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Pregled bibliografske jedinice broj: 428786

Structural aspects of flavonoids as inhibitors of human butyrylcholinesterase


Katalinić, Maja; Rusak, Gordana; Domaćinović Barović, Jelena; Šinko, Goran; Jelić, Dubravko; Antolović, Roberto; Kovarik, Zrinka
Structural aspects of flavonoids as inhibitors of human butyrylcholinesterase // 10th International Meeting on Cholinesterases, Šibenik, Hrvatska, Programme and Abstracts / Kovarik, Zrinka (ur.).
Zagreb: Hrvatsko društvo za biokemiju i molekularnu biologiju, 2009. str. 99-99 (poster, međunarodna recenzija, sažetak, znanstveni)


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Naslov
Structural aspects of flavonoids as inhibitors of human butyrylcholinesterase

Autori
Katalinić, Maja ; Rusak, Gordana ; Domaćinović Barović, Jelena ; Šinko, Goran ; Jelić, Dubravko ; Antolović, Roberto ; Kovarik, Zrinka

Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni

Izvornik
10th International Meeting on Cholinesterases, Šibenik, Hrvatska, Programme and Abstracts / Kovarik, Zrinka - Zagreb : Hrvatsko društvo za biokemiju i molekularnu biologiju, 2009, 99-99

ISBN
978-953-95551-3-7

Skup
10th International Meeting on Cholinesterases

Mjesto i datum
Šibenik, Hrvatska, 20-25.09.2009

Vrsta sudjelovanja
Poster

Vrsta recenzije
Međunarodna recenzija

Ključne riječi
Acetylcholinesterase; Cholinesterase; Cytotoxicity; Flavonoids; UV-VIS spectra; Reversible inhibition

Sažetak
Selected flavonoids: galangin, kaempferol, quercetin, myricetin, fisetin, apigenin, luteolin and rutin, reversibly inhibited human butyrylcholinesterase (BChE, EC 3.1.1.8). Inhibition potency of the flavonoids we attributed to their chemical structure, i.e., the number of OH groups and their side on the phenyl ring. The most potent BChE inhibitor among the tested flavonoids was galangin, which showed 12 times higher preference for binding to BChE (Ki = 7 μ mol/L) than to the related enzyme human acetylcholinesterase (AChE, EC 3.1.1.7). Docking study showed that flavonoids bind to the BChE active site by forming multiple hydrogen bonds and π -π interactions. The UV-VIS (200-500 nm) absorption spectra of the flavonoid phosphate buffer solution (pH 7.4), with the exception of rutin, revealed time dependant changes indicating precipitation of flavonoids or in the case of myricetin, a change in the chemical structure resulting in a BChE non-inhibiting specie. Selected flavonoids showed no cytotoxic effect on HepG2 and A549 cell lines at concentrations up to 200 μ mol/L. Cytotoxicity was observed only for fisetin, apigenin and luteolin in the THP-1 cell line with IC50 of 30, 60 and 70 μ mol/L, respectively. Galangin is therefore singled out as a promising hit in the search for new BChE inhibitors.

Izvorni jezik
Engleski

Znanstvena područja
Kemija, Biologija



POVEZANOST RADA


Projekti:
022-0222148-2889 - Interakcije organofosfata, karbamata i određenih liganada s esterazama (Kovarik, Zrinka, MZOS ) ( POIROT)
119-1191192-1213 - Flavonoidi i molekularni mehanizmi njihovih bioloških učinaka (Rusak, Gordana, MZOS ) ( POIROT)

Ustanove:
Institut za medicinska istraživanja i medicinu rada, Zagreb,
Prirodoslovno-matematički fakultet, Zagreb

Citiraj ovu publikaciju

Katalinić, Maja; Rusak, Gordana; Domaćinović Barović, Jelena; Šinko, Goran; Jelić, Dubravko; Antolović, Roberto; Kovarik, Zrinka
Structural aspects of flavonoids as inhibitors of human butyrylcholinesterase // 10th International Meeting on Cholinesterases, Šibenik, Hrvatska, Programme and Abstracts / Kovarik, Zrinka (ur.).
Zagreb: Hrvatsko društvo za biokemiju i molekularnu biologiju, 2009. str. 99-99 (poster, međunarodna recenzija, sažetak, znanstveni)
Katalinić, M., Rusak, G., Domaćinović Barović, J., Šinko, G., Jelić, D., Antolović, R. & Kovarik, Z. (2009) Structural aspects of flavonoids as inhibitors of human butyrylcholinesterase. U: Kovarik, Z. (ur.)10th International Meeting on Cholinesterases, Šibenik, Hrvatska, Programme and Abstracts.
@article{article, editor = {Kovarik, Z.}, year = {2009}, pages = {99-99}, keywords = {Acetylcholinesterase, Cholinesterase, Cytotoxicity, Flavonoids, UV-VIS spectra, Reversible inhibition}, isbn = {978-953-95551-3-7}, title = {Structural aspects of flavonoids as inhibitors of human butyrylcholinesterase}, keyword = {Acetylcholinesterase, Cholinesterase, Cytotoxicity, Flavonoids, UV-VIS spectra, Reversible inhibition}, publisher = {Hrvatsko dru\v{s}tvo za biokemiju i molekularnu biologiju}, publisherplace = {\v{S}ibenik, Hrvatska} }
@article{article, editor = {Kovarik, Z.}, year = {2009}, pages = {99-99}, keywords = {Acetylcholinesterase, Cholinesterase, Cytotoxicity, Flavonoids, UV-VIS spectra, Reversible inhibition}, isbn = {978-953-95551-3-7}, title = {Structural aspects of flavonoids as inhibitors of human butyrylcholinesterase}, keyword = {Acetylcholinesterase, Cholinesterase, Cytotoxicity, Flavonoids, UV-VIS spectra, Reversible inhibition}, publisher = {Hrvatsko dru\v{s}tvo za biokemiju i molekularnu biologiju}, publisherplace = {\v{S}ibenik, Hrvatska} }




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