| Literature DB >> 33926051 |
Marcin Magacz1,2, Maria Oszajca3, Izabela Nawrot-Hadzik4, Ryszard Drożdż1, Anna Jurczak5, Jakub Hadzik6, Aleksander Smakosz4, Wirginia Krzyściak1.
Abstract
Lactoperoxidase (LPO) together with its (pseudo)halogenation cycle substrates, H2O2 and thiocyanate ions oxidized to hypothiocyanite ions, form one of the main systems involved in antimicrobial defense within the oral cavity. In bacterial diseases such as dental caries, lactoperoxidase is oxidized to a form known as Compound II, which is characterized by its inability to oxidize SCN-, resulting in a decreased generation of antimicrobial products. Reynoutria sp. rizome extracts, due to their high polyphenol content, have been tested as a source of compounds able to regenerate the antimicrobial activity of lactoperoxidase through converting the Compound II to the native LPO state. In the presented study, acetone extracts of R. japonica, R. sachalinensis, and R. x bohemica, together with their five fractions and four selected polyphenols dominating in the studied in extracts, were tested toward lactoperoxidase reactivating potential. For this purpose, IC50, EC50, and activation percentage were determined by Ellman's method. Furthermore, the rate constants for the conversion of Compound I-Compound II and Compound II-native-LPO in the presence of extracts, extracts fractions, and selected polyphenols were determined. Finally, the ability to enhance the antimicrobial properties of the lactoperoxidase system was tested against Streptococcus mutans. We proved that Reynoutria sp. rhizome is the source of lactoperoxidase peroxidation cycle substrates, which can act as activators and inhibitors of the antimicrobial properties of that system. The presented study shows that the reactivation of lactoperoxidase could become a potential therapeutic target in prevention and treatment support in some infectious oral diseases.Entities:
Keywords: Reynoutria; Streptococcus mutans; dental caries; lactoperoxidase; lactoperoxidase reactivators; peroxidase; polyphenols; stopped-flow spectroscopy
Year: 2021 PMID: 33926051 DOI: 10.3390/antiox10050676
Source DB: PubMed Journal: Antioxidants (Basel) ISSN: 2076-3921