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THE EFFECT OF AROMATIC AMINES IN THE THIYL- INDUCED REACTIONS OF POLYUNSATURATED FATTY ACIDS (CROSBI ID 627606)

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Mihaljević, Branka ; Tartaro Bujak, Ivana THE EFFECT OF AROMATIC AMINES IN THE THIYL- INDUCED REACTIONS OF POLYUNSATURATED FATTY ACIDS // 13th Tihany Symposium on Radiation Chemistry / Wojnarovits, Laszlo ; Takacs, Erzsebet (ur.). 2015. str. P55-P55

Podaci o odgovornosti

Mihaljević, Branka ; Tartaro Bujak, Ivana

engleski

THE EFFECT OF AROMATIC AMINES IN THE THIYL- INDUCED REACTIONS OF POLYUNSATURATED FATTY ACIDS

Lipid peroxidation and geometrical isomerization are two main classes of reactions that are known in the context of reactivity of lipids toward free radicals. Both processes peroxidation and isomerization were detected in biomimetic model of linoleic acid in the presence of oxygen and thiols.1 Thiols are known repairing agents in case of lipid peroxidation, due to the H-donation towards peroxyl radicals. In doing so, thiols are precursors of thiyl radicals that can act as isomerizing agents for the fatty acid double bonds. The double-sward character of thiols towards biomolecules has been increasingly addressed in the last decade. Whether these processes can occur together or influence each other in the presence of some common antioxidant, such as aromatic amines and phenols, is presently unknown. We were interested in extending the investigation of the reactivity of thiols involving diphenylamine in aerobic conditions. We investigated the interaction of diphenylamine and 2-mercaptoethanol in the radical stress induced to linoleic acid under biomimetic conditions. As a measure of lipid peroxidation in model systems of linoleic acid we determined hydroperoxides of linoleic acid initiated by thiyl radicals which were generated by gamma radiolysis.2 The role of diphenylamine in protecting from linoleic acid geometrical isomerization was determined simultaneously by gas chromatography.3 The mechanistic scenario was defined contributing to a better understanding of complex interactions related to free radical stress and antioxidant activity, as well as of the mechanisms of aromatic amines reactivity. References: [1] B. Mihaljević, I. Tartaro, C. Ferreri, C. Chatgilialoglu, Org. Biomol. Chem. 9 (2011) 3541–3548. [2] B. Mihaljević, B. Katušin-Ražem, D. Ražem, Free Radical Biol. Med. 21 (1996) 53–63. [3] C. Ferreri, S. Kratzsch, O. Brede, B. Marciniak, C. Chatgilialoglu, Free Radical Biol. Med. 38 (2005) 1180–1187.

diphenylamine; lipid hydroperoxides; cis-trans isomers; thiyl radicals

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Podaci o prilogu

P55-P55.

2015.

objavljeno

Podaci o matičnoj publikaciji

13th Tihany Symposium on Radiation Chemistry

Wojnarovits, Laszlo ; Takacs, Erzsebet

Podaci o skupu

13th Tihany Symposium on Radiation Chemistry

poster

29.08.2015-03.09.2015

Balatonalmádi, Mađarska

Povezanost rada

Kemija