Antioxidant activity of catecholamines during the oxidation of methyl linoleoate in Triton X-100 micelles
- Authors: Ryabkova V.A.1, Tikhonov I.V.1, Pliss E.M.1
- 
							Affiliations: 
							- Demidov Yaroslavl State University
 
- Issue: Vol 43, No 9 (2024)
- Pages: 35-41
- Section: Kinetics and mechanism of chemical reactions, catalysis
- URL: https://cardiosomatics.ru/0207-401X/article/view/680964
- DOI: https://doi.org/10.31857/S0207401X24090042
- ID: 680964
Cite item
Abstract
The effect of catecholamines on the oxidation of methyl linoleate in Triton X-100 micelles was studied. It has been established that catecholamines do not inhibit oxidation at a pH 7.4. Inhibition is only possible in the presence of the superoxide dismutase enzyme or at lower pH levels. The reason for this effect is the interaction of anionic forms of phenols and phenoxyl radicals with oxygen with the formation of superoxide anions. High values of inhibition coefficients for catecholamines in the presence of superoxide dismutase are due to the reactions of the resulting ortho-quinones, leading to the regeneration of OH groups.
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	                        About the authors
V. A. Ryabkova
Demidov Yaroslavl State University
														Email: tikhonoviv.ysu@gmail.com
				                					                																			                												                	Russian Federation, 							Yaroslavl						
I. V. Tikhonov
Demidov Yaroslavl State University
							Author for correspondence.
							Email: tikhonoviv.ysu@gmail.com
				                					                																			                												                	Russian Federation, 							Yaroslavl						
E. M. Pliss
Demidov Yaroslavl State University
														Email: tikhonoviv.ysu@gmail.com
				                					                																			                												                	Russian Federation, 							Yaroslavl						
References
- I. Tikhonov, V. Roginsky, and E. Pliss, Int. J. Chem. Kinet. 41, 92 (2008). https://doi.org/10.1002/kin.20377
- I. Tichonov, V. Roginsky, and E. Pliss, Eur. J. Lipid Sci. Technol. 112, 887 (2010). https://doi.org/10.1002/ejlt.200900282
- V. Roginsky, Arch. Biochem. Biophys. 414, 261 (2003). https://doi.org/10.1016/S0003-9861(03)00143-7
- V. Roginsky, and E.A. Lissi, Food Chem. 92, 235 (2005). https://doi.org/10.1016/j.foodchem.2004.08.004
- K. Jodko-Piorecka, and G. Litwinienko, Free Radic. Biol. Med. 83, 1 (2015). https://doi.org/10.1016/j.freeradbiomed.2015.02.006
- D. Loshadkin, V. Roginsky, and E. Pliss, Int. J. Chem. Kinet. 34, 162 (2002). https://doi.org/10.1002/kin.10041
- V. Roginsky, and T. Barsukova, Chem. Phys. Lipids 111, 87 (2001). https://doi.org/10.1016/S0009-3084(01)00148-7
- V. Roginsky, T. Barsukova, D. Loshadkin, and E. Pliss, Chem. Phys. Lipids 125, 49 (2003). https://doi.org/10.1016/S0009-3084(03)00068-9
- V. Roginsky, Free Radic. Res. 35, 55 (2001). https://doi.org/10.1080/10715760100300591
- I.V. Moskalenko, and I.V. Tikhonov, Russ. J. Phys. Chem. B 16, 602 (2022). https://doi.org/10.1134/S1990793122040121
- V.M. Costa, R. Silva, L.M. Ferreira, P.S. Branco, F. Carvalho, M.L. Bastos, R.A. Carvalho, M. Carvalho, and F. Remiao, Chem. Res. Toxicol. 20, 1183 (2007). https://doi.org/10.1021/tx7000916
- T.V. Sirota, Biophysics. 65, 548 (2020). https://doi.org/10.1134/S0006350920040223
- N.A. Mautjana, J. Estes, J.R. Eyler, and A. Brajter-Toth, Electroanalysis 20, 1959 (2008). https://doi.org/10.1002/elan.200804279
- I. Iftikhar, K. Abou El-Nour, and A. Brajter-Toth, Electrochim. Acta 249, 145 (2017). https://doi.org/10.1016/j.electacta.2017.07.087
- I.F. Rusina, T.L. Veprintsev, and R.F. Vasil’ev, Russ. J. Phys. Chem. B 16, 50 (2022). https://doi.org/10.1134/S1990793122010274
- F. Mack, and H. Bonisch, Naunyn-Schmiedeberg’s Arch. Pharmacol. 310, 1 (1979). https://doi.org/10.1007/BF00499868
- N.Yu. Gerasimov, O.V. Nevrova, I.V. Zhigacheva, I.P. Generozova, and A.N. Goloshchapov, Russ. J. Phys. Chem. B 17, 135 (2023). https://doi.org/10.1134/S1990793123010049
- L.N. Shishkina, M.V. Kozlov, T.V. Konstantinova, A.N. Smirnova, and V.O. Shvydkiy, Russ. J. Phys. Chem. B 17, 141 (2023). https://doi.org/10.1134/S1990793123010104
- K. Jodko-Piorecka, B. Sikora, M. Kluzek, P. Przybylski, and G. Litwinienko, J. Org. Chem. 87, 1791 (2022). https://doi.org/10.1021/acs.joc.1c02308
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