The gut microbiota attenuates muscle wasting by regulating energy metabolism in chemotherapy-induced malnutrition rats

Background Malnutrition is a common clinical symptom in cancer patients after chemotherapy, which is characterized by muscle wasting and metabolic dysregulation. The regulation of muscle metabolism by gut microbiota has been studied recently. However, there is no direct convincing evidence proving t...

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Veröffentlicht in:Cancer chemotherapy and pharmacology 2020-06, Vol.85 (6), p.1049-1062
Hauptverfasser: Chen, Haitao, Xu, Chao, Zhang, Fan, Liu, Yu, Guo, Yong, Yao, Qinghua
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Xu, Chao
Zhang, Fan
Liu, Yu
Guo, Yong
Yao, Qinghua
description Background Malnutrition is a common clinical symptom in cancer patients after chemotherapy, which is characterized by muscle wasting and metabolic dysregulation. The regulation of muscle metabolism by gut microbiota has been studied recently. However, there is no direct convincing evidence proving that manipulating gut microbiota homeostasis could regulate muscle metabolic disorder caused by chemotherapy. Here, we investigate the potential role of gut microbiota in the regulation of the muscle metabolism in 5-fluorouracil (5-Fu)-induced malnutrition rat model. Methods Male Sprague–Dawley rats were randomly divided into two groups ( n  = 8/group): control group and 5-Fu group. In the 5-Fu group, rats received 5-Fu (40 mg/kg/day) by intraperitoneal injection for 4 days, and all rats were raised for 8 days. Nutritional status, muscle function, muscle metabolites, and gut microbiota were assessed. Fecal microbiota transplantation (FMT) was applied to explore the potential regulation of gut microbiota on muscle metabolism. Results 5-Fu-treated rats exhibited loss of body weight and food intake compared to control group. 5-Fu decreased the levels of total protein and albumin in serum, and significantly increased the levels of IL-6 and TNF-α in muscle tissue. Rats that received 5-Fu displayed concurrent reduction of muscle function and fiber size. Moreover, 5-Fu group showed a distinct profile of gut microbiota compared to control group, including the relative lower abundance of Firmicutes and a higher abundance of Proteobacteria and Verrucomicrobia . Fourteen differential muscle metabolites were identified between two groups, which were mainly related to glycolysis, amino acid metabolism, and TCA cycle pathway. Furthermore, fecal transplantation from healthy rats improved nutritional status and muscle function in 5-Fu-treated rats. Notably, FMT inhibited the inflammatory response in muscle, and reversed the changes of several differential muscle metabolites and energy metabolism in 5-Fu-treated rats. Conclusions Our study demonstrated that gut microbiota played an important role in the regulation of muscle metabolism and promoting muscle energy production in 5-Fu-induced malnutrition rats, suggesting the potential attenuation of chemotherapy-induced muscle wasting by manipulating gut microbiota homeostasis.
