Effect of chromium source on tissue concentration of chromium in pigs

The concentration of Cr in several tissues in response to high-level, short-term supplementation was used to determine the relative bioavailability among 4 organic Cr sources and to assess the relative safety of high levels of supplementation. Crossbred pigs (n = 40; mean BW = 48.1 ± 0.9 kg) were al...

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Veröffentlicht in:Journal of animal science 2008-11, Vol.86 (11), p.2971-2978
Hauptverfasser: Lindemann, M.D, Cromwell, G.L, Monegue, H.J, Purser, K.W
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container_end_page 2978
container_issue 11
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container_title Journal of animal science
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creator Lindemann, M.D
Cromwell, G.L
Monegue, H.J
Purser, K.W
description The concentration of Cr in several tissues in response to high-level, short-term supplementation was used to determine the relative bioavailability among 4 organic Cr sources and to assess the relative safety of high levels of supplementation. Crossbred pigs (n = 40; mean BW = 48.1 ± 0.9 kg) were allotted to 5 diets: a control diet with no added Cr, or 5,000 μg/kg of Cr from Cr tripicolinate (CrTP), Cr propionate (CrPrp), Cr methionine (CrMet), or Cr yeast (CrY). Twenty gilts were housed individually and barrows were housed in pairs. Average duration of feeding before slaughter was 75 d. For the total experiment, pigs fed the unsupplemented diet had less ADG than pigs fed CrY (P < 0.05). Serum clinical chemistry values, obtained during the final week of the experiment, demonstrated few effects with no responses that would raise concern about metabolic changes in response to the Cr sources. The effects of the forms of Cr fed on carcass measurements and meat quality were also minimal. All Cr sources reduced cooler shrink (P < 0.05) and most resulted in some meat color change on d 1 postslaughter. For tissue Cr content, 4 of 5 tissues (bone, kidney, liver, and ovary) were increased (P < 0.05) in Cr content by supplementation with CrTP and CrMet, whereas only 2 tissues (bone and kidney) were increased (P < 0.05) by CrY, and none were increased by CrPrp. In all tissues of response, CrTP exceeded CrMet and CrMet exceeded CrY. Comparing the relative increase in tissue Cr for all responsive tissues (bone, kidney, liver, and ovary) gave a range of responses, for which the mean bioavailability relative to CrTP across tissues was 13.1% for CrPrp (0.2 to 19.0%), 50.5% for CrMet (36.2 to 79.1%), and 22.8% for CrY (2.5 to 47.9%). In summation, these results show very clear Cr effects on multiple tissues, which is conclusive evidence of absorption and deposition. The lack of a negative response in growth performance, carcass measures, and clinical chemistry at the increased quantities used herein provides assurance that normal quantities of addition are extremely safe.
doi_str_mv 10.2527/jas.2008-0888
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Crossbred pigs (n = 40; mean BW = 48.1 ± 0.9 kg) were allotted to 5 diets: a control diet with no added Cr, or 5,000 μg/kg of Cr from Cr tripicolinate (CrTP), Cr propionate (CrPrp), Cr methionine (CrMet), or Cr yeast (CrY). Twenty gilts were housed individually and barrows were housed in pairs. Average duration of feeding before slaughter was 75 d. For the total experiment, pigs fed the unsupplemented diet had less ADG than pigs fed CrY (P &lt; 0.05). Serum clinical chemistry values, obtained during the final week of the experiment, demonstrated few effects with no responses that would raise concern about metabolic changes in response to the Cr sources. The effects of the forms of Cr fed on carcass measurements and meat quality were also minimal. All Cr sources reduced cooler shrink (P &lt; 0.05) and most resulted in some meat color change on d 1 postslaughter. For tissue Cr content, 4 of 5 tissues (bone, kidney, liver, and ovary) were increased (P &lt; 0.05) in Cr content by supplementation with CrTP and CrMet, whereas only 2 tissues (bone and kidney) were increased (P &lt; 0.05) by CrY, and none were increased by CrPrp. In all tissues of response, CrTP