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Opioid-induced gut microbial disruption and bile dysregulation leads to gut barrier compromise and sustained systemic inflammation
Morphine and its pharmacological derivatives are the most prescribed analgesics for moderate to severe pain management. However, chronic use of morphine reduces pathogen clearance and induces bacterial translocation across the gut barrier. The enteric microbiome has been shown to play a critical rol...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4996771/ https://www.ncbi.nlm.nih.gov/pubmed/26906406 http://dx.doi.org/10.1038/mi.2016.9 |
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author | Banerjee, Santanu Sindberg, Gregory Wang, Fuyuan Meng, Jingjing Sharma, Umakant Zhang, Li Dauer, Patricia Chen, Chi Dalluge, Joseph Johnson, Timothy Roy, Sabita |
author_facet | Banerjee, Santanu Sindberg, Gregory Wang, Fuyuan Meng, Jingjing Sharma, Umakant Zhang, Li Dauer, Patricia Chen, Chi Dalluge, Joseph Johnson, Timothy Roy, Sabita |
author_sort | Banerjee, Santanu |
collection | PubMed |
description | Morphine and its pharmacological derivatives are the most prescribed analgesics for moderate to severe pain management. However, chronic use of morphine reduces pathogen clearance and induces bacterial translocation across the gut barrier. The enteric microbiome has been shown to play a critical role in the preservation of the mucosal barrier function and metabolic homeostasis. Here, we show for the first time, using bacterial 16s rDNA sequencing, that chronic morphine treatment significantly alters the gut microbial composition and induces preferential expansion of gram-positive pathogenic and reduction in bile-deconjugating bacterial strains. A significant reduction in both primary and secondary bile acid levels was seen in the gut, but not in the liver with morphine treatment. Morphine induced microbial dysbiosis and gut barrier disruption was rescued by transplanting placebo-treated microbiota into morphine-treated animals, indicating that microbiome modulation could be exploited as a therapeutic strategy for patients using morphine for pain management. |
format | Online Article Text |
id | pubmed-4996771 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
record_format | MEDLINE/PubMed |
spelling | pubmed-49967712016-10-14 Opioid-induced gut microbial disruption and bile dysregulation leads to gut barrier compromise and sustained systemic inflammation Banerjee, Santanu Sindberg, Gregory Wang, Fuyuan Meng, Jingjing Sharma, Umakant Zhang, Li Dauer, Patricia Chen, Chi Dalluge, Joseph Johnson, Timothy Roy, Sabita Mucosal Immunol Article Morphine and its pharmacological derivatives are the most prescribed analgesics for moderate to severe pain management. However, chronic use of morphine reduces pathogen clearance and induces bacterial translocation across the gut barrier. The enteric microbiome has been shown to play a critical role in the preservation of the mucosal barrier function and metabolic homeostasis. Here, we show for the first time, using bacterial 16s rDNA sequencing, that chronic morphine treatment significantly alters the gut microbial composition and induces preferential expansion of gram-positive pathogenic and reduction in bile-deconjugating bacterial strains. A significant reduction in both primary and secondary bile acid levels was seen in the gut, but not in the liver with morphine treatment. Morphine induced microbial dysbiosis and gut barrier disruption was rescued by transplanting placebo-treated microbiota into morphine-treated animals, indicating that microbiome modulation could be exploited as a therapeutic strategy for patients using morphine for pain management. 2016-02-24 2016-11 /pmc/articles/PMC4996771/ /pubmed/26906406 http://dx.doi.org/10.1038/mi.2016.9 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Banerjee, Santanu Sindberg, Gregory Wang, Fuyuan Meng, Jingjing Sharma, Umakant Zhang, Li Dauer, Patricia Chen, Chi Dalluge, Joseph Johnson, Timothy Roy, Sabita Opioid-induced gut microbial disruption and bile dysregulation leads to gut barrier compromise and sustained systemic inflammation |
title | Opioid-induced gut microbial disruption and bile dysregulation leads
to gut barrier compromise and sustained systemic inflammation |
title_full | Opioid-induced gut microbial disruption and bile dysregulation leads
to gut barrier compromise and sustained systemic inflammation |
title_fullStr | Opioid-induced gut microbial disruption and bile dysregulation leads
to gut barrier compromise and sustained systemic inflammation |
title_full_unstemmed | Opioid-induced gut microbial disruption and bile dysregulation leads
to gut barrier compromise and sustained systemic inflammation |
title_short | Opioid-induced gut microbial disruption and bile dysregulation leads
to gut barrier compromise and sustained systemic inflammation |
title_sort | opioid-induced gut microbial disruption and bile dysregulation leads
to gut barrier compromise and sustained systemic inflammation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4996771/ https://www.ncbi.nlm.nih.gov/pubmed/26906406 http://dx.doi.org/10.1038/mi.2016.9 |
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