Meier T, Allenbacher A, Mueller E, Multhoff G, Botzler C, Wiesnet M, Issels R
GSF-Institut für Klinische Hämatologie, München, Germany.
Anticancer Drugs. 1994 Aug;5(4):403-9. doi: 10.1097/00001813-199408000-00003.
We studied the effects of ifosfamide and major metabolites on intracellular glutathione (GSH) levels in human peripheral blood lymphocytes (PBL). In vitro exposure of PBL to 4-hydroperoxyifosfamide (4-OOH-IF), acrolein or chloroacetaldehyde at 37 degrees C for 60 min led to a concentration dependent depletion of intracellular GSH. The concentration of the three metabolites to cause a 50% depletion of GSH in PBL was in the micromolar range (acrolein: 16 +/- 4 microM; 4-OOH-IF: 22 +/- 9 microM; chloroacetaldehyde: 30 +/- 7 microM). Exposure to ifosfamide, the non-activated drug, had no effects on the intracellular GSH levels. Pretreatment with 4-OOH-IF suppressed dose-dependently the interleukin-2-induced proliferation of PBL. Incubation of PBL together with 2-mercaptoethanesulfonate (mesna) and 4-OOH-IF, acrolein or chloroacetaldehyde prevented the GSH depletion. The protecting effect of mesna in combination with 4-OOH-IF was independent of GSH biosynthesis, because addition of buthionine sulfoximine had no significant influence on this effect. These findings indicate a novel protective mechanism of mesna against intracellular GSH depletion of PBL during exposure to metabolites of ifosfamide.
我们研究了异环磷酰胺及其主要代谢产物对人外周血淋巴细胞(PBL)内谷胱甘肽(GSH)水平的影响。在37℃下将PBL体外暴露于4 - 氢过氧异环磷酰胺(4 - OOH - IF)、丙烯醛或氯乙醛60分钟,导致细胞内GSH浓度依赖性耗竭。使PBL中GSH耗竭50%的这三种代谢产物的浓度处于微摩尔范围(丙烯醛:16±4μM;4 - OOH - IF:22±9μM;氯乙醛:30±7μM)。暴露于未活化药物异环磷酰胺对细胞内GSH水平无影响。用4 - OOH - IF预处理可剂量依赖性抑制白细胞介素 - 2诱导的PBL增殖。将PBL与2 - 巯基乙烷磺酸盐(美司钠)和4 - OOH - IF、丙烯醛或氯乙醛一起孵育可防止GSH耗竭。美司钠与4 - OOH - IF联合的保护作用与GSH生物合成无关,因为添加丁硫氨酸亚砜胺对该作用无显著影响。这些发现表明美司钠在暴露于异环磷酰胺代谢产物期间对PBL细胞内GSH耗竭具有一种新的保护机制。