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Dual effects of a high-protein diet on DSS-treated mice during colitis resolution phase
The impact of the dietary protein level on the process of colonic mucosal inflammation and subsequent recovery remains largely unknown. In this study, we fed DSS-treated mice with either a normoproteic (NP) or a high-protein (HP) isocaloric diet from the beginning of the 5-day dextran sulfate sodium...
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Published in: | American journal of physiology: Gastrointestinal and liver physiology 2016-10, Vol.311 (4), p.G624-G633 |
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container_title | American journal of physiology: Gastrointestinal and liver physiology |
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creator | Lan, Annaïg Blais, Anne Coelho, Desire Capron, Juliette Maarouf, Manar Benamouzig, Robert Lancha, Jr, Antonio H Walker, Francine Tomé, Daniel Blachier, François |
description | The impact of the dietary protein level on the process of colonic mucosal inflammation and subsequent recovery remains largely unknown. In this study, we fed DSS-treated mice with either a normoproteic (NP) or a high-protein (HP) isocaloric diet from the beginning of the 5-day dextran sulfate sodium (DSS) treatment to 14 days later. Measurements of colitis indicators (colon weight:length ratio, myeloperoxidase activity, cytokine expressions) showed a similar level of colonic inflammation in both DSS groups during the colitis induction phase. However, during the colitis resolution phase, inflammation intensity was higher in the DSS-HP group than in the DSS-NP group as evidenced by higher inflammatory score and body weight loss. This coincided with a higher mortality rate. In surviving animals, an increase in colonic crypt height associated with a higher number of colon epithelial cells per crypt, and TGF-β3 content was observed in the DSS-HP vs. DSS-NP group. Moreover, colonic expression patterns of tight junction proteins and E-cadherin were also different according to the diet. Altogether, our results indicate that the HP diet, when given during both the induction and resolution periods of DSS-induced colitis, showed deleterious effects during the post-induction phase. However, HP diet ingestion was also associated with morphological and biochemical differences compatible with higher colonic epithelium restoration in surviving animals, indicating an effect of the dietary protein level on colonic crypt repair after acute inflammation. These data highlight the potential impact of the dietary protein amount during the colitis course. |
doi_str_mv | 10.1152/ajpgi.00433.2015 |
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In this study, we fed DSS-treated mice with either a normoproteic (NP) or a high-protein (HP) isocaloric diet from the beginning of the 5-day dextran sulfate sodium (DSS) treatment to 14 days later. Measurements of colitis indicators (colon weight:length ratio, myeloperoxidase activity, cytokine expressions) showed a similar level of colonic inflammation in both DSS groups during the colitis induction phase. However, during the colitis resolution phase, inflammation intensity was higher in the DSS-HP group than in the DSS-NP group as evidenced by higher inflammatory score and body weight loss. This coincided with a higher mortality rate. In surviving animals, an increase in colonic crypt height associated with a higher number of colon epithelial cells per crypt, and TGF-β3 content was observed in the DSS-HP vs. DSS-NP group. Moreover, colonic expression patterns of tight junction proteins and E-cadherin were also different according to the diet. Altogether, our results indicate that the HP diet, when given during both the induction and resolution periods of DSS-induced colitis, showed deleterious effects during the post-induction phase. However, HP diet ingestion was also associated with morphological and biochemical differences compatible with higher colonic epithelium restoration in surviving animals, indicating an effect of the dietary protein level on colonic crypt repair after acute inflammation. These data highlight the potential impact of the dietary protein amount during the colitis course.