Liu T Z, Lin T F, Hung I J, Wei J S, Chiu D T
Chang Gung College of Medicine & Technology, School of Medical Technology, Tao-yuan, Taiwan.
Life Sci. 1994;55(3):PL55-60. doi: 10.1016/0024-3205(94)00888-4.
It has been hypothesized that enhanced oxidant sensitivity of glucose-6-phosphate dehydrogenase (G6PD) deficient red cells(RBCs) is the underlying mechanism for drug- or chemical-induced hemolytic crises in G6PD-deficiency. To further test this hypothesis, we used an alloxan-glutathione system to mimic oxidative stress and see how oxidative damage might affect RBC deformability. RBC deformability, a major determinant of RBC survival in vivo, was monitored by a laser viscodiffractometer. Under our experimental conditions, GSH alone had very little effect on the deformability of either normal or G6PD-deficient RBCs. In contrast, alloxan alone induced a small but significant decrease in the deformability of either normal or G6PD-deficient RBCs. Interestingly, alloxan and GSH together induced a further decrease in the deformability of either normal or G6PD-deficient RBCs. The decrease in deformability in G6PD-deficient RBCs was much more profound than in normal RBCs. In addition, an alloxan-vitamin C system produced a similar deleterious effect on RBC deformability as that produced by the alloxan-GSH system. Appreciable amount of hydroxyl radicals was generated by both alloxan-GSH and alloxan-vitamin C systems as evidenced by the production of hydroxylated products of salicylate which was used as a radical trap. Moreover, salicylate could ameliorate the deleterious effect of the alloxan system on the deformability of RBCs. Taken together, our results demonstrated that G6PD-deficient RBCs were particularly susceptible to oxidant-induced damage leading to a dramatic decrease in their deformability and thus provided strong support for the hypothesis that enhanced oxidant sensitivity of G6PD-deficient RBCs is the underlying mechanism for accelerated destruction of these RBCs in vivo.
据推测,葡萄糖-6-磷酸脱氢酶(G6PD)缺乏的红细胞(RBC)对氧化剂敏感性增强是G6PD缺乏症中药物或化学物质诱导的溶血性危机的潜在机制。为了进一步验证这一假设,我们使用了一种四氧嘧啶-谷胱甘肽系统来模拟氧化应激,并观察氧化损伤如何影响红细胞的变形性。红细胞变形性是红细胞在体内存活的主要决定因素,通过激光粘度衍射仪进行监测。在我们的实验条件下,单独的谷胱甘肽(GSH)对正常或G6PD缺乏的红细胞的变形性影响很小。相比之下,单独的四氧嘧啶会导致正常或G6PD缺乏的红细胞的变形性出现轻微但显著的下降。有趣的是,四氧嘧啶和谷胱甘肽一起会导致正常或G6PD缺乏的红细胞的变形性进一步下降。G6PD缺乏的红细胞中变形性的下降比正常红细胞中更为显著。此外,四氧嘧啶-维生素C系统对红细胞变形性产生了与四氧嘧啶-GSH系统类似的有害影响。四氧嘧啶-GSH和四氧嘧啶-维生素C系统均产生了可观数量的羟基自由基,以用作自由基捕获剂的水杨酸酯的羟基化产物的产生为证据。此外,水杨酸酯可以改善四氧嘧啶系统对红细胞变形性的有害影响。综上所述,我们的结果表明,G6PD缺乏的红细胞对氧化剂诱导的损伤特别敏感,导致其变形性急剧下降,从而为以下假设提供了有力支持:G6PD缺乏的红细胞对氧化剂敏感性增强是这些红细胞在体内加速破坏的潜在机制。