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乙醛诱导的人血红细胞氧化修饰和形态变化:一项体外研究。

Acetaldehyde-induced oxidative modifications and morphological changes in isolated human erythrocytes: an in vitro study.

机构信息

Department of Biochemistry, Faculty of Medicine, J. N. Medical College, Aligarh Muslim University, Aligarh, UP, India.

Department of Clinical Biochemistry, King Khalid University, Abha, Saudi Arabia.

出版信息

Environ Sci Pollut Res Int. 2020 May;27(14):16268-16281. doi: 10.1007/s11356-020-08044-4. Epub 2020 Mar 2.

Abstract

Acetaldehyde is a toxic, mutagenic and carcinogenic metabolite of alcohol which can bind to proteins, DNA and several other cellular macromolecules. Chronic alcohol consumption increases intracellular acetaldehyde levels which enhances the generation of reactive oxygen and nitrogen species (ROS and RNS). In this study, we have examined the effect of acetaldehyde on human erythrocytes under in vitro conditions. Treatment of human erythrocytes with different concentrations of acetaldehyde (0.05-2 mM) for 24 h at 37 °C increased intracellular generation of ROS and RNS. It also increased oxidation of proteins and lipids but decreased glutathione, total sulphhydryl and free amino group content. Methemoglobin level was increased accompanied by a decrease in methemoglobin reductase activity. Acetaldehyde impaired the antioxidant defence system and lowered the total antioxidant capacity of the cell. It decreased the activity of metabolic and membrane-bound enzymes and altered erythrocyte morphology. Our results show that acetaldehyde enhances the generation of ROS and RNS that results in oxidative modification of cellular components. This will lower the oxygen transporting ability of blood and shorten erythrocyte lifespan (red cell senescence).

摘要

乙醛是酒精的一种有毒、致突变和致癌的代谢物,可与蛋白质、DNA 和几种其他细胞大分子结合。长期饮酒会增加细胞内乙醛水平,从而增强活性氧和活性氮物质 (ROS 和 RNS) 的产生。在这项研究中,我们在体外条件下检查了乙醛对人红细胞的影响。在 37°C 下用不同浓度的乙醛(0.05-2 mM)处理人红细胞 24 小时,会增加细胞内 ROS 和 RNS 的产生。它还会氧化蛋白质和脂质,但会降低谷胱甘肽、总巯基和游离氨基含量。高铁血红蛋白水平升高伴随着高铁血红蛋白还原酶活性降低。乙醛会损害抗氧化防御系统并降低细胞的总抗氧化能力。它会降低代谢酶和膜结合酶的活性,并改变红细胞的形态。我们的结果表明,乙醛会增强 ROS 和 RNS 的产生,导致细胞成分的氧化修饰。这会降低血液的携氧能力并缩短红细胞寿命(红细胞衰老)。

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