Pregled bibliografske jedinice broj: 485899
Antiaggregatory activity of flavonoids
Antiaggregatory activity of flavonoids // Periodicum Biologorumv - 6th Croatian Congress of Pharmacology with international participation / Boban, M ; i sur. (ur.).
Zagreb: Hrvatsko prirodoslovno društvo, 2010. str. 50-50 (pozvano predavanje, međunarodna recenzija, sažetak, znanstveni)
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Naslov
Antiaggregatory activity of flavonoids
Autori
Debeljak, Željko ; Bojić, Mirza ; Medić-Šarić, Marica
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Periodicum Biologorumv - 6th Croatian Congress of Pharmacology with international participation
/ Boban, M ; i sur. - Zagreb : Hrvatsko prirodoslovno društvo, 2010, 50-50
Skup
6th Congress of Pharmacology with International Participation
Mjesto i datum
Opatija, Hrvatska, 15.09.2010. - 18.09.2010
Vrsta sudjelovanja
Pozvano predavanje
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
antiaggregatory activity; flavonoids
Sažetak
Introduction: Antiaggregatory activity of flavonoids is well known property of these compounds. However, the results of a systematic search for highly potent members of this family are still missing. Moreover, different mechanisms of antiaggregatory action of this group of compounds were proposed. Material and methods: In order to analyze the antiaggregatory activity of series of flavonoids platelet impedance aggregation in whole blood has been selected while the ADP has been used as an aggregation agonist. For the analysis of possible mechanism of antiaggregatory action of the most potent compounds other aggregation agonists were also tested. Results: The following members among analyzed flavonoids show the most potent antiaggregatory effect: syringetin, 3, 6-dihydroxyflavone, rhamnethin. Besides inhibition of aggregation induced by ADP these compounds also inhibit the aggregation induced by collagen to some extent. Conclusions: Among the analyzed flavonoids the most potent members posses following structural properties: double bond on position C2-C3 and hydroxyl fgroup on position C3 of the ring C (flavonols). According to our results inhibition of phosphatidyl-inositol synthesis is the most likely explanation for antiaggregatory action throught interference with one or more common platelet signaling pathways.
Izvorni jezik
Engleski
Znanstvena područja
Farmacija
POVEZANOST RADA
Projekti:
006-0061117-1237 - Biološki aktivni spojevi, metaboliti i QSAR (Medić-Šarić, Marica, MZOS ) ( CroRIS)
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