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Individual and combined effects of subclinical doses of deoxynivalenol and fumonisins in piglets

Scope: Deoxynivalenol (DON) and fumonisins (FB) are the most frequently encountered mycotoxins produced by Fusarium species and most commonly co-occur in animal diets. These mycotoxins were studied for their toxicity in piglets on several parameters including plasma biochemistry, organ histopatholog...

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Published in:Molecular nutrition & food research 2011-05, Vol.55 (5), p.761-771
Main Authors: Grenier, Bertrand, Loureiro-Bracarense, Ana-Paula, Lucioli, Joelma, Pacheco, Graziela Drociunas, Cossalter, Anne-Marie, Moll, Wulf-Dieter, Schatzmayr, Gerd, Oswald, Isabelle P
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cited_by cdi_FETCH-LOGICAL-c6092-dce7946232cbd5368e75dbcdbac9ff4e8c4a9cf7ba7657189235f6911a7b3d273
cites cdi_FETCH-LOGICAL-c6092-dce7946232cbd5368e75dbcdbac9ff4e8c4a9cf7ba7657189235f6911a7b3d273
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container_issue 5
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container_title Molecular nutrition & food research
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creator Grenier, Bertrand
Loureiro-Bracarense, Ana-Paula
Lucioli, Joelma
Pacheco, Graziela Drociunas
Cossalter, Anne-Marie
Moll, Wulf-Dieter
Schatzmayr, Gerd
Oswald, Isabelle P
description Scope: Deoxynivalenol (DON) and fumonisins (FB) are the most frequently encountered mycotoxins produced by Fusarium species and most commonly co-occur in animal diets. These mycotoxins were studied for their toxicity in piglets on several parameters including plasma biochemistry, organ histopathology and immune response. Methods and results: Twenty-four 5-wk-old animals were randomly assigned to four different groups, receiving separate diets for 5 wk, a control diet, a diet contaminated with either DON (3 mg/kg) or FB (6 mg/kg) or both toxins. At days 4 and 16 of the trial, the animals were subcutaneously immunized with ovalbumin to assess their specific immune response. The different diets did not affect animal performance and had minimal effect on hematological and biochemical blood parameters. By contrast, DON and FB induced histopathological lesions in the liver, the lungs and the kidneys of exposed animals. The liver was significantly more affected when the two mycotoxins were present simultaneously. The contaminated diets also altered the specific immune response upon vaccination as measured by reduced anti-ovalbumin IgG level in the plasma and reduced lymphocyte proliferation upon antigenic stimulation. Because cytokines play a key role in immunity, the expression levels of IL-8, IL-1β, IL-6 and macrophage inflammatory protein-1β were measured by RT-PCR at the end of the experiment. The expression of these four cytokines was significantly decreased in the spleen of piglets exposed to multi-contaminated diet. Conclusion: Taken together, our data indicate that ingestion of multi-contaminated diet induces greater histopathological lesions and higher immune suppression than ingestion of mono-contaminated diets.