exceeded CrMet and CrMet exceeded CrY. Comparing the relative increase in tissue Cr for all responsive tissues (bone, kidney, liver, and ovary) gave a range of responses, for which the mean bioavailability relative to CrTP across tissues was 13.1% for CrPrp (0.2 to 19.0%), 50.5% for CrMet (36.2 to 79.1%), and 22.8% for CrY (2.5 to 47.9%). In summation, these results show very clear Cr effects on multiple tissues, which is conclusive evidence of absorption and deposition. The lack of a negative response in growth performance, carcass measures, and clinical chemistry at the increased quantities used herein provides assurance that normal quantities of addition are extremely safe.</description><identifier>ISSN: 0021-8812</identifier><identifier>EISSN: 1525-3163</identifier><identifier>DOI: 10.2527/jas.2008-0888</identifier><identifier>PMID: 18599670</identifier><language>eng</language><publisher>Savoy, IL: American Society of Animal Science</publisher><subject>Animal productions ; animal tissues ; Animals ; average daily gain ; Biological and medical sciences ; Blood Chemical Analysis ; carcass characteristics ; carcass quality ; chromium ; Chromium - administration &amp; dosage ; Chromium - analysis ; Chromium - metabolism ; Chromium - pharmacology ; crude glycerin ; dietary minerals ; dietary nutrient sources ; Dietary Supplements - analysis ; experimental diets ; Female ; food analysis ; Fundamental and applied biological sciences. Psychology ; Male ; Meat - standards ; meat composition ; meat quality ; Minerals - analysis ; nutrient availability ; Picolinic Acids - administration &amp; dosage ; Picolinic Acids - pharmacology ; pig carcasses ; pork ; swine ; Swine - growth &amp; development ; Swine - metabolism ; Terrestrial animal productions ; tissue analysis ; Vertebrates ; Weight Gain - drug effects</subject><ispartof>Journal of animal science, 2008-11, Vol.86 (11), p.2971-2978</ispartof><rights>2008 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,27929,27930</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=20825302$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18599670$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lindemann, M.D</creatorcontrib><creatorcontrib>Cromwell, G.L</creatorcontrib><creatorcontrib>Monegue, H.J</creatorcontrib><creatorcontrib>Purser, K.W</creatorcontrib><title>Effect of chromium source on tissue concentration of chromium in pigs</title><title>Journal of animal science</title><addtitle>J Anim Sci</addtitle><description>The concentration of Cr in several tissues in response to high-level, short-term supplementation was used to determine the relative bioavailability among 4 organic Cr sources and to assess the relative safety of high levels of supplementation. Crossbred pigs (n = 40; mean BW = 48.1 ± 0.9 kg) were allotted to 5 diets: a control diet with no added Cr, or 5,000 μg/kg of Cr from Cr tripicolinate (CrTP), Cr propionate (CrPrp), Cr methionine (CrMet), or Cr yeast (CrY). Twenty gilts were housed individually and barrows were housed in pairs. Average duration of feeding before slaughter was 75 d. For the total experiment, pigs fed the unsupplemented diet had less ADG than pigs fed CrY (P &lt; 0.05). Serum clinical chemistry values, obtained during the final week of the experiment, demonstrated few effects with no responses that would raise concern about metabolic changes in response to the Cr sources. The effects of the forms of Cr fed on carcass measurements and meat quality were also minimal. All Cr sources reduced cooler shrink (P &lt; 0.05) and most resulted in some meat color change on d 1 postslaughter. For tissue Cr content, 4 of 5 tissues (bone, kidney, liver, and ovary) were increased (P &lt; 0.05) in Cr content by supplementation with CrTP and CrMet, whereas only 2 tissues (bone and kidney) were increased (P &lt; 0.05) by CrY, and none were increased by CrPrp. In all tissues of response, CrTP exceeded CrMet and CrMet exceeded CrY. Comparing the relative increase in tissue Cr for all responsive tissues (bone, kidney, liver, and ovary) gave a range of responses, for which the mean bioavailability relative to CrTP across tissues was 13.1% for CrPrp (0.2 to 19.0%), 50.5% for CrMet (36.2 to 79.1%), and 22.8% for CrY (2.5 to 47.9%). In summation, these results show very clear Cr effects on multiple tissues, which is conclusive evidence of absorption and deposition. The lack of a negative response in growth performance, carcass measures, and clinical chemistry at the increased quantities used herein provides assurance that normal quantities of addition are extremely safe.</description><subject>Animal productions</subject><subject>animal tissues</subject><subject>Animals</subject><subject>average daily gain</subject><subject>Biological and medical sciences</subject><subject>Blood Chemical Analysis</subject><subject>carcass characteristics</subject><subject>carcass quality</subject><subject>chromium</subject><subject>Chromium - administration &amp; dosage</subject><subject>Chromium - analysis</subject><subject>Chromium - metabolism</subject><subject>Chromium - pharmacology</subject><subject>crude glycerin</subject><subject>dietary minerals</subject><subject>dietary nutrient sources</subject><subject>Dietary Supplements - analysis</subject><subject>experimental diets</subject><subject>Female</subject><subject>food analysis</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Male</subject><subject>Meat - standards</subject><subject>meat composition</subject><subject>meat quality</subject><subject>Minerals - analysis</subject><subject>nutrient availability</subject><subject>Picolinic Acids - administration &amp; dosage</subject><subject>Picolinic Acids - pharmacology</subject><subject>pig carcasses</subject><subject>pork</subject><subject>swine</subject><subject>Swine - growth &amp; development</subject><subject>Swine - metabolism</subject><subject>Terrestrial animal productions</subject><subject>tissue analysis</subject><subject>Vertebrates</subject><subject>Weight Gain - drug effects</subject><issn>0021-8812</issn><issn>1525-3163</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpN0E1rGzEQBmARGhLn49hru5ekp3VGI0srHUtw0kCgh8ZnMauVbIX9cKVdQv59N9gtPQ0MD-_LDGOfOSxRYnX3SnmJALoErfUJW3CJshRciU9sAYC81JrjObvI-RWAozTyjJ1zLY1RFSzYeh2Cd2MxhMLt0tDFqSvyMCXni6Evxpjz5As39M73Y6Ixzsv_aeyLfdzmK3YaqM3--jgv2eZh_XL_o3z--fh0__25DGjkWJIDaURQoYFQk_eNc0oZJUSjDFS-Dlp6rJ2sASqx0oiBqiYQcbUyJBHFJbs95O7T8HvyebRdzM63LfV-mLJVpuJamdUMvxzhVHe-sfsUO0rv9u_hM7g5AsqO2pCodzH_cwgapYCPxm8Ht4vb3VtM3uaO2naO5XZ-vVaWc4tz7Sy_HmSgwdI2zWmbXwhcAJeVUhzEH4ACfgY</recordid><startdate>20081101</startdate><enddate>20081101</enddate><creator>Lindemann, M.D</creator><creator>Cromwell, G.L</creator><creator>Monegue, H.J</creator><creator>Purser, K.W</creator><general>American Society of Animal Science</general><general>Am Soc Animal Sci</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>7X8</scope></search><sort><creationdate>20081101</creationdate><title>Effect of chromium source on tissue concentration of chromium in pigs</title><author>Lindemann, M.D ; Cromwell, G.L ; Monegue, H.J ; Purser, K.W</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-f295t-ac0593f6fd0fbaeedcc669633d6907ebf85e2bc5b00734822fa7dfaa1649a5223</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Animal productions</topic><topic>animal tissues</topic><topic>Animals</topic><topic>average daily gain</topic><topic>Biological and medical sciences</topic><topic>Blood Chemical Analysis</topic><topic>carcass characteristics</topic><topic>carcass quality</topic><topic>chromium</topic><topic>Chromium - administration &amp; dosage</topic><topic>Chromium - analysis</topic><topic>Chromium - metabolism</topic><topic>Chromium - pharmacology</topic><topic>crude glycerin</topic><topic>dietary minerals</topic><topic>dietary nutrient sources</topic><topic>Dietary Supplements - analysis</topic><topic>experimental diets</topic><topic>Female</topic><topic>food analysis</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Male</topic><topic>Meat - standards</topic><topic>meat composition</topic><topic>meat quality</topic><topic>Minerals - analysis</topic><topic>nutrient availability</topic><topic>Picolinic Acids - administration &amp; dosage</topic><topic>Picolinic Acids - pharmacology</topic><topic>pig carcasses</topic><topic>pork</topic><topic>swine</topic><topic>Swine - growth &amp; development</topic><topic>Swine - metabolism</topic><topic>Terrestrial animal productions</topic><topic>tissue analysis</topic><topic>Vertebrates</topic><topic>Weight Gain - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lindemann, M.D</creatorcontrib><creatorcontrib>Cromwell, G.L</creatorcontrib><creatorcontrib>Monegue, H.J</creatorcontrib><creatorcontrib>Purser, K.W</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>MEDLINE - Academic</collection><jtitle>Journal of animal science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lindemann, M.D</au><au>Cromwell, G.L</au><au>Monegue, H.J</au><au>Purser, K.W</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of chromium source on tissue concentration of chromium in pigs</atitle><jtitle>Journal of animal science</jtitle><addtitle>J Anim Sci</addtitle><date>2008-11-01</date><risdate>2008</risdate><volume>86</volume><issue>11</issue><spage>2971</spage><epage>2978</epage><pages>2971-2978</pages><issn>0021-8812</issn><eissn>1525-3163</eissn><abstract>The concentration of Cr in several tissues in response to high-level, short-term supplementation was used to determine the relative bioavailability among 4 organic Cr sources and to assess the relative safety of high levels of supplementation. Crossbred pigs (n = 40; mean BW = 48.1 ± 0.9 kg) were allotted to 5 diets: a control diet with no added Cr, or 5,000 μg/kg of Cr from Cr tripicolinate (CrTP), Cr propionate (CrPrp), Cr methionine (CrMet), or Cr yeast (CrY). Twenty gilts were housed individually and barrows were housed in pairs. Average duration of feeding before slaughter was 75 d. For the total experiment, pigs fed the unsupplemented diet had less ADG than pigs fed CrY (P &lt; 0.05). Serum clinical chemistry values, obtained during the final week of the experiment, demonstrated few effects with no responses that would raise concern about metabolic changes in response to the Cr sources. The effects of the forms of Cr fed on carcass measurements and meat quality were also minimal. All Cr sources reduced cooler shrink (P &lt; 0.05) and most resulted in some meat color change on d 1 postslaughter. For tissue Cr content, 4 of 5 tissues (bone, kidney, liver, and ovary) were increased (P &lt; 0.05) in Cr content by supplementation with CrTP and CrMet, whereas only 2 tissues (bone and kidney) were increased (P &lt; 0.05) by CrY, and none were increased by CrPrp. In all tissues of response, CrTP exceeded CrMet and CrMet exceeded CrY. Comparing the relative increase in tissue Cr for all responsive tissues (bone, kidney, liver, and ovary) gave a range of responses, for which the mean bioavailability relative to CrTP across tissues was 13.1% for CrPrp (0.2 to 19.0%), 50.5% for CrMet (36.2 to 79.1%), and 22.8% for CrY (2.5 to 47.9%). In summation, these results show very clear Cr effects on multiple tissues, which is conclusive evidence of absorption and deposition. The lack of a negative response in growth performance, carcass measures, and clinical chemistry at the increased quantities used herein provides assurance that normal quantities of addition are extremely safe.</abstract><cop>Savoy, IL</cop><pub>American Society of Animal Science</pub><pmid>18599670</pmid><doi>10.2527/jas.2008-0888</doi><tpages>8</tpages></addata></record>
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source MEDLINE; Oxford University Press Journals All Titles (1996-Current)
subjects Animal productions
animal tissues
Animals
average daily gain
Biological and medical sciences
Blood Chemical Analysis
carcass characteristics
carcass quality
chromium
Chromium - administration & dosage
Chromium - analysis
Chromium - metabolism
Chromium - pharmacology
crude glycerin
dietary minerals
dietary nutrient sources
Dietary Supplements - analysis
experimental diets
Female
food analysis
Fundamental and applied biological sciences. Psychology
Male
Meat - standards
meat composition
meat quality
Minerals - analysis
nutrient availability
Picolinic Acids - administration & dosage
Picolinic Acids - pharmacology
pig carcasses
pork
swine
Swine - growth & development
Swine - metabolism
Terrestrial animal productions
tissue analysis
Vertebrates
Weight Gain - drug effects
title Effect of chromium source on tissue concentration of chromium in pigs
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