Kinetics and Mechanisms of Oxidative Hemolysis of Erythrocytes under the Action of Azo- and Peroxide Initiator

被引:0
作者
Sokolova E.M. [1 ]
Dubenskaia N.A. [2 ]
Psikha B.L. [1 ]
Neshev N.I. [1 ]
机构
[1] Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry, Russian Academy of Sciences, 1 prosp. Akademika Semenova, Moscow oblast, Chernogolovka
[2] Faculty of Fundamental Physical and Chemical Engineering, Lomonosov Moscow State University, Moscow
关键词
erythrocytes; hemoglobin; lipid peroxidation; oxidative hemolysis;
D O I
10.1134/S0006350923040206
中图分类号
学科分类号
摘要
Abstract: The kinetics of oxidative hemolysis of the 0.2% mouse erythrocytes suspension has been studied over a wide range of concentrations under the action of radical-forming initiators 2,2'-azobis(2-amidinopropan) dihydrochloride and tert-butyl hydroperoxide. Hemolysis of erythrocytes proceeded upon activation lipid peroxidation in erythrocyte membranes. In the case of tert-butyl hydroperoxide, oxidative processes also developed in the soluble part of the cell, leading to the formation of insoluble hemoglobin aggregates. Period of hemolysis induction (time of reaching 10% hemolysis) under the influence of 2,2'-azobis(2-amidinopropane) dihydrochloride decreases inversely to the square root of the initiator concentration, which is consistent with the classical theory of radical chain oxidation of hydrocarbons. In the case of tert-butyl hydroperoxide this pattern is not observed. In the erythrocyte model of testing natural and synthetic compounds for antioxidant activity it is preferable to use 2,2'-azobis (2-amidinopropane) dihydrochloride as the initiator of lipid peroxidation. © 2023, Pleiades Publishing, Inc.
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页码:570 / 575
页数:5
相关论文
共 14 条
[1]  
Burlakova E.B., Usp. Khim., 44, (1975)
[2]  
Shevchenko O.G., Shishkina L.N., Usp. Sovrem. Biol., 134, (2014)
[3]  
Semchikov Y.D., High Molecular Weight Compounds, (2010)
[4]  
Young J.D., Leong L.G., DiNome M.A., Cohn Z.A., Anal. Biochem., 154, (1986)
[5]  
Stocks J., Dormandy T.L., Br. J. Haematol., 20, (1971)
[6]  
Wahl R.U.R., Zeng L., Madison S.A., J. Chem. Soc., Perkin Trans, 2, (1998)
[7]  
Lopez-Alarcon C., Fuentes-Lemus E., Figueroa J.D., Free Radical Biol. Med., 160, (2020)
[8]  
Deuticke B., Heller K.B., Haest C.W., Biochim. Biophys. Acta, 854, (1986)
[9]  
Trotta R.J., Sullivan S.G., Stern A., Biochem. J., 204, (1982)
[10]  
Domanskii A.V., Lapshina E.A., Zavodnik I.B., Biochemistry (Moscow), 70, (2005)