Effects of vitamin E and selenium deficiencies on rat immune function

The effects of dietary restriction of vitamin E and selenium were studied in male Long-Evans hooded rats. Weanling animals were maintained for 5-6 weeks on torula yeast-based diets, with or without the addition of vitamin E (150 IU/kg) or selenium (0.5 mg/kg), to form the following dietary groups: +...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Immunology 1985, Vol.54 (1), p.173-180
Hauptverfasser: ESKEW, M. L, SCHOLZ, R. W, REDDY, C. C, TODHUNTER, D. A, ZARKOWER, A
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 180
container_issue 1
container_start_page 173
container_title Immunology
container_volume 54
creator ESKEW, M. L
SCHOLZ, R. W
REDDY, C. C
TODHUNTER, D. A
ZARKOWER, A
description The effects of dietary restriction of vitamin E and selenium were studied in male Long-Evans hooded rats. Weanling animals were maintained for 5-6 weeks on torula yeast-based diets, with or without the addition of vitamin E (150 IU/kg) or selenium (0.5 mg/kg), to form the following dietary groups: +E, +Se; +E, -Se; -E, +Se; -E, -Se, and a fifth group pair-fed with the -E, -Se group. This latter group exhibited a decreased rate of growth similar to the -E, -Se group. Lymphocyte blastogenesis in response to mitogens was decreased in animals fed the diets deficient in either vitamin E or selenium, and also in the pair-fed group. Very marked suppression of mitogen responses was seen in the doubly deficient group, as well as a greater loss of viability during culture. Spleen cell-mediated antibody-dependent lysis of chicken erythrocytes was increased in the doubly deficient group, although this difference could be abolished by the addition of catalase, but not indomethacin, to the culture medium. Dietary deficiency of vitamin E and selenium had no discernible effects on alveolar macrophage function, as measured by cell-mediated antibody-dependent cytolysis, killing of Staphylococcus aureus or regulation of T-lymphocyte blastogenesis.
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_1454841</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>75989997</sourcerecordid><originalsourceid>FETCH-LOGICAL-p321t-b844e18ffdabe4e804c3a3c52fa8b8fc47371b5efcf680781fa382d2f6044d4d3</originalsourceid><addsrcrecordid>eNqFkEtLxDAUhYMo4zj6E4QsxF0hzybZCDLUBwy40XVJ0xuNtOnYpIL_3oJl0JWLy-FyPg6Hc4TWlJeyYLJUx2hNCDUF00SeorOU3ueXEylXaMWNYoLTNaoq78HlhAePP0O2fYi4wja2OEEHMUw9bsEHFyDON2MRjzbj0PdTBOyn6HIY4jk68bZLcLHoBr3cVc_bh2L3dP-4vd0Ve85oLhotBFDtfWsbEKCJcNxyJ5m3utHeCcUVbSR450tNlKbecs1a5ksiRCtavkE3P7n7qemhdRDzaLt6P4bejl_1YEP914nhrX4dPmsqpNCCzgHXS8A4fEyQct2H5KDrbIRhSrWSRhtj1L8gFURzw-UMXv6udOiyLDz7V4tvk7OdH-08ZDpghlHGlOHfrVGGfA</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>14083935</pqid></control><display><type>article</type><title>Effects of vitamin E and selenium deficiencies on rat immune function</title><source>MEDLINE</source><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><creator>ESKEW, M. L ; SCHOLZ, R. W ; REDDY, C. C ; TODHUNTER, D. A ; ZARKOWER, A</creator><creatorcontrib>ESKEW, M. L ; SCHOLZ, R. W ; REDDY, C. C ; TODHUNTER, D. A ; ZARKOWER, A</creatorcontrib><description>The effects of dietary restriction of vitamin E and selenium were studied in male Long-Evans hooded rats. Weanling animals were maintained for 5-6 weeks on torula yeast-based diets, with or without the addition of vitamin E (150 IU/kg) or selenium (0.5 mg/kg), to form the following dietary groups: +E, +Se; +E, -Se; -E, +Se; -E, -Se, and a fifth group pair-fed with the -E, -Se group. This latter group exhibited a decreased rate of growth similar to the -E, -Se group. Lymphocyte blastogenesis in response to mitogens was decreased in animals fed the diets deficient in either vitamin E or selenium, and also in the pair-fed group. Very marked suppression of mitogen responses was seen in the doubly deficient group, as well as a greater loss of viability during culture. Spleen cell-mediated antibody-dependent lysis of chicken erythrocytes was increased in the doubly deficient group, although this difference could be abolished by the addition of catalase, but not indomethacin, to the culture medium. Dietary deficiency of vitamin E and selenium had no discernible effects on alveolar macrophage function, as measured by cell-mediated antibody-dependent cytolysis, killing of Staphylococcus aureus or regulation of T-lymphocyte blastogenesis.