In Vitro anti-inflammatory activity of iridoids and triterpenoid compounds isolated from Phillyrea latifolia L.
Two iridoids, oleuropeoside and ligustroside, and two triterpenoid compounds, oleanolic acid and ursolic acid, ha re been isolated from the leaves of Phillyrea latifolia L. (Oleaceae). These compounds were tested for interactions with the cyclooxygenase (COX) and 5-lipoxygenase (5-LOX) pathways of a...
| Autores: | , , , , , , |
|---|---|
| Tipo de recurso: | artículo |
| Fecha de publicación: | 2000 |
| País: | España |
| Institución: | Universidad de Alcalá (UAH) |
| Repositorio: | e_Buah Biblioteca Digital Universidad de Alcalá |
| Idioma: | inglés |
| OAI Identifier: | oai:ebuah.uah.es:10017/64382 |
| Acceso en línea: | http://hdl.handle.net/10017/64382 https://dx.doi.org/10.1248/bpb.23.1307 |
| Access Level: | acceso abierto |
| Palabra clave: | Phillyrea latifolia Iridoid Triterpenoid PGE(2) LTC4 TXB2 Farmacia Pharmacy |
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In Vitro anti-inflammatory activity of iridoids and triterpenoid compounds isolated from Phillyrea latifolia L.Díaz Lanza, Ana María|||0000-0002-4216-3997Abad, María JoséFernández Matellano, LidiaRecuero, CristinaVillaescusa Castillo, Lucinda|||0000-0001-7187-5515Silván, Ana MaríaBermejo, PaulinaPhillyrea latifoliaIridoidTriterpenoidPGE(2)LTC4TXB2FarmaciaPharmacyTwo iridoids, oleuropeoside and ligustroside, and two triterpenoid compounds, oleanolic acid and ursolic acid, ha re been isolated from the leaves of Phillyrea latifolia L. (Oleaceae). These compounds were tested for interactions with the cyclooxygenase (COX) and 5-lipoxygenase (5-LOX) pathways of arachidonate metabolism in calcium ionophore-stimulated mouse peritoneal macrophages and human platelets, and for their effect on cell viability Structure-activity relationships obtained for in vitro screening results were discussed, These compounds ale capable of exerting inhibitory actions on enzymes of the arachidonate cascade,,ill compounds assayed showed a significant effect on prostaglandin E-2 (PGE(2))-release, with inhibition percentages similar to the reference drug indomethacin (IC50 = 0.95 muM). The IC50 values of the active compounds ate: oleuropeoside 47 muM, ligustroside 38.53 muM, oleanolic acid 23.51 muM and ursolic acid 60.91 muM;. In the leukotriene C-4 (LTC4)-assay, only oleanolic acid showed a significant effect (IC50 = 16.79 muM). We also investigated the action of compounds on thromborane B-2 (TXB2)-release induced by calcium ionophore in human platelets. Of all the tested compounds, only. ligustroside (IC50 = 122.63 muM) and ursolic acid (IC50 = 50.21 muM) showed a significant effect, although with less potency than the reference drug ibuprofen (IC50 = 1.27 muM). Thus, our compounds possess an array of potentially beneficial anti-inflammatory properties which may, alongside other constituents, contribute to the claimed therapeutic properties of the plant from which they are derived.20002000-10-01journal articlehttp://purl.org/coar/resource_type/c_6501NAhttp://purl.org/coar/version/c_be7fb7dd8ff6fe43info:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10017/64382https://dx.doi.org/10.1248/bpb.23.1307reponame:e_Buah Biblioteca Digital Universidad de Alcaláinstname:Universidad de Alcalá (UAH)Inglésengopen accesshttp://purl.org/coar/access_right/c_abf2Attribution-NonCommercial-ShareAlike 4.0 Internationalhttp://creativecommons.org/licenses/by-nc-sa/4.0/info:eu-repo/semantics/openAccessoai:ebuah.uah.es:10017/643822026-06-18T11:13:07Z |
| dc.title.none.fl_str_mv |
In Vitro anti-inflammatory activity of iridoids and triterpenoid compounds isolated from Phillyrea latifolia L. |
| title |
In Vitro anti-inflammatory activity of iridoids and triterpenoid compounds isolated from Phillyrea latifolia L. |
| spellingShingle |
In Vitro anti-inflammatory activity of iridoids and triterpenoid compounds isolated from Phillyrea latifolia L. Díaz Lanza, Ana María|||0000-0002-4216-3997 Phillyrea latifolia Iridoid Triterpenoid PGE(2) LTC4 TXB2 Farmacia Pharmacy |
| title_short |
In Vitro anti-inflammatory activity of iridoids and triterpenoid compounds isolated from Phillyrea latifolia L. |
| title_full |
In Vitro anti-inflammatory activity of iridoids and triterpenoid compounds isolated from Phillyrea latifolia L. |
| title_fullStr |
In Vitro anti-inflammatory activity of iridoids and triterpenoid compounds isolated from Phillyrea latifolia L. |
| title_full_unstemmed |
