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Varied doses and chemical forms of selenium supplementation differentially affect mouse intestinal physiology.

Identifieur interne : 000299 ( Main/Exploration ); précédent : 000298; suivant : 000300

Varied doses and chemical forms of selenium supplementation differentially affect mouse intestinal physiology.

Auteurs : Qixiao Zhai [République populaire de Chine] ; Yue Xiao [République populaire de Chine] ; Peng Li [République populaire de Chine] ; Fengwei Tian [République populaire de Chine] ; Jianxin Zhao [République populaire de Chine] ; Hao Zhang [République populaire de Chine] ; Wei Chen [République populaire de Chine]

Source :

RBID : pubmed:31397465

Descripteurs français

English descriptors

Abstract

In this study, the effects of three doses (diets containing <0.01, 0.15, 0.40 mg kg-1 Se) and two forms (sodium selenite and selenomethionine) of dietary Se supplementation on the intestinal physiology of untreated, dextran sodium sulfate-treated, and Salmonella typhimurium-infected mice were evaluated. The underlying modes of action of the varied doses and forms of Se supplementation were analyzed using fecal metabolomic and jejunal proteomic approaches. Compared with adequate Se (0.15 mg kg-1 Se) supplementation, Se-deficiency supplementation adversely affected the gut barrier and intestinal immune responses of the untreated mice and increased their susceptibility to experimental colitis and pathogen infection. In contrast, supranutritional Se (0.40 mg kg-1 Se) supplementation improved mouse intestinal physiology compared with adequate Se supplementation. Varied doses of Se supplementation differentially perturbed the fecal metabolic profiles of and jejunal protein expression in mice. Further, both forms of dietary Se supplementation, i.e., sodium selenite and selenomethionine, showed similar effects on the gut barrier and intestinal immune homeostasis but differentially affected fecal metabolites, such as neurosubstances and immunomodulators, and induced significant proteomic variations in various pathways, including the xenobiotic detoxification pathway and glutathione metabolism. Our results indicate that the doses and chemical forms of Se should be considered when developing dietary nutritional supplements for gut health.

DOI: 10.1039/c9fo00278b
PubMed: 31397465


Affiliations:


