Planta Med 2006; 72(8): 727-734
DOI: 10.1055/s-2006-931588
Original Paper
Biochemistry and Molecular Biology
© Georg Thieme Verlag KG Stuttgart · New York

Gingerol Metabolite and a Synthetic Analogue Capsarol™ Inhibit Macrophage NF-κB-Mediated iNOS Gene Expression and Enzyme Activity

Fugen Aktan1 , 2 , Sheridan Henness1 , Van H. Tran1 , Colin C. Duke1 , Basil D. Roufogalis1 , Alaina J. Ammit1
  • 1Faculty of Pharmacy, University of Sydney, New South Wales, Australia
  • 2Present address: Faculty of Pharmacy, Ankara University, Tandogan, Ankara, Turkey
Further Information

Publication History

Received: October 27, 2005

Accepted: February 21, 2006

Publication Date:
29 May 2006 (online)

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Abstract

Ginger (Zingiber officinale) is widely used in traditional Chinese medicine, with beneficial effects reported in numerous diseases, including inflammation. Inducible nitric oxide synthase (iNOS), a proinflammatory enzyme responsible for the generation of nitric oxide (NO), has been implicated in the pathogenesis of inflammatory diseases. Gingerols, the main pungent principles of ginger, have anti-inflammatory properties in vitro. In this study we examine the inhibitory effect of a stable [6]-gingerol metabolite, rac-[6]-dihydroparadol ([6]-DHP) and a closely related gingerol analogue, rac-2-hydroxy-1-(4-hydroxy-3-methoxyphenyl)dodecan-3-one [a capsaicin/gingerol (Capsarol™) analogue referred to as ZTX42] on NO production, inducible nitric oxide synthase (iNOS) activity and protein expression levels in a murine macrophage cell line, RAW 264.7. Both ZTX42 and [6]-DHP significantly inhibited lipopolysaccharide-induced NO production in a concentration-dependent manner, with an IC50 of 1.45 ± 0.03 μM and 7.24 ± 0.22 μM, respectively (P < 0.05). Although both compounds partially inhibited the catalytic activity of iNOS, their inhibitory effect was predominantly due to attenuation of iNOS protein production. This occurred at the transcriptional level, since the gingerol compounds decreased LPS-induced IκB-α degradation, prevented nuclear translocation of NF-κB p65 and reduced NF-κB activity in a concentration-dependent manner. Taken together, these results show that ZTX42 and [6]-DHP suppress NO production in murine macrophages by partially inhibiting iNOS enzymatic activity and reducing iNOS protein production, via attenuation of NF-κB-mediated iNOS gene expression, providing a rationale for the anti-inflammatory activity reported for this class of compounds.

Abbreviations

ZTX42:rac-2-hydroxy-1-(4-hydroxy-3-methoxyphenyl)dodecan-3-one

COX:cyclo-oxygenase

[6]-DHP:rac-[6]-dihydroparadol

LPS:lipopolysaccharide

MTT:3-(3,4-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide

NF-κB:nuclear factor-κB

NO:nitric oxide

NOS:nitric oxide synthase

PDTC:pyrrolidine dithiocarbamate

TRPV1:vanilloid receptor 1

References

Alaina J. Ammit

Faculty of Pharmacy

Building A15, Room S222

University of Sydney

Sydney

NSW 2006

Australia

Phone: +61-2-9351-6099

Fax: +61-2-9351-4391

Email: ajammit@pharm.usyd.edu.au