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Identification and pharmacological characterization of the anti-inflammatory principal of the leaves of dwarf elder (Sambucus ebulus L.)

AIM OF THE STUDY: The performed investigations aimed on the identification of the anti-inflammatory principal of extracts of leaves of Sambucus ebulus L. (dwarf elder) in order to rationalize the traditional use of this plant for the treatment of chronically inflammatory diseases. MATERIALS AND METH...

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Autores principales: Schwaiger, Stefan, Zeller, Iris, Pölzelbauer, Petra, Frotschnig, Sandra, Laufer, Günther, Messner, Barbara, Pieri, Valerio, Stuppner, Hermann, Bernhard, David
Formato: Texto
Lenguaje:English
Publicado: Elsevier Sequoia 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3029555/
https://www.ncbi.nlm.nih.gov/pubmed/21040770
http://dx.doi.org/10.1016/j.jep.2010.10.049
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author Schwaiger, Stefan
Zeller, Iris
Pölzelbauer, Petra
Frotschnig, Sandra
Laufer, Günther
Messner, Barbara
Pieri, Valerio
Stuppner, Hermann
Bernhard, David
author_facet Schwaiger, Stefan
Zeller, Iris
Pölzelbauer, Petra
Frotschnig, Sandra
Laufer, Günther
Messner, Barbara
Pieri, Valerio
Stuppner, Hermann
Bernhard, David
author_sort Schwaiger, Stefan
collection PubMed
description AIM OF THE STUDY: The performed investigations aimed on the identification of the anti-inflammatory principal of extracts of leaves of Sambucus ebulus L. (dwarf elder) in order to rationalize the traditional use of this plant for the treatment of chronically inflammatory diseases. MATERIALS AND METHODS: Dwarf elder leaf extract was subjected to activity guided fractionation using inhibition of TNFα induced expression of vascular cell adhesion molecule 1 (VCAM-1) on the surface of human umbilical vein endothelial cells (HUVECs) as monitoring tool (positive control: parthenolide 10 μM, VCAM-1 expression (% of control): 5.35 ± 0.38%). RESULTS: Bio-guided isolation resulted in identification of ursolic acid as anti-inflammatory principal. Besides its inhibitory effects against TNFα induced expression of VCAM-1 (IC(50) 6.25 μM), ursolic acid inhibits also TNFα induced expression of ICAM-1 (IC(50) value between 3.13 and 6.25 μM) (positive control: parthenolide 10 μM, ICAM-1 expression (% of control): 38.89 ± 16.6%). Toxic effects of ursolic acid on HUVECs can be drastically reduced using an enriched extract instead of the pure compound. CONCLUSIONS: Our findings suggest an additional mechanism of the anti-inflammatory activity of ursolic acid by demonstrating its ability to inhibit TNFα-stimulated expression of VCAM-1 and ICAM-1 and support the traditional use of extracts and preparations of Sambucus ebulus L., rich in ursolic acid, for the treatment of chronically inflammatory processes.
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spelling pubmed-30295552011-02-10 Identification and pharmacological characterization of the anti-inflammatory principal of the leaves of dwarf elder (Sambucus ebulus L.) Schwaiger, Stefan Zeller, Iris Pölzelbauer, Petra Frotschnig, Sandra Laufer, Günther Messner, Barbara Pieri, Valerio Stuppner, Hermann Bernhard, David J Ethnopharmacol Article AIM OF THE STUDY: The performed investigations aimed on the identification of the anti-inflammatory principal of extracts of leaves of Sambucus ebulus L. (dwarf elder) in order to rationalize the traditional use of this plant for the treatment of chronically inflammatory diseases. MATERIALS AND METHODS: Dwarf elder leaf extract was subjected to activity guided fractionation using inhibition of TNFα induced expression of vascular cell adhesion molecule 1 (VCAM-1) on the surface of human umbilical vein endothelial cells (HUVECs) as monitoring tool (positive control: parthenolide 10 μM, VCAM-1 expression (% of control): 5.35 ± 0.38%). RESULTS: Bio-guided isolation resulted in identification of ursolic acid as anti-inflammatory principal. Besides its inhibitory effects against TNFα induced expression of VCAM-1 (IC(50) 6.25 μM), ursolic acid inhibits also TNFα induced expression of ICAM-1 (IC(50) value between 3.13 and 6.25 μM) (positive control: parthenolide 10 μM, ICAM-1 expression (% of control): 38.89 ± 16.6%). Toxic effects of ursolic acid on HUVECs can be drastically reduced using an enriched extract instead of the pure compound. CONCLUSIONS: Our findings suggest an additional mechanism of the anti-inflammatory activity of ursolic acid by demonstrating its ability to inhibit TNFα-stimulated expression of VCAM-1 and ICAM-1 and support the traditional use of extracts and preparations of Sambucus ebulus L., rich in ursolic acid, for the treatment of chronically inflammatory processes. Elsevier Sequoia 2011-01-27 /pmc/articles/PMC3029555/ /pubmed/21040770 http://dx.doi.org/10.1016/j.jep.2010.10.049 Text en © 2011 Elsevier Ireland Ltd. https://creativecommons.org/licenses/by-nc-nd/3.0/ Open Access under CC BY-NC-ND 3.0 (https://creativecommons.org/licenses/by-nc-nd/3.0/) license
spellingShingle Article
Schwaiger, Stefan
Zeller, Iris
Pölzelbauer, Petra
Frotschnig, Sandra
Laufer, Günther
Messner, Barbara
Pieri, Valerio
Stuppner, Hermann
Bernhard, David
Identification and pharmacological characterization of the anti-inflammatory principal of the leaves of dwarf elder (Sambucus ebulus L.)
title Identification and pharmacological characterization of the anti-inflammatory principal of the leaves of dwarf elder (Sambucus ebulus L.)
title_full Identification and pharmacological characterization of the anti-inflammatory principal of the leaves of dwarf elder (Sambucus ebulus L.)
title_fullStr Identification and pharmacological characterization of the anti-inflammatory principal of the leaves of dwarf elder (Sambucus ebulus L.)
title_full_unstemmed Identification and pharmacological characterization of the anti-inflammatory principal of the leaves of dwarf elder (Sambucus ebulus L.)
title_short Identification and pharmacological characterization of the anti-inflammatory principal of the leaves of dwarf elder (Sambucus ebulus L.)
title_sort identification and pharmacological characterization of the anti-inflammatory principal of the leaves of dwarf elder (sambucus ebulus l.)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3029555/
https://www.ncbi.nlm.nih.gov/pubmed/21040770
http://dx.doi.org/10.1016/j.jep.2010.10.049
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