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缺铁和去铁胺对人细胞DNA合成的影响。

Effect of iron deficiency and desferrioxamine on DNA synthesis in human cells.

作者信息

Hoffbrand A V, Ganeshaguru K, Hooton J W, Tattersall M H

出版信息

Br J Haematol. 1976 Aug;33(4):517-26. doi: 10.1111/j.1365-2141.1976.tb03570.x.

Abstract

Desferrioxamine (10(-3) M) caused a fall in the deoxyadenosine triphosphate level after 4 h incubation in normal phytohaemagglutinin-stimulated lymphocytes. There was a rise in the concentrations of the other three deoxyribonucleoside triphosphates (deoxythymidine-,deoxycytidine-and deoxyguanosine-triphosphate). The changes are similar to those caused by hydroxyurea, a known inhibitor of ribonucleotide reductase. Desferrioxamine (10(-3 M) was found to inhibit human lymphocyte ribonucleotide reductase to a mean of 11% of control activity after 45 min incubation. Both drugs, desferrioxamine and hydroxyurea, inhibited incorporation of [3H]thymidine DNA into lymphocytes in the presence or absence of deoxyuridine, and inhibited production of lymphocytic thymidine kinase, having opposite effects to methotrexate on both [3H]thymidine incorporation and thymidine kinase activity. Phytohaemagglutinin-stimulated lymphocytes from patients with chronic iron deficiency showed lower levels of all our deoxyribonucleoside triphosphates than normal lymphocytes. It is suggested that this may be due to reduced ribnucleotide reductase activity of the iron-deficient cells.

摘要

去铁胺(10⁻³M)在正常植物血凝素刺激的淋巴细胞中孵育4小时后,导致三磷酸脱氧腺苷水平下降。其他三种三磷酸脱氧核糖核苷(三磷酸脱氧胸苷、三磷酸脱氧胞苷和三磷酸脱氧鸟苷)的浓度有所上升。这些变化与已知的核糖核苷酸还原酶抑制剂羟基脲所引起的变化相似。发现去铁胺(10⁻³M)在孵育45分钟后可将人淋巴细胞核糖核苷酸还原酶抑制至对照活性的平均11%。去铁胺和羟基脲这两种药物,无论有无脱氧尿苷存在,均抑制[³H]胸苷掺入淋巴细胞DNA,并抑制淋巴细胞胸苷激酶的产生,在[³H]胸苷掺入和胸苷激酶活性方面对甲氨蝶呤具有相反的作用。慢性缺铁患者经植物血凝素刺激的淋巴细胞显示,所有三磷酸脱氧核糖核苷的水平均低于正常淋巴细胞。提示这可能是由于缺铁细胞的核糖核苷酸还原酶活性降低所致。

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