Effects of glutamine administration on inflammatory responses in chronic ethanol-fed rats
The purpose of this study was to investigate the effects of glutamine supplementation on inflammatory responses in chronic ethanol-fed rats. Male Wistar rats weighing about 160 g were divided into five groups. Two groups were fed a normal liquid diet and three groups were fed a glutamine-containing...
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description | The purpose of this study was to investigate the effects of glutamine supplementation on inflammatory responses in chronic ethanol-fed rats. Male Wistar rats weighing about 160 g were divided into five groups. Two groups were fed a normal liquid diet and three groups were fed a glutamine-containing liquid diet. After 1 week, one of the normal liquid diet groups was fed an ethanol-containing liquid diet (CE), and the other group served as the control (CC) group. At the same time, one of the glutamine-containing liquid diet groups was continually fed the same diet (GCG), but the other two groups were fed ethanol-containing diet supplemented with glutamine (GEG) or without glutamine (GE). The following items were analyzed: (1) liver function, (2) cytokine contents, and (3) hepatic oxidative stress. The activities of aspartate transaminase (AST) and alanine transaminase (ALT) and levels of tumor necrosis factor (TNF)-α and interleukin (IL)-1β in the CE group had significantly increased. In addition, hepatic cytochrome P450 2E1 (CYP2E1) expression had significantly increased in the CE, GE and GEG groups. However, the activities of AST and ALT and levels of TNF-α and IL-1β in the GE group were significantly lower than those of the CE group. The results suggest that the plasma inflammatory responses of rats fed an ethanol-containing liquid diet for 7 weeks significantly increased. However, pretreatment with glutamine improved the plasma inflammatory responses induced by ethanol. |
doi_str_mv | 10.1016/j.jnutbio.2010.02.006 |
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Male Wistar rats weighing about 160 g were divided into five groups. Two groups were fed a normal liquid diet and three groups were fed a glutamine-containing liquid diet. After 1 week, one of the normal liquid diet groups was fed an ethanol-containing liquid diet (CE), and the other group served as the control (CC) group. At the same time, one of the glutamine-containing liquid diet groups was continually fed the same diet (GCG), but the other two groups were fed ethanol-containing diet supplemented with glutamine (GEG) or without glutamine (GE). The following items were analyzed: (1) liver function, (2) cytokine contents, and (3) hepatic oxidative stress. The activities of aspartate transaminase (AST) and alanine transaminase (ALT) and levels of tumor necrosis factor (TNF)-α and interleukin (IL)-1β in the CE group had significantly increased. In addition, hepatic cytochrome P450 2E1 (CYP2E1) expression had significantly increased in the CE, GE and GEG groups. However, the activities of AST and ALT and levels of TNF-α and IL-1β in the GE group were significantly lower than those of the CE group. The results suggest that the plasma inflammatory responses of rats fed an ethanol-containing liquid diet for 7 weeks significantly increased. However, pretreatment with glutamine improved the plasma inflammatory responses induced by ethanol.</description><identifier>ISSN: 0955-2863</identifier><identifier>EISSN: 1873-4847</identifier><identifier>DOI: 10.1016/j.jnutbio.2010.02.006</identifier><identifier>PMID: 20573494</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Alanine Transaminase - metabolism ; Alcoholic liver disease ; Animals ; Aspartate Aminotransferases - metabolism ; Biological and medical sciences ; Cholesterol - analysis ; Cytochrome P-450 CYP2E1 - metabolism ; Dietary Supplements ; Ethanol - administration & dosage ; Ethanol - toxicity ; Feeding. Feeding behavior ; Fundamental and applied biological sciences. Psychology ; Glutamine ; Glutamine - pharmacology ; Inflammation - pathology ; Interleukin-1beta - analysis ; Lipid Metabolism ; Liver - metabolism ; Liver Diseases, Alcoholic - prevention & control ; Male ; Oxidative Stress ; Rats ; Rats, Wistar ; Triglycerides - analysis ; Tumor Necrosis Factor-alpha - analysis ; Vertebrates: anatomy and physiology, studies on body, several organs or systems</subject><ispartof>The Journal of nutritional biochemistry, 2011-03, Vol.22 (3), p.282-288</ispartof><rights>2011 Elsevier Inc.