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.
Author supplied keywords
Cite
CITATION STYLE
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
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.