Pentacyclic triterpenoids and ceramide mediate the vasorelaxant activity of Vitex cienkowskii via involvement of NO/cGMP pathway in isolated rat aortic rings
Dongmo AB, Azebaze AGB, Donfack FM, Dimo T, Nkeng-Efouet PA, Devkota KP, Sontia B, Wagner H, Sewald N, Vierling W (2011)
Journal of Ethnopharmacology 133(1): 204-212.
Zeitschriftenaufsatz
| Veröffentlicht | Englisch
Download
Es wurden keine Dateien hochgeladen. Nur Publikationsnachweis!
Autor*in
Dongmo, Alain Bertrand;
Azebaze, Anatole Guy Blaise;
Donfack, Flaure Metchi;
Dimo, Theophile;
Nkeng-Efouet, Pepin Alango;
Devkota, Krishna Prasad;
Sontia, Bruno;
Wagner, Hildebert;
Sewald, NorbertUniBi ;
Vierling, Wolfgang
Einrichtung
Abstract / Bemerkung
Ethnopharmacological relevance: Vitex cienkowskii Kotschy & Peyritsch is a deciduous tree, prescribed by Cameroonian traditional healers as one of the most popular plant widely used in many disorders including cardiovascular diseases. The preliminary pharmacological studies carried out on Vitex cienkowskii showed its vasorelaxant activities on guinea-pig aortic rings. Aim of the study: The present work evaluated the vasorelaxant activity of extract and isolated compounds from Vitex cienkowskii. Materials and methods: Rat aortic rings were used to evaluate the in vitro vascular effect of the extract. The antioxidant activity was determined by measuring the reduction of the free radical 1,1-diphenyl-1-picryl-hydrazyl (DPPH). Results: Vitex cienkowskii induced significant relaxation in a concentration- and endothelium-dependent manner (EC50 = 12.12 mu g/ml, CH2Cl2-MeOH, 1:1) and did not produce a vasorelaxant effect on contraction evoked by KCl (60 mM). In order to determine its mode of action, Vitex cienkowskii-induced relaxant effect was evaluated in the presence of indomethacin (10 mu M), L-NAME (100 mu M), ODQ (1 mu M) and SQ22356 (100 mu M). Relaxation was significantly blocked by L-NAME and ODQ. These results indicate that Vitex cienkowskii-mediated relaxation is endothelium dependent, probably due to NO release, and the consequent activation of vascular smooth muscle soluble guanylate cyclase (sGC), a signal transduction enzyme that forms the second messenger cGMP. Bio-guided study of Vitex cienkowskii allowed the isolation of the known pentacyclic triterpenoids and a ceramide. It is the first report of salvin A, maslinic acid and a ceramide from Vitex cienkowskii. The activity induced by these compounds indicated that they may be partly responsible for the vasorelaxant effect of the plant extract. A dose of 40 mg/kg of CH2Cl2-MeOH (1:1) extract administered intravenously induced a decrease of mean arterial pressure but did not affect the heart rate. Moreover the plant extracts were found to be highly active in the DPPH radical scavenging assay. Conclusion: Vitex cienkowskii extract possesses antioxidant property, vasorelaxing, and hypotensive effect linked to the endothelium related factors, where nitric oxide is involved. (C) 2010 Elsevier Ireland Ltd. All rights reserved.
Stichworte
cGMP;
Pentacyclic triterpenoids;
Vitex cienkowskii;
Relaxation;
muscle;
Aortic smooth;
Nitric oxide
Erscheinungsjahr
2011
Zeitschriftentitel
Journal of Ethnopharmacology
Band
133
Ausgabe
1
Seite(n)
204-212
ISSN
0378-8741
Page URI
https://pub.uni-bielefeld.de/record/2003168
Zitieren
Dongmo AB, Azebaze AGB, Donfack FM, et al. Pentacyclic triterpenoids and ceramide mediate the vasorelaxant activity of Vitex cienkowskii via involvement of NO/cGMP pathway in isolated rat aortic rings. Journal of Ethnopharmacology. 2011;133(1):204-212.
Dongmo, A. B., Azebaze, A. G. B., Donfack, F. M., Dimo, T., Nkeng-Efouet, P. A., Devkota, K. P., Sontia, B., et al. (2011). Pentacyclic triterpenoids and ceramide mediate the vasorelaxant activity of Vitex cienkowskii via involvement of NO/cGMP pathway in isolated rat aortic rings. Journal of Ethnopharmacology, 133(1), 204-212. https://doi.org/10.1016/j.jep.2010.09.033
Dongmo, Alain Bertrand, Azebaze, Anatole Guy Blaise, Donfack, Flaure Metchi, Dimo, Theophile, Nkeng-Efouet, Pepin Alango, Devkota, Krishna Prasad, Sontia, Bruno, Wagner, Hildebert, Sewald, Norbert, and Vierling, Wolfgang. 2011. “Pentacyclic triterpenoids and ceramide mediate the vasorelaxant activity of Vitex cienkowskii via involvement of NO/cGMP pathway in isolated rat aortic rings”. Journal of Ethnopharmacology 133 (1): 204-212.
