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dc.date.accessioned2020-05-17T18:48:18Z
dc.date.available2020-05-17T18:48:18Z
dc.date.created2019-10-28T14:54:01Z
dc.date.issued2019
dc.identifier.citationZabirnyk, Arsenii Ferrer, Miguel David Bogdanova, Maria A Perez, MM Salcedo, C Kaljusto, Mari-Liis Kvitting, John Peder Escobar Stensløkken, Kåre-Olav Perello, Joan Vaage, Ingvar Jarle . SNF472, a novel anti-crystallization agent, inhibits induced calcification in an in vitro model of human aortic valve calcification. Vascular pharmacology. 2019
dc.identifier.urihttp://hdl.handle.net/10852/75858
dc.description.abstractThe purpose of the present study was to investigate whether SNF472, the hexasodium salt of myo-inositol hexaphosphate (IP6 or phytate): 1. Inhibits induced calcification in cultured aortic valve interstitial cells (VIC) as an in vitro model of aortic valve stenosis and 2. Whether inhibition is different in VIC obtained from healthy and calcified aortic valves. VIC from healthy (n = 5) and calcified (n = 7) human aortic valves were seeded in basic growth medium, osteogenic differentiation medium alone, or in osteogenic medium with SNF472 (3, 10, and 30 μM) and cultivated for 3 weeks. Calcification was quantified spectrophotometrically after Alizarin Red staining. In VIC from calcified valves, a complete inhibition of calcification was observed with SNF472 concentrations of 10 and 30 μM (p < .01), significantly stronger than in VIC from healthy valves. When SNF472 was added to VIC after 1 week in osteogenic medium, 30 and 100 μM SNF472 inhibited the progression of ongoing calcification by 81 and 100% (p < .01), respectively. The same concentrations of SNF472 given after 2 weeks reduced calcification by 35 and 40% respectively (not significant). SNF472 inhibited both the formation and the progression of calcification with the strongest effect in VIC from calcified valves.en_US
dc.languageEN
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.titleSNF472, a novel anti-crystallization agent, inhibits induced calcification in an in vitro model of human aortic valve calcificationen_US
dc.typeJournal articleen_US
dc.creator.authorZabirnyk, Arsenii
dc.creator.authorFerrer, Miguel David
dc.creator.authorBogdanova, Maria A
dc.creator.authorPerez, MM
dc.creator.authorSalcedo, C
dc.creator.authorKaljusto, Mari-Liis
dc.creator.authorKvitting, John Peder Escobar
dc.creator.authorStensløkken, Kåre-Olav
dc.creator.authorPerello, Joan
dc.creator.authorVaage, Ingvar Jarle
cristin.unitcode185,51,12,51
cristin.unitnameHjertefysiologigruppen
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.cristin1741279
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Vascular pharmacology&rft.volume=&rft.spage=&rft.date=2019
dc.identifier.jtitleVascular pharmacology
dc.identifier.volume122-123
dc.identifier.doihttps://doi.org/10.1016/j.vph.2019.106583
dc.identifier.urnURN:NBN:no-78949
dc.type.documentTidsskriftartikkelen_US
dc.type.peerreviewedPeer reviewed
dc.source.issn1537-1891
dc.identifier.fulltextFulltext https://www.duo.uio.no/bitstream/handle/10852/75858/2/SNF472%252C%2Ba%2Bnovel%2Banti-crystallization%2Bagent%252C.pdf
dc.type.versionPublishedVersion
cristin.articleid106583


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