RSS-Feed abonnieren
DOI: 10.1055/s-2006-957467
© Georg Thieme Verlag Stuttgart · New York
Inhibition of Lipopolysaccharide (LPS)-lnduced Endothelial Cytotoxicity by Selected Flavonoids
Publikationsverlauf
1997
1998
Publikationsdatum:
04. Januar 2007 (online)
Abstract
The cytotoxic effect of lipopolysaccharide (LPS) was examined on bovine aortic endothelial cell proliferation in vitro. This LPS-induced cytotoxicity (IC50 = 22 ng/ml) was attenuated by selected flavonoids, such as catechin, myricetin, quercetin, hesperitin, and rutin. No inhibitory effect was induced by flavones, morin, kaempferol, chrysin and naringin. The isoflavone genistein, and the synthetic tyrphostin B46, both known inhibitors of tyrosine kinases, also attenuated the toxic LPS effect. The hypothesis was framed that the inhibition of LPS-induced cytotoxicity in bovine aortic endothelial cell cultures by flavonoids could be mediated via inhibition of specific tyrosine kinases.
Key words
Flavonoids - endothelial cells - lipopolysaccharides - toxicity - tyrosine kinases