Antioxidant activity of catecholamines during the oxidation of methyl linoleoate in Triton X-100 micelles
- Autores: Ryabkova V.A.1, Tikhonov I.V.1, Pliss E.M.1
- 
							Afiliações: 
							- Demidov Yaroslavl State University
 
- Edição: Volume 43, Nº 9 (2024)
- Páginas: 35-41
- Seção: 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
Citar
Texto integral
 Acesso aberto
		                                Acesso aberto Acesso está concedido
						Acesso está concedido Acesso é pago ou somente para assinantes
		                                							Acesso é pago ou somente para assinantes
		                                					Resumo
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.
Palavras-chave
Texto integral
 
												
	                        Sobre autores
V. Ryabkova
Demidov Yaroslavl State University
														Email: tikhonoviv.ysu@gmail.com
				                					                																			                												                	Rússia, 							Yaroslavl						
I. Tikhonov
Demidov Yaroslavl State University
							Autor responsável pela correspondência
							Email: tikhonoviv.ysu@gmail.com
				                					                																			                												                	Rússia, 							Yaroslavl						
E. Pliss
Demidov Yaroslavl State University
														Email: tikhonoviv.ysu@gmail.com
				                					                																			                												                	Rússia, 							Yaroslavl						
Bibliografia
- 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
Arquivos suplementares
 
				
			 
						 
						 
					 
						 
						 
									

 
  
  
  Enviar artigo por via de e-mail
			Enviar artigo por via de e-mail 




