Planta Med 2010; 76(14): 1536-1543
DOI: 10.1055/s-0029-1241013
Pharmacology
Original Papers
© Georg Thieme Verlag KG Stuttgart · New York

Xanthohumol and Related Prenylated Flavonoids Inhibit Inflammatory Cytokine Production in LPS-Activated THP-1 Monocytes: Structure-Activity Relationships and In Silico Binding to Myeloid Differentiation Protein-2 (MD-2)

Michael R. Peluso1 , 2 , Cristobal L. Miranda1 , 2 , Deborah J. Hobbs1 , Rosita R. Proteau2 , Jan Frederik Stevens1 , 2
  • 1Linus Pauling Institute, Oregon State University, Corvallis, Oregon, USA
  • 2Department of Pharmaceutical Sciences, Oregon State University, Corvallis, Oregon, USA
Further Information

Publication History

received Dec. 20, 2009 revised February 14, 2010

accepted February 24, 2010

Publication Date:
22 March 2010 (online)

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Abstract

Xanthohumol (XN) is a prenylated chalcone-type flavonoid found in hops and beer. Our objective of this study was to determine the anti-inflammatory activities of XN, isoxanthohumol (IX), and 15 related prenylated chalcones and flavanones, as well as their structure-activity relationships. The anti-inflammatory activities of the flavonoids were measured by their ability to inhibit lipopolysaccharide (LPS)-induced cytokine production in human monocytic THP-1 cells. The position, number, and length of the prenyl groups had a marked influence on the inhibitory activity of the prenylfavonoids towards MCP-1 and IL-6 production. The α,β-unsaturated carbonyl moiety present in chalcones such as XN was not an absolute requirement for inhibitory activity, as the saturated XN derivative, tetrahydroxanthohumol (TX), showed inhibitory activity comparable to XN. With the aim to determine the mechanism of the observed anti-inflammatory effects, cellular protein levels of Toll-like receptor 4 (TLR4) were measured by Western blot 24 h following coexposure of THP-1 cells to LPS and either XN, TX, or IX. Only XN reduced the cellular TLR4 protein content. Therefore, an additional hypothesis was developed for an anti-inflammatory mechanism that involves the TLR4 coreceptor myeloid differentiation protein-2 (MD-2), which provides the actual binding site for LPS. Molecular docking studies showed that the complementarity of prenylated flavonoids with the hydrophobic MD-2 pocket (indicating goodness of fit) directly predicted their relative ability to inhibit MCP-1 and IL-6 production. In conclusion, prenylated flavonoids may suppress LPS-induced TLR4 activation at least partly by interfering with LPS binding to the TLR4 coreceptor MD-2, and XN (but not other prenylflavonoids) exerts an additional anti-inflammatory effect by downregulating the cellular TLR4 protein content.

References

Prof. Ph.D. Jan Frederik Stevens

Oregon State University
Pharmaceutical Sciences 203 Pharmacy Building

1601 SW Jefferson

Corvallis, OR 97331

United States

Phone: + 1 54 17 37 95 34

Fax: + 1 54 17 37 39 99

Email: fred.stevens@oregonstate.edu