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Characterization of the Metabolic Fate of Datura metel Seed Extract and Its Main Constituents in Rats
Datura metel L. has been frequently used in Chinese traditional medicine. However, little is known on the chemical composition and in vivo metabolism of its seeds. In this study, using the strategy “chemical analysis, metabolism of single representative compounds, and metabolism of extract at clinic...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6546908/ https://www.ncbi.nlm.nih.gov/pubmed/31191311 http://dx.doi.org/10.3389/fphar.2019.00571 |
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author | Xia, Cong Liu, Yan Qi, Hai Niu, Lulu Zhu, Yuxuan Lu, Wanying Xu, Xinyi Su, Yongjian Yang, Bingyou Wang, Qi |
author_facet | Xia, Cong Liu, Yan Qi, Hai Niu, Lulu Zhu, Yuxuan Lu, Wanying Xu, Xinyi Su, Yongjian Yang, Bingyou Wang, Qi |
author_sort | Xia, Cong |
collection | PubMed |
description | Datura metel L. has been frequently used in Chinese traditional medicine. However, little is known on the chemical composition and in vivo metabolism of its seeds. In this study, using the strategy “chemical analysis, metabolism of single representative compounds, and metabolism of extract at clinical dosage” that we propose here, 42 constituents were characterized from D. metel seeds water extract. Furthermore, the metabolic pathways of 13 representative bioactive compounds of D. metel seeds were studied in rats after the oral administration of D. metel seeds water extract at a clinical dosage (0.15 g/kg). These included three withanolides, two withanolide glucosides, four amides, one indole, one triterpenoid, one steroid, and one sesquiterpenoid, and with regard to phase II metabolism, hydroxylation, (de)methylation, and dehydrogenation reactions were dominant. Furthermore, the metabolism of D. metel seeds water extract provided to rats at a clinical dosage was investigated by liquid chromatography-tandem mass spectrometry based on the above metabolic pathways. Sixty-one compounds were detected in plasma, 83 in urine, and 76 in fecal samples. Among them, withanolides exhibited higher plasma exposure than the other types. To our knowledge, this is the first systematic study on the chemical profiling and metabolite identification of D. metel seeds, including all compounds instead of single constituents. |
format | Online Article Text |
id | pubmed-6546908 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-65469082019-06-12 Characterization of the Metabolic Fate of Datura metel Seed Extract and Its Main Constituents in Rats Xia, Cong Liu, Yan Qi, Hai Niu, Lulu Zhu, Yuxuan Lu, Wanying Xu, Xinyi Su, Yongjian Yang, Bingyou Wang, Qi Front Pharmacol Pharmacology Datura metel L. has been frequently used in Chinese traditional medicine. However, little is known on the chemical composition and in vivo metabolism of its seeds. In this study, using the strategy “chemical analysis, metabolism of single representative compounds, and metabolism of extract at clinical dosage” that we propose here, 42 constituents were characterized from D. metel seeds water extract. Furthermore, the metabolic pathways of 13 representative bioactive compounds of D. metel seeds were studied in rats after the oral administration of D. metel seeds water extract at a clinical dosage (0.15 g/kg). These included three withanolides, two withanolide glucosides, four amides, one indole, one triterpenoid, one steroid, and one sesquiterpenoid, and with regard to phase II metabolism, hydroxylation, (de)methylation, and dehydrogenation reactions were dominant. Furthermore, the metabolism of D. metel seeds water extract provided to rats at a clinical dosage was investigated by liquid chromatography-tandem mass spectrometry based on the above metabolic pathways. Sixty-one compounds were detected in plasma, 83 in urine, and 76 in fecal samples. Among them, withanolides exhibited higher plasma exposure than the other types. To our knowledge, this is the first systematic study on the chemical profiling and metabolite identification of D. metel seeds, including all compounds instead of single constituents. Frontiers Media S.A. 2019-05-28 /pmc/articles/PMC6546908/ /pubmed/31191311 http://dx.doi.org/10.3389/fphar.2019.00571 Text en Copyright © 2019 Xia, Liu, Qi, Niu, Zhu, Lu, Xu, Su, Yang and Wang. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Pharmacology Xia, Cong Liu, Yan Qi, Hai Niu, Lulu Zhu, Yuxuan Lu, Wanying Xu, Xinyi Su, Yongjian Yang, Bingyou Wang, Qi Characterization of the Metabolic Fate of Datura metel Seed Extract and Its Main Constituents in Rats |
title | Characterization of the Metabolic Fate of Datura metel Seed Extract and Its Main Constituents in Rats |
title_full | Characterization of the Metabolic Fate of Datura metel Seed Extract and Its Main Constituents in Rats |
title_fullStr | Characterization of the Metabolic Fate of Datura metel Seed Extract and Its Main Constituents in Rats |
title_full_unstemmed | Characterization of the Metabolic Fate of Datura metel Seed Extract and Its Main Constituents in Rats |
title_short | Characterization of the Metabolic Fate of Datura metel Seed Extract and Its Main Constituents in Rats |
title_sort | characterization of the metabolic fate of datura metel seed extract and its main constituents in rats |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6546908/ https://www.ncbi.nlm.nih.gov/pubmed/31191311 http://dx.doi.org/10.3389/fphar.2019.00571 |
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