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PXR as a mediator of herb–drug interaction

Medicinal herbs have been a part of human medicine for thousands of years. The herb–drug interaction is an extension of drug–drug interaction, in which the consumptions of herbs cause alterations in the metabolism of drugs the patients happen to take at the same time. The pregnane X receptor (PXR) h...

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Autores principales: Hogle, Brett C., Guan, Xiudong, Folan, M. Maggie, Xie, Wen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taiwan Food and Drug Administration 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9326879/
https://www.ncbi.nlm.nih.gov/pubmed/29703383
http://dx.doi.org/10.1016/j.jfda.2017.11.007
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author Hogle, Brett C.
Guan, Xiudong
Folan, M. Maggie
Xie, Wen
author_facet Hogle, Brett C.
Guan, Xiudong
Folan, M. Maggie
Xie, Wen
author_sort Hogle, Brett C.
collection PubMed
description Medicinal herbs have been a part of human medicine for thousands of years. The herb–drug interaction is an extension of drug–drug interaction, in which the consumptions of herbs cause alterations in the metabolism of drugs the patients happen to take at the same time. The pregnane X receptor (PXR) has been established as one of the most important transcriptional factors that regulate the expression of phase I enzymes, phase II enzymes, and drug transporters in the xenobiotic responses. Since its initial discovery, PXR has been implicated in multiple herb–drug interactions that can lead to alterations of the drug’s pharmacokinetic properties and cause fluctuating therapeutic efficacies, possibly leading to complications. Regions of the world that heavily incorporate herbalism into their primary health care and people turning to alternative medicines as a personal choice could be at risk for adverse reactions or unintended results from these interactions. This article is intended to highlight our understanding of the PXR-mediated herb–drug interactions.
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spelling pubmed-93268792022-08-09 PXR as a mediator of herb–drug interaction Hogle, Brett C. Guan, Xiudong Folan, M. Maggie Xie, Wen J Food Drug Anal Review Article Medicinal herbs have been a part of human medicine for thousands of years. The herb–drug interaction is an extension of drug–drug interaction, in which the consumptions of herbs cause alterations in the metabolism of drugs the patients happen to take at the same time. The pregnane X receptor (PXR) has been established as one of the most important transcriptional factors that regulate the expression of phase I enzymes, phase II enzymes, and drug transporters in the xenobiotic responses. Since its initial discovery, PXR has been implicated in multiple herb–drug interactions that can lead to alterations of the drug’s pharmacokinetic properties and cause fluctuating therapeutic efficacies, possibly leading to complications. Regions of the world that heavily incorporate herbalism into their primary health care and people turning to alternative medicines as a personal choice could be at risk for adverse reactions or unintended results from these interactions. This article is intended to highlight our understanding of the PXR-mediated herb–drug interactions. Taiwan Food and Drug Administration 2017-12-19 /pmc/articles/PMC9326879/ /pubmed/29703383 http://dx.doi.org/10.1016/j.jfda.2017.11.007 Text en © 2018 Taiwan Food and Drug Administration https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC-BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ).
spellingShingle Review Article
Hogle, Brett C.
Guan, Xiudong
Folan, M. Maggie
Xie, Wen
PXR as a mediator of herb–drug interaction
title PXR as a mediator of herb–drug interaction
title_full PXR as a mediator of herb–drug interaction
title_fullStr PXR as a mediator of herb–drug interaction
title_full_unstemmed PXR as a mediator of herb–drug interaction
title_short PXR as a mediator of herb–drug interaction
title_sort pxr as a mediator of herb–drug interaction
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9326879/
https://www.ncbi.nlm.nih.gov/pubmed/29703383
http://dx.doi.org/10.1016/j.jfda.2017.11.007
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