Decomposition of α-tocopheryl glycosides in rat tissues

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Abstract

Background: The aim of our investigation was to estimate the stability of α-tocopheryl O-glycosides in relation to activity of exoglycosidases in selected rat tissues. Material and Methods: Acetylated glycosides were obtained in glucosidation of α-tocopherol using the Helferich method. The activity of exoglycosidases was determined by the Zwierz et al. method. Protein concentrations were determined by the biuret method. The concentration of released α-tocopherol was determined with the HPLC method. Results: The comparison of the amount of released α-tocopherol with the amount of released p-nitrophenol shows that glycoside bound in 2a-5a derivatives of α-tocopherol undergoes hydrolysis significantly harder than in appropriate 2b-5b p-nitrophenyl derivatives. Conclusion: The results indicate that tocopheryl O-glycosides are more resistant to enzymatic hydrolysis than appropriate p-nitrophenol O-glycosides 2a-5a. Among examined tocopheryl O-glycosides, galactoside 4 is the only compound that caused the significant increase in tocopherol concentration, as compared to its endogenic content.

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Knaś, M., Wałejko, P., Maj, J., Hryniewicka, A., Witkowski, S., Borzym-Kluczyk, M., … Zwierz, K. (2008). Decomposition of α-tocopheryl glycosides in rat tissues. Toxicology Mechanisms and Methods, 18(6), 491–496. https://doi.org/10.1080/15376510802164519

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