Preventive effects of bovine colostrum supplementation in TNBS-induced colitis in mice

Inflammatory bowel disease (IBD) is a chronic inflammatory disorder for which the current medical therapy is not completely effective. Bovine colostrum (BC) is a biological fluid rich in bioactive molecules that may have beneficial effects on several gastrointestinal disorders. The objectives of thi...

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Veröffentlicht in:PloS one 2018-08, Vol.13 (8), p.e0202929
Hauptverfasser: Filipescu, Iulia Elena, Leonardi, Leonardo, Menchetti, Laura, Guelfi, Gabriella, Traina, Giovanna, Casagrande-Proietti, Patrizia, Piro, Federica, Quattrone, Alda, Barbato, Olimpia, Brecchia, Gabriele
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creator Filipescu, Iulia Elena
Leonardi, Leonardo
Menchetti, Laura
Guelfi, Gabriella
Traina, Giovanna
Casagrande-Proietti, Patrizia
Piro, Federica
Quattrone, Alda
Barbato, Olimpia
Brecchia, Gabriele
description Inflammatory bowel disease (IBD) is a chronic inflammatory disorder for which the current medical therapy is not completely effective. Bovine colostrum (BC) is a biological fluid rich in bioactive molecules that may have beneficial effects on several gastrointestinal disorders. The objectives of this study were to assess the preventive effects of BC supplementation in a mouse model of 2,4,6 trinitrobenzene sulfonic acid (TNBS)-induced colitis using a multidisciplinary approach. Specifically, the following parameters were evaluated: (i) disease activity index (DAI), (ii) histological score, (iii) expression levels of TLR4, anti- and pro-inflammatory cytokines, and (iv) count of some bacterial species of the intestinal microbiota. Mice received a daily suspension of BC (BC group, n = 12) or saline solution (control, CN group, n = 12) for 21 days before the intrarectal inoculation with 1% of TNBS solution. BC was well tolerated and did not induce any histological damage or clinical symptoms. After TNBS treatment, BC group showed a reduction of body weight (BW) loss (P
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Bovine colostrum (BC) is a biological fluid rich in bioactive molecules that may have beneficial effects on several gastrointestinal disorders. The objectives of this study were to assess the preventive effects of BC supplementation in a mouse model of 2,4,6 trinitrobenzene sulfonic acid (TNBS)-induced colitis using a multidisciplinary approach. Specifically, the following parameters were evaluated: (i) disease activity index (DAI), (ii) histological score, (iii) expression levels of TLR4, anti- and pro-inflammatory cytokines, and (iv) count of some bacterial species of the intestinal microbiota. Mice received a daily suspension of BC (BC group, n = 12) or saline solution (control, CN group, n = 12) for 21 days before the intrarectal inoculation with 1% of TNBS solution. BC was well tolerated and did not induce any histological damage or clinical symptoms. After TNBS treatment, BC group showed a reduction of body weight (BW) loss (P<0.01) and histological score (P<0.05) compared to CN. Moreover, the expression levels of TLR4 (P<0.05), IL-1β (P<0.001), IL-8 (P<0.001), and IL-10 (P<0.001) were lower in mice administered with BC, while the concentrations of TNF-α did not show any differences between groups. Finally, the supplementation with BC resulted in a differential response to TNBS treatment in the bacterial count. In CN group, E. coli and Enterococci increased (P<0.001), while Anaerobes (P<0.01), Lactobacilli, and Bifidobacteria (P<0.001) reduced. Conversely, no significant changes in bacterial load were found after the inoculation of TNBS in BC pre-treated mice. This study confirms that TNBS-induced colitis model in mice is useful for studying the mechanisms involved in IBD pathogenesis and shows that pre-treatment with BC reduces the intestinal damages and clinical signs of the colitis. Molecular mechanisms and intestinal microflora could be involved in the protective effect of colostrum.]]></description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0202929</identifier><identifier>PMID: 30138385</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Anaerobes ; Animals ; Antigens ; Bacteria ; Bacterial Load ; Binding sites ; Biology and Life Sciences ; Body weight ; Care and treatment ; Cattle ; Colitis ; Colitis - chemically induced ; Colitis - prevention &amp; control ; Colostrum ; Cytokines ; Cytokines - metabolism ; Damage tolerance ; Disease ; E coli ; Gastrointestinal diseases ; Gastrointestinal Microbiome ; Gene expression ; Genetic aspects ; Health aspects ; Homeostasis ; Immune system ; Immunology ; Inflammation ; Inflammatory bowel disease ; Inflammatory bowel diseases ; Inflammatory diseases ; Inoculation ; Interleukin 10 ; Interleukin 8 ; Intestinal microflora ; Intestine ; Lactobacilli ; Lymphocytes ; Male ; Medicine and Health Sciences ; Mice ; Microbiota ; Molecular modelling ; Pathogenesis ; Permeability ; Properties ; Protective Agents - therapeutic use ; Proteins ; Research and Analysis Methods ; Rodents ; Saline solutions ; Sulfonic acid ; Sulfonic acids ; Supplements ; TLR4 protein ; Toll-Like Receptor 4 - metabolism ; Toll-like receptors ; Trinitrobenzenesulfonic Acid ; Tumor necrosis factor-α ; Veterinary medicine ; Weight reduction</subject><ispartof>PloS one, 2018-08, Vol.13 (8), p.e0202929</ispartof><rights>COPYRIGHT 2018 Public Library of Science</rights><rights>2018 Filipescu et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. 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Bovine colostrum (BC) is a biological fluid rich in bioactive molecules that may have beneficial effects on several gastrointestinal disorders. The objectives of this study were to assess the preventive effects of BC supplementation in a mouse model of 2,4,6 trinitrobenzene sulfonic acid (TNBS)-induced colitis using a multidisciplinary approach. Specifically, the following parameters were evaluated: (i) disease activity index (DAI), (ii) histological score, (iii) expression levels of TLR4, anti- and pro-inflammatory cytokines, and (iv) count of some bacterial species of the intestinal microbiota. Mice received a daily suspension of BC (BC group, n = 12) or saline solution (control, CN group, n = 12) for 21 days before the intrarectal inoculation with 1% of TNBS solution. BC was well tolerated and did not induce any histological damage or clinical symptoms. After TNBS treatment, BC group showed a reduction of body weight (BW) loss (P<0.01) and histological score (P<0.05) compared to CN. Moreover, the expression levels of TLR4 (P<0.05), IL-1β (P<0.001), IL-8 (P<0.001), and IL-10 (P<0.001) were lower in mice administered with BC, while the concentrations of TNF-α did not show any differences between groups. Finally, the supplementation with BC resulted in a differential response to TNBS treatment in the bacterial count. In CN group, E. coli and Enterococci increased (P<0.001), while Anaerobes (P<0.01), Lactobacilli, and Bifidobacteria (P<0.001) reduced. Conversely, no significant changes in bacterial load were found after the inoculation of TNBS in BC pre-treated mice. This study confirms that TNBS-induced colitis model in mice is useful for studying the mechanisms involved in IBD pathogenesis and shows that pre-treatment with BC reduces the intestinal damages and clinical signs of the colitis. Molecular mechanisms and intestinal microflora could be involved in the protective effect of colostrum.]]></description><subject>Anaerobes</subject><subject>Animals</subject><subject>Antigens</subject><subject>Bacteria</subject><subject>Bacterial Load</subject><subject>Binding sites</subject><subject>Biology and Life Sciences</subject><subject>Body weight</subject><subject>Care and treatment</subject><subject>Cattle</subject><subject>Colitis</subject><subject>Colitis - chemically induced</subject><subject>Colitis - prevention &amp; control</subject><subject>Colostrum</subject><subject>Cytokines</subject><subject>Cytokines - metabolism</subject><subject>Damage tolerance</subject><subject>Disease</subject><subject>E coli</subject><subject>Gastrointestinal diseases</subject><subject>Gastrointestinal Microbiome</subject><subject>Gene expression</subject><subject>Genetic aspects</subject><subject>Health aspects</subject><subject>Homeostasis</subject><subject>Immune system</subject><subject>Immunology</subject><subject>Inflammation</subject><subject>Inflammatory bowel disease</subject><subject>Inflammatory bowel diseases</subject><subject>Inflammatory diseases</subject><subject>Inoculation</subject><subject>Interleukin 10</subject><subject>Interleukin 8</subject><subject>Intestinal microflora</subject><subject>Intestine</subject><subject>Lactobacilli</subject><subject>Lymphocytes</subject><subject>Male</subject><subject>Medicine and Health Sciences</subject><subject>Mice</subject><subject>Microbiota</subject><subject>Molecular modelling</subject><subject>Pathogenesis</subject><subject>Permeability</subject><subject>Properties</subject><subject>Protective Agents - 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Academic</collection><collection>ProQuest Engineering Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Agricultural Science Database</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Engineering Database</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>Advanced Technologies &amp; Aerospace Database</collection><collection>ProQuest Advanced Technologies &amp; Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environmental Science Database</collection><collection>Materials