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In vitro human fecal microbial metabolism of Forsythoside A and biological activities of its metabolites
The present study aimed to investigate the metabolism of Forsythoside A (FTA) by human fecal bacteria to clarify the relationship between its intestinal metabolism and its pharmacological activities. FTA was incubated with human fecal microflora in vitro to investigate its metabolic process, and hig...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier B.V.
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7126381/ https://www.ncbi.nlm.nih.gov/pubmed/25281775 http://dx.doi.org/10.1016/j.fitote.2014.09.018 |
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author | Xing, Shihua Peng, Ying Wang, Mengyue Chen, Daofeng Li, Xiaobo |
author_facet | Xing, Shihua Peng, Ying Wang, Mengyue Chen, Daofeng Li, Xiaobo |
author_sort | Xing, Shihua |
collection | PubMed |
description | The present study aimed to investigate the metabolism of Forsythoside A (FTA) by human fecal bacteria to clarify the relationship between its intestinal metabolism and its pharmacological activities. FTA was incubated with human fecal microflora in vitro to investigate its metabolic process, and highly sensitive and specific ultra-performance liquid chromatography/quadrupole time-of-flight mass spectrometry (UPLC–Q-TOF/MS) was performed using MetaboLynx™ software for metabolite analysis. Caffeic acid (CA) and hydroxytyrosol (HT) were obtained by hydrolysis of FTA, and CA was further hydrogenated to form 3,4-dihydroxybenzenepropionic acid (DCA). The anticomplementary, antimicrobial and antiendotoxin activities of FTA and its metabolites by human fecal microflora were evaluated in vitro with a hemolysis assay, the agar disc-diffusion method, the MIC value and the gel clot LAL assay, respectively. The metabolites showed higher biological activity than FTA, especially HT and DCA. Orally administered FTA may be metabolized to HT and DCA, and the pharmacological effects of FTA may be dependent on intestinal bacterial metabolism. |
format | Online Article Text |
id | pubmed-7126381 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71263812020-04-08 In vitro human fecal microbial metabolism of Forsythoside A and biological activities of its metabolites Xing, Shihua Peng, Ying Wang, Mengyue Chen, Daofeng Li, Xiaobo Fitoterapia Article The present study aimed to investigate the metabolism of Forsythoside A (FTA) by human fecal bacteria to clarify the relationship between its intestinal metabolism and its pharmacological activities. FTA was incubated with human fecal microflora in vitro to investigate its metabolic process, and highly sensitive and specific ultra-performance liquid chromatography/quadrupole time-of-flight mass spectrometry (UPLC–Q-TOF/MS) was performed using MetaboLynx™ software for metabolite analysis. Caffeic acid (CA) and hydroxytyrosol (HT) were obtained by hydrolysis of FTA, and CA was further hydrogenated to form 3,4-dihydroxybenzenepropionic acid (DCA). The anticomplementary, antimicrobial and antiendotoxin activities of FTA and its metabolites by human fecal microflora were evaluated in vitro with a hemolysis assay, the agar disc-diffusion method, the MIC value and the gel clot LAL assay, respectively. The metabolites showed higher biological activity than FTA, especially HT and DCA. Orally administered FTA may be metabolized to HT and DCA, and the pharmacological effects of FTA may be dependent on intestinal bacterial metabolism. Elsevier B.V. 2014-12 2014-10-02 /pmc/articles/PMC7126381/ /pubmed/25281775 http://dx.doi.org/10.1016/j.fitote.2014.09.018 Text en Copyright © 2014 Elsevier B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Xing, Shihua Peng, Ying Wang, Mengyue Chen, Daofeng Li, Xiaobo In vitro human fecal microbial metabolism of Forsythoside A and biological activities of its metabolites |
title | In vitro human fecal microbial metabolism of Forsythoside A and biological activities of its metabolites |
title_full | In vitro human fecal microbial metabolism of Forsythoside A and biological activities of its metabolites |
title_fullStr | In vitro human fecal microbial metabolism of Forsythoside A and biological activities of its metabolites |
title_full_unstemmed | In vitro human fecal microbial metabolism of Forsythoside A and biological activities of its metabolites |
title_short | In vitro human fecal microbial metabolism of Forsythoside A and biological activities of its metabolites |
title_sort | in vitro human fecal microbial metabolism of forsythoside a and biological activities of its metabolites |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7126381/ https://www.ncbi.nlm.nih.gov/pubmed/25281775 http://dx.doi.org/10.1016/j.fitote.2014.09.018 |
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