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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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 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_2414911295</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2414911295</sourcerecordid><originalsourceid>FETCH-LOGICAL-c375t-4c291d86cc4e3610f4b41b2ef00a60528323da47cdad7c8915a2716e221643683</originalsourceid><addsrcrecordid>eNp9kEtrGzEQx0VpqZ20X6CHIOh509FjX8dikjZg6CU9C612vJbZ1Tp6xPjbV7Hd5JbDMAzzf8CPkG8MbhlA_SMA8AYK4HkkVFAcPpAlk4IX0EjxkSxBSFmUNcgFuQphBwCSCfGZLASXrBSyXZLnxy3SIUU6WePnzs5RUx0juqQjBjqlYEakBx2idQPtjtTjkEZ9utChH450wqi7ebRhotZRs8Vpjlv0en8srOuTwZ5OenQpehvt7KjXMXwhnzZ6DPj1sq_J3_u7x9XvYv3n18Pq57owoi5jIQ1vWd9UxkgUFYON7CTrOG4AdAUlbwQXvZa16XVfm6ZlpeY1q5BzVklRNeKafD_n7v38lDBEtZuTd7lSZQSyZYy3ZVbxsyojCMHjRu29nbQ_KgbqBbU6o1YZtTqhVodsurlEp27C_tXyn20WiLMg5Jcb0L91vxP7Dwhpi8Q</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2414911295</pqid></control><display><type>article</type><title>The gut microbiota attenuates muscle wasting by regulating energy metabolism in chemotherapy-induced malnutrition rats</title><source>MEDLINE</source><source>Springer Nature - Complete Springer Journals</source><creator>Chen, Haitao ; Xu, Chao ; Zhang, Fan ; Liu, Yu ; Guo, Yong ; Yao, Qinghua</creator><creatorcontrib>Chen, Haitao ; Xu, Chao ; Zhang, Fan ; Liu, Yu ; Guo, Yong ; Yao, Qinghua</creatorcontrib><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><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 & 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</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 & control</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Metabolic disorders</subject><subject>Metabolism</subject><subject>Metabolites</subject><subject>Microbiota</subject><subject>Muscle function</subject><subject>Muscles</subject><subject>Muscular Atrophy - chemically induced</subject><subject>Muscular Atrophy - metabolism</subject><subject>Muscular Atrophy - pathology</subject><subject>Muscular Atrophy - therapy</subject><subject>Nutritional status</subject><subject>Oncology</subject><subject>Original Article</subject><subject>Pharmacology/Toxicology</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Regulations</subject><subject>Transplantation</subject><subject>Tricarboxylic acid cycle</subject><subject>Tumor necrosis factor-α</subject><issn>0344-5704</issn><issn>1432-0843</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp9kEtrGzEQx0VpqZ20X6CHIOh509FjX8dikjZg6CU9C612vJbZ1Tp6xPjbV7Hd5JbDMAzzf8CPkG8MbhlA_SMA8AYK4HkkVFAcPpAlk4IX0EjxkSxBSFmUNcgFuQphBwCSCfGZLASXrBSyXZLnxy3SIUU6WePnzs5RUx0juqQjBjqlYEakBx2idQPtjtTjkEZ9utChH450wqi7ebRhotZRs8Vpjlv0en8srOuTwZ5OenQpehvt7KjXMXwhnzZ6DPj1sq_J3_u7x9XvYv3n18Pq57owoi5jIQ1vWd9UxkgUFYON7CTrOG4AdAUlbwQXvZa16XVfm6ZlpeY1q5BzVklRNeKafD_n7v38lDBEtZuTd7lSZQSyZYy3ZVbxsyojCMHjRu29nbQ_KgbqBbU6o1YZtTqhVodsurlEp27C_tXyn20WiLMg5Jcb0L91vxP7Dwhpi8Q</recordid><startdate>20200601</startdate><enddate>20200601</enddate><creator>Chen, Haitao</creator><creator>Xu, Chao</creator><creator>Zhang, Fan</creator><creator>Liu, Yu</creator><creator>Guo, Yong</creator><creator>Yao, Qinghua</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><orcidid>https://orcid.org/0000-0002-0302-4433</orcidid></search><sort><creationdate>20200601</creationdate><title>The gut microbiota attenuates muscle wasting by regulating energy metabolism in chemotherapy-induced malnutrition rats</title><author>Chen, Haitao ; 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 & control</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Metabolic disorders</topic><topic>Metabolism</topic><topic>Metabolites</topic><topic>Microbiota</topic><topic>Muscle function</topic><topic>Muscles</topic><topic>Muscular Atrophy - chemically induced</topic><topic>Muscular Atrophy - metabolism</topic><topic>Muscular Atrophy - pathology</topic><topic>Muscular Atrophy - therapy</topic><topic>Nutritional status</topic><topic>Oncology</topic><topic>Original Article</topic><topic>Pharmacology/Toxicology</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Regulations</topic><topic>Transplantation</topic><topic>Tricarboxylic acid cycle</topic><topic>Tumor necrosis factor-α</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chen, Haitao</creatorcontrib><creatorcontrib>Xu, Chao</creatorcontrib><creatorcontrib>Zhang, Fan</creatorcontrib><creatorcontrib>Liu, Yu</creatorcontrib><creatorcontrib>Guo, Yong</creatorcontrib><creatorcontrib>Yao, Qinghua</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><jtitle>Cancer chemotherapy and pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chen, Haitao</au><au>Xu, Chao</au><au>Zhang, Fan</au><au>Liu, Yu</au><au>Guo, Yong</au><au>Yao, Qinghua</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The gut microbiota attenuates muscle wasting by regulating energy metabolism in chemotherapy-induced malnutrition rats</atitle><jtitle>Cancer chemotherapy and pharmacology</jtitle><stitle>Cancer Chemother Pharmacol</stitle><addtitle>Cancer Chemother Pharmacol</addtitle><date>2020-06-01</date><risdate>2020</risdate><volume>85</volume><issue>6</issue><spage>1049</spage><epage>1062</epage><pages>1049-1062</pages><issn>0344-5704</issn><eissn>1432-0843</eissn><abstract>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.</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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