Morrison H, Hammarskiöld V, Jernström B
Chem Biol Interact. 1983 Jul 15;45(2):235-42. doi: 10.1016/0009-2797(83)90071-6.
The intracellular level of reduced glutathione (GSH) and GSH conjugation have been investigated in primary cell cultures of hepatocytes isolated from control rats, phenobarbitone (PB) and 3-methylcholanthrene (MC) treated rats. The data demonstrate that in all cell cultures the GSH concentrations show a triphasic pattern: (i) within 1 h of culture an initial marked decrease to 50% of the levels found in fresh hepatocytes; (ii) recovery of GSH concentrations to above the levels observed in fresh cells. This occurs after 6 h in culture with control cells and after 10-24 h with cells from either PB or MC treated rats and was most prominent in cells from PB-treated rats. (iii) A slow decline to between 30 and 40 nmol GSH/mg protein from 24 to 96 h in culture. Synthesis of GSH was slower in cultured cells from PB treated rats and this was confirmed by the resynthesis rates when diethylmaleate (DEM) was used to deplete GSH. The formation of GSH conjugates with racemic 7 beta,8 alpha-dihydroxy-9 alpha,10 alpha-epoxy-7,8,9,10-tetrahydrobenzo[a]pyrene (BPDE) was measured in control cells in suspension and after 3 and 24 h in culture. Despite the decrease in GSH concentrations observed between 1 and 4 h after culture, the conjugation rates were not decreased.
在从对照大鼠、苯巴比妥(PB)和3-甲基胆蒽(MC)处理的大鼠分离出的肝细胞原代细胞培养物中,研究了还原型谷胱甘肽(GSH)的细胞内水平和GSH结合情况。数据表明,在所有细胞培养物中,GSH浓度呈现三相模式:(i)培养1小时内,初始显著下降至新鲜肝细胞中发现水平的50%;(ii)GSH浓度恢复至高于新鲜细胞中观察到的水平。对照细胞培养6小时后,以及PB或MC处理的大鼠来源的细胞培养10 - 24小时后发生这种情况,在PB处理的大鼠来源的细胞中最为明显。(iii)培养24至96小时期间,缓慢下降至30至40 nmol GSH/mg蛋白质。PB处理的大鼠来源的培养细胞中GSH的合成较慢,当使用马来酸二乙酯(DEM)耗尽GSH时,再合成速率证实了这一点。在悬浮的对照细胞以及培养3小时和24小时后,测量了GSH与外消旋7β,8α - 二羟基 - 9α,10α - 环氧 - 7,8,9,10 - 四氢苯并[a]芘(BPDE)的结合物形成情况。尽管培养后1至4小时观察到GSH浓度下降,但结合速率并未降低。