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Docetaxel does not impair skeletal muscle force production in a murine model of cancer chemotherapy

Chemotherapy drugs such as docetaxel are commonly used to treat cancer. Cancer patients treated with chemotherapy experience decreased physical fitness, muscle weakness and fatigue. To date, it is unclear whether these symptoms result only from cancer‐derived factors or from the combination of cance...

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Autores principales: Chaillou, Thomas, McPeek, Ashley, Lanner, Johanna T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5471428/
https://www.ncbi.nlm.nih.gov/pubmed/28583990
http://dx.doi.org/10.14814/phy2.13261
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author Chaillou, Thomas
McPeek, Ashley
Lanner, Johanna T.
author_facet Chaillou, Thomas
McPeek, Ashley
Lanner, Johanna T.
author_sort Chaillou, Thomas
collection PubMed
description Chemotherapy drugs such as docetaxel are commonly used to treat cancer. Cancer patients treated with chemotherapy experience decreased physical fitness, muscle weakness and fatigue. To date, it is unclear whether these symptoms result only from cancer‐derived factors or from the combination of cancer disease and cancer treatments, such as chemotherapy. In this study, we aimed at determining the impact of chemotherapy per se on force production of hind limb muscles from healthy mice treated with docetaxel. We hypothesized that docetaxel will decrease maximal force, exacerbate the force decline during repeated contractions and impair recovery after fatiguing stimulations. We examined the function of soleus and extensor digitorum longus (EDL) muscles 24 h and 72 h after a single injection of docetaxel (acute treatment), and 7 days after the third weekly injection of docetaxel (repeated treatment). Docetaxel was administrated by intravenous injection (20 mg/kg) in female FVB/NRj mice and control mice were injected with saline solution. Our results show that neither acute nor repeated docetaxel treatment significantly alters force production during maximal contractions, repeated contractions or recovery. Only a tendency to decreased peak specific force was observed in soleus muscles 24 h after a single injection of docetaxel (−17%, P = 0.13). In conclusion, docetaxel administered intravenously does not impair force production in hind limb muscles from healthy mice. It remains to be clarified whether docetaxel, or other chemotherapy drugs, affect muscle function in subjects with cancer and whether the side effects associated with chemotherapy (neurotoxicity, central fatigue, decreased physical activity, etc.) are responsible for the experienced muscle weakness and fatigue.
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spelling pubmed-54714282017-06-21 Docetaxel does not impair skeletal muscle force production in a murine model of cancer chemotherapy Chaillou, Thomas McPeek, Ashley Lanner, Johanna T. Physiol Rep Original Research Chemotherapy drugs such as docetaxel are commonly used to treat cancer. Cancer patients treated with chemotherapy experience decreased physical fitness, muscle weakness and fatigue. To date, it is unclear whether these symptoms result only from cancer‐derived factors or from the combination of cancer disease and cancer treatments, such as chemotherapy. In this study, we aimed at determining the impact of chemotherapy per se on force production of hind limb muscles from healthy mice treated with docetaxel. We hypothesized that docetaxel will decrease maximal force, exacerbate the force decline during repeated contractions and impair recovery after fatiguing stimulations. We examined the function of soleus and extensor digitorum longus (EDL) muscles 24 h and 72 h after a single injection of docetaxel (acute treatment), and 7 days after the third weekly injection of docetaxel (repeated treatment). Docetaxel was administrated by intravenous injection (20 mg/kg) in female FVB/NRj mice and control mice were injected with saline solution. Our results show that neither acute nor repeated docetaxel treatment significantly alters force production during maximal contractions, repeated contractions or recovery. Only a tendency to decreased peak specific force was observed in soleus muscles 24 h after a single injection of docetaxel (−17%, P = 0.13). In conclusion, docetaxel administered intravenously does not impair force production in hind limb muscles from healthy mice. It remains to be clarified whether docetaxel, or other chemotherapy drugs, affect muscle function in subjects with cancer and whether the side effects associated with chemotherapy (neurotoxicity, central fatigue, decreased physical activity, etc.) are responsible for the experienced muscle weakness and fatigue. John Wiley and Sons Inc. 2017-06-05 /pmc/articles/PMC5471428/ /pubmed/28583990 http://dx.doi.org/10.14814/phy2.13261 Text en © 2017 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of The Physiological Society and the American Physiological Society This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Chaillou, Thomas
McPeek, Ashley
Lanner, Johanna T.
Docetaxel does not impair skeletal muscle force production in a murine model of cancer chemotherapy
title Docetaxel does not impair skeletal muscle force production in a murine model of cancer chemotherapy
title_full Docetaxel does not impair skeletal muscle force production in a murine model of cancer chemotherapy
title_fullStr Docetaxel does not impair skeletal muscle force production in a murine model of cancer chemotherapy
title_full_unstemmed Docetaxel does not impair skeletal muscle force production in a murine model of cancer chemotherapy
title_short Docetaxel does not impair skeletal muscle force production in a murine model of cancer chemotherapy
title_sort docetaxel does not impair skeletal muscle force production in a murine model of cancer chemotherapy
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5471428/
https://www.ncbi.nlm.nih.gov/pubmed/28583990
http://dx.doi.org/10.14814/phy2.13261
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