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The Blood-Brain Barrier Permeability of Lignans and Malabaricones from the Seeds of Myristica fragrans in the MDCK-pHaMDR Cell Monolayer Model
The blood-brain barrier (BBB) permeability of twelve lignans and three phenolic malabaricones from the seeds of Myristica fragrans (nutmeg) were studied with the MDCK-pHaMDR cell monolayer model. The samples were measured by high-performance liquid chromatography and the apparent permeability coeffi...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6274353/ https://www.ncbi.nlm.nih.gov/pubmed/26805808 http://dx.doi.org/10.3390/molecules21020134 |
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author | Wu, Ni Xu, Wei Cao, Gui-Yun Yang, Yan-Fang Yang, Xin-Bao Yang, Xiu-Wei |
author_facet | Wu, Ni Xu, Wei Cao, Gui-Yun Yang, Yan-Fang Yang, Xin-Bao Yang, Xiu-Wei |
author_sort | Wu, Ni |
collection | PubMed |
description | The blood-brain barrier (BBB) permeability of twelve lignans and three phenolic malabaricones from the seeds of Myristica fragrans (nutmeg) were studied with the MDCK-pHaMDR cell monolayer model. The samples were measured by high-performance liquid chromatography and the apparent permeability coefficients (P(app)) were calculated. Among the fifteen test compounds, benzonfuran-type, dibenzylbutane-type and arylnaphthalene-type lignans showed poor to moderate permeabilities with P(app) values at 10(−8)–10(−6) cm/s; those of 8-O-4′-neolignan and tetrahydrofuran-lignan were at 10(−6)–10(−5) cm/s, meaning that their permeabilities are moderate to high; the permeabilities of malabaricones were poor as their P(app) values were at 10(−8)–10(−7) cm/s. To 5-methoxy-dehydrodiisoeugenol (2), erythro-2-(4-allyl-2,6-dimethoxyphenoxy)-1-(3,4-dimethoxyphenyl)-propan-1-ol acetate (6), verrucosin (8), and nectandrin B (9), an efflux way was involved and the main transporter for 6, 8 and 9 was demonstrated to be P-glycoprotein. The time and concentration dependency experiments indicated the main transport mechanism for neolignans dehydrodiisoeugenol (1), myrislignan (7) and 8 was passive diffusion. This study summarized the relationship between the BBB permeability and structure parameters of the test compounds, which could be used to preliminarily predict the transport of a compound through BBB. The results provide a significant molecular basis for better understanding the potential central nervous system effects of nutmeg. |
format | Online Article Text |
id | pubmed-6274353 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62743532018-12-28 The Blood-Brain Barrier Permeability of Lignans and Malabaricones from the Seeds of Myristica fragrans in the MDCK-pHaMDR Cell Monolayer Model Wu, Ni Xu, Wei Cao, Gui-Yun Yang, Yan-Fang Yang, Xin-Bao Yang, Xiu-Wei Molecules Article The blood-brain barrier (BBB) permeability of twelve lignans and three phenolic malabaricones from the seeds of Myristica fragrans (nutmeg) were studied with the MDCK-pHaMDR cell monolayer model. The samples were measured by high-performance liquid chromatography and the apparent permeability coefficients (P(app)) were calculated. Among the fifteen test compounds, benzonfuran-type, dibenzylbutane-type and arylnaphthalene-type lignans showed poor to moderate permeabilities with P(app) values at 10(−8)–10(−6) cm/s; those of 8-O-4′-neolignan and tetrahydrofuran-lignan were at 10(−6)–10(−5) cm/s, meaning that their permeabilities are moderate to high; the permeabilities of malabaricones were poor as their P(app) values were at 10(−8)–10(−7) cm/s. To 5-methoxy-dehydrodiisoeugenol (2), erythro-2-(4-allyl-2,6-dimethoxyphenoxy)-1-(3,4-dimethoxyphenyl)-propan-1-ol acetate (6), verrucosin (8), and nectandrin B (9), an efflux way was involved and the main transporter for 6, 8 and 9 was demonstrated to be P-glycoprotein. The time and concentration dependency experiments indicated the main transport mechanism for neolignans dehydrodiisoeugenol (1), myrislignan (7) and 8 was passive diffusion. This study summarized the relationship between the BBB permeability and structure parameters of the test compounds, which could be used to preliminarily predict the transport of a compound through BBB. The results provide a significant molecular basis for better understanding the potential central nervous system effects of nutmeg. MDPI 2016-01-22 /pmc/articles/PMC6274353/ /pubmed/26805808 http://dx.doi.org/10.3390/molecules21020134 Text en © 2016 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons by Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Wu, Ni Xu, Wei Cao, Gui-Yun Yang, Yan-Fang Yang, Xin-Bao Yang, Xiu-Wei The Blood-Brain Barrier Permeability of Lignans and Malabaricones from the Seeds of Myristica fragrans in the MDCK-pHaMDR Cell Monolayer Model |
title | The Blood-Brain Barrier Permeability of Lignans and Malabaricones from the Seeds of Myristica fragrans in the MDCK-pHaMDR Cell Monolayer Model |
title_full | The Blood-Brain Barrier Permeability of Lignans and Malabaricones from the Seeds of Myristica fragrans in the MDCK-pHaMDR Cell Monolayer Model |
title_fullStr | The Blood-Brain Barrier Permeability of Lignans and Malabaricones from the Seeds of Myristica fragrans in the MDCK-pHaMDR Cell Monolayer Model |
title_full_unstemmed | The Blood-Brain Barrier Permeability of Lignans and Malabaricones from the Seeds of Myristica fragrans in the MDCK-pHaMDR Cell Monolayer Model |
title_short | The Blood-Brain Barrier Permeability of Lignans and Malabaricones from the Seeds of Myristica fragrans in the MDCK-pHaMDR Cell Monolayer Model |
title_sort | blood-brain barrier permeability of lignans and malabaricones from the seeds of myristica fragrans in the mdck-phamdr cell monolayer model |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6274353/ https://www.ncbi.nlm.nih.gov/pubmed/26805808 http://dx.doi.org/10.3390/molecules21020134 |
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