Phillips T L, Mitchell J B, DeGraff W G, Russo A, Albright N, Rajpal R
Radiation Oncology Branch, National Cancer Institute.
Int J Radiat Oncol Biol Phys. 1989 May;16(5):1335-9. doi: 10.1016/0360-3016(89)90310-6.
This series of experiments employed the hypoxic cell sensitizer SR 2508 in concentrations ranging from 0.1 to 10 mM and V-79 cells irradiated in air or made hypoxic in glass syringes, then irradiated with 15 MV X rays. Using a series of survival curves measured at the various concentrations, K curves relating sensitizer enhancement ratio (SER) to SR 2508 concentration were calculated with normal GSH levels or with depletion of GSH to 0% using 1 mM buthionine sulfoximine (BSO) or elevation to 200% of normal using 1 mM oxothiazolidine carboxylate (OTZ). Survival curves were fitted by computer, allowing calculation of standard errors for the SER values. The depletion of GSH by BSO sensitized hypoxic and aerated cells significantly and caused more than additive enhancement of SR 2508 sensitization in hypoxic cells. Elevation of GSH with OTZ protects cells irradiated in air or hypoxia and reduces the SER obtained with SR 2508. The results further support the importance of GSH levels in influencing sensitization by nitroimidazoles.
本系列实验使用了浓度范围为0.1至10 mM的缺氧细胞增敏剂SR 2508,以及在空气中照射或在玻璃注射器中制成缺氧状态后再用15 MV X射线照射的V - 79细胞。利用在不同浓度下测得的一系列存活曲线,计算了在正常谷胱甘肽(GSH)水平下或使用1 mM丁硫氨酸亚砜胺(BSO)将GSH耗尽至0% ,或使用1 mM氧噻唑烷羧酸盐(OTZ)将其提高至正常水平的200%时,增敏剂增强比(SER)与SR 2508浓度的K曲线。通过计算机拟合存活曲线,从而能够计算SER值的标准误差。BSO使缺氧和通气细胞中的GSH耗尽,显著增强了缺氧细胞中SR 2508的增敏作用,且这种增强作用超过了相加效应。OTZ使GSH水平升高,对在空气中或缺氧状态下照射的细胞起到保护作用,并降低了SR 2508获得的SER。这些结果进一步支持了GSH水平在影响硝基咪唑类药物增敏作用方面的重要性。