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在酸性pH值下从转铁蛋白释放的铁可催化低密度脂蛋白的氧化。

Iron released from transferrin at acidic pH can catalyse the oxidation of low density lipoprotein.

作者信息

Lamb D J, Leake D S

机构信息

Department of Biochemistry and Physiology, School of Animal and Microbial Sciences, University of Reading, Berks, UK.

出版信息

FEBS Lett. 1994 Sep 19;352(1):15-8. doi: 10.1016/0014-5793(94)00903-1.

Abstract

Low density lipoprotein (LDL) oxidation within the arterial wall may contribute to the disease of atherosclerosis. We have investigated the conditions under which transferrin (the major iron-carrying protein in plasma) may release iron ions to catalyse the oxidation of LDL. Transferrin that had been incubated at pH 5.5 released approximately 10% of its bound iron in 24 h, as measured by ultrafiltration and atomic absorption spectroscopy. Furthermore, transferrin co-incubated with LDL and L-cysteine at pH 5.5 resulted in the oxidation of the LDL as measured by thiobarbituric acid-reactive substances and electrophoretic mobility. This effect was observed at transferrin concentrations as low as 40% of its average plasma concentration. The release of iron from transferrin in atherosclerotic lesions due to a localised acidic pH may help to explain why LDL oxidation occurs in these lesions.

摘要

动脉壁内的低密度脂蛋白(LDL)氧化可能会导致动脉粥样硬化疾病。我们研究了转铁蛋白(血浆中主要的铁转运蛋白)在何种条件下可能释放铁离子以催化LDL的氧化。通过超滤和原子吸收光谱法测定,在pH 5.5下孵育的转铁蛋白在24小时内释放了约10%的结合铁。此外,在pH 5.5下与LDL和L-半胱氨酸共同孵育的转铁蛋白导致LDL氧化,这通过硫代巴比妥酸反应性物质和电泳迁移率来测定。在转铁蛋白浓度低至其平均血浆浓度的40%时就观察到了这种效应。由于局部酸性pH,转铁蛋白在动脉粥样硬化病变中释放铁可能有助于解释为什么这些病变中会发生LDL氧化。

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