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Cocaine Induces Inflammatory Gut Milieu by Compromising the Mucosal Barrier Integrity and Altering the Gut Microbiota Colonization

Cocaine use disorder (CUD), a major health crisis, has traditionally been considered a complication of the CNS; however, it is also closely associated with malnourishment and deteriorating gut health. In light of emerging studies on the potential role of gut microbiota in neurological disorders, we...

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Autores principales: Chivero, Ernest T., Ahmad, Rizwan, Thangaraj, Annadurai, Periyasamy, Palsamy, Kumar, Balawant, Kroeger, Elisa, Feng, Dan, Guo, Ming-Lei, Roy, Sabita, Dhawan, Punita, Singh, Amar B., Buch, Shilpa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6704112/
https://www.ncbi.nlm.nih.gov/pubmed/31434922
http://dx.doi.org/10.1038/s41598-019-48428-2
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author Chivero, Ernest T.
Ahmad, Rizwan
Thangaraj, Annadurai
Periyasamy, Palsamy
Kumar, Balawant
Kroeger, Elisa
Feng, Dan
Guo, Ming-Lei
Roy, Sabita
Dhawan, Punita
Singh, Amar B.
Buch, Shilpa
author_facet Chivero, Ernest T.
Ahmad, Rizwan
Thangaraj, Annadurai
Periyasamy, Palsamy
Kumar, Balawant
Kroeger, Elisa
Feng, Dan
Guo, Ming-Lei
Roy, Sabita
Dhawan, Punita
Singh, Amar B.
Buch, Shilpa
author_sort Chivero, Ernest T.
collection PubMed
description Cocaine use disorder (CUD), a major health crisis, has traditionally been considered a complication of the CNS; however, it is also closely associated with malnourishment and deteriorating gut health. In light of emerging studies on the potential role of gut microbiota in neurological disorders, we sought to understand the causal association between CUD and gut dysbiosis. Using a comprehensive approach, we confirmed that cocaine administration in mice resulted in alterations of the gut microbiota. Furthermore, cocaine-mediated gut dysbiosis was associated with upregulation of proinflammatory mediators including NF-κB and IL-1β. In vivo and in vitro analyses confirmed that cocaine altered gut-barrier composition of the tight junction proteins while also impairing epithelial permeability by potentially involving the MAPK/ERK1/2 signaling. Taken together, our findings unravel a causal link between CUD, gut-barrier dysfunction and dysbiosis and set a stage for future development of supplemental strategies for the management of CUD-associated gut complications.
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spelling pubmed-67041122019-08-23 Cocaine Induces Inflammatory Gut Milieu by Compromising the Mucosal Barrier Integrity and Altering the Gut Microbiota Colonization Chivero, Ernest T. Ahmad, Rizwan Thangaraj, Annadurai Periyasamy, Palsamy Kumar, Balawant Kroeger, Elisa Feng, Dan Guo, Ming-Lei Roy, Sabita Dhawan, Punita Singh, Amar B. Buch, Shilpa Sci Rep Article Cocaine use disorder (CUD), a major health crisis, has traditionally been considered a complication of the CNS; however, it is also closely associated with malnourishment and deteriorating gut health. In light of emerging studies on the potential role of gut microbiota in neurological disorders, we sought to understand the causal association between CUD and gut dysbiosis. Using a comprehensive approach, we confirmed that cocaine administration in mice resulted in alterations of the gut microbiota. Furthermore, cocaine-mediated gut dysbiosis was associated with upregulation of proinflammatory mediators including NF-κB and IL-1β. In vivo and in vitro analyses confirmed that cocaine altered gut-barrier composition of the tight junction proteins while also impairing epithelial permeability by potentially involving the MAPK/ERK1/2 signaling. Taken together, our findings unravel a causal link between CUD, gut-barrier dysfunction and dysbiosis and set a stage for future development of supplemental strategies for the management of CUD-associated gut complications. Nature Publishing Group UK 2019-08-21 /pmc/articles/PMC6704112/ /pubmed/31434922 http://dx.doi.org/10.1038/s41598-019-48428-2 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Chivero, Ernest T.
Ahmad, Rizwan
Thangaraj, Annadurai
Periyasamy, Palsamy
Kumar, Balawant
Kroeger, Elisa
Feng, Dan
Guo, Ming-Lei
Roy, Sabita
Dhawan, Punita
Singh, Amar B.
Buch, Shilpa
Cocaine Induces Inflammatory Gut Milieu by Compromising the Mucosal Barrier Integrity and Altering the Gut Microbiota Colonization
title Cocaine Induces Inflammatory Gut Milieu by Compromising the Mucosal Barrier Integrity and Altering the Gut Microbiota Colonization
title_full Cocaine Induces Inflammatory Gut Milieu by Compromising the Mucosal Barrier Integrity and Altering the Gut Microbiota Colonization
title_fullStr Cocaine Induces Inflammatory Gut Milieu by Compromising the Mucosal Barrier Integrity and Altering the Gut Microbiota Colonization
title_full_unstemmed Cocaine Induces Inflammatory Gut Milieu by Compromising the Mucosal Barrier Integrity and Altering the Gut Microbiota Colonization
title_short Cocaine Induces Inflammatory Gut Milieu by Compromising the Mucosal Barrier Integrity and Altering the Gut Microbiota Colonization
title_sort cocaine induces inflammatory gut milieu by compromising the mucosal barrier integrity and altering the gut microbiota colonization
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6704112/
https://www.ncbi.nlm.nih.gov/pubmed/31434922
http://dx.doi.org/10.1038/s41598-019-48428-2
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