doi_str_mv 10.1007/s00280-020-04060-w
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The regulation of muscle metabolism by gut microbiota has been studied recently. However, there is no direct convincing evidence proving that manipulating gut microbiota homeostasis could regulate muscle metabolic disorder caused by chemotherapy. Here, we investigate the potential role of gut microbiota in the regulation of the muscle metabolism in 5-fluorouracil (5-Fu)-induced malnutrition rat model. Methods Male Sprague–Dawley rats were randomly divided into two groups ( n  = 8/group): control group and 5-Fu group. In the 5-Fu group, rats received 5-Fu (40 mg/kg/day) by intraperitoneal injection for 4 days, and all rats were raised for 8 days. Nutritional status, muscle function, muscle metabolites, and gut microbiota were assessed. Fecal microbiota transplantation (FMT) was applied to explore the potential regulation of gut microbiota on muscle metabolism. Results 5-Fu-treated rats exhibited loss of body weight and food intake compared to control group. 5-Fu decreased the levels of total protein and albumin in serum, and significantly increased the levels of IL-6 and TNF-α in muscle tissue. Rats that received 5-Fu displayed concurrent reduction of muscle function and fiber size. Moreover, 5-Fu group showed a distinct profile of gut microbiota compared to control group, including the relative lower abundance of Firmicutes and a higher abundance of Proteobacteria and Verrucomicrobia . Fourteen differential muscle metabolites were identified between two groups, which were mainly related to glycolysis, amino acid metabolism, and TCA cycle pathway. Furthermore, fecal transplantation from healthy rats improved nutritional status and muscle function in 5-Fu-treated rats. Notably, FMT inhibited the inflammatory response in muscle, and reversed the changes of several differential muscle metabolites and energy metabolism in 5-Fu-treated rats. Conclusions Our study demonstrated that gut microbiota played an important role in the regulation of muscle metabolism and promoting muscle energy production in 5-Fu-induced malnutrition rats, suggesting the potential attenuation of chemotherapy-induced muscle wasting by manipulating gut microbiota homeostasis.</description><identifier>ISSN: 0344-5704</identifier><identifier>EISSN: 1432-0843</identifier><identifier>DOI: 10.1007/s00280-020-04060-w</identifier><identifier>PMID: 32415349</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>5-Fluorouracil ; Albumins ; Amino acids ; Animal tissues ; Animals ; Antimetabolites, Antineoplastic - adverse effects ; Attenuation ; Body Weight ; Body weight loss ; Cancer Research ; Chemotherapy ; Energy Metabolism ; Fecal Microbiota Transplantation - methods ; Fecal microflora ; Fluorouracil - adverse effects ; Food intake ; Gastrointestinal Microbiome ; Glycolysis ; Homeostasis ; Inflammation ; Inflammatory response ; Interleukin 6 ; Intestinal microflora ; Male ; Malnutrition ; Malnutrition - chemically induced ; Malnutrition - metabolism ; Malnutrition - pathology ; Malnutrition - prevention &amp; control ; Medicine ; Medicine &amp; Public Health ; Metabolic disorders ; Metabolism ; Metabolites ; Microbiota ; Muscle function ; Muscles ; Muscular Atrophy - chemically induced ; Muscular Atrophy - metabolism ; Muscular Atrophy - pathology ; Muscular Atrophy - therapy ; Nutritional status ; Oncology ; Original Article ; Pharmacology/Toxicology ; Rats ; Rats, Sprague-Dawley ; Regulations ; Transplantation ; Tricarboxylic acid cycle ; Tumor necrosis factor-α</subject><ispartof>Cancer chemotherapy and pharmacology, 2020-06, Vol.85 (6), p.1049-1062</ispartof><rights>Springer-Verlag GmbH Germany, part of Springer Nature 2020</rights><rights>Springer-Verlag GmbH Germany, part of Springer Nature 2020.