Science Collection</collection><collection>Publicly Available Content 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><collection>Engineering Collection</collection><collection>Environmental Science Collection</collection><collection>Genetics Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Filipescu, Iulia Elena</au><au>Leonardi, Leonardo</au><au>Menchetti, Laura</au><au>Guelfi, Gabriella</au><au>Traina, Giovanna</au><au>Casagrande-Proietti, Patrizia</au><au>Piro, Federica</au><au>Quattrone, Alda</au><au>Barbato, Olimpia</au><au>Brecchia, Gabriele</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Preventive effects of bovine colostrum supplementation in TNBS-induced colitis in mice</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2018-08-23</date><risdate>2018</risdate><volume>13</volume><issue>8</issue><spage>e0202929</spage><pages>e0202929-</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract><![CDATA[Inflammatory bowel disease (IBD) is a chronic inflammatory disorder for which the current medical therapy is not completely effective. Bovine colostrum (BC) is a biological fluid rich in bioactive molecules that may have beneficial effects on several gastrointestinal disorders. The objectives of this study were to assess the preventive effects of BC supplementation in a mouse model of 2,4,6 trinitrobenzene sulfonic acid (TNBS)-induced colitis using a multidisciplinary approach. Specifically, the following parameters were evaluated: (i) disease activity index (DAI), (ii) histological score, (iii) expression levels of TLR4, anti- and pro-inflammatory cytokines, and (iv) count of some bacterial species of the intestinal microbiota. Mice received a daily suspension of BC (BC group, n = 12) or saline solution (control, CN group, n = 12) for 21 days before the intrarectal inoculation with 1% of TNBS solution. BC was well tolerated and did not induce any histological damage or clinical symptoms. After TNBS treatment, BC group showed a reduction of body weight (BW) loss (P<0.01) and histological score (P<0.05) compared to CN. Moreover, the expression levels of TLR4 (P<0.05), IL-1β (P<0.001), IL-8 (P<0.001), and IL-10 (P<0.001) were lower in mice administered with BC, while the concentrations of TNF-α did not show any differences between groups. Finally, the supplementation with BC resulted in a differential response to TNBS treatment in the bacterial count. In CN group, E. coli and Enterococci increased (P<0.001), while Anaerobes (P<0.01), Lactobacilli, and Bifidobacteria (P<0.001) reduced. Conversely, no significant changes in bacterial load were found after the inoculation of TNBS in BC pre-treated mice. This study confirms that TNBS-induced colitis model in mice is useful for studying the mechanisms involved in IBD pathogenesis and shows that pre-treatment with BC reduces the intestinal damages and clinical signs of the colitis. Molecular mechanisms and intestinal microflora could be involved in the protective effect of colostrum.]]></abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>30138385</pmid><doi>10.1371/journal.pone.0202929</doi><tpages>e0202929</tpages><orcidid>https://orcid.org/0000-0001-8500-7970</orcidid><orcidid>https://orcid.org/0000-0003-1147-2540</orcidid><oa>free_for_read</oa></addata></record>
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identifier ISSN: 1932-6203
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issn 1932-6203
1932-6203
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source MEDLINE; DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; Free Full-Text Journals in Chemistry; Public Library of Science (PLoS)
subjects Anaerobes
Animals
Antigens
Bacteria
Bacterial Load
Binding sites
Biology and Life Sciences
Body weight
Care and treatment
Cattle
Colitis
Colitis - chemically induced
Colitis - prevention & control
Colostrum
Cytokines
Cytokines - metabolism
Damage tolerance
Disease
E coli
Gastrointestinal diseases
Gastrointestinal Microbiome
Gene expression
Genetic aspects
Health aspects
Homeostasis
Immune system
Immunology
Inflammation
Inflammatory bowel disease
Inflammatory bowel diseases
Inflammatory diseases
Inoculation
Interleukin 10
Interleukin 8
Intestinal microflora
Intestine
Lactobacilli
Lymphocytes
Male
Medicine and Health Sciences
Mice
Microbiota
Molecular modelling
Pathogenesis
Permeability
Properties
Protective Agents - therapeutic use
Proteins
Research and Analysis Methods
Rodents
Saline solutions
Sulfonic acid
Sulfonic acids
Supplements
TLR4 protein
Toll-Like Receptor 4 - metabolism
Toll-like receptors
Trinitrobenzenesulfonic Acid
Tumor necrosis factor-α
Veterinary medicine
Weight reduction
title Preventive effects of bovine colostrum supplementation in TNBS-induced colitis in mice
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