Olive P L
Radiat Res. 1987 Mar;109(3):490-9.
The binding of misonidazole (MISO) in Chinese hamster V79 spheroids was increased several-fold in the presence of an equimolar concentration of AF-2 (2-[2-furyl]-3-[5-nitro-2-furyl]-acrylamide) or several other electron-affinic drugs. This results was unexpected since AF-2 is much more electron affinic than MISO and should therefore compete more effectively for electrons (i.e., AF-2 should inhibit MISO binding). Enhanced MISO binding by AF-2 occurred for both ring-labeled and side chain-labeled MISO, was proportional to AF-2 concentration, and was greatest under anoxia. However, as the ratio of MISO to AF-2 increased, the effectiveness of AF-2 in enhancing MISO binding decreased. In contrast, MISO, even at high concentrations, did not affect AF-2 binding. Since AF-2 enhanced MISO binding significantly only when both drugs were present simultaneously, electron transfer processes are implicated. These results suggest that the sensitivity of MISO as a hypoxia probe may be significantly improved by the simultaneous administration of AF-2 or other nitrofurans.
在等摩尔浓度的AF-2(2-[2-呋喃基]-3-[5-硝基-2-呋喃基]-丙烯酰胺)或其他几种亲电子药物存在的情况下,甲硝唑(MISO)在中国仓鼠V79球体中的结合增加了几倍。这一结果出人意料,因为AF-2比MISO的亲电子性强得多,因此应该能更有效地竞争电子(即AF-2应该抑制MISO的结合)。AF-2对环标记和侧链标记的MISO都能增强其结合,与AF-2浓度成正比,并且在缺氧条件下最大。然而,随着MISO与AF-2比例的增加,AF-2增强MISO结合的效果会降低。相反,即使在高浓度下,MISO也不会影响AF-2的结合。由于只有当两种药物同时存在时,AF-2才会显著增强MISO的结合,因此涉及电子转移过程。这些结果表明,通过同时给予AF-2或其他硝基呋喃,MISO作为缺氧探针的敏感性可能会显著提高。