doi_str_mv 10.1002/mnfr.201000402
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These mycotoxins were studied for their toxicity in piglets on several parameters including plasma biochemistry, organ histopathology and immune response. Methods and results: Twenty-four 5-wk-old animals were randomly assigned to four different groups, receiving separate diets for 5 wk, a control diet, a diet contaminated with either DON (3 mg/kg) or FB (6 mg/kg) or both toxins. At days 4 and 16 of the trial, the animals were subcutaneously immunized with ovalbumin to assess their specific immune response. The different diets did not affect animal performance and had minimal effect on hematological and biochemical blood parameters. By contrast, DON and FB induced histopathological lesions in the liver, the lungs and the kidneys of exposed animals. The liver was significantly more affected when the two mycotoxins were present simultaneously. The contaminated diets also altered the specific immune response upon vaccination as measured by reduced anti-ovalbumin IgG level in the plasma and reduced lymphocyte proliferation upon antigenic stimulation. Because cytokines play a key role in immunity, the expression levels of IL-8, IL-1β, IL-6 and macrophage inflammatory protein-1β were measured by RT-PCR at the end of the experiment. The expression of these four cytokines was significantly decreased in the spleen of piglets exposed to multi-contaminated diet. Conclusion: Taken together, our data indicate that ingestion of multi-contaminated diet induces greater histopathological lesions and higher immune suppression than ingestion of mono-contaminated diets.</description><identifier>ISSN: 1613-4125</identifier><identifier>ISSN: 1613-4133</identifier><identifier>EISSN: 1613-4133</identifier><identifier>DOI: 10.1002/mnfr.201000402</identifier><identifier>PMID: 21259430</identifier><language>eng</language><publisher>Weinheim: Wiley-VCH Verlag</publisher><subject>animal performance ; Animals ; Biological and medical sciences ; Blood ; Co-contamination ; cytokines ; Cytokines - genetics ; Data processing ; Deoxynivalenol ; diet ; dietary exposure ; Diets ; feed contamination ; Food industries ; Food toxicology ; Fumonisins ; Fumonisins - toxicity ; Fundamental and applied biological sciences. Psychology ; Fusarium ; histopathology ; Immune response ; Immune System - drug effects ; Immunity ; Immunoglobulin G ; Inflammation ; ingestion ; Interleukin 6 ; Interleukin 8 ; interleukin-1 ; Kidney ; Kidney - drug effects ; Kidney - pathology ; kidneys ; lesions (animal) ; Life Sciences ; Liver ; Liver - drug effects ; Liver - pathology ; Lung ; Lung - drug effects ; Lung - pathology ; lungs ; lymphocyte proliferation ; Lymphocytes ; Macrophages ; Male ; Mycotoxins ; Ovalbumin ; piglet feeding ; piglets ; Polymerase chain reaction ; Spleen ; Subclinical doses ; Swine ; Toxicity ; toxicity testing ; Trichothecenes - toxicity ; Vaccination ; Vomitoxin ; Weight Gain - drug effects</subject><ispartof>Molecular nutrition &amp; food research, 2011-05, Vol.55 (5), p.761-771</ispartof><rights>Copyright © 2011 WILEY‐VCH Verlag GmbH &amp; Co. KGaA, Weinheim</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2011 WILEY-VCH Verlag GmbH &amp; Co. KGaA, Weinheim.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c6092-dce7946232cbd5368e75dbcdbac9ff4e8c4a9cf7ba7657189235f6911a7b3d273</citedby><cites>FETCH-LOGICAL-c6092-dce7946232cbd5368e75dbcdbac9ff4e8c4a9cf7ba7657189235f6911a7b3d273</cites><orcidid>0000-0001-9918-277X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,777,781,882,27905,27906</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=24165748$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21259430$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.inrae.fr/hal-02644751$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Grenier, Bertrand</creatorcontrib><creatorcontrib>Loureiro-Bracarense, Ana-Paula</creatorcontrib><creatorcontrib>Lucioli, Joelma</creatorcontrib><creatorcontrib>Pacheco, Graziela