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Phytochemical Study of Tapirira guianensis Leaves Guided by Vasodilatory and Antioxidant Activities

The aim of this research was to perform a phytochemical study of the methanol leaves extract of T. guianensis (MET) guided by vasodilatory and antioxidant activities. The chemical profile of MET and the ethyl acetate fraction (EA fraction) was determined by HPLC-UV-MS and EA fraction guided fraction...

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Autores principales: Rodrigues, Amélia M. G., Guimarães, Denise O., Konno, Tatiana U. P., Tinoco, Luzineide W., Barth, Thiago, Aguiar, Fernando A., Lopes, Norberto P., Leal, Ivana C. R., Raimundo, Juliana M., Muzitano, Michelle F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6155791/
https://www.ncbi.nlm.nih.gov/pubmed/28218702
http://dx.doi.org/10.3390/molecules22020304
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author Rodrigues, Amélia M. G.
Guimarães, Denise O.
Konno, Tatiana U. P.
Tinoco, Luzineide W.
Barth, Thiago
Aguiar, Fernando A.
Lopes, Norberto P.
Leal, Ivana C. R.
Raimundo, Juliana M.
Muzitano, Michelle F.
author_facet Rodrigues, Amélia M. G.
Guimarães, Denise O.
Konno, Tatiana U. P.
Tinoco, Luzineide W.
Barth, Thiago
Aguiar, Fernando A.
Lopes, Norberto P.
Leal, Ivana C. R.
Raimundo, Juliana M.
Muzitano, Michelle F.
author_sort Rodrigues, Amélia M. G.
collection PubMed
description The aim of this research was to perform a phytochemical study of the methanol leaves extract of T. guianensis (MET) guided by vasodilatory and antioxidant activities. The chemical profile of MET and the ethyl acetate fraction (EA fraction) was determined by HPLC-UV-MS and EA fraction guided fractionation by reverse-phase chromatography. The vasorelaxant effects of MET, fractions, sub-fractions and constituents were assessed on rat aorta pre-contracted with phenylephrine. Antioxidant activity was evaluated by using a DPPH assay. The results show that MET-induced vasodilation was dependent on NO/cGMP; and that the PI3K/Akt pathway seems to be the main route involved in eNOS activation. The EA fraction showed greater vasodilatory and antioxidant potency and was submitted to further fractionation. This allowed the isolation and characterization of quercetin, quercetin 3-O-(6″-O-galloyl)-β-d-galactopyranoside and 1,4,6-tri-O-galloyl-β-d-glucose. Also, galloyl-HHDP-hexoside and myricetin deoxyhexoside were identified by HPLC-UV-MS. These compounds are being described for the first time for T. guianensis. 1,4,6-tri-O-galloyl-β-d-glucose and quercetin 3-O-(6″-O-galloyl)-β-d-galactopyranoside showed no vasodilatory activity. Quercetin and myricetin glycoside seems to contribute to the MET activity, since they have been reported as vasodilatory flavonoids. MET-induced vasodilation could contribute to the hypotensive effect of T. guianensis previously reported.
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spelling pubmed-61557912018-11-13 Phytochemical Study of Tapirira guianensis Leaves Guided by Vasodilatory and Antioxidant Activities Rodrigues, Amélia M. G. Guimarães, Denise O. Konno, Tatiana U. P. Tinoco, Luzineide W. Barth, Thiago Aguiar, Fernando A. Lopes, Norberto P. Leal, Ivana C. R. Raimundo, Juliana M. Muzitano, Michelle F. Molecules Article The aim of this research was to perform a phytochemical study of the methanol leaves extract of T. guianensis (MET) guided by vasodilatory and antioxidant activities. The chemical profile of MET and the ethyl acetate fraction (EA fraction) was determined by HPLC-UV-MS and EA fraction guided fractionation by reverse-phase chromatography. The vasorelaxant effects of MET, fractions, sub-fractions and constituents were assessed on rat aorta pre-contracted with phenylephrine. Antioxidant activity was evaluated by using a DPPH assay. The results show that MET-induced vasodilation was dependent on NO/cGMP; and that the PI3K/Akt pathway seems to be the main route involved in eNOS activation. The EA fraction showed greater vasodilatory and antioxidant potency and was submitted to further fractionation. This allowed the isolation and characterization of quercetin, quercetin 3-O-(6″-O-galloyl)-β-d-galactopyranoside and 1,4,6-tri-O-galloyl-β-d-glucose. Also, galloyl-HHDP-hexoside and myricetin deoxyhexoside were identified by HPLC-UV-MS. These compounds are being described for the first time for T. guianensis. 1,4,6-tri-O-galloyl-β-d-glucose and quercetin 3-O-(6″-O-galloyl)-β-d-galactopyranoside showed no vasodilatory activity. Quercetin and myricetin glycoside seems to contribute to the MET activity, since they have been reported as vasodilatory flavonoids. MET-induced vasodilation could contribute to the hypotensive effect of T. guianensis previously reported. MDPI 2017-02-18 /pmc/articles/PMC6155791/ /pubmed/28218702 http://dx.doi.org/10.3390/molecules22020304 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Rodrigues, Amélia M. G.
Guimarães, Denise O.
Konno, Tatiana U. P.
Tinoco, Luzineide W.
Barth, Thiago
Aguiar, Fernando A.
Lopes, Norberto P.
Leal, Ivana C. R.
Raimundo, Juliana M.
Muzitano, Michelle F.
Phytochemical Study of Tapirira guianensis Leaves Guided by Vasodilatory and Antioxidant Activities
title Phytochemical Study of Tapirira guianensis Leaves Guided by Vasodilatory and Antioxidant Activities
title_full Phytochemical Study of Tapirira guianensis Leaves Guided by Vasodilatory and Antioxidant Activities
title_fullStr Phytochemical Study of Tapirira guianensis Leaves Guided by Vasodilatory and Antioxidant Activities
title_full_unstemmed Phytochemical Study of Tapirira guianensis Leaves Guided by Vasodilatory and Antioxidant Activities
title_short Phytochemical Study of Tapirira guianensis Leaves Guided by Vasodilatory and Antioxidant Activities
title_sort phytochemical study of tapirira guianensis leaves guided by vasodilatory and antioxidant activities
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6155791/
https://www.ncbi.nlm.nih.gov/pubmed/28218702
http://dx.doi.org/10.3390/molecules22020304
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