Cellerino R, Guidi G, Perona G
Scand J Haematol. 1976 Aug;17(2):111-6.
The red cell glutathione-peroxidase (GSH-Px) activity of 9 normal subjects is compared with that of 15 cases of iron deficiency anaemia and with 13 cases of heterozygous beta-thalassemia with the same degree of anaemia and hypochromia. 2 cases of sideroblastic anaemia with high serum iron levels were also examined. Enzymatic activity was found to be significantly decreased in iron deficiency anaemia (about 55% of normal range), while it was not affected in heterozygous beta thalassaemia and it was increased in the 2 cases of sideroblastic anaemia. Moreover, GSH-Px activity exhibited a significant correlation with serum iron levels in all the patients studied. The observed modifications in GSH-Px activity are not correlated with erythrocyte ageing because reticulocyte-poor fractions exhibited GSH-Px activity which was not significantly reduced in respect of the reticulocyte-rich ones. These data seem to suggest that iron has a crucial connection with erythrocyte GSH-Px and that the enzyme deficiency may be of some importance in explaining the decreased red cell survival observed in severe iron-deficiency anaemias.
将9名正常受试者的红细胞谷胱甘肽过氧化物酶(GSH-Px)活性与15例缺铁性贫血患者以及13例具有相同贫血程度和低色素性的杂合子β地中海贫血患者的进行比较。还检查了2例血清铁水平高的铁粒幼细胞贫血患者。发现缺铁性贫血患者的酶活性显著降低(约为正常范围的55%),而杂合子β地中海贫血患者的酶活性未受影响,2例铁粒幼细胞贫血患者的酶活性增加。此外,在所研究的所有患者中,GSH-Px活性与血清铁水平呈显著相关。观察到的GSH-Px活性变化与红细胞衰老无关,因为缺乏网织红细胞的部分所表现出的GSH-Px活性相对于富含网织红细胞的部分并未显著降低。这些数据似乎表明铁与红细胞GSH-Px有至关重要的联系,并且该酶缺乏在解释严重缺铁性贫血中观察到的红细胞存活降低方面可能具有一定重要性。