Inhibition of lipopolysaccharide (LPS)-induced endothelial cytotoxicity by selected flavonoids

被引:10
作者
Melzig, MF
Loose, R
机构
[1] Humboldt Univ, Inst Pharm, D-13086 Berlin, Germany
[2] Res Inst Mol Pharmacol, Berlin, Germany
关键词
flavonoids; endothelial cells; lipopolysaccharides; toxicity; tyrosine kinases;
D O I
10.1055/s-2006-957467
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
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 846, 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.
引用
收藏
页码:397 / 399
页数:3
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