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氧衍生自由基和钙对人红细胞膜流动性的影响

Alterations of human erythrocyte membrane fluidity by oxygen-derived free radicals and calcium.

作者信息

Watanabe H, Kobayashi A, Yamamoto T, Suzuki S, Hayashi H, Yamazaki N

机构信息

Third Department of Internal Medicine, Hamamatsu University School of Medicine, Japan.

出版信息

Free Radic Biol Med. 1990;8(6):507-14. doi: 10.1016/0891-5849(90)90150-h.

Abstract

Two possible reasons for the structural alterations of cell membranes caused by free radicals are lipid peroxidation and an increase in the intracellular calcium ion concentration. To characterize the alterations in membrane molecular dynamics caused by oxygen-derived free radicals and calcium, human erythrocytes were spin-labeled with 5-doxyl stearic acid, and alterations in membrane fluidity were quantified by electron spin resonance spectrometry. The in vitro generation of oxygen free radicals, using hypoxanthine (0.43 mM) plus xanthine oxidase (0.07 U/mL) decreased membrane fluidity, and the addition of superoxide dismutase and catalase inhibited the effect on membrane fluidity of the hypoxanthine-xanthine oxidase system. Hydrogen peroxide (0.1 and 1 mM) also decreased membrane fluidity and caused alterations to erythrocyte morphology. In addition, a decrease in membrane fluidity was observed in erythrocytes incubated with 2.8 mM CaCl2. On the other hand, incubation of erythrocytes with calcium-free solution decreased the changes in membrane fluidity caused by hydrogen peroxide. These results suggest that changes in membrane fluidity are directly due to lipid peroxidation and are indirectly the result of increased intracellular calcium concentration. We support the hypothesis that alterations of the biophysical properties of membranes caused by free radicals play an important role in cell injury, and that the accumulation of calcium amplifies the damage to membranes weakened by free radicals.

摘要

自由基导致细胞膜结构改变的两个可能原因是脂质过氧化和细胞内钙离子浓度升高。为了表征由氧衍生自由基和钙引起的膜分子动力学变化,用人红细胞与5-硬脂酸基氮氧自由基进行自旋标记,并通过电子自旋共振光谱法定量膜流动性的变化。使用次黄嘌呤(0.43 mM)加黄嘌呤氧化酶(0.07 U/mL)体外产生氧自由基会降低膜流动性,添加超氧化物歧化酶和过氧化氢酶可抑制次黄嘌呤-黄嘌呤氧化酶系统对膜流动性的影响。过氧化氢(0.1和1 mM)也会降低膜流动性并导致红细胞形态改变。此外,在与2.8 mM氯化钙孵育的红细胞中观察到膜流动性降低。另一方面,用无钙溶液孵育红细胞可减少过氧化氢引起的膜流动性变化。这些结果表明,膜流动性的变化直接归因于脂质过氧化,间接是细胞内钙浓度升高的结果。我们支持这样的假设,即自由基引起的膜生物物理性质改变在细胞损伤中起重要作用,并且钙的积累会放大自由基对膜的损伤。

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