</description><identifier>ISSN: 0193-1857</identifier><identifier>EISSN: 1522-1547</identifier><identifier>DOI: 10.1152/ajpgi.00433.2015</identifier><identifier>PMID: 27562061</identifier><identifier>CODEN: APGPDF</identifier><language>eng</language><publisher>United States: American Physiological Society</publisher><subject>Animals ; Colitis - chemically induced ; Colitis - diet therapy ; Colitis - metabolism ; Colon - drug effects ; Colon - metabolism ; Dextran Sulfate ; Diet ; Dietary Proteins - administration & dosage ; Dietary Proteins - therapeutic use ; Disease Models, Animal ; Effects ; Food and Nutrition ; Humans ; Inflammation - chemically induced ; Inflammation - diet therapy ; Inflammation - metabolism ; Inflammatory bowel disease ; Intestinal Mucosa - drug effects ; Intestinal Mucosa - metabolism ; Life Sciences ; Male ; Mice ; Proteins ; Rodents ; Transforming Growth Factor beta3 - metabolism</subject><ispartof>American journal of physiology: Gastrointestinal and liver physiology, 2016-10, Vol.311 (4), p.G624-G633</ispartof><rights>Copyright © 2016 the American Physiological Society.</rights><rights>Copyright American Physiological Society Oct 1, 2016</rights><rights>Copyright</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c469t-bca63401c4d0044d971c9fe06c5ea4e8419d31e392bcd0c1732e6c932920b6cf3</citedby><cites>FETCH-LOGICAL-c469t-bca63401c4d0044d971c9fe06c5ea4e8419d31e392bcd0c1732e6c932920b6cf3</cites><orcidid>0000-0003-1952-6830</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27562061$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://agroparistech.hal.science/hal-01488439$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Lan, Annaïg</creatorcontrib><creatorcontrib>Blais, Anne</creatorcontrib><creatorcontrib>Coelho, Desire</creatorcontrib><creatorcontrib>Capron, Juliette</creatorcontrib><creatorcontrib>Maarouf, Manar</creatorcontrib><creatorcontrib>Benamouzig, Robert</creatorcontrib><creatorcontrib>Lancha, Jr, Antonio H</creatorcontrib><creatorcontrib>Walker, Francine</creatorcontrib><creatorcontrib>Tomé, Daniel</creatorcontrib><creatorcontrib>Blachier, François</creatorcontrib><title>Dual effects of a high-protein diet on DSS-treated mice during colitis resolution phase</title><title>American journal of physiology: Gastrointestinal and liver physiology</title><addtitle>Am J Physiol Gastrointest Liver Physiol</addtitle><description>The impact of the dietary protein level on the process of colonic mucosal inflammation and subsequent recovery remains largely unknown. In this study, we fed DSS-treated mice with either a normoproteic (NP) or a high-protein (HP) isocaloric diet from the beginning of the 5-day dextran sulfate sodium (DSS) treatment to 14 days later. Measurements of colitis indicators (colon weight:length ratio, myeloperoxidase activity, cytokine expressions) showed a similar level of colonic inflammation in both DSS groups during the colitis induction phase. However, during the colitis resolution phase, inflammation intensity was higher in the DSS-HP group than in the DSS-NP group as evidenced by higher inflammatory score and body weight loss. This coincided with a higher mortality rate. In surviving animals, an increase in colonic crypt height associated with a higher number of colon epithelial cells per crypt, and TGF-β3 content was observed in the DSS-HP vs. DSS-NP group. Moreover, colonic expression patterns of tight junction proteins and E-cadherin were also different according to the diet. Altogether, our results indicate that the HP diet, when given during both the induction and resolution periods of DSS-induced colitis, showed deleterious effects during the post-induction phase. However, HP diet ingestion was also associated with morphological and biochemical differences compatible with higher colonic epithelium restoration in surviving animals, indicating an effect of the dietary protein level on colonic crypt repair after acute inflammation. These data highlight the potential impact of the dietary protein amount during the colitis course.