</description><identifier>ISSN: 0019-2805</identifier><identifier>EISSN: 1365-2567</identifier><identifier>PMID: 3972431</identifier><identifier>CODEN: IMMUAM</identifier><language>eng</language><publisher>Oxford: Blackwell</publisher><subject>Analysis of the immune response. Humoral and cellular immunity ; Animals ; Antibody-Dependent Cell Cytotoxicity - drug effects ; Biological and medical sciences ; Body Weight ; Catalase - pharmacology ; Cell Survival ; Cells, Cultured ; Fundamental and applied biological sciences. Psychology ; Fundamental immunology ; Immunobiology ; Indomethacin - pharmacology ; Lymphocyte Activation ; Macrophages - immunology ; Male ; Organs and cells involved in the immune response ; Rats ; Selenium - deficiency ; Spleen - pathology ; Vitamin E Deficiency - immunology ; Vitamin E Deficiency - pathology</subject><ispartof>Immunology, 1985, Vol.54 (1), p.173-180</ispartof><rights>1985 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1454841/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1454841/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,4021,53789,53791</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=9212279$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/3972431$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>ESKEW, M. L</creatorcontrib><creatorcontrib>SCHOLZ, R. W</creatorcontrib><creatorcontrib>REDDY, C. C</creatorcontrib><creatorcontrib>TODHUNTER, D. A</creatorcontrib><creatorcontrib>ZARKOWER, A</creatorcontrib><title>Effects of vitamin E and selenium deficiencies on rat immune function</title><title>Immunology</title><addtitle>Immunology</addtitle><description>The effects of dietary restriction of vitamin E and selenium were studied in male Long-Evans hooded rats. Weanling animals were maintained for 5-6 weeks on torula yeast-based diets, with or without the addition of vitamin E (150 IU/kg) or selenium (0.5 mg/kg), to form the following dietary groups: +E, +Se; +E, -Se; -E, +Se; -E, -Se, and a fifth group pair-fed with the -E, -Se group. This latter group exhibited a decreased rate of growth similar to the -E, -Se group. Lymphocyte blastogenesis in response to mitogens was decreased in animals fed the diets deficient in either vitamin E or selenium, and also in the pair-fed group. Very marked suppression of mitogen responses was seen in the doubly deficient group, as well as a greater loss of viability during culture. Spleen cell-mediated antibody-dependent lysis of chicken erythrocytes was increased in the doubly deficient group, although this difference could be abolished by the addition of catalase, but not indomethacin, to the culture medium. Dietary deficiency of vitamin E and selenium had no discernible effects on alveolar macrophage function, as measured by cell-mediated antibody-dependent cytolysis, killing of Staphylococcus aureus or regulation of T-lymphocyte blastogenesis.</description><subject>Analysis of the immune response. Humoral and cellular immunity</subject><subject>Animals</subject><subject>Antibody-Dependent Cell Cytotoxicity - drug effects</subject><subject>Biological and medical sciences</subject><subject>Body Weight</subject><subject>Catalase - pharmacology</subject><subject>Cell Survival</subject><subject>Cells, Cultured</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Fundamental immunology</subject><subject>Immunobiology</subject><subject>Indomethacin - pharmacology</subject><subject>Lymphocyte Activation</subject><subject>Macrophages - immunology</subject><subject>Male</subject><subject>Organs and cells involved in the immune response</subject><subject>Rats</subject><subject>Selenium - deficiency</subject><subject>Spleen - pathology</subject><subject>Vitamin E Deficiency - immunology</subject><subject>Vitamin E Deficiency - pathology</subject><issn>0019-2805</issn><issn>1365-2567</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1985</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkEtLxDAUhYMo4zj6E4QsxF0hzybZCDLUBwy40XVJ0xuNtOnYpIL_3oJl0JWLy-FyPg6Hc4TWlJeyYLJUx2hNCDUF00SeorOU3ueXEylXaMWNYoLTNaoq78HlhAePP0O2fYi4wja2OEEHMUw9bsEHFyDON2MRjzbj0PdTBOyn6HIY4jk68bZLcLHoBr3cVc_bh2L3dP-4vd0Ve85oLhotBFDtfWsbEKCJcNxyJ5m3utHeCcUVbSR450tNlKbecs1a5ksiRCtavkE3P7n7qemhdRDzaLt6P4bejl_1YEP914nhrX4dPmsqpNCCzgHXS8A4fEyQct2H5KDrbIRhSrWSRhtj1L8gFURzw-UMXv6udOiyLDz7V4tvk7OdH-08ZDpghlHGlOHfrVGGfA</recordid><startdate>1985</startdate><enddate>1985</enddate><creator>ESKEW, M. L</creator><creator>SCHOLZ, R. W</creator><creator>REDDY, C. C</creator><creator>TODHUNTER, D. A</creator><creator>ZARKOWER, A</creator><general>Blackwell</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7QL</scope><scope>7T5</scope><scope>C1K</scope><scope>H94</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>1985</creationdate><title>Effects of vitamin E and selenium deficiencies on rat immune function</title><author>ESKEW, M. L ; SCHOLZ, R. W ; REDDY, C. C ; TODHUNTER, D. A ; ZARKOWER, A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p321t-b844e18ffdabe4e804c3a3c52fa8b8fc47371b5efcf680781fa382d2f6044d4d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1985</creationdate><topic>Analysis of the immune response. Humoral and cellular immunity</topic><topic>Animals</topic><topic>Antibody-Dependent Cell Cytotoxicity - drug effects</topic><topic>Biological and medical sciences</topic><topic>Body Weight</topic><topic>Catalase - pharmacology</topic><topic>Cell Survival</topic><topic>Cells, Cultured</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Fundamental immunology</topic><topic>Immunobiology</topic><topic>Indomethacin - pharmacology</topic><topic>Lymphocyte Activation</topic><topic>Macrophages - immunology</topic><topic>Male</topic><topic>Organs and cells involved in the immune response</topic><topic>Rats</topic><topic>Selenium - deficiency</topic><topic>Spleen - pathology</topic><topic>Vitamin E Deficiency - immunology</topic><topic>Vitamin E Deficiency - pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>ESKEW, M. L</creatorcontrib><creatorcontrib>SCHOLZ, R. W</creatorcontrib><creatorcontrib>REDDY, C. C</creatorcontrib><creatorcontrib>TODHUNTER, D. A</creatorcontrib><creatorcontrib>ZARKOWER, A</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Immunology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>ESKEW, M. L</au><au>SCHOLZ, R. W</au><au>REDDY, C. C</au><au>TODHUNTER, D. A</au><au>ZARKOWER, A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of vitamin E and selenium deficiencies on rat immune function</atitle><jtitle>Immunology</jtitle><addtitle>Immunology</addtitle><date>1985</date><risdate>1985</risdate><volume>54</volume><issue>1</issue><spage>173</spage><epage>180</epage><pages>173-180</pages><issn>0019-2805</issn><eissn>1365-2567</eissn><coden>IMMUAM</coden><abstract>The effects of dietary restriction of vitamin E and selenium were studied in male Long-Evans hooded rats. Weanling animals were maintained for 5-6 weeks on torula yeast-based diets, with or without the addition of vitamin E (150 IU/kg) or selenium (0.5 mg/kg), to form the following dietary groups: +E, +Se; +E, -Se; -E, +Se; -E, -Se, and a fifth group pair-fed with the -E, -Se group. This latter group exhibited a decreased rate of growth similar to the -E, -Se group. Lymphocyte blastogenesis in response to mitogens was decreased in animals fed the diets deficient in either vitamin E or selenium, and also in the pair-fed group. Very marked suppression of mitogen responses was seen in the doubly deficient group, as well as a greater loss of viability during culture. Spleen cell-mediated antibody-dependent lysis of chicken erythrocytes was increased in the doubly deficient group, although this difference could be abolished by the addition of catalase, but not indomethacin, to the culture medium. Dietary deficiency of vitamin E and selenium had no discernible effects on alveolar macrophage function, as measured by cell-mediated antibody-dependent cytolysis, killing of Staphylococcus aureus or regulation of T-lymphocyte blastogenesis.</abstract><cop>Oxford</cop><pub>Blackwell</pub><pmid>3972431</pmid><tpages>8</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0019-2805
ispartof Immunology, 1985, Vol.54 (1), p.173-180
issn 0019-2805
1365-2567
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_1454841
source MEDLINE; EZB-FREE-00999 freely available EZB journals; PubMed Central
subjects Analysis of the immune response. Humoral and cellular immunity
Animals
Antibody-Dependent Cell Cytotoxicity - drug effects
Biological and medical sciences
Body Weight
Catalase - pharmacology
Cell Survival
Cells, Cultured
Fundamental and applied biological sciences. Psychology
Fundamental immunology
Immunobiology
Indomethacin - pharmacology
Lymphocyte Activation
Macrophages - immunology
Male
Organs and cells involved in the immune response
Rats
Selenium - deficiency
Spleen - pathology
Vitamin E Deficiency - immunology
Vitamin E Deficiency - pathology
title Effects of vitamin E and selenium deficiencies on rat immune function
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-14T01%3A04%3A38IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Effects%20of%20vitamin%20E%20and%20selenium%20deficiencies%20on%20rat%20immune%20function&rft.jtitle=Immunology&rft.au=ESKEW,%20M.%20L&rft.date=1985&rft.volume=54&rft.issue=1&rft.spage=173&rft.epage=180&rft.pages=173-180&rft.issn=0019-2805&rft.eissn=1365-2567&rft.coden=IMMUAM&rft_id=info:doi/&rft_dat=%3Cproquest_pubme%3E75989997%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=14083935&rft_id=info:pmid/3972431&rfr_iscdi=true