Drociunas</creatorcontrib><creatorcontrib>Cossalter, Anne-Marie</creatorcontrib><creatorcontrib>Moll, Wulf-Dieter</creatorcontrib><creatorcontrib>Schatzmayr, Gerd</creatorcontrib><creatorcontrib>Oswald, Isabelle P</creatorcontrib><title>Individual and combined effects of subclinical doses of deoxynivalenol and fumonisins in piglets</title><title>Molecular nutrition &amp; food research</title><addtitle>Mol. Nutr. Food Res</addtitle><description>Scope: Deoxynivalenol (DON) and fumonisins (FB) are the most frequently encountered mycotoxins produced by Fusarium species and most commonly co-occur in animal diets. These mycotoxins were studied for their toxicity in piglets on several parameters including plasma biochemistry, organ histopathology and immune response. Methods and results: Twenty-four 5-wk-old animals were randomly assigned to four different groups, receiving separate diets for 5 wk, a control diet, a diet contaminated with either DON (3 mg/kg) or FB (6 mg/kg) or both toxins. At days 4 and 16 of the trial, the animals were subcutaneously immunized with ovalbumin to assess their specific immune response. The different diets did not affect animal performance and had minimal effect on hematological and biochemical blood parameters. By contrast, DON and FB induced histopathological lesions in the liver, the lungs and the kidneys of exposed animals. The liver was significantly more affected when the two mycotoxins were present simultaneously. The contaminated diets also altered the specific immune response upon vaccination as measured by reduced anti-ovalbumin IgG level in the plasma and reduced lymphocyte proliferation upon antigenic stimulation. Because cytokines play a key role in immunity, the expression levels of IL-8, IL-1β, IL-6 and macrophage inflammatory protein-1β were measured by RT-PCR at the end of the experiment. The expression of these four cytokines was significantly decreased in the spleen of piglets exposed to multi-contaminated diet. Conclusion: Taken together, our data indicate that ingestion of multi-contaminated diet induces greater histopathological lesions and higher immune suppression than ingestion of mono-contaminated diets.</description><subject>animal performance</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Blood</subject><subject>Co-contamination</subject><subject>cytokines</subject><subject>Cytokines - genetics</subject><subject>Data processing</subject><subject>Deoxynivalenol</subject><subject>diet</subject><subject>dietary exposure</subject><subject>Diets</subject><subject>feed contamination</subject><subject>Food industries</subject><subject>Food toxicology</subject><subject>Fumonisins</subject><subject>Fumonisins - toxicity</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Fusarium</subject><subject>histopathology</subject><subject>Immune response</subject><subject>Immune System - drug effects</subject><subject>Immunity</subject><subject>Immunoglobulin G</subject><subject>Inflammation</subject><subject>ingestion</subject><subject>Interleukin 6</subject><subject>Interleukin 8</subject><subject>interleukin-1</subject><subject>Kidney</subject><subject>Kidney - drug effects</subject><subject>Kidney - pathology</subject><subject>kidneys</subject><subject>lesions (animal)</subject><subject>Life Sciences</subject><subject>Liver</subject><subject>Liver - drug effects</subject><subject>Liver - pathology</subject><subject>Lung</subject><subject>Lung - drug effects</subject><subject>Lung - pathology</subject><subject>lungs</subject><subject>lymphocyte proliferation</subject><subject>Lymphocytes</subject><subject>Macrophages</subject><subject>Male</subject><subject>Mycotoxins</subject><subject>Ovalbumin</subject><subject>piglet feeding</subject><subject>piglets</subject><subject>Polymerase chain reaction</subject><subject>Spleen</subject><subject>Subclinical doses</subject><subject>Swine</subject><subject>Toxicity</subject><subject>toxicity testing</subject><subject>Trichothecenes - toxicity</subject><subject>Vaccination</subject><subject>Vomitoxin</subject><subject>Weight Gain - drug effects</subject><issn>1613-4125</issn><issn>1613-4133</issn><issn>1613-4133</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNqFkUtv1DAUhSMEoqWwZQnZVIJFBr8dL6uKPtBQJKBUYmMcP4ohsQd7MnT-PR4yBHasfHX0neP7qKqnECwgAOjVEFxaIFBqQAC6Vx1CBnFDIMb35xrRg-pRzt8AwBAR_LA6QEUTBIPD6stlMH7jzaj6WgVT6zh0PlhTW-esXuc6ujqPne598LowJmb7WzQ23m2D36jehjh53TjE4LMPufahXvnb3q7z4-qBU322T_bvUXV99vrj6UWzfHd-eXqybDQDAjVGWy4IQxjpzlDMWsup6bTplBbOEdtqooR2vFOcUQ5bgTB1TECoeIcN4vioejnlflW9XCU_qLSVUXl5cbKUOw0gRgincAML-2JiVyn-GG1ey8FnbfteBRvHLCFALUCgRaygiwnVKeacrJuzIZC7C8jdBeR8gWJ4ts8eu8GaGf-z8gIc7wGVy0ZdUkH7_JcjsAxI2sKJifvpe7v9z7fy7dXZ-3-baCavz2t7N3tV-i4Zx5zKm6tz-QnfCEbeUPm58M8n3qko1W0q_Vx_KHEYQEEZoAT_AlvDt80</recordid><startdate>201105</startdate><enddate>201105</enddate><creator>Grenier, Bertrand</creator><creator>Loureiro-Bracarense, Ana-Paula</creator><creator>Lucioli, Joelma</creator><creator>Pacheco, Graziela Drociunas</creator><creator>Cossalter, Anne-Marie</creator><creator>Moll, Wulf-Dieter</creator><creator>Schatzmayr, Gerd</creator><creator>Oswald, Isabelle P</creator><general>Wiley-VCH Verlag</general><general>WILEY-VCH Verlag</general><general>WILEY‐VCH Verlag</general><general>Wiley</general><scope>FBQ</scope><scope>BSCLL</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>M7N</scope><scope>1XC</scope><scope>VOOES</scope><orcidid>https://orcid.org/0000-0001-9918-277X</orcidid></search><sort><creationdate>201105</creationdate><title>Individual and combined effects of subclinical doses of deoxynivalenol and fumonisins in piglets</title><author>Grenier, Bertrand ; Loureiro-Bracarense, Ana-Paula ; Lucioli, Joelma ; Pacheco, Graziela Drociunas ; Cossalter, Anne-Marie ; Moll, Wulf-Dieter ; Schatzmayr, Gerd ; Oswald, Isabelle P</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c6092-dce7946232cbd5368e75dbcdbac9ff4e8c4a9cf7ba7657189235f6911a7b3d273</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>animal performance</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Blood</topic><topic>Co-contamination</topic><topic>cytokines</topic><topic>Cytokines - genetics</topic><topic>Data processing</topic><topic>Deoxynivalenol</topic><topic>diet</topic><topic>dietary exposure</topic><topic>Diets</topic><topic>feed contamination</topic><topic>Food industries</topic><topic>Food toxicology</topic><topic>Fumonisins</topic><topic>Fumonisins - toxicity</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Fusarium</topic><topic>histopathology</topic><topic>Immune response</topic><topic>Immune System - drug effects</topic><topic>Immunity</topic><topic>Immunoglobulin G</topic><topic>Inflammation</topic><topic>ingestion</topic><topic>Interleukin 6</topic><topic>Interleukin 8</topic><topic>interleukin-1</topic><topic>Kidney</topic><topic>Kidney - drug effects</topic><topic>Kidney - pathology</topic><topic>kidneys</topic><topic>lesions (animal)</topic><topic>Life Sciences</topic><topic>Liver</topic><topic>Liver - drug effects</topic><topic>Liver - pathology</topic><topic>Lung</topic><topic>Lung - drug effects</topic><topic>Lung - pathology</topic><topic>lungs</topic><topic>lymphocyte proliferation</topic><topic>Lymphocytes</topic><topic>Macrophages</topic><topic>Male</topic><topic>Mycotoxins</topic><topic>Ovalbumin</topic><topic>piglet feeding</topic><topic>piglets</topic><topic>Polymerase chain reaction</topic><topic>Spleen</topic><topic>Subclinical doses</topic><topic>Swine</topic><topic>Toxicity</topic><topic>toxicity testing</topic><topic>Trichothecenes - toxicity</topic><topic>Vaccination</topic><topic>Vomitoxin</topic><topic>Weight Gain - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Grenier, Bertrand</creatorcontrib><creatorcontrib>Loureiro-Bracarense, Ana-Paula</creatorcontrib><creatorcontrib>Lucioli, Joelma</creatorcontrib><creatorcontrib>Pacheco, Graziela Drociunas</creatorcontrib><creatorcontrib>Cossalter, Anne-Marie</creatorcontrib><creatorcontrib>Moll, Wulf-Dieter</creatorcontrib><creatorcontrib>Schatzmayr, Gerd</creatorcontrib><creatorcontrib>Oswald, Isabelle P</creatorcontrib><collection>AGRIS</collection><collection>Istex</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>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><jtitle>Molecular