</description><subject>Animals</subject><subject>Colitis - chemically induced</subject><subject>Colitis - diet therapy</subject><subject>Colitis - metabolism</subject><subject>Colon - drug effects</subject><subject>Colon - metabolism</subject><subject>Dextran Sulfate</subject><subject>Diet</subject><subject>Dietary Proteins - administration & dosage</subject><subject>Dietary Proteins - therapeutic use</subject><subject>Disease Models, Animal</subject><subject>Effects</subject><subject>Food and Nutrition</subject><subject>Humans</subject><subject>Inflammation - chemically induced</subject><subject>Inflammation - diet therapy</subject><subject>Inflammation - metabolism</subject><subject>Inflammatory bowel disease</subject><subject>Intestinal Mucosa - drug effects</subject><subject>Intestinal Mucosa - metabolism</subject><subject>Life Sciences</subject><subject>Male</subject><subject>Mice</subject><subject>Proteins</subject><subject>Rodents</subject><subject>Transforming Growth Factor beta3 - metabolism</subject><issn>0193-1857</issn><issn>1522-1547</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNpdkU1vEzEQhi1ERUPhzglZ4gKHTT3-WK-PVQu0UqQeCuJoOd7ZxNFmHWwvUv89TlN64DTS6HlH8-oh5AOwJYDil2532IQlY1KIJWegXpFFXfMGlNSvyYKBEQ10Sp-TtznvGGOKA7wh51yrlrMWFuTXzexGisOAvmQaB-roNmy2zSHFgmGifcBC40RvHh6aktAV7Ok-eKT9nMK0oT6OoYRME-Y4ziVU9LB1Gd-Rs8GNGd8_zwvy89vXH9e3zer--9311arxsjWlWXvXCsnAy762kL3R4M2ArPUKncROgukFoDB87XvmQQuOrTeCG87WrR_EBflyurt1oz2ksHfp0UYX7O3Vyh53DGTXSWH-QGU_n9ha7veMudh9yB7H0U0Y52yhE0p0oLWq6Kf_0F2c01SbVIpr0RnQslLsRPkUc044vHwAzB4F2SdB9kmQPQqqkY_Ph-f1HvuXwD8j4i_eLIpf</recordid><startdate>20161001</startdate><enddate>20161001</enddate><creator>Lan, Annaïg</creator><creator>Blais, Anne</creator><creator>Coelho, Desire</creator><creator>Capron, Juliette</creator><creator>Maarouf, Manar</creator><creator>Benamouzig, Robert</creator><creator>Lancha, Jr, Antonio H</creator><creator>Walker, Francine</creator><creator>Tomé, Daniel</creator><creator>Blachier, François</creator><general>American Physiological Society</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>7X8</scope><scope>1XC</scope><scope>VOOES</scope><orcidid>https://orcid.org/0000-0003-1952-6830</orcidid></search><sort><creationdate>20161001</creationdate><title>Dual effects of a high-protein diet on DSS-treated mice during colitis resolution phase</title><author>Lan, Annaïg ; 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In this study, we fed DSS-treated mice with either a normoproteic (NP) or a high-protein (HP) isocaloric diet from the beginning of the 5-day dextran sulfate sodium (DSS) treatment to 14 days later. Measurements of colitis indicators (colon weight:length ratio, myeloperoxidase activity, cytokine expressions) showed a similar level of colonic inflammation in both DSS groups during the colitis induction phase. However, during the colitis resolution phase, inflammation intensity was higher in the DSS-HP group than in the DSS-NP group as evidenced by higher inflammatory score and body weight loss. This coincided with a higher mortality rate. In surviving animals, an increase in colonic crypt height associated with a higher number of colon epithelial cells per crypt, and TGF-β3 content was observed in the DSS-HP vs. DSS-NP group. Moreover, colonic expression patterns of tight junction proteins and E-cadherin were also different according to the diet. Altogether, our results indicate that the HP diet, when given during both the induction and resolution periods of DSS-induced colitis, showed deleterious effects during the post-induction phase. However, HP diet ingestion was also associated with morphological and biochemical differences compatible with higher colonic epithelium restoration in surviving animals, indicating an effect of the dietary protein level on colonic crypt repair after acute inflammation. These data highlight the potential impact of the dietary protein amount during the colitis course.</abstract><cop>United States</cop><pub>American Physiological Society</pub><pmid>27562061</pmid><doi>10.1152/ajpgi.00433.2015</doi><orcidid>https://orcid.org/0000-0003-1952-6830</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Animals Colitis - chemically induced Colitis - diet therapy Colitis - metabolism Colon - drug effects Colon - metabolism Dextran Sulfate Diet Dietary Proteins - administration & dosage Dietary Proteins - therapeutic use Disease Models, Animal Effects Food and Nutrition Humans Inflammation - chemically induced Inflammation - diet therapy Inflammation - metabolism Inflammatory bowel disease Intestinal Mucosa - drug effects Intestinal Mucosa - metabolism Life Sciences Male Mice Proteins Rodents Transforming Growth Factor beta3 - metabolism |
title | Dual effects of a high-protein diet on DSS-treated mice during colitis resolution phase |
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