</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2011 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c517t-45a1f1bad729d51d7a68687bc6152f39a7740979c47a3eb973b4385240f09a373</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.jnutbio.2010.02.006$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27922,27923,45993</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=23953394$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20573494$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Peng, Hsiang-Chi</creatorcontrib><creatorcontrib>Chen, Ya-Ling</creatorcontrib><creatorcontrib>Chen, Jiun-Rong</creatorcontrib><creatorcontrib>Yang, Sien-Sing</creatorcontrib><creatorcontrib>Huang, Kuan-Hsun</creatorcontrib><creatorcontrib>Wu, Yi-Chin</creatorcontrib><creatorcontrib>Lin, Yun-Ho</creatorcontrib><creatorcontrib>Yang, Suh-Ching</creatorcontrib><title>Effects of glutamine administration on inflammatory responses in chronic ethanol-fed rats</title><title>The Journal of nutritional biochemistry</title><addtitle>J Nutr Biochem</addtitle><description>The purpose of this study was to investigate the effects of glutamine supplementation on inflammatory responses in chronic ethanol-fed rats. Male Wistar rats weighing about 160 g were divided into five groups. Two groups were fed a normal liquid diet and three groups were fed a glutamine-containing liquid diet. After 1 week, one of the normal liquid diet groups was fed an ethanol-containing liquid diet (CE), and the other group served as the control (CC) group. At the same time, one of the glutamine-containing liquid diet groups was continually fed the same diet (GCG), but the other two groups were fed ethanol-containing diet supplemented with glutamine (GEG) or without glutamine (GE). The following items were analyzed: (1) liver function, (2) cytokine contents, and (3) hepatic oxidative stress. The activities of aspartate transaminase (AST) and alanine transaminase (ALT) and levels of tumor necrosis factor (TNF)-α and interleukin (IL)-1β in the CE group had significantly increased. In addition, hepatic cytochrome P450 2E1 (CYP2E1) expression had significantly increased in the CE, GE and GEG groups. However, the activities of AST and ALT and levels of TNF-α and IL-1β in the GE group were significantly lower than those of the CE group. The results suggest that the plasma inflammatory responses of rats fed an ethanol-containing liquid diet for 7 weeks significantly increased. However, pretreatment with glutamine improved the plasma inflammatory responses induced by ethanol.</description><subject>Alanine Transaminase - metabolism</subject><subject>Alcoholic liver disease</subject><subject>Animals</subject><subject>Aspartate Aminotransferases - metabolism</subject><subject>Biological and medical sciences</subject><subject>Cholesterol - analysis</subject><subject>Cytochrome P-450 CYP2E1 - metabolism</subject><subject>Dietary Supplements</subject><subject>Ethanol - administration & dosage</subject><subject>Ethanol - toxicity</subject><subject>Feeding. Feeding behavior</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Glutamine</subject><subject>Glutamine - pharmacology</subject><subject>Inflammation - pathology</subject><subject>Interleukin-1beta - analysis</subject><subject>Lipid Metabolism</subject><subject>Liver - metabolism</subject><subject>Liver Diseases, Alcoholic - prevention & control</subject><subject>Male</subject><subject>Oxidative Stress</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Triglycerides - analysis</subject><subject>Tumor Necrosis Factor-alpha - analysis</subject><subject>Vertebrates: anatomy and physiology, studies on body, several organs or systems</subject><issn>0955-2863</issn><issn>1873-4847</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1rFTEUhoNY7LX6E9TZiG7mms_JZFWkVC0UXGgXrsKZTNLmMpNck4zQf2_Ge9VdC4EDh-fNOTwHoVcEbwkm3YfddheWMvi4pbj2MN1i3D1BG9JL1vKey6dog5UQLe07doqe57zDGFMuumfolGIhGVd8g35cOmdNyU10ze20FJh9sA2MtfhcEhQfQ1OfD26CeYYS032TbN7HkG2u7cbcpRi8aWy5gxCn1tmxqbn8Ap04mLJ9eaxn6ObT5feLL-31189XFx-vWyOILC0XQBwZYJRUjYKMErq-6-VgOiKoYwqk5FhJZbgEZgcl2cBZLyjHDitgkp2hd4d_9yn-XGwuevbZ2GmCYOOSdS8YpYLKlXz_IEmk6Clbp1dUHFCTYs7JOr1PfoZ0rwnWq3-900f_evWvMdXVf829Po5YhtmO_1J_hVfg7RGAbGByCYLx-T_HlGDsD_fmwDmIGm5TZW6-1UkME8U7TNcVzw-ErXJ_eZt0Nt4GY0ef6kX1GP0jy_4GliWvPg</recordid><startdate>20110301</startdate><enddate>20110301</enddate><creator>Peng, Hsiang-Chi</creator><creator>Chen, Ya-Ling</creator><creator>Chen, Jiun-Rong</creator><creator>Yang, Sien-Sing</creator><creator>Huang, Kuan-Hsun</creator><creator>Wu, Yi-Chin</creator><creator>Lin, Yun-Ho</creator><creator>Yang, Suh-Ching</creator><general>Elsevier Inc</general><general>New York, NY: Elsevier Science</general><general>Elsevier</general><scope>FBQ</scope><scope>IQODW</scope><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>7U7</scope><scope>C1K</scope><scope>7X8</scope></search><sort><creationdate>20110301</creationdate><title>Effects of glutamine administration on inflammatory responses in chronic ethanol-fed rats</title><author>Peng, Hsiang-Chi ; Chen, Ya-Ling ; Chen, Jiun-Rong ; Yang, Sien-Sing ; Huang, Kuan-Hsun ; Wu, Yi-Chin ; Lin, Yun-Ho ; Yang, Suh-Ching</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c517t-45a1f1bad729d51d7a68687bc6152f39a7740979c47a3eb973b4385240f09a373</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Alanine Transaminase - metabolism</topic><topic>Alcoholic liver disease</topic><topic>Animals</topic><topic>Aspartate Aminotransferases - metabolism</topic><topic>Biological and medical sciences</topic><topic>Cholesterol - analysis</topic><topic>Cytochrome P-450 CYP2E1 - metabolism</topic><topic>Dietary Supplements</topic><topic>Ethanol - administration & dosage</topic><topic>Ethanol - toxicity</topic><topic>Feeding. Feeding behavior</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Glutamine</topic><topic>Glutamine - pharmacology</topic><topic>Inflammation - pathology</topic><topic>Interleukin-1beta - analysis</topic><topic>Lipid Metabolism</topic><topic>Liver - metabolism</topic><topic>Liver Diseases, Alcoholic - prevention & control</topic><topic>Male</topic><topic>Oxidative Stress</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Triglycerides - analysis</topic><topic>Tumor Necrosis Factor-alpha - analysis</topic><topic>Vertebrates: anatomy and physiology, studies on body, several organs or systems</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Peng, Hsiang-Chi</creatorcontrib><creatorcontrib>Chen, Ya-Ling</creatorcontrib><creatorcontrib>Chen, Jiun-Rong</creatorcontrib><creatorcontrib>Yang, Sien-Sing</creatorcontrib><creatorcontrib>Huang, Kuan-Hsun</creatorcontrib><creatorcontrib>Wu, Yi-Chin</creatorcontrib><creatorcontrib>Lin, Yun-Ho</creatorcontrib><creatorcontrib>Yang, Suh-Ching</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of nutritional biochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Peng, Hsiang-Chi</au><au>Chen, Ya-Ling</au><au>Chen, Jiun-Rong</au><au>Yang, Sien-Sing</au><au>Huang, Kuan-Hsun</au><au>Wu, Yi-Chin</au><au>Lin, Yun-Ho</au><au>Yang, Suh-Ching</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of glutamine administration on inflammatory responses in chronic ethanol-fed rats</atitle><jtitle>The Journal of nutritional biochemistry</jtitle><addtitle>J Nutr Biochem</addtitle><date>2011-03-01</date><risdate>2011</risdate><volume>22</volume><issue>3</issue><spage>282</spage><epage>288</epage><pages>282-288</pages><issn>0955-2863</issn><eissn>1873-4847</eissn><abstract>The purpose of this study was to investigate the effects of glutamine supplementation on inflammatory responses in chronic ethanol-fed rats. Male Wistar rats weighing about 160 g were divided into five groups. Two groups were fed a normal liquid diet and three groups were fed a glutamine-containing liquid diet. After 1 week, one of the normal liquid diet groups was fed an ethanol-containing liquid diet (CE), and the other group served as the control (CC) group. At the same time, one of the glutamine-containing liquid diet groups was continually fed the same diet (GCG), but the other two groups were fed ethanol-containing diet supplemented with glutamine (GEG) or without glutamine (GE). The following items were analyzed: (1) liver function, (2) cytokine contents, and (3) hepatic oxidative stress. The activities of aspartate transaminase (AST) and alanine transaminase (ALT) and levels of tumor necrosis factor (TNF)-α and interleukin (IL)-1β in the CE group had significantly increased. In addition, hepatic cytochrome P450 2E1 (CYP2E1) expression had significantly increased in the CE, GE and GEG groups. However, the activities of AST and ALT and levels of TNF-α and IL-1β in the GE group were significantly lower than those of the CE group. The results suggest that the plasma inflammatory responses of rats fed an ethanol-containing liquid diet for 7 weeks significantly increased. However, pretreatment with glutamine improved the plasma inflammatory responses induced by ethanol.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>20573494</pmid><doi>10.1016/j.jnutbio.2010.02.006</doi><tpages>7</tpages></addata></record> |
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subjects | Alanine Transaminase - metabolism Alcoholic liver disease Animals Aspartate Aminotransferases - metabolism Biological and medical sciences Cholesterol - analysis Cytochrome P-450 CYP2E1 - metabolism Dietary Supplements Ethanol - administration & dosage Ethanol - toxicity Feeding. Feeding behavior Fundamental and applied biological sciences. Psychology Glutamine Glutamine - pharmacology Inflammation - pathology Interleukin-1beta - analysis Lipid Metabolism Liver - metabolism Liver Diseases, Alcoholic - prevention & control Male Oxidative Stress Rats Rats, Wistar Triglycerides - analysis Tumor Necrosis Factor-alpha - analysis Vertebrates: anatomy and physiology, studies on body, several organs or systems |
title | Effects of glutamine administration on inflammatory responses in chronic ethanol-fed rats |
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