nutrition &amp; food research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Grenier, Bertrand</au><au>Loureiro-Bracarense, Ana-Paula</au><au>Lucioli, Joelma</au><au>Pacheco, Graziela Drociunas</au><au>Cossalter, Anne-Marie</au><au>Moll, Wulf-Dieter</au><au>Schatzmayr, Gerd</au><au>Oswald, Isabelle P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Individual and combined effects of subclinical doses of deoxynivalenol and fumonisins in piglets</atitle><jtitle>Molecular nutrition &amp; food research</jtitle><addtitle>Mol. Nutr. Food Res</addtitle><date>2011-05</date><risdate>2011</risdate><volume>55</volume><issue>5</issue><spage>761</spage><epage>771</epage><pages>761-771</pages><issn>1613-4125</issn><issn>1613-4133</issn><eissn>1613-4133</eissn><abstract>Scope: Deoxynivalenol (DON) and fumonisins (FB) are the most frequently encountered mycotoxins produced by Fusarium species and most commonly co-occur in animal diets. These mycotoxins were studied for their toxicity in piglets on several parameters including plasma biochemistry, organ histopathology and immune response. Methods and results: Twenty-four 5-wk-old animals were randomly assigned to four different groups, receiving separate diets for 5 wk, a control diet, a diet contaminated with either DON (3 mg/kg) or FB (6 mg/kg) or both toxins. At days 4 and 16 of the trial, the animals were subcutaneously immunized with ovalbumin to assess their specific immune response. The different diets did not affect animal performance and had minimal effect on hematological and biochemical blood parameters. By contrast, DON and FB induced histopathological lesions in the liver, the lungs and the kidneys of exposed animals. The liver was significantly more affected when the two mycotoxins were present simultaneously. The contaminated diets also altered the specific immune response upon vaccination as measured by reduced anti-ovalbumin IgG level in the plasma and reduced lymphocyte proliferation upon antigenic stimulation. Because cytokines play a key role in immunity, the expression levels of IL-8, IL-1β, IL-6 and macrophage inflammatory protein-1β were measured by RT-PCR at the end of the experiment. The expression of these four cytokines was significantly decreased in the spleen of piglets exposed to multi-contaminated diet. Conclusion: Taken together, our data indicate that ingestion of multi-contaminated diet induces greater histopathological lesions and higher immune suppression than ingestion of mono-contaminated diets.</abstract><cop>Weinheim</cop><pub>Wiley-VCH Verlag</pub><pmid>21259430</pmid><doi>10.1002/mnfr.201000402</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0001-9918-277X</orcidid><oa>free_for_read</oa></addata></record>
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ispartof Molecular nutrition & food research, 2011-05, Vol.55 (5), p.761-771
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source Wiley-Blackwell Read & Publish Collection
subjects animal performance
Animals
Biological and medical sciences
Blood
Co-contamination
cytokines
Cytokines - genetics
Data processing
Deoxynivalenol
diet
dietary exposure
Diets
feed contamination
Food industries
Food toxicology
Fumonisins
Fumonisins - toxicity
Fundamental and applied biological sciences. Psychology
Fusarium
histopathology
Immune response
Immune System - drug effects
Immunity
Immunoglobulin G
Inflammation
ingestion
Interleukin 6
Interleukin 8
interleukin-1
Kidney
Kidney - drug effects
Kidney - pathology
kidneys
lesions (animal)
Life Sciences
Liver
Liver - drug effects
Liver - pathology
Lung
Lung - drug effects
Lung - pathology
lungs
lymphocyte proliferation
Lymphocytes
Macrophages
Male
Mycotoxins
Ovalbumin
piglet feeding
piglets
Polymerase chain reaction
Spleen
Subclinical doses
Swine
Toxicity
toxicity testing
Trichothecenes - toxicity
Vaccination
Vomitoxin
Weight Gain - drug effects
title Individual and combined effects of subclinical doses of deoxynivalenol and fumonisins in piglets
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