起孵育,之后彻底洗涤细胞,并测定特异性外周型BZD放射性配体[3H]Ro5 - 4864的结合情况。暴露于外周型BZD Ro7 - 3351使[3H]Ro5 - 4864结合位点的数量从324 fmol/10(6)细胞减少至41 fmol/10(6)细胞,亲和力未发生变化。下调似乎需要活跃的细胞过程,因为当在4℃而非37℃下暴露于BZD时,下调被阻断。此外,虽然在由下调细胞制备的膜制剂中[3H]Ro5 - 4864结合显著减少,但当对照细胞的膜制剂暴露于BZD时,结合情况并未改变。下调的时间进程相当迅速,在数分钟内即可发生。相比之下,位点的恢复需要数天时间,并且位点的恢复与新细胞的生长之间存在密切关系。BZDs下调的能力与对外周型位点的亲和力的相关性比与生物活性的相关性更紧密。发生下调的能力是受体的特征,其出现表明外周型BZD结合位点是功能性受体。