Copper deficiency affects selenoglutathione peroxidase and selenodeiodinase activities and antioxidant defense in weanling rats
Copper deficiency has been postulated to result in low selenoglutathione peroxidase (Se-GSHPx) activity, secondary to alterations in the antioxidant defense system. Type I iodothyronine 5′-deiodinase contains selenium; because it is not part of the antioxidant defense system its measurement provides...
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Veröffentlicht in: | The American journal of clinical nutrition 1994-03, Vol.59 (3), p.654-658 |
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description | Copper deficiency has been postulated to result in low selenoglutathione peroxidase (Se-GSHPx) activity, secondary to alterations in the antioxidant defense system. Type I iodothyronine 5′-deiodinase contains selenium; because it is not part of the antioxidant defense system its measurement provides a way to evaluate the influence of copper on selenoenzymes independent of the antioxidant system. Weanling rats were fed the control diet (125.9 nmol Cu/g diet), copper-deficient diet (7.9 nmol Cu/g diet), or the control diet restricted to the intake of the deficient rats (restrict-fed), for 21 d. Rats fed the copper-deficient diet had cardiomegaly, low hematocrit values, and low tissue copper concentrations, but normal liver selenium concentrations. Liver and plasma Se-GSHPx activities were lowest in the deficient rats. Non-Se-GSHPx activity was similar between control and copper-deficient groups. Liver selenodeiodinase activity was lowest in the copper-deficient rats; this reduction was functionally significant as evidenced by low plasma 3,3′,5-triiodothyronine and high plasma 3,3′,5′-triiodothyronine concentrations. |
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Type I iodothyronine 5′-deiodinase contains selenium; because it is not part of the antioxidant defense system its measurement provides a way to evaluate the influence of copper on selenoenzymes independent of the antioxidant system. Weanling rats were fed the control diet (125.9 nmol Cu/g diet), copper-deficient diet (7.9 nmol Cu/g diet), or the control diet restricted to the intake of the deficient rats (restrict-fed), for 21 d. Rats fed the copper-deficient diet had cardiomegaly, low hematocrit values, and low tissue copper concentrations, but normal liver selenium concentrations. Liver and plasma Se-GSHPx activities were lowest in the deficient rats. Non-Se-GSHPx activity was similar between control and copper-deficient groups. Liver selenodeiodinase activity was lowest in the copper-deficient rats; this reduction was functionally significant as evidenced by low plasma 3,3′,5-triiodothyronine and high plasma 3,3′,5′-triiodothyronine concentrations.</description><identifier>ISSN: 0002-9165</identifier><identifier>EISSN: 1938-3207</identifier><identifier>DOI: 10.1093/ajcn/59.3.654</identifier><identifier>PMID: 8116544</identifier><identifier>CODEN: AJCNAC</identifier><language>eng</language><publisher>Bethesda, MD: Elsevier Inc</publisher><subject>3,3′,5-triiodothyronine ; Animals ; Antioxidants - metabolism ; Biological and medical sciences ; Brain - drug effects ; Brain - enzymology ; Brain - metabolism ; Cardiomegaly ; Copper ; Copper - deficiency ; Copper - metabolism ; Copper - pharmacology ; deiodinase ; Diet ; Enzymes ; Glutathione - analogs & derivatives ; Glutathione - metabolism ; Glutathione Disulfide ; glutathione peroxidase ; Glutathione Peroxidase - metabolism ; Hormones ; Iodide Peroxidase - metabolism ; Liver - drug effects ; Liver - enzymology ; Liver - metabolism ; Medical sciences ; Metabolic diseases ; Other nutritional diseases (malnutrition, nutritional and vitamin deficiencies...) ; Rats ; Rats, Sprague-Dawley ; Reference Values ; Rodents ; selenium ; selenoglutathione peroxidase ; thyroid hormones ; Trace Elements - metabolism ; Weaning</subject><ispartof>The American journal of clinical nutrition, 1994-03, Vol.59 (3), p.654-658</ispartof><rights>1994 American Society for Nutrition.