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Dysbiosis in gastrointestinal pathophysiology: Role of the gut microbiome in Gulf War Illness

Gulf War Illness (GWI) has been reported in 25%–35% of veterans returned from the Gulf war. Symptoms of GWI are varied and include both neurological and gastrointestinal symptoms as well as chronic fatigue. Development of GWI has been associated with chemical exposure particularly with exposure to p...

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Autores principales: Slevin, Elise, Koyama, Sachiko, Harrison, Kelly, Wan, Ying, Klaunig, James E., Wu, Chaodong, Shetty, Ashok K., Meng, Fanyin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10064030/
https://www.ncbi.nlm.nih.gov/pubmed/36716094
http://dx.doi.org/10.1111/jcmm.17631
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author Slevin, Elise
Koyama, Sachiko
Harrison, Kelly
Wan, Ying
Klaunig, James E.
Wu, Chaodong
Shetty, Ashok K.
Meng, Fanyin
author_facet Slevin, Elise
Koyama, Sachiko
Harrison, Kelly
Wan, Ying
Klaunig, James E.
Wu, Chaodong
Shetty, Ashok K.
Meng, Fanyin
author_sort Slevin, Elise
collection PubMed
description Gulf War Illness (GWI) has been reported in 25%–35% of veterans returned from the Gulf war. Symptoms of GWI are varied and include both neurological and gastrointestinal symptoms as well as chronic fatigue. Development of GWI has been associated with chemical exposure particularly with exposure to pyridostigmine bromide (PB) and permethrin. Recent studies have found that the pathology of GWI is connected to changes in the gut microbiota, that is the gut dysbiosis. In studies using animal models, the exposure to PB and permethrin resulted in similar changes in the gut microbiome as these found in GW veterans with GWI. Studies using animal models have also shown that phytochemicals like curcumin are beneficial in reducing the symptoms and that the extracellular vesicles (EV) released from gut bacteria and from the intestinal epithelium can both promote diseases and suppress diseases through the intercellular communication mechanisms. The intestinal epithelium cells produce EVs and these EVs of intestinal epithelium origin are found to suppress inflammatory bowel disease severity, suggesting the benefits of utilizing EV in treatments. On the contrary, EV from the plasma of septic mice enhanced the level of proinflammatory cytokines in vitro and neutrophils and macrophages in vivo, suggesting differences in the EV depending on the types of cells they were originated and/or influences of environmental changes. These studies suggest that targeting the EV that specifically have positive influences may become a new therapeutic strategy in the treatment of veterans with GWI.
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spelling pubmed-100640302023-04-01 Dysbiosis in gastrointestinal pathophysiology: Role of the gut microbiome in Gulf War Illness Slevin, Elise Koyama, Sachiko Harrison, Kelly Wan, Ying Klaunig, James E. Wu, Chaodong Shetty, Ashok K. Meng, Fanyin J Cell Mol Med Reviews Gulf War Illness (GWI) has been reported in 25%–35% of veterans returned from the Gulf war. Symptoms of GWI are varied and include both neurological and gastrointestinal symptoms as well as chronic fatigue. Development of GWI has been associated with chemical exposure particularly with exposure to pyridostigmine bromide (PB) and permethrin. Recent studies have found that the pathology of GWI is connected to changes in the gut microbiota, that is the gut dysbiosis. In studies using animal models, the exposure to PB and permethrin resulted in similar changes in the gut microbiome as these found in GW veterans with GWI. Studies using animal models have also shown that phytochemicals like curcumin are beneficial in reducing the symptoms and that the extracellular vesicles (EV) released from gut bacteria and from the intestinal epithelium can both promote diseases and suppress diseases through the intercellular communication mechanisms. The intestinal epithelium cells produce EVs and these EVs of intestinal epithelium origin are found to suppress inflammatory bowel disease severity, suggesting the benefits of utilizing EV in treatments. On the contrary, EV from the plasma of septic mice enhanced the level of proinflammatory cytokines in vitro and neutrophils and macrophages in vivo, suggesting differences in the EV depending on the types of cells they were originated and/or influences of environmental changes. These studies suggest that targeting the EV that specifically have positive influences may become a new therapeutic strategy in the treatment of veterans with GWI. John Wiley and Sons Inc. 2023-01-30 /pmc/articles/PMC10064030/ /pubmed/36716094 http://dx.doi.org/10.1111/jcmm.17631 Text en © 2023 The Authors. Journal of Cellular and Molecular Medicine published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Reviews
Slevin, Elise
Koyama, Sachiko
Harrison, Kelly
Wan, Ying
Klaunig, James E.
Wu, Chaodong
Shetty, Ashok K.
Meng, Fanyin
Dysbiosis in gastrointestinal pathophysiology: Role of the gut microbiome in Gulf War Illness
title Dysbiosis in gastrointestinal pathophysiology: Role of the gut microbiome in Gulf War Illness
title_full Dysbiosis in gastrointestinal pathophysiology: Role of the gut microbiome in Gulf War Illness
title_fullStr Dysbiosis in gastrointestinal pathophysiology: Role of the gut microbiome in Gulf War Illness
title_full_unstemmed Dysbiosis in gastrointestinal pathophysiology: Role of the gut microbiome in Gulf War Illness
title_short Dysbiosis in gastrointestinal pathophysiology: Role of the gut microbiome in Gulf War Illness
title_sort dysbiosis in gastrointestinal pathophysiology: role of the gut microbiome in gulf war illness
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10064030/
https://www.ncbi.nlm.nih.gov/pubmed/36716094
http://dx.doi.org/10.1111/jcmm.17631
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