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携带血红蛋白S个体红细胞中的氧化过程。

Oxidative process in erythrocytes of individuals with hemoglobin S.

作者信息

Chaves Michele Ana Flores, Leonart Maria Suely Soares, do Nascimento Aguinaldo José

机构信息

Programa de Pós-Graduação em Ciências Farmacêuticas da Universidade Federal do Paraná, Avenida Lothário Meissner, 3400, Jardim Botânico, CEP 80210-170, Curitiba, PR, Brazil.

出版信息

Hematology. 2008 Jun;13(3):187-92. doi: 10.1179/102453308X343356.

Abstract

The understanding of the oxidative stress mechanisms helps to explain many of the processes of cellular lesion and death, especially those related to the hemolytic diseases. Sickle cell anemia, thalassemias and G6-PD deficiency are among the more frequent genetic anomalies accompanied by oxidative stress. In the sickle cells, one of the factors that predisposes to the hemolytic process is the oxidative degradation of the hemoglobin S due to its deoxigenation leading to hemichrome formation and precipitation as Heinz bodies. The oxidative stress contributes to the sickle process and shortening of the erythrocyte survival. Here we analyzed the oxidative process in erythrocytes of patients with two different genotypes for HbS (AS and SS). Units of blood from donors of the Center of Hematology and Hemotherapy of Paraná (HEMEPAR), from normal individuals (AA) and from heterozygote individuals (AS), and venous blood collected from patients with sickle cell anemia (SS) were analyzed. In order to evaluate the protective action of the vitamins C and E in oxidative stress, erythrocytes were treated with antioxidant substances, vitamin C and vitamin E, and then treated with the oxidant tert-butilhydroperoxide (TBHP). The oxidative action induced by TBHP was observed in erythrocytes AA<AS<SS, by the increase in the content of Heinz bodies, methemoglobin, hemolysis, GSH depletion and lowering activities of the enzymes G6-PD and GR. The protective actions of the vitamins C and E for the oxidative stress induced by TBHP were observed for the erythrocytes in the lowering Heinz bodies, methemoglobin, hemolysis, and partial recovery of GSH more efficiently in AS and SS erythrocytes. Recovery was not observed in the levels of the activities of the enzymes G6-PD and GR, under the vitamins actions. The results obtained confirmed the higher susceptibility of the sickle erythrocyte to oxidation which necessitates precaution in the transfusion adequacy of AS erythrocytes. On the other hand, the protective effect of the vitamins C and E over the oxidative stress observed in erythrocytes AS and SS open perspectives for their use for treatment of patients with sickle cell anemias, as well as in the preservation of transfusional erythrocyte bag units.

摘要

对氧化应激机制的理解有助于解释许多细胞损伤和死亡过程,尤其是那些与溶血性疾病相关的过程。镰状细胞贫血、地中海贫血和葡萄糖-6-磷酸脱氢酶(G6-PD)缺乏症是伴随氧化应激的较为常见的遗传异常。在镰状细胞中,导致溶血过程的因素之一是血红蛋白S因脱氧而发生氧化降解,导致高铁血红素形成并沉淀为海因茨小体。氧化应激促进镰状化过程并缩短红细胞存活期。在此,我们分析了两种不同HbS基因型(AS和SS)患者红细胞中的氧化过程。对来自巴拉那州血液学和血液疗法中心(HEMEPAR)的正常个体(AA)供体、杂合子个体(AS)的血液单位,以及镰状细胞贫血患者(SS)采集的静脉血进行了分析。为了评估维生素C和E在氧化应激中的保护作用,用抗氧化物质维生素C和维生素E处理红细胞,然后用氧化剂叔丁基过氧化氢(TBHP)处理。通过海因茨小体、高铁血红蛋白含量增加、溶血、谷胱甘肽(GSH)消耗以及G6-PD和谷胱甘肽还原酶(GR)酶活性降低,观察到TBHP在红细胞中诱导的氧化作用为AA<AS<SS。在降低海因茨小体、高铁血红蛋白、溶血以及更有效地部分恢复AS和SS红细胞中的GSH方面,观察到维生素C和E对TBHP诱导的氧化应激具有保护作用。在维生素作用下,未观察到G6-PD和GR酶活性水平的恢复。获得的结果证实了镰状红细胞对氧化的更高易感性,这使得在AS红细胞的输血充足性方面需要谨慎。另一方面,维生素C和E对AS和SS红细胞中观察到的氧化应激的保护作用为其用于治疗镰状细胞贫血患者以及保存输血红细胞袋单位开辟了前景。

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