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c375t-4c291d86cc4e3610f4b41b2ef00a60528323da47cdad7c8915a2716e221643683</citedby><cites>FETCH-LOGICAL-c375t-4c291d86cc4e3610f4b41b2ef00a60528323da47cdad7c8915a2716e221643683</cites><orcidid>0000-0002-0302-4433</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00280-020-04060-w$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00280-020-04060-w$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32415349$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chen, Haitao</creatorcontrib><creatorcontrib>Xu, Chao</creatorcontrib><creatorcontrib>Zhang, Fan</creatorcontrib><creatorcontrib>Liu, Yu</creatorcontrib><creatorcontrib>Guo, Yong</creatorcontrib><creatorcontrib>Yao, Qinghua</creatorcontrib><title>The gut microbiota attenuates muscle wasting by regulating energy metabolism in chemotherapy-induced malnutrition rats</title><title>Cancer chemotherapy and pharmacology</title><addtitle>Cancer Chemother Pharmacol</addtitle><addtitle>Cancer Chemother Pharmacol</addtitle><description>Background Malnutrition is a common clinical symptom in cancer patients after chemotherapy, which is characterized by muscle wasting and metabolic dysregulation. The regulation of muscle metabolism by gut microbiota has been studied recently. However, there is no direct convincing evidence proving that manipulating gut microbiota homeostasis could regulate muscle metabolic disorder caused by chemotherapy. Here, we investigate the potential role of gut microbiota in the regulation of the muscle metabolism in 5-fluorouracil (5-Fu)-induced malnutrition rat model. Methods Male Sprague–Dawley rats were randomly divided into two groups ( n  = 8/group): control group and 5-Fu group. In the 5-Fu group, rats received 5-Fu (40 mg/kg/day) by intraperitoneal injection for 4 days, and all rats were raised for 8 days. Nutritional status, muscle function, muscle metabolites, and gut microbiota were assessed. Fecal microbiota transplantation (FMT) was applied to explore the potential regulation of gut microbiota on muscle metabolism. Results 5-Fu-treated rats exhibited loss of body weight and food intake compared to control group. 5-Fu decreased the levels of total protein and albumin in serum, and significantly increased the levels of IL-6 and TNF-α in muscle tissue. Rats that received 5-Fu displayed concurrent reduction of muscle function and fiber size. Moreover, 5-Fu group showed a distinct profile of gut microbiota compared to control group, including the relative lower abundance of Firmicutes and a higher abundance of Proteobacteria and Verrucomicrobia . Fourteen differential muscle metabolites were identified between two groups, which were mainly related to glycolysis, amino acid metabolism, and TCA cycle pathway. Furthermore, fecal transplantation from healthy rats improved nutritional status and muscle function in 5-Fu-treated rats. Notably, FMT inhibited the inflammatory response in muscle, and reversed the changes of several differential muscle metabolites and energy metabolism in 5-Fu-treated rats. Conclusions Our study demonstrated that gut microbiota played an important role in the regulation of muscle metabolism and promoting muscle energy production in 5-Fu-induced malnutrition rats, suggesting the potential attenuation of chemotherapy-induced muscle wasting by manipulating gut microbiota homeostasis.</description><subject>5-Fluorouracil</subject><subject>Albumins</subject><subject>Amino acids</subject><subject>Animal tissues</subject><subject>Animals</subject><subject>Antimetabolites, Antineoplastic - adverse effects</subject><subject>Attenuation</subject><subject>Body Weight</subject><subject>Body weight loss</subject><subject>Cancer Research</subject><subject>Chemotherapy</subject><subject>Energy Metabolism</subject><subject>Fecal Microbiota Transplantation - methods</subject><subject>Fecal microflora</subject><subject>Fluorouracil - adverse effects</subject><subject>Food intake</subject><subject>Gastrointestinal Microbiome</subject><subject>Glycolysis</subject><subject>Homeostasis</subject><subject>Inflammation</subject><subject>Inflammatory response</subject><subject>Interleukin 6</subject><subject>Intestinal microflora</subject><subject>Male</subject><subject>Malnutrition</subject><subject>Malnutrition - chemically induced</subject><subject>Malnutrition - metabolism</subject><subject>Malnutrition - pathology</subject><subject>Malnutrition - prevention &amp; 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Xu, Chao ; Zhang, Fan ; Liu, Yu ; Guo, Yong ; Yao, Qinghua</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c375t-4c291d86cc4e3610f4b41b2ef00a60528323da47cdad7c8915a2716e221643683</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>5-Fluorouracil</topic><topic>Albumins</topic><topic>Amino acids</topic><topic>Animal tissues</topic><topic>Animals</topic><topic>Antimetabolites, Antineoplastic - adverse