Effect of phosphorylated mannans and pharmacological additions of zinc oxide on growth and immunocompetence of weanling pigs

Three experiments were conducted to evaluate the efficacy of phosphorylated mannans (MAN) and pharmacological levels of ZnO on performance and immunity when added to nursery pig diets. Pigs (216 in each experiment), averaging 19 d of age and 6.2, 4.6, and 5.6 kg of BW in Exp. 1, 2, and 3, respective...

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Veröffentlicht in:Journal of animal science 2004-02, Vol.82 (2), p.581-587
Hauptverfasser: Davis, M.E, Brown, D.C, Maxwell, C.V, Johnson, Z.B, Kegley, E.B, Dvorak, R.A
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container_start_page 581
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Brown, D.C
Maxwell, C.V
Johnson, Z.B
Kegley, E.B
Dvorak, R.A
description Three experiments were conducted to evaluate the efficacy of phosphorylated mannans (MAN) and pharmacological levels of ZnO on performance and immunity when added to nursery pig diets. Pigs (216 in each experiment), averaging 19 d of age and 6.2, 4.6, and 5.6 kg of BW in Exp. 1, 2, and 3, respectively, were blocked by BW in each experiment, and penned in groups of six. A lymphocyte blastogenesis assay was performed in each experiment to measure in vitro lymphocyte proliferation response. In Exp. 1, diets were arranged as a 2 x 2 factorial with two levels of Zn (200 and 2,500 ppm) and two levels of MAN (0 and 0.3% from d 0 to 10, and 0 and 0.2% from d 10 to 38). Zinc oxide increased (P < 0.05) ADG, ADFI, and G:F from d 0 to 10, and ADG and ADFI from d 10 to 24. In Exp. 2, diets were arranged as a 2 x 3 factorial with two levels of Zn (200 and 2,500 ppm) and three levels of MAN (0, 0.2, and 0.3%). Pigs fed 2,500 ppm Zn from d 0 to 10 had greater (P < 0.05) ADG, ADFI, and G:F than pigs fed 200 ppm Zn. From d 10 to 24, ADG was similar when pigs were fed 200 ppm Zn, regardless of MAN supplementation; however, ADG increased (P < 0.05) when 0.2% MAN was added to diets containing 2,500 ppm Zn (MAN x Zn interaction, P < 0.05). In Exp. 3, diets were arranged as a 2 x 3 factorial with two levels of MAN (0 and 0.3%) and three levels of Zn (200, 500, and 2,500 ppm). Zinc was maintained at 200 ppm from d 21 to 35, so only two dietary treatments (0 and 0.3% MAN) were fed during this period. Average daily gain was greater (P < 0.05) from d 7 to 21 when pigs were fed 2,500 ppm Zn compared with pigs fed 200 or 500 ppm Zn. The addition of MAN improved (P < 0.05) G:F from d 7 to 21 and d 0 to 35. Lymphocyte proliferation of unstimulated cells and phytohemagglutinin-stimulated cells was decreased (P < 0.05) in cells isolated from pigs fed MAN compared with cells isolated from pigs fed diets without MAN. Lymphocyte proliferation of pokeweed mitogen-stimulated cells isolated from pigs fed MAN was less (P < 0.05) than for pigs fed diets devoid of MAN when diets contained 200 ppm Zn; however, MAN had no effect on lymphocyte proliferation when the diet contained 500 or 2,500 ppm Zn (MAN x Zn interaction, P < 0.05). Although the magnitude of response to MAN was not equivalent to that of pharmacological concentrations of Zn, MAN may improve growth response when pharmacological Zn levels are restricted.
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Pigs (216 in each experiment), averaging 19 d of age and 6.2, 4.6, and 5.6 kg of BW in Exp. 1, 2, and 3, respectively, were blocked by BW in each experiment, and penned in groups of six. A lymphocyte blastogenesis assay was performed in each experiment to measure in vitro lymphocyte proliferation response. In Exp. 1, diets were arranged as a 2 x 2 factorial with two levels of Zn (200 and 2,500 ppm) and two levels of MAN (0 and 0.3% from d 0 to 10, and 0 and 0.2% from d 10 to 38). Zinc oxide increased (P < 0.05) ADG, ADFI, and G:F from d 0 to 10, and ADG and ADFI from d 10 to 24. In Exp. 2, diets were arranged as a 2 x 3 factorial with two levels of Zn (200 and 2,500 ppm) and three levels of MAN (0, 0.2, and 0.3%). Pigs fed 2,500 ppm Zn from d 0 to 10 had greater (P < 0.05) ADG, ADFI, and G:F than pigs fed 200 ppm Zn. From d 10 to 24, ADG was similar when pigs were fed 200 ppm Zn, regardless of MAN supplementation; however, ADG increased (P < 0.05) when 0.2% MAN was added to diets containing 2,500 ppm Zn (MAN x Zn interaction, P < 0.05). In Exp. 3, diets were arranged as a 2 x 3 factorial with two levels of MAN (0 and 0.3%) and three levels of Zn (200, 500, and 2,500 ppm). Zinc was maintained at 200 ppm from d 21 to 35, so only two dietary treatments (0 and 0.3% MAN) were fed during this period. Average daily gain was greater (P < 0.05) from d 7 to 21 when pigs were fed 2,500 ppm Zn compared with pigs fed 200 or 500 ppm Zn. The addition of MAN improved (P < 0.05) G:F from d 7 to 21 and d 0 to 35. Lymphocyte proliferation of unstimulated cells and phytohemagglutinin-stimulated cells was decreased (P < 0.05) in cells isolated from pigs fed MAN compared with cells isolated from pigs fed diets without MAN. Lymphocyte proliferation of pokeweed mitogen-stimulated cells isolated from pigs fed MAN was less (P < 0.05) than for pigs fed diets devoid of MAN when diets contained 200 ppm Zn; however, MAN had no effect on lymphocyte proliferