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Alkaloids in Erythrina by UPLC-ESI-MS and In Vivo Hypotensive Potential of Extractive Preparations
Erythrina species are used in popular medicine as sedative, anxiolytic, anti-inflammatory, and antihypertensive. In this work, we investigated the chemical composition of extracts obtained from leaves of E. falcata and E. crista-galli. The hypotensive potential of E. falcata and the mechanism of act...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4556073/ https://www.ncbi.nlm.nih.gov/pubmed/26356581 http://dx.doi.org/10.1155/2015/959081 |
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author | Merlugo, Liara Santos, Marí C. Sant'Anna, Liane S. Cordeiro, Everson W. F. Batista, Luiz A. C. Miotto, Silvia T. S. Garcia, Cássia V. Moreira, Cleci M. Mendez, Andreas S. L. |
author_facet | Merlugo, Liara Santos, Marí C. Sant'Anna, Liane S. Cordeiro, Everson W. F. Batista, Luiz A. C. Miotto, Silvia T. S. Garcia, Cássia V. Moreira, Cleci M. Mendez, Andreas S. L. |
author_sort | Merlugo, Liara |
collection | PubMed |
description | Erythrina species are used in popular medicine as sedative, anxiolytic, anti-inflammatory, and antihypertensive. In this work, we investigated the chemical composition of extracts obtained from leaves of E. falcata and E. crista-galli. The hypotensive potential of E. falcata and the mechanism of action were also studied. The extracts were obtained by maceration and infusion. The total content of phenolic compounds and flavonoids was estimated by spectrophotometric methods. The chemical constituents were studied performing a chromatographic analysis by UPLC-ESI-MS. For in vivo protocols, blood pressure and heart rate were measured by the invasive hemodynamic monitoring method. Different concentrations of extracts and drugs such as L-NAME, losartan, hexamethonium, and propranolol were administrated i.v. The results of total phenolic contents for E. falcata and E. crista-galli were 1.3193–1.4989 mgGAE/mL for maceration and 0.8771–0.9506 mgGAE/mL for infusion. In total flavonoids, the content was 7.7829–8.1976 mg RE/g for maceration and 9.3471–10.4765 RE mg/g for infusion. The chemical composition was based on alkaloids, suggesting the presence of erythristemine, 11β-methoxyglucoerysodine, erysothiopine, 11β-hydroxyerysodine-glucose, and 11-hydroxyerysotinone-rhamnoside. A potent dose-dependent hypotensive effect was observed for E. falcata, which may be related to the route of β-adrenergic receptors. |
format | Online Article Text |
id | pubmed-4556073 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-45560732015-09-09 Alkaloids in Erythrina by UPLC-ESI-MS and In Vivo Hypotensive Potential of Extractive Preparations Merlugo, Liara Santos, Marí C. Sant'Anna, Liane S. Cordeiro, Everson W. F. Batista, Luiz A. C. Miotto, Silvia T. S. Garcia, Cássia V. Moreira, Cleci M. Mendez, Andreas S. L. Evid Based Complement Alternat Med Research Article Erythrina species are used in popular medicine as sedative, anxiolytic, anti-inflammatory, and antihypertensive. In this work, we investigated the chemical composition of extracts obtained from leaves of E. falcata and E. crista-galli. The hypotensive potential of E. falcata and the mechanism of action were also studied. The extracts were obtained by maceration and infusion. The total content of phenolic compounds and flavonoids was estimated by spectrophotometric methods. The chemical constituents were studied performing a chromatographic analysis by UPLC-ESI-MS. For in vivo protocols, blood pressure and heart rate were measured by the invasive hemodynamic monitoring method. Different concentrations of extracts and drugs such as L-NAME, losartan, hexamethonium, and propranolol were administrated i.v. The results of total phenolic contents for E. falcata and E. crista-galli were 1.3193–1.4989 mgGAE/mL for maceration and 0.8771–0.9506 mgGAE/mL for infusion. In total flavonoids, the content was 7.7829–8.1976 mg RE/g for maceration and 9.3471–10.4765 RE mg/g for infusion. The chemical composition was based on alkaloids, suggesting the presence of erythristemine, 11β-methoxyglucoerysodine, erysothiopine, 11β-hydroxyerysodine-glucose, and 11-hydroxyerysotinone-rhamnoside. A potent dose-dependent hypotensive effect was observed for E. falcata, which may be related to the route of β-adrenergic receptors. Hindawi Publishing Corporation 2015 2015-08-18 /pmc/articles/PMC4556073/ /pubmed/26356581 http://dx.doi.org/10.1155/2015/959081 Text en Copyright © 2015 Liara Merlugo et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Merlugo, Liara Santos, Marí C. Sant'Anna, Liane S. Cordeiro, Everson W. F. Batista, Luiz A. C. Miotto, Silvia T. S. Garcia, Cássia V. Moreira, Cleci M. Mendez, Andreas S. L. Alkaloids in Erythrina by UPLC-ESI-MS and In Vivo Hypotensive Potential of Extractive Preparations |
title | Alkaloids in Erythrina by UPLC-ESI-MS and In Vivo Hypotensive Potential of Extractive Preparations |
title_full | Alkaloids in Erythrina by UPLC-ESI-MS and In Vivo Hypotensive Potential of Extractive Preparations |
title_fullStr | Alkaloids in Erythrina by UPLC-ESI-MS and In Vivo Hypotensive Potential of Extractive Preparations |
title_full_unstemmed | Alkaloids in Erythrina by UPLC-ESI-MS and In Vivo Hypotensive Potential of Extractive Preparations |
title_short | Alkaloids in Erythrina by UPLC-ESI-MS and In Vivo Hypotensive Potential of Extractive Preparations |
title_sort | alkaloids in erythrina by uplc-esi-ms and in vivo hypotensive potential of extractive preparations |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4556073/ https://www.ncbi.nlm.nih.gov/pubmed/26356581 http://dx.doi.org/10.1155/2015/959081 |
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