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The Impact of the Gut Microbiota on Drug Metabolism and Clinical Outcome

The significance of the gut microbiota as a determinant of drug pharmacokinetics and accordingly therapeutic response is of increasing importance with the advent of modern medicines characterised by low solubility and/or permeability, or modified-release. These physicochemical properties and release...

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Detalles Bibliográficos
Autores principales: Enright, Elaine F., Gahan, Cormac G.M., Joyce, Susan A., Griffin, Brendan T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: YJBM 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5045146/
https://www.ncbi.nlm.nih.gov/pubmed/27698621
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author Enright, Elaine F.
Gahan, Cormac G.M.
Joyce, Susan A.
Griffin, Brendan T.
author_facet Enright, Elaine F.
Gahan, Cormac G.M.
Joyce, Susan A.
Griffin, Brendan T.
author_sort Enright, Elaine F.
collection PubMed
description The significance of the gut microbiota as a determinant of drug pharmacokinetics and accordingly therapeutic response is of increasing importance with the advent of modern medicines characterised by low solubility and/or permeability, or modified-release. These physicochemical properties and release kinetics prolong drug residence times within the gastrointestinal tract, wherein biotransformation by commensal microbes can occur. As the evidence base in support of this supplementary metabolic “organ” expands, novel opportunities to engineer the microbiota for clinical benefit have emerged. This review provides an overview of microbe-mediated alteration of drug pharmacokinetics, with particular emphasis on studies demonstrating proof of concept in vivo. Additionally, recent advances in modulating the microbiota to improve clinical response to therapeutics are explored.
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spelling pubmed-50451462016-10-03 The Impact of the Gut Microbiota on Drug Metabolism and Clinical Outcome Enright, Elaine F. Gahan, Cormac G.M. Joyce, Susan A. Griffin, Brendan T. Yale J Biol Med Mini-Review The significance of the gut microbiota as a determinant of drug pharmacokinetics and accordingly therapeutic response is of increasing importance with the advent of modern medicines characterised by low solubility and/or permeability, or modified-release. These physicochemical properties and release kinetics prolong drug residence times within the gastrointestinal tract, wherein biotransformation by commensal microbes can occur. As the evidence base in support of this supplementary metabolic “organ” expands, novel opportunities to engineer the microbiota for clinical benefit have emerged. This review provides an overview of microbe-mediated alteration of drug pharmacokinetics, with particular emphasis on studies demonstrating proof of concept in vivo. Additionally, recent advances in modulating the microbiota to improve clinical response to therapeutics are explored. YJBM 2016-09-30 /pmc/articles/PMC5045146/ /pubmed/27698621 Text en Copyright ©2016, Yale Journal of Biology and Medicine https://creativecommons.org/licenses/by-nc/3.0/ This is an open access article distributed under the terms of the Creative Commons CC BY-NC license, which permits use, distribution, and reproduction in any medium, provided the original work is properly cited. You may not use the material for commercial purposes.
spellingShingle Mini-Review
Enright, Elaine F.
Gahan, Cormac G.M.
Joyce, Susan A.
Griffin, Brendan T.
The Impact of the Gut Microbiota on Drug Metabolism and Clinical Outcome
title The Impact of the Gut Microbiota on Drug Metabolism and Clinical Outcome
title_full The Impact of the Gut Microbiota on Drug Metabolism and Clinical Outcome
title_fullStr The Impact of the Gut Microbiota on Drug Metabolism and Clinical Outcome
title_full_unstemmed The Impact of the Gut Microbiota on Drug Metabolism and Clinical Outcome
title_short The Impact of the Gut Microbiota on Drug Metabolism and Clinical Outcome
title_sort impact of the gut microbiota on drug metabolism and clinical outcome
topic Mini-Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5045146/
https://www.ncbi.nlm.nih.gov/pubmed/27698621
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