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Antibiotic treatment inhibits paclitaxel chemotherapy-induced activity deficits in female mice

Chemotherapy, a mainstay in the treatment of cancer, is associated with severe and debilitating side effects. Side effects can be physical (e.g., gastrointestinal distress, anemia, and hair loss) or mental (e.g., fatigue, cognitive dysfunction). Chemotherapy is known to alter the gut microbiota; thu...

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Autores principales: Grant, Corena V., Jordan, Kelley, Seng, Melina M., Pyter, Leah M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10174578/
https://www.ncbi.nlm.nih.gov/pubmed/37167214
http://dx.doi.org/10.1371/journal.pone.0284365
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author Grant, Corena V.
Jordan, Kelley
Seng, Melina M.
Pyter, Leah M.
author_facet Grant, Corena V.
Jordan, Kelley
Seng, Melina M.
Pyter, Leah M.
author_sort Grant, Corena V.
collection PubMed
description Chemotherapy, a mainstay in the treatment of cancer, is associated with severe and debilitating side effects. Side effects can be physical (e.g., gastrointestinal distress, anemia, and hair loss) or mental (e.g., fatigue, cognitive dysfunction). Chemotherapy is known to alter the gut microbiota; thus, communication through the gut-brain axis may influence behavioral side effects. Here, we used a clinically-relevant paclitaxel chemotherapy regimen in combination with antibiotics to test the hypothesis that gut microbes contribute to chemotherapy-associated fatigue-like behaviors in female mice. Data presented suggest that chemotherapy-altered gut microbes contribute to fatigue-like behaviors in mice by disrupting energy homeostasis.
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spelling pubmed-101745782023-05-12 Antibiotic treatment inhibits paclitaxel chemotherapy-induced activity deficits in female mice Grant, Corena V. Jordan, Kelley Seng, Melina M. Pyter, Leah M. PLoS One Research Article Chemotherapy, a mainstay in the treatment of cancer, is associated with severe and debilitating side effects. Side effects can be physical (e.g., gastrointestinal distress, anemia, and hair loss) or mental (e.g., fatigue, cognitive dysfunction). Chemotherapy is known to alter the gut microbiota; thus, communication through the gut-brain axis may influence behavioral side effects. Here, we used a clinically-relevant paclitaxel chemotherapy regimen in combination with antibiotics to test the hypothesis that gut microbes contribute to chemotherapy-associated fatigue-like behaviors in female mice. Data presented suggest that chemotherapy-altered gut microbes contribute to fatigue-like behaviors in mice by disrupting energy homeostasis. Public Library of Science 2023-05-11 /pmc/articles/PMC10174578/ /pubmed/37167214 http://dx.doi.org/10.1371/journal.pone.0284365 Text en © 2023 Grant et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Grant, Corena V.
Jordan, Kelley
Seng, Melina M.
Pyter, Leah M.
Antibiotic treatment inhibits paclitaxel chemotherapy-induced activity deficits in female mice
title Antibiotic treatment inhibits paclitaxel chemotherapy-induced activity deficits in female mice
title_full Antibiotic treatment inhibits paclitaxel chemotherapy-induced activity deficits in female mice
title_fullStr Antibiotic treatment inhibits paclitaxel chemotherapy-induced activity deficits in female mice
title_full_unstemmed Antibiotic treatment inhibits paclitaxel chemotherapy-induced activity deficits in female mice
title_short Antibiotic treatment inhibits paclitaxel chemotherapy-induced activity deficits in female mice
title_sort antibiotic treatment inhibits paclitaxel chemotherapy-induced activity deficits in female mice
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10174578/
https://www.ncbi.nlm.nih.gov/pubmed/37167214
http://dx.doi.org/10.1371/journal.pone.0284365
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