In Vitro anti-inflammatory activity of iridoids and triterpenoid compounds isolated from Phillyrea latifolia L. |
| title_sort |
In Vitro anti-inflammatory activity of iridoids and triterpenoid compounds isolated from Phillyrea latifolia L. |
| dc.creator.none.fl_str_mv |
Díaz Lanza, Ana María|||0000-0002-4216-3997 Abad, María José Fernández Matellano, Lidia Recuero, Cristina Villaescusa Castillo, Lucinda|||0000-0001-7187-5515 Silván, Ana María Bermejo, Paulina |
| author |
Díaz Lanza, Ana María|||0000-0002-4216-3997 |
| author_facet |
Díaz Lanza, Ana María|||0000-0002-4216-3997 Abad, María José Fernández Matellano, Lidia Recuero, Cristina Villaescusa Castillo, Lucinda|||0000-0001-7187-5515 Silván, Ana María Bermejo, Paulina |
| author_role |
author |
| author2 |
Abad, María José Fernández Matellano, Lidia Recuero, Cristina Villaescusa Castillo, Lucinda|||0000-0001-7187-5515 Silván, Ana María Bermejo, Paulina |
| author2_role |
author author author author author author |
| dc.subject.none.fl_str_mv |
Phillyrea latifolia Iridoid Triterpenoid PGE(2) LTC4 TXB2 Farmacia Pharmacy |
| topic |
Phillyrea latifolia Iridoid Triterpenoid PGE(2) LTC4 TXB2 Farmacia Pharmacy |
| description |
Two iridoids, oleuropeoside and ligustroside, and two triterpenoid compounds, oleanolic acid and ursolic acid, ha re been isolated from the leaves of Phillyrea latifolia L. (Oleaceae). These compounds were tested for interactions with the cyclooxygenase (COX) and 5-lipoxygenase (5-LOX) pathways of arachidonate metabolism in calcium ionophore-stimulated mouse peritoneal macrophages and human platelets, and for their effect on cell viability Structure-activity relationships obtained for in vitro screening results were discussed, These compounds ale capable of exerting inhibitory actions on enzymes of the arachidonate cascade,,ill compounds assayed showed a significant effect on prostaglandin E-2 (PGE(2))-release, with inhibition percentages similar to the reference drug indomethacin (IC50 = 0.95 muM). The IC50 values of the active compounds ate: oleuropeoside 47 muM, ligustroside 38.53 muM, oleanolic acid 23.51 muM and ursolic acid 60.91 muM;. In the leukotriene C-4 (LTC4)-assay, only oleanolic acid showed a significant effect (IC50 = 16.79 muM). We also investigated the action of compounds on thromborane B-2 (TXB2)-release induced by calcium ionophore in human platelets. Of all the tested compounds, only. ligustroside (IC50 = 122.63 muM) and ursolic acid (IC50 = 50.21 muM) showed a significant effect, although with less potency than the reference drug ibuprofen (IC50 = 1.27 muM). Thus, our compounds possess an array of potentially beneficial anti-inflammatory properties which may, alongside other constituents, contribute to the claimed therapeutic properties of the plant from which they are derived. |
| publishDate |
2000 |
| dc.date.none.fl_str_mv |
2000 2000-10-01 |
| dc.type.none.fl_str_mv |
journal article http://purl.org/coar/resource_type/c_6501 NA http://purl.org/coar/version/c_be7fb7dd8ff6fe43 |
| dc.type.openaire.fl_str_mv |
info:eu-repo/semantics/article |
| format |
article |
| dc.identifier.none.fl_str_mv |
http://hdl.handle.net/10017/64382 https://dx.doi.org/10.1248/bpb.23.1307 |
| url |
http://hdl.handle.net/10017/64382 https://dx.doi.org/10.1248/bpb.23.1307 |
| dc.language.none.fl_str_mv |
Inglés eng |
| language_invalid_str_mv |
Inglés |
| language |
eng |
| dc.rights.none.fl_str_mv |
open access http://purl.org/coar/access_right/c_abf2 Attribution-NonCommercial-ShareAlike 4.0 International http://creativecommons.org/licenses/by-nc-sa/4.0/ |
| dc.rights.openaire.fl_str_mv |
info:eu-repo/semantics/openAccess |
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open access http://purl.org/coar/access_right/c_abf2 Attribution-NonCommercial-ShareAlike 4.0 International http://creativecommons.org/licenses/by-nc-sa/4.0/ |
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openAccess |
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application/pdf |
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reponame:e_Buah Biblioteca Digital Universidad de Alcalá instname:Universidad de Alcalá (UAH) |
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Universidad de Alcalá (UAH) |
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e_Buah Biblioteca Digital Universidad de Alcalá |
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e_Buah Biblioteca Digital Universidad de Alcalá |
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