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Luteolin,quercetin, genistein and quercetagetin inhibit the effects of lipopolysaccharide obtained from <Emphasis Type="Italic">Porphyromonas gingivalis</Emphasis> in H9c2 cardiomyoblasts
Authors:Gloria Gutiérrez-Venegas  Alfredo Torras-Ceballos  Juan Arturo Gómez-Mora  Berenice Fernández-Rojas
Institution:1.Laboratorio de Bioquímica de la División de Estudios de Posgrado de la Facultad de Odontología,Universidad Nacional Autónoma de México Ciudad Universitaria,México DF,Mexico
Abstract:

Background

One of the microorganisms from dental plaque associated with severe inflammatory responses in infectious endocarditis is Porphyromonas gingivalis. It is a Gram-negative bacteria harvested from chronic periodontitis patients. Lipopolysaccharide (LPS) obtained from P. gingivalis promotes the expressions of interleukin-1 (IL-1), IL-6 and tumor necrosis factor alpha (TNF-α). Flavonoids are thought to participate in processes that control inflammation, such as the expression of cyclooxygenase-2 (COX-2).

Methods

We investigated the effects of luteolin, quercetin, genistein and quercetagetin on cardiomyoblasts treated with LPS alone or in combination with following inhibitors p38 (SB203580), ERK (PD98059), JNK (SP600125) and PKC (Calphostin C) for 1 h. The kinase activation and COX-2 expression levels were determined at the gene and protein levels.

Results

These flavonoids are considered to inhibit the activation of mitogen-activated protein kinase (MAPK) and the degradation of inhibitor of kappa B-alpha (IκB-α). They also play a role in COX-2 expression.

Conclusion

We conclude that the tested flavonoids inhibit inflammatory responses induced by LPS in H9c2 cells.
Keywords:
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