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Comparative effect of genistein and daidzein on the expression of MCP-1, eNOS, and cell adhesion molecules in TNF-α-stimulated HUVECs. | LitMetric

AI Article Synopsis

  • The study compared genistein and daidzein's effects on chemokines, cell adhesion molecules, and eNOS in human umbilical vascular endothelial cells triggered by TNF-α.
  • Genistein significantly reduced the production of MCP-1 and VCAM-1, while daidzein had a minor effect on MCP-1 and neither substantially impacted CAM expression.
  • Both compounds enhanced eNOS expression and nitric oxide production, with low concentrations of isoflavones inhibiting NFκB activation, suggesting genistein is more effective than daidzein in this context.

Article Abstract

We compared the effects of genistein and daidzein on the expression of chemokines, cell adhesion molecules (CAMs), and endothelial nitric oxide synthase (eNOS) in tumor necrosis factor (TNF)-α-stimulated human umbilical vascular endothelial cells (HUVECs). TNF-α exposure significantly increased expression of monocyte chemoattractant protein (MCP)-1, vascular adhesion molecule (VCAM)-1, and intercellular adhesion molecule-1. Genistein significantly decreased MCP-1 and VCAM-1 production in a dose-dependent manner, whereas CAM expression was not significantly lowered by genistein treatment. However, daidzein slightly decreased MCP-1 production. The effects of genistein and daidzein on MCP-1 secretion coincided with mRNA expression. Pre-treatment with either genistein or daidzein elevated eNOS expression and nitric oxide production disturbed by TNF-α exposure. A low concentration of isoflavones significantly inhibited nuclear factor (NF)κB activation, whereas a high dose slightly ameliorated these inhibitive effects. These results suggest that genistein had a stronger effect on MCP-1 and eNOS expression than that of daidzein. Additionally, NFκB transactivation might be partially related to the down-regulation of these mRNAs in TNF-α-stimulated HUVECs.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3221822PMC
http://dx.doi.org/10.4162/nrp.2011.5.5.381DOI Listing

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