effects</topic><topic>Attenuation</topic><topic>Body Weight</topic><topic>Body weight loss</topic><topic>Cancer Research</topic><topic>Chemotherapy</topic><topic>Energy Metabolism</topic><topic>Fecal Microbiota Transplantation - methods</topic><topic>Fecal microflora</topic><topic>Fluorouracil - adverse effects</topic><topic>Food intake</topic><topic>Gastrointestinal Microbiome</topic><topic>Glycolysis</topic><topic>Homeostasis</topic><topic>Inflammation</topic><topic>Inflammatory response</topic><topic>Interleukin 6</topic><topic>Intestinal microflora</topic><topic>Male</topic><topic>Malnutrition</topic><topic>Malnutrition - chemically induced</topic><topic>Malnutrition - metabolism</topic><topic>Malnutrition - pathology</topic><topic>Malnutrition - prevention &amp; 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The regulation of muscle metabolism by gut microbiota has been studied recently. However, there is no direct convincing evidence proving that manipulating gut microbiota homeostasis could regulate muscle metabolic disorder caused by chemotherapy. Here, we investigate the potential role of gut microbiota in the regulation of the muscle metabolism in 5-fluorouracil (5-Fu)-induced malnutrition rat model. Methods Male Sprague–Dawley rats were randomly divided into two groups ( n  = 8/group): control group and 5-Fu group. In the 5-Fu group, rats received 5-Fu (40 mg/kg/day) by intraperitoneal injection for 4 days, and all rats were raised for 8 days. Nutritional status, muscle function, muscle metabolites, and gut microbiota were assessed. Fecal microbiota transplantation (FMT) was applied to explore the potential regulation of gut microbiota on muscle metabolism. Results 5-Fu-treated rats exhibited loss of body weight and food intake compared to control group. 5-Fu decreased the levels of total protein and albumin in serum, and significantly increased the levels of IL-6 and TNF-α in muscle tissue. Rats that received 5-Fu displayed concurrent reduction of muscle function and fiber size. Moreover, 5-Fu group showed a distinct profile of gut microbiota compared to control group, including the relative lower abundance of Firmicutes and a higher abundance of Proteobacteria and Verrucomicrobia . Fourteen differential muscle metabolites were identified between two groups, which were mainly related to glycolysis, amino acid metabolism, and TCA cycle pathway. Furthermore, fecal transplantation from healthy rats improved nutritional status and muscle function in 5-Fu-treated rats. Notably, FMT inhibited the inflammatory response in muscle, and reversed the changes of several differential muscle metabolites and energy metabolism in 5-Fu-treated rats. Conclusions Our study demonstrated that gut microbiota played an important role in the regulation of muscle metabolism and promoting muscle energy production in 5-Fu-induced malnutrition rats, suggesting the potential attenuation of chemotherapy-induced muscle wasting by manipulating gut microbiota homeostasis.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>32415349</pmid><doi>10.1007/s00280-020-04060-w</doi><tpages>14</tpages><orcidid>https://orcid.org/0000-0002-0302-4433</orcidid></addata></record>
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subjects 5-Fluorouracil
Albumins
Amino acids
Animal tissues
Animals
Antimetabolites, Antineoplastic - adverse effects
Attenuation
Body Weight
Body weight loss
Cancer Research
Chemotherapy
Energy Metabolism
Fecal Microbiota Transplantation - methods
Fecal microflora
Fluorouracil - adverse effects
Food intake
Gastrointestinal Microbiome
Glycolysis
Homeostasis
Inflammation
Inflammatory response
Interleukin 6
Intestinal microflora
Male
Malnutrition
Malnutrition - chemically induced
Malnutrition - metabolism
Malnutrition - pathology
Malnutrition - prevention & control
Medicine
Medicine & Public Health
Metabolic disorders
Metabolism
Metabolites
Microbiota
Muscle function
Muscles
Muscular Atrophy - chemically induced
Muscular Atrophy - metabolism
Muscular Atrophy - pathology
Muscular Atrophy - therapy
Nutritional status
Oncology
Original Article
Pharmacology/Toxicology
Rats
Rats, Sprague-Dawley
Regulations
Transplantation
Tricarboxylic acid cycle
Tumor necrosis factor-α
title The gut microbiota attenuates muscle wasting by regulating energy metabolism in chemotherapy-induced malnutrition rats
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