Pregled bibliografske jedinice broj: 1092732
INACTIVATION KINETICS OF CYTOCHROME P450 3A4 BY ACACETIN
INACTIVATION KINETICS OF CYTOCHROME P450 3A4 BY ACACETIN // Archives of Industrial Hygiene and Toxicology: Abstracts of the 3rd International Congress on Food Safety and Quality / Šostar, Zvonimir ; Šikić, Sandra ; Krivohlavek, Adela ; Bošnir, Jasna (ur.).
Zagreb: Institut za medicinska istraživanja i medicinu rada, 2020. str. 44-44 (poster, domaća recenzija, sažetak, znanstveni)
CROSBI ID: 1092732 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
INACTIVATION KINETICS OF CYTOCHROME P450 3A4 BY
ACACETIN
Autori
Kondža, Martin ; Maleš, Željan ; Antolić, Andrea ; Bojić, Mirza
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Archives of Industrial Hygiene and Toxicology: Abstracts of the 3rd International Congress on Food Safety and Quality
/ Šostar, Zvonimir ; Šikić, Sandra ; Krivohlavek, Adela ; Bošnir, Jasna - Zagreb : Institut za medicinska istraživanja i medicinu rada, 2020, 44-44
Skup
3. međunarodni kongres o sigurnosti i kvaliteti hrane = 3rd International Congress on Food Safety and Quality
Mjesto i datum
Opatija, Hrvatska, 11.11.2020. - 13.11.2020
Vrsta sudjelovanja
Poster
Vrsta recenzije
Domaća recenzija
Ključne riječi
flavonoids, cytochrome P450 3A4, inhibition, kinetics, acacetin
Sažetak
Flavonoids are secondary plant metabolites found in fruits and vegetables. Cytochrome P450 enzymes are the most significant metabolic enzymes of xenobiotics, including food constituents, toxic substances, medications. Some flavonoids can interact with other drugs by inhibiting cytochrome P450 enzymes. The objective of this study was to determine inhibition kinetics of cytochrome P450 3A4 by acacetin. Acacetin is one of the major polyphenols present in honey, which is believed to be associated with the prevention of heart disease. Enzyme activity was determined using testosterone and nifedipine as marker substrates, and generation of respective metabolites 6β-hydroxytestosterone and nifedipine-oxide was monitored by high performance liquid chromatography coupled with diode array detector. In testosterone assay the values of inactivation kinetic parameters were as follows: IC50 value of 10.9 ± 0.3 µM, inhibition constant 6 ± 3 µM, inhibition rate constant 0.036 ± 0.006 per min Similar results were obtained in nifedipine assay. Further in vitro studies are needed to determine the reactive intermediate responsible for inactivation of cytochrome P450 3A4 enzyme, as well as in vivo studies to determine possible clinical significance of this inhibition.
Izvorni jezik
Engleski
Znanstvena područja
Farmacija
POVEZANOST RADA
Ustanove:
Farmaceutsko-biokemijski fakultet, Zagreb
Citiraj ovu publikaciju:
Časopis indeksira:
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE