Effects of copper, iron, and ascorbic acid on manganese availability to rats

Four experiments were done to characterize the interactions of copper, iron, and ascorbic acid with manganese in rats. All experiments were factorially arranged Dietary Mn concentrations were less than 1 micrograms/g (Mn0) and 50 micrograms/g (Mn+). Dietary Cu was less than 1 mg/g (Cu0) and 5 microg...

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Veröffentlicht in:Experimental biology and medicine (Maywood, N.J.) N.J.), 1992-04, Vol.199 (4), p.470-480
Hauptverfasser: Johnson, Phyllis E, Korynta, Eugene D
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description Four experiments were done to characterize the interactions of copper, iron, and ascorbic acid with manganese in rats. All experiments were factorially arranged Dietary Mn concentrations were less than 1 micrograms/g (Mn0) and 50 micrograms/g (Mn+). Dietary Cu was less than 1 mg/g (Cu0) and 5 micrograms/g (Cu+); dietary Fe was 10 micrograms/g (Fe10) and 140 micrograms/g (Fe140). Ascorbic acid (Asc) was not added to the diet or added at a concentration of 10 g/kg diet. Experiment 1 had two variables, Mn and Cu; in Experiment 2, the variables were Mn and Asc. In Experiment 3, the variables were Mn, Cu, and Asc; in Experiment 4, they were Mn, Cu, and Fe. Definite interactions between Mn and Cu were observed, but they tended to be less pronounced than interactions between Mn and Fe. Cu depressed absorption of 54Mn and accelerated its turnover. In addition, adequate Cu (Cu+), compared with Cu0, depressed liver, plasma, and whole blood Mn of rats. Absorption of 67Cu was higher in animals fed Mn0 diets than in those fed Mn+. Ascorbic acid depressed Mn superoxide dismutase activity and increased Cu superoxide dismutase activity in the heart. The addition of ascorbic acid to the diet did not affect Mn concentration in the liver or blood. Absorption of 54Mn was depressed in rats fed Fe140 compared with those fed Fe10. Interactions among Fe, Cu, and Mn resulted in a tendency for Mn superoxide dismutase activity to be lower in rats fed Fe140 than in rats fed Fe10. Within the physiologic range of dietary concentrations, Mn and Cu have opposite effects on many factors that tend to balance one another. The effects of ascorbic acid on Mn metabolism are much less pronounced than effects of dietary Cu, which in turn affects Mn metabolism less than does Fe.
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All experiments were factorially arranged Dietary Mn concentrations were less than 1 micrograms/g (Mn0) and 50 micrograms/g (Mn+). Dietary Cu was less than 1 mg/g (Cu0) and 5 micrograms/g (Cu+); dietary Fe was 10 micrograms/g (Fe10) and 140 micrograms/g (Fe140). Ascorbic acid (Asc) was not added to the diet or added at a concentration of 10 g/kg diet. Experiment 1 had two variables, Mn and Cu; in Experiment 2, the variables were Mn and Asc. In Experiment 3, the variables were Mn, Cu, and Asc; in Experiment 4, they were Mn, Cu, and Fe. Definite interactions between Mn and Cu were observed, but they tended to be less pronounced than interactions between Mn and Fe. Cu depressed absorption of 54Mn and accelerated its turnover. In addition, adequate Cu (Cu+), compared with Cu0, depressed liver, plasma, and whole blood Mn of rats. Absorption of 67Cu was higher in animals fed Mn0 diets than in those fed Mn+. Ascorbic acid depressed Mn superoxide dismutase activity and increased Cu superoxide dismutase activity in the heart. The addition of ascorbic acid to the diet did not affect Mn concentration in the liver or blood. Absorption of 54Mn was depressed in rats fed Fe140 compared with those fed Fe10. Interactions among Fe, Cu, and Mn resulted in a tendency for Mn superoxide dismutase activity to be lower in rats fed Fe140 than in rats fed Fe10. Within the physiologic range of dietary concentrations, Mn and Cu have opposite effects on many factors that tend to balance one another. The effects of ascorbic acid on Mn metabolism are much less pronounced than effects of dietary Cu, which in turn affects Mn metabolism less than does Fe.</description><identifier>ISSN: 0037-9727</identifier><identifier>ISSN: 1535-3702</identifier><identifier>EISSN: 1525-1373</identifier><identifier>EISSN: 1535-3699</identifier><identifier>DOI: 10.3181/00379727-199-43383</identifier><identifier>PMID: 1549627</identifier><identifier>CODEN: PSEBAA</identifier><language>eng</language><publisher>London, England: SAGE Publications</publisher><subject>Absorption ; animal models ; Animals ; ascorbic acid ; Ascorbic Acid - pharmacology ; Biological and medical sciences ; Biological Availability ; copper ; Copper - metabolism ; Copper - pharmacology ; dietary minerals ; Fundamental and applied biological sciences. Psychology ; intestinal absorption ; iron ; Iron - metabolism ; Iron - pharmacology ; manganese ; Manganese - metabolism ; Metabolisms and neurohumoral controls ; mineral metabolism ; nutrient availability ; nutrient intake ; nutrient-nutrient interactions ; nutritional adequacy ; Rats ; Rats, Inbred Strains ; Superoxide Dismutase - analysis ; Vertebrates: anatomy and physiology, studies on body, several organs or systems ; vitamins ; Water and mineral metabolism. Osmoregulation. Acidobasic balance</subject><ispartof>Experimental biology and medicine (Maywood, N.J.), 1992-04, Vol.199 (4), p.470-480</ispartof><rights>1992 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c391t-72ac368df7d89e7e4bd9f267a677a7566389208c8c4b8ffcd44523d91d5369e73</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=5556555$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1549627$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Johnson, Phyllis E</creatorcontrib><creatorcontrib>Korynta, Eugene D</creatorcontrib><title>Effects of copper, iron, and ascorbic acid on manganese availability to rats</title><title>Experimental biology and medicine (Maywood, N.J.)</title><addtitle>Proc Soc Exp Biol Med</addtitle><description>Four experiments were done to characterize the interactions of copper, iron, and ascorbic acid with manganese in rats. All experiments were factorially arranged Dietary Mn concentrations were less than 1 micrograms/g (Mn0) and 50 micrograms/g (Mn+). Dietary Cu was less than 1 mg/g (Cu0) and 5 micrograms/g (Cu+); dietary Fe was 10 micrograms/g (Fe10) and 140 micrograms/g (Fe140). Ascorbic acid (Asc) was not added to the diet or added at a concentration of 10 g/kg diet. Experiment 1 had two variables, Mn and Cu; in Experiment 2, the variables were Mn and Asc. In Experiment 3, the variables were Mn, Cu, and Asc; in Experiment 4, they were Mn, Cu, and Fe. Definite interactions between Mn and Cu were observed, but they tended to be less pronounced than interactions between Mn and Fe. Cu depressed absorption of 54Mn and accelerated its turnover. In addition, adequate Cu (Cu+), compared with Cu0, depressed liver, plasma, and whole blood Mn of rats. Absorption of 67Cu was higher in animals fed Mn0 diets than in those fed Mn+. Ascorbic acid depressed Mn superoxide dismutase activity and increased Cu superoxide dismutase activity in the heart. The addition of ascorbic acid to the diet did not affect Mn concentration in the liver or blood. Absorption of 54Mn was depressed in rats fed Fe140 compared with those fed Fe10. Interactions among Fe, Cu, and Mn resulted in a tendency for Mn superoxide dismutase activity to be lower in rats fed Fe140 than in rats fed Fe10. Within the physiologic range of dietary concentrations, Mn and Cu have opposite effects on many factors that tend to balance one another. The effects of ascorbic acid on Mn metabolism are much less pronounced than effects of dietary Cu, which in turn affects Mn metabolism less than does Fe.</description><subject>Absorption</subject><subject>animal models</subject><subject>Animals</subject><subject>ascorbic acid</subject><subject>Ascorbic Acid - pharmacology</subject><subject>Biological and medical sciences</subject><subject>Biological Availability</subject><subject>copper</subject><subject>Copper - metabolism</subject><subject>Copper - pharmacology</subject><subject>dietary minerals</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>intestinal absorption</subject><subject>iron</subject><subject>Iron - metabolism</subject><subject>Iron - pharmacology</subject><subject>manganese</subject><subject>Manganese - metabolism</subject><subject>Metabolisms and neurohumoral controls</subject><subject>mineral metabolism</subject><subject>nutrient availability</subject><subject>nutrient intake</subject><subject>nutrient-nutrient interactions</subject><subject>nutritional adequacy</subject><subject>Rats</subject><subject>Rats, Inbred Strains</subject><subject>Superoxide Dismutase - analysis</subject><subject>Vertebrates: anatomy and physiology, studies on body, several organs or systems</subject><subject>vitamins</subject><subject>Water and mineral metabolism. Osmoregulation. Acidobasic balance</subject><issn>0037-9727</issn><issn>1535-3702</issn><issn>1525-1373</issn><issn>1535-3699</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1992</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kMtqHDEQRUVIsCdOfiBgooXJym3r0XotjXEeMJBF7LWo1mOQ6WlNpJ6A_96a9NjZZVFoUefeEgehT5RccarpNSFcGcVUR43pes41f4NWVDDRUa74W7Q6AN2BOEXva30khEjCyAk6oaI3kqkVWt_FGNxccY7Y5d0ulEucSp4uMUweQ3W5DMlhcMnjPOEtTBuYQg0Y_kAaYUhjmp_wnHGBuX5A7yKMNXw8vmfo4evd_e33bv3z24_bm3XnuKFzpxg4LrWPymsTVOgHbyKTCqRSoISUXBtGtNOuH3SMzve9YNwb6gWXLcDP0Jeld1fy732os92m6sI4tq_lfbWKacEMow1kC-hKrrWEaHclbaE8WUrsQaF9UWibQvtXYQudH9v3wzb4f5HFWdtfHPdND4yxwORSfcWEELJNw64XrMIm2Me8L1Nz8v_Dn5dEhGxhU1rpwy9GKCfUCNoLyZ8BhGGORg</recordid><startdate>19920401</startdate><enddate>19920401</enddate><creator>Johnson, Phyllis E</creator><creator>Korynta, Eugene D</creator><general>SAGE Publications</general><general>Blackwell Science</general><scope>FBQ</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>7X8</scope></search><sort><creationdate>19920401</creationdate><title>Effects of copper, iron, and ascorbic acid on manganese availability to rats</title><author>Johnson, Phyllis E ; Korynta, Eugene D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c391t-72ac368df7d89e7e4bd9f267a677a7566389208c8c4b8ffcd44523d91d5369e73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1992</creationdate><topic>Absorption</topic><topic>animal models</topic><topic>Animals</topic><topic>ascorbic acid</topic><topic>Ascorbic Acid - pharmacology</topic><topic>Biological and medical sciences</topic><topic>Biological Availability</topic><topic>copper</topic><topic>Copper - metabolism</topic><topic>Copper - pharmacology</topic><topic>dietary minerals</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>intestinal absorption</topic><topic>iron</topic><topic>Iron - metabolism</topic><topic>Iron - pharmacology</topic><topic>manganese</topic><topic>Manganese - metabolism</topic><topic>Metabolisms and neurohumoral controls</topic><topic>mineral metabolism</topic><topic>nutrient availability</topic><topic>nutrient intake</topic><topic>nutrient-nutrient interactions</topic><topic>nutritional adequacy</topic><topic>Rats</topic><topic>Rats, Inbred Strains</topic><topic>Superoxide Dismutase - analysis</topic><topic>Vertebrates: anatomy and physiology, studies on body, several organs or systems</topic><topic>vitamins</topic><topic>Water and mineral metabolism. Osmoregulation. Acidobasic balance</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Johnson, Phyllis E</creatorcontrib><creatorcontrib>Korynta, Eugene D</creatorcontrib><collection>AGRIS</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>MEDLINE - Academic</collection><jtitle>Experimental biology and medicine (Maywood, N.J.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Johnson, Phyllis E</au><au>Korynta, Eugene D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of copper, iron, and ascorbic acid on manganese availability to rats</atitle><jtitle>Experimental biology and medicine (Maywood, N.J.)</jtitle><addtitle>Proc Soc Exp Biol Med</addtitle><date>1992-04-01</date><risdate>1992</risdate><volume>199</volume><issue>4</issue><spage>470</spage><epage>480</epage><pages>470-480</pages><issn>0037-9727</issn><issn>1535-3702</issn><eissn>1525-1373</eissn><eissn>1535-3699</eissn><coden>PSEBAA</coden><abstract>Four experiments were done to characterize the interactions of copper, iron, and ascorbic acid with manganese in rats. All experiments were factorially arranged Dietary Mn concentrations were less than 1 micrograms/g (Mn0) and 50 micrograms/g (Mn+). Dietary Cu was less than 1 mg/g (Cu0) and 5 micrograms/g (Cu+); dietary Fe was 10 micrograms/g (Fe10) and 140 micrograms/g (Fe140). Ascorbic acid (Asc) was not added to the diet or added at a concentration of 10 g/kg diet. Experiment 1 had two variables, Mn and Cu; in Experiment 2, the variables were Mn and Asc. In Experiment 3, the variables were Mn, Cu, and Asc; in Experiment 4, they were Mn, Cu, and Fe. Definite interactions between Mn and Cu were observed, but they tended to be less pronounced than interactions between Mn and Fe. Cu depressed absorption of 54Mn and accelerated its turnover. In addition, adequate Cu (Cu+), compared with Cu0, depressed liver, plasma, and whole blood Mn of rats. Absorption of 67Cu was higher in animals fed Mn0 diets than in those fed Mn+. Ascorbic acid depressed Mn superoxide dismutase activity and increased Cu superoxide dismutase activity in the heart. The addition of ascorbic acid to the diet did not affect Mn concentration in the liver or blood. Absorption of 54Mn was depressed in rats fed Fe140 compared with those fed Fe10. Interactions among Fe, Cu, and Mn resulted in a tendency for Mn superoxide dismutase activity to be lower in rats fed Fe140 than in rats fed Fe10. Within the physiologic range of dietary concentrations, Mn and Cu have opposite effects on many factors that tend to balance one another. The effects of ascorbic acid on Mn metabolism are much less pronounced than effects of dietary Cu, which in turn affects Mn metabolism less than does Fe.</abstract><cop>London, England</cop><pub>SAGE Publications</pub><pmid>1549627</pmid><doi>10.3181/00379727-199-43383</doi><tpages>11</tpages></addata></record>
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ispartof Experimental biology and medicine (Maywood, N.J.), 1992-04, Vol.199 (4), p.470-480
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subjects Absorption
animal models
Animals
ascorbic acid
Ascorbic Acid - pharmacology
Biological and medical sciences
Biological Availability
copper
Copper - metabolism
Copper - pharmacology
dietary minerals
Fundamental and applied biological sciences. Psychology
intestinal absorption
iron
Iron - metabolism
Iron - pharmacology
manganese
Manganese - metabolism
Metabolisms and neurohumoral controls
mineral metabolism
nutrient availability
nutrient intake
nutrient-nutrient interactions
nutritional adequacy
Rats
Rats, Inbred Strains
Superoxide Dismutase - analysis
Vertebrates: anatomy and physiology, studies on body, several organs or systems
vitamins
Water and mineral metabolism. Osmoregulation. Acidobasic balance
title Effects of copper, iron, and ascorbic acid on manganese availability to rats
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