Dongmo, A. B., Azebaze, A. G. B., Donfack, F. M., Dimo, T., Nkeng-Efouet, P. A., Devkota, K. P., Sontia, B., Wagner, H., Sewald, N., and Vierling, W. (2011). Pentacyclic triterpenoids and ceramide mediate the vasorelaxant activity of Vitex cienkowskii via involvement of NO/cGMP pathway in isolated rat aortic rings. Journal of Ethnopharmacology 133, 204-212.
Dongmo, A.B., et al., 2011. Pentacyclic triterpenoids and ceramide mediate the vasorelaxant activity of Vitex cienkowskii via involvement of NO/cGMP pathway in isolated rat aortic rings. Journal of Ethnopharmacology, 133(1), p 204-212.
A.B. Dongmo, et al., “Pentacyclic triterpenoids and ceramide mediate the vasorelaxant activity of Vitex cienkowskii via involvement of NO/cGMP pathway in isolated rat aortic rings”, Journal of Ethnopharmacology, vol. 133, 2011, pp. 204-212.
Dongmo, A.B., Azebaze, A.G.B., Donfack, F.M., Dimo, T., Nkeng-Efouet, P.A., Devkota, K.P., Sontia, B., Wagner, H., Sewald, N., Vierling, W.: Pentacyclic triterpenoids and ceramide mediate the vasorelaxant activity of Vitex cienkowskii via involvement of NO/cGMP pathway in isolated rat aortic rings. Journal of Ethnopharmacology. 133, 204-212 (2011).
Dongmo, Alain Bertrand, Azebaze, Anatole Guy Blaise, Donfack, Flaure Metchi, Dimo, Theophile, Nkeng-Efouet, Pepin Alango, Devkota, Krishna Prasad, Sontia, Bruno, Wagner, Hildebert, Sewald, Norbert, and Vierling, Wolfgang. “Pentacyclic triterpenoids and ceramide mediate the vasorelaxant activity of Vitex cienkowskii via involvement of NO/cGMP pathway in isolated rat aortic rings”. Journal of Ethnopharmacology 133.1 (2011): 204-212.
Daten bereitgestellt von European Bioinformatics Institute (EBI)
CHEBI
1 Eintrag gefunden, die diesen Artikel zitieren
6 Zitationen in Europe PMC
Daten bereitgestellt von Europe PubMed Central.
Vascular Endothelium-Dependent and Independent Actions of Oleanolic Acid and Its Synthetic Oleanane Derivatives as Possible Mechanisms for Hypotensive Effects.
Madlala HP, Metzinger T, van Heerden FR, Musabayane CT, Mubagwa K, Dessy C., PLoS One 11(1), 2016
PMID: 26799746
Madlala HP, Metzinger T, van Heerden FR, Musabayane CT, Mubagwa K, Dessy C., PLoS One 11(1), 2016
PMID: 26799746
Changes in Renal Function and Oxidative Status Associated with the Hypotensive Effects of Oleanolic Acid and Related Synthetic Derivatives in Experimental Animals.
Madlala HP, Van Heerden FR, Mubagwa K, Musabayane CT., PLoS One 10(6), 2015
PMID: 26046776
Madlala HP, Van Heerden FR, Mubagwa K, Musabayane CT., PLoS One 10(6), 2015
PMID: 26046776
Biotransformations of diterpenoids and triterpenoids: a review.
Bhatti HN, Khera RA., J Asian Nat Prod Res 16(1), 2014
PMID: 24266458
Bhatti HN, Khera RA., J Asian Nat Prod Res 16(1), 2014
PMID: 24266458
Maslinic acid protects vascular smooth muscle cells from oxidative stress through Akt/Nrf2/HO-1 pathway.
Qin X, Qiu C, Zhao L., Mol Cell Biochem 390(1-2), 2014
PMID: 24553817
Qin X, Qiu C, Zhao L., Mol Cell Biochem 390(1-2), 2014
PMID: 24553817
Cameroonian medicinal plants: a bioactivity versus ethnobotanical survey and chemotaxonomic classification.
Ntie-Kang F, Lifongo LL, Mbaze LM, Ekwelle N, Owono Owono LC, Megnassan E, Judson PN, Sippl W, Efange SM., BMC Complement Altern Med 13(), 2013
PMID: 23802859
Ntie-Kang F, Lifongo LL, Mbaze LM, Ekwelle N, Owono Owono LC, Megnassan E, Judson PN, Sippl W, Efange SM., BMC Complement Altern Med 13(), 2013
PMID: 23802859
Preliminary evaluation of the wound healing effect of Vitex doniana sweet (Verbenaceae) in mice.
Amegbor K, Metowogo K, Eklu-Gadegbeku K, Agbonon A, Aklikokou KA, Napo-Koura G, Gbeassor M., Afr J Tradit Complement Altern Med 9(4), 2012
PMID: 23983395
Amegbor K, Metowogo K, Eklu-Gadegbeku K, Agbonon A, Aklikokou KA, Napo-Koura G, Gbeassor M., Afr J Tradit Complement Altern Med 9(4), 2012
PMID: 23983395
References
Daten bereitgestellt von Europe PubMed Central.
Export
Markieren/ Markierung löschen
Markierte Publikationen
Web of Science
Dieser Datensatz im Web of Science®Quellen
PMID: 20920567
PubMed | Europe PMC
Suchen in