Insights from pharmacokinetic models of host-microbiome drug metabolism

Increasing evidence suggests a role of the gut microbiota in patients’ response to medicinal drugs. In our recent study, we combined genomics of human gut commensals and gnotobiotic animal experiments to quantify microbiota and host contributions to drug metabolism. Informed by experimental data, we...

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Main Authors: Maria Zimmermann-Kogadeeva, Michael Zimmermann, Andrew L. Goodman
Format: Article
Language:English
Published: Taylor & Francis Group 2020-05-01
Series:Gut Microbes
Subjects:
Online Access:http://dx.doi.org/10.1080/19490976.2019.1667724
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spelling doaj-3e0bf2b0230940a696273ed3e321338d2021-01-04T18:02:36ZengTaylor & Francis GroupGut Microbes1949-09761949-09842020-05-0111358759610.1080/19490976.2019.16677241667724Insights from pharmacokinetic models of host-microbiome drug metabolismMaria Zimmermann-Kogadeeva0Michael Zimmermann1Andrew L. Goodman2Yale University School of MedicineYale University School of MedicineYale University School of MedicineIncreasing evidence suggests a role of the gut microbiota in patients’ response to medicinal drugs. In our recent study, we combined genomics of human gut commensals and gnotobiotic animal experiments to quantify microbiota and host contributions to drug metabolism. Informed by experimental data, we built a physiology-based pharmacokinetic model of drug metabolism that includes intestinal compartments with microbiome drug-metabolizing activity. This model successfully predicted serum levels of metabolites of three different drugs, quantified microbial contribution to systemic drug metabolite exposure, and simulated the effect of different parameters on host and microbiota drug metabolism. In this addendum, we expand these simulations to assess the effect of microbiota on the systemic drug and metabolite levels under conditions of altered host physiology, microbiota drug-metabolizing activity or physico-chemical properties of drugs. This work illustrates how and under which circumstances the gut microbiome may influence drug pharmacokinetics, and discusses broader implications of expanded pharmacokinetic models.http://dx.doi.org/10.1080/19490976.2019.1667724gut microbiotadrug metabolismphysiology-based pharmacokinetic modeling
collection DOAJ
language English
format Article
sources DOAJ
author Maria Zimmermann-Kogadeeva
Michael Zimmermann
Andrew L. Goodman
spellingShingle Maria Zimmermann-Kogadeeva
Michael Zimmermann
Andrew L. Goodman
Insights from pharmacokinetic models of host-microbiome drug metabolism
Gut Microbes
gut microbiota
drug metabolism
physiology-based pharmacokinetic modeling
author_facet Maria Zimmermann-Kogadeeva
Michael Zimmermann
Andrew L. Goodman
author_sort Maria Zimmermann-Kogadeeva
title Insights from pharmacokinetic models of host-microbiome drug metabolism
title_short Insights from pharmacokinetic models of host-microbiome drug metabolism
title_full Insights from pharmacokinetic models of host-microbiome drug metabolism
title_fullStr Insights from pharmacokinetic models of host-microbiome drug metabolism
title_full_unstemmed Insights from pharmacokinetic models of host-microbiome drug metabolism
title_sort insights from pharmacokinetic models of host-microbiome drug metabolism
publisher Taylor & Francis Group
series Gut Microbes
issn 1949-0976
1949-0984
publishDate 2020-05-01
description Increasing evidence suggests a role of the gut microbiota in patients’ response to medicinal drugs. In our recent study, we combined genomics of human gut commensals and gnotobiotic animal experiments to quantify microbiota and host contributions to drug metabolism. Informed by experimental data, we built a physiology-based pharmacokinetic model of drug metabolism that includes intestinal compartments with microbiome drug-metabolizing activity. This model successfully predicted serum levels of metabolites of three different drugs, quantified microbial contribution to systemic drug metabolite exposure, and simulated the effect of different parameters on host and microbiota drug metabolism. In this addendum, we expand these simulations to assess the effect of microbiota on the systemic drug and metabolite levels under conditions of altered host physiology, microbiota drug-metabolizing activity or physico-chemical properties of drugs. This work illustrates how and under which circumstances the gut microbiome may influence drug pharmacokinetics, and discusses broader implications of expanded pharmacokinetic models.
topic gut microbiota
drug metabolism
physiology-based pharmacokinetic modeling
url http://dx.doi.org/10.1080/19490976.2019.1667724
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