</rights><rights>1994 INIST-CNRS</rights><rights>Copyright American Society for Clinical Nutrition, Inc. Mar 1994</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c431t-35d1851e18c6aa795c7c088389c65041bc2d9975873fa4bd3d42badf74e4a5a93</citedby><cites>FETCH-LOGICAL-c431t-35d1851e18c6aa795c7c088389c65041bc2d9975873fa4bd3d42badf74e4a5a93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=3984221$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8116544$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Olin, KL</creatorcontrib><creatorcontrib>Walter, RM</creatorcontrib><creatorcontrib>Keen, CL</creatorcontrib><title>Copper deficiency affects selenoglutathione peroxidase and selenodeiodinase activities and antioxidant defense in weanling rats</title><title>The American journal of clinical nutrition</title><addtitle>Am J Clin Nutr</addtitle><description>Copper deficiency has been postulated to result in low selenoglutathione peroxidase (Se-GSHPx) activity, secondary to alterations in the antioxidant defense system. Type I iodothyronine 5′-deiodinase contains selenium; because it is not part of the antioxidant defense system its measurement provides a way to evaluate the influence of copper on selenoenzymes independent of the antioxidant system. Weanling rats were fed the control diet (125.9 nmol Cu/g diet), copper-deficient diet (7.9 nmol Cu/g diet), or the control diet restricted to the intake of the deficient rats (restrict-fed), for 21 d. Rats fed the copper-deficient diet had cardiomegaly, low hematocrit values, and low tissue copper concentrations, but normal liver selenium concentrations. Liver and plasma Se-GSHPx activities were lowest in the deficient rats. Non-Se-GSHPx activity was similar between control and copper-deficient groups. Liver selenodeiodinase activity was lowest in the copper-deficient rats; this reduction was functionally significant as evidenced by low plasma 3,3′,5-triiodothyronine and high plasma 3,3′,5′-triiodothyronine concentrations.</description><subject>3,3′,5-triiodothyronine</subject><subject>Animals</subject><subject>Antioxidants - metabolism</subject><subject>Biological and medical sciences</subject><subject>Brain - drug effects</subject><subject>Brain - enzymology</subject><subject>Brain - metabolism</subject><subject>Cardiomegaly</subject><subject>Copper</subject><subject>Copper - deficiency</subject><subject>Copper - metabolism</subject><subject>Copper - pharmacology</subject><subject>deiodinase</subject><subject>Diet</subject><subject>Enzymes</subject><subject>Glutathione - analogs & derivatives</subject><subject>Glutathione - metabolism</subject><subject>Glutathione Disulfide</subject><subject>glutathione peroxidase</subject><subject>Glutathione Peroxidase - metabolism</subject><subject>Hormones</subject><subject>Iodide Peroxidase - metabolism</subject><subject>Liver - drug effects</subject><subject>Liver - enzymology</subject><subject>Liver - metabolism</subject><subject>Medical sciences</subject><subject>Metabolic diseases</subject><subject>Other nutritional diseases (malnutrition, nutritional and vitamin deficiencies...)</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Reference Values</subject><subject>Rodents</subject><subject>selenium</subject><subject>selenoglutathione peroxidase</subject><subject>thyroid hormones</subject><subject>Trace Elements - metabolism</subject><subject>Weaning</subject><issn>0002-9165</issn><issn>1938-3207</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp10cGKFDEQBuAgyjquHj0KjcjeejbpJJ3kKIOuwoIXPYeapHrN0JOMSfeue_LVzcw0exA8FVR9FEX9hLxldM2o4dewc_FamjVf91I8IytmuG55R9VzsqKUdq1hvXxJXpWyo5R1QvcX5EKz2hRiRf5s0uGAufE4BBcwuscGhgHdVJqCI8Z0N84TTD9DithUmH4HDwUbiH4BHkPyIZ6abgr3YQpYTnOIUzj5OB33Y6wkxOYBIY4h3jUZpvKavBhgLPhmqZfkx-dP3zdf2ttvN183H29bJzibWi4905Ih064HUEY65ajWXBvXSyrY1nXeGCW14gOIrededFvwgxIoQILhl-TqvPeQ068Zy2T3oTgcR4iY5mJVz1XPelXh-3_gLs051ttsx1n9pdJ9Re0ZuZxKyTjYQw57yI-WUXtMxR5TsdJYbuufq3-3LJ23e_RPeomhzj8scygOxiFDdKE8MW606DpWmTozrJ-6D5htOWWGPuQamfUp_OeAv86yqwM</recordid><startdate>19940301</startdate><enddate>19940301</enddate><creator>Olin, KL</creator><creator>Walter, RM</creator><creator>Keen, CL</creator><general>Elsevier Inc</general><general>American Society for Clinical Nutrition</general><general>American Society for Clinical Nutrition, Inc</general><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>7QP</scope><scope>7T7</scope><scope>7TS</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>19940301</creationdate><title>Copper deficiency affects selenoglutathione peroxidase and selenodeiodinase activities and antioxidant defense in weanling rats</title><author>Olin, KL ; Walter, RM ; Keen, CL</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c431t-35d1851e18c6aa795c7c088389c65041bc2d9975873fa4bd3d42badf74e4a5a93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1994</creationdate><topic>3,3′,5-triiodothyronine</topic><topic>Animals</topic><topic>Antioxidants - metabolism</topic><topic>Biological and medical sciences</topic><topic>Brain - drug effects</topic><topic>Brain - enzymology</topic><topic>Brain - metabolism</topic><topic>Cardiomegaly</topic><topic>Copper</topic><topic>Copper - deficiency</topic><topic>Copper - metabolism</topic><topic>Copper - pharmacology</topic><topic>deiodinase</topic><topic>Diet</topic><topic>Enzymes</topic><topic>Glutathione - analogs & derivatives</topic><topic>Glutathione - metabolism</topic><topic>Glutathione Disulfide</topic><topic>glutathione peroxidase</topic><topic>Glutathione Peroxidase - metabolism</topic><topic>Hormones</topic><topic>Iodide Peroxidase - metabolism</topic><topic>Liver - drug effects</topic><topic>Liver - enzymology</topic><topic>Liver - metabolism</topic><topic>Medical sciences</topic><topic>Metabolic diseases</topic><topic>Other nutritional diseases (malnutrition, nutritional and vitamin deficiencies...)</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Reference Values</topic><topic>Rodents</topic><topic>selenium</topic><topic>selenoglutathione peroxidase</topic><topic>thyroid hormones</topic><topic>Trace Elements - metabolism</topic><topic>Weaning</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Olin, KL</creatorcontrib><creatorcontrib>Walter, RM</creatorcontrib><creatorcontrib>Keen, CL</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>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Physical Education Index</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>The American journal of clinical nutrition</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Olin, KL</au><au>Walter, RM</au><au>Keen, CL</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Copper deficiency affects selenoglutathione peroxidase and selenodeiodinase activities and antioxidant defense in weanling rats</atitle><jtitle>The American journal of clinical nutrition</jtitle><addtitle>Am J Clin Nutr</addtitle><date>1994-03-01</date><risdate>1994</risdate><volume>59</volume><issue>3</issue><spage>654</spage><epage>658</epage><pages>654-658</pages><issn>0002-9165</issn><eissn>1938-3207</eissn><coden>AJCNAC</coden><abstract>Copper deficiency has been postulated to result in low selenoglutathione peroxidase (Se-GSHPx) activity, secondary to alterations in the antioxidant defense system. Type I iodothyronine 5′-deiodinase contains selenium; because it is not part of the antioxidant defense system its measurement provides a way to evaluate the influence of copper on selenoenzymes independent of the antioxidant system. Weanling rats were fed the control diet (125.9 nmol Cu/g diet), copper-deficient diet (7.9 nmol Cu/g diet), or the control diet restricted to the intake of the deficient rats (restrict-fed), for 21 d. Rats fed the copper-deficient diet had cardiomegaly, low hematocrit values, and low tissue copper concentrations, but normal liver selenium concentrations. Liver and plasma Se-GSHPx activities were lowest in the deficient rats. Non-Se-GSHPx activity was similar between control and copper-deficient groups. Liver selenodeiodinase activity was lowest in the copper-deficient rats; this reduction was functionally significant as evidenced by low plasma 3,3′,5-triiodothyronine and high plasma 3,3′,5′-triiodothyronine concentrations.</abstract><cop>Bethesda, MD</cop><pub>Elsevier Inc</pub><pmid>8116544</pmid><doi>10.1093/ajcn/59.3.654</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 3,3′,5-triiodothyronine Animals Antioxidants - metabolism Biological and medical sciences Brain - drug effects Brain - enzymology Brain - metabolism Cardiomegaly Copper Copper - deficiency Copper - metabolism Copper - pharmacology deiodinase Diet Enzymes Glutathione - analogs & derivatives Glutathione - metabolism Glutathione Disulfide glutathione peroxidase Glutathione Peroxidase - metabolism Hormones Iodide Peroxidase - metabolism Liver - drug effects Liver - enzymology Liver - metabolism Medical sciences Metabolic diseases Other nutritional diseases (malnutrition, nutritional and vitamin deficiencies...) Rats Rats, Sprague-Dawley Reference Values Rodents selenium selenoglutathione peroxidase thyroid hormones Trace Elements - metabolism Weaning |
title | Copper deficiency affects selenoglutathione peroxidase and selenodeiodinase activities and antioxidant defense in weanling rats |
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