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<div type="abstract" xml:lang="en">In this study, the effects of three doses (diets containing <0.01, 0.15, 0.40 mg kg
<sup>-1</sup>
Se) and two forms (sodium selenite and selenomethionine) of dietary Se supplementation on the intestinal physiology of untreated, dextran sodium sulfate-treated, and Salmonella typhimurium-infected mice were evaluated. The underlying modes of action of the varied doses and forms of Se supplementation were analyzed using fecal metabolomic and jejunal proteomic approaches. Compared with adequate Se (0.15 mg kg
<sup>-1</sup>
Se) supplementation, Se-deficiency supplementation adversely affected the gut barrier and intestinal immune responses of the untreated mice and increased their susceptibility to experimental colitis and pathogen infection. In contrast, supranutritional Se (0.40 mg kg
<sup>-1</sup>
Se) supplementation improved mouse intestinal physiology compared with adequate Se supplementation. Varied doses of Se supplementation differentially perturbed the fecal metabolic profiles of and jejunal protein expression in mice. Further, both forms of dietary Se supplementation, i.e., sodium selenite and selenomethionine, showed similar effects on the gut barrier and intestinal immune homeostasis but differentially affected fecal metabolites, such as neurosubstances and immunomodulators, and induced significant proteomic variations in various pathways, including the xenobiotic detoxification pathway and glutathione metabolism. Our results indicate that the doses and chemical forms of Se should be considered when developing dietary nutritional supplements for gut health.</div>
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<AbstractText>In this study, the effects of three doses (diets containing <0.01, 0.15, 0.40 mg kg
<sup>-1</sup>
Se) and two forms (sodium selenite and selenomethionine) of dietary Se supplementation on the intestinal physiology of untreated, dextran sodium sulfate-treated, and Salmonella typhimurium-infected mice were evaluated. The underlying modes of action of the varied doses and forms of Se supplementation were analyzed using fecal metabolomic and jejunal proteomic approaches. Compared with adequate Se (0.15 mg kg
<sup>-1</sup>
Se) supplementation, Se-deficiency supplementation adversely affected the gut barrier and intestinal immune responses of the untreated mice and increased their susceptibility to experimental colitis and pathogen infection. In contrast, supranutritional Se (0.40 mg kg
<sup>-1</sup>
Se) supplementation improved mouse intestinal physiology compared with adequate Se supplementation. Varied doses of Se supplementation differentially perturbed the fecal metabolic profiles of and jejunal protein expression in mice. Further, both forms of dietary Se supplementation, i.e., sodium selenite and selenomethionine, showed similar effects on the gut barrier and intestinal immune homeostasis but differentially affected fecal metabolites, such as neurosubstances and immunomodulators, and induced significant proteomic variations in various pathways, including the xenobiotic detoxification pathway and glutathione metabolism. Our results indicate that the doses and chemical forms of Se should be considered when developing dietary nutritional supplements for gut health.</AbstractText>
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<AffiliationInfo>
<Affiliation>State Key Laboratory of Food Science and Technology, Jiangnan University, Wuxi, Jiangsu 214122, P. R. China. chenwei66@jiangnan.edu.cn and School of Food Science and Technology, Jiangnan University, Wuxi, Jiangsu 214122, P. R. China and National Engineering Research Center for Functional Food, Jiangnan University, Wuxi, Jiangsu 214122, P. R. China and Beijing Innovation Center of Food Nutrition and Human Health, Beijing Technology and Business University (BTBU), Beijing 100048, P. R. China.</Affiliation>
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<QualifierName UI="Q000382" MajorTopicYN="N">microbiology</QualifierName>
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<MeshHeading>
<DescriptorName UI="D012486" MajorTopicYN="N">Salmonella typhimurium</DescriptorName>
<QualifierName UI="Q000502" MajorTopicYN="N">physiology</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D012645" MajorTopicYN="N">Selenomethionine</DescriptorName>
<QualifierName UI="Q000008" MajorTopicYN="Y">administration & dosage</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D018038" MajorTopicYN="N">Sodium Selenite</DescriptorName>
<QualifierName UI="Q000008" MajorTopicYN="Y">administration & dosage</QualifierName>
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</MedlineCitation>
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<Day>10</Day>
<Hour>6</Hour>
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<Month>2</Month>
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<Hour>6</Hour>
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<Year>2019</Year>
<Month>8</Month>
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<country>
<li>République populaire de Chine</li>
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<li>Pékin</li>
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<country name="République populaire de Chine">
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<name sortKey="Zhai, Qixiao" sort="Zhai, Qixiao" uniqKey="Zhai Q" first="Qixiao" last="Zhai">Qixiao Zhai</name>
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<name sortKey="Chen, Wei" sort="Chen, Wei" uniqKey="Chen W" first="Wei" last="Chen">Wei Chen</name>
<name sortKey="Li, Peng" sort="Li, Peng" uniqKey="Li P" first="Peng" last="Li">Peng Li</name>
<name sortKey="Tian, Fengwei" sort="Tian, Fengwei" uniqKey="Tian F" first="Fengwei" last="Tian">Fengwei Tian</name>
<name sortKey="Xiao, Yue" sort="Xiao, Yue" uniqKey="Xiao Y" first="Yue" last="Xiao">Yue Xiao</name>
<name sortKey="Zhang, Hao" sort="Zhang, Hao" uniqKey="Zhang H" first="Hao" last="Zhang">Hao Zhang</name>
<name sortKey="Zhao, Jianxin" sort="Zhao, Jianxin" uniqKey="Zhao J" first="Jianxin" last="Zhao">Jianxin Zhao</name>
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