Planta Med 2015; 81(14): 1270-1276
DOI: 10.1055/s-0035-1546242
Biological and Pharmacological Activity
Original Papers
Georg Thieme Verlag KG Stuttgart · New York

Inhibition of COX-2 and NF-κB1 Gene Expression, NO Production, 5-LOX, and COX-1 and COX-2 Enzymes by Extracts and Constituents of Onopordum acanthium

Ildikó Lajter
1   Department of Pharmacognosy, University of Szeged, Szeged, Hungary
,
San-Po Pan
2   Institute of Pharmaceutical Sciences, Department of Pharmacognosy, Karl-Franzens University Graz, Graz, Austria
,
Stefanie Nikles
2   Institute of Pharmaceutical Sciences, Department of Pharmacognosy, Karl-Franzens University Graz, Graz, Austria
,
Sabine Ortmann
2   Institute of Pharmaceutical Sciences, Department of Pharmacognosy, Karl-Franzens University Graz, Graz, Austria
,
Andrea Vasas
1   Department of Pharmacognosy, University of Szeged, Szeged, Hungary
,
Boglárka Csupor-Löffler
1   Department of Pharmacognosy, University of Szeged, Szeged, Hungary
,
Peter Forgó
1   Department of Pharmacognosy, University of Szeged, Szeged, Hungary
,
Judit Hohmann
1   Department of Pharmacognosy, University of Szeged, Szeged, Hungary
,
Rudolf Bauer
2   Institute of Pharmaceutical Sciences, Department of Pharmacognosy, Karl-Franzens University Graz, Graz, Austria
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Weitere Informationen

Publikationsverlauf

received 29. Dezember 2014
revised 24. Mai 2015

accepted 01. Juni 2015

Publikationsdatum:
18. September 2015 (online)

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Abstract

The present study focused on the investigation of the inhibition of cyclooxygenase-2 and nuclear factor kappa B1 gene expression, nitric oxide production, leukotriene biosynthesis (5-lipoxygenase), and cyclooxygenase-1 and cyclooxygenase-2 enzymes of Onopordum acanthium, and the isolation and identification of its active compounds. From the chloroform soluble part of the MeOH extract prepared from aerial parts, lignans [pinoresinol (1), syringaresinol (2), and medioresinol (3)] and flavonoids [hispidulin (4), nepetin (5), apigenin (6), and luteolin (7)] were isolated by a combination of different chromatographic methods. The structures of the compounds were determined by means of mass spectrometry and 1D- and 2D-nuclear magnetic resonance spectroscopy, and by comparison of the spectral data with literature values. Extracts of different polarity and the isolated compounds obtained from the aerial parts, together with those previously isolated from the roots of the plant [4β,15-dihydro-3-dehydrozaluzanin C (8), zaluzanin C (9), 4β,15,11β,13-tetrahydrozaluzanin C (10), nitidanin diisovalerianate (11), 24-methylenecholesterol (12), and 13-oxo-9Z,11E-octadecadienoic acid (13)], were evaluated for their inhibitory effects on cyclooxygenase-2 and nuclear factor kappa B1 gene expression, inducible nitric oxide synthase, 5-lipoxygenase, and cyclooxygenase-1 and cyclooxygenase-2 enzymes in in vitro assays. It was found that O. acanthium extracts exert strong inhibitory activities in vitro and some lignans, flavonoids, and sesquiterpenes may play a role in these activities. 4β,15-Dihydro-3-dehydrozaluzanin C and zaluzanin C at 20 µM were the most active constituents tested against lipopolysaccharide/interferon-γ-induced nitric oxide production (100.4 ± 0.5 % and 99.4 ± 0.8 %) in the inhibition of cyclooxygenase-2 (98.6 ± 0.2 % and 97.0 ± 1.1 %) and nuclear factor kappa B1 gene expression (76.7 ± 7.3 % and 69.9 ± 3.4 %). Furthermore, it was shown that these inhibitory effects are not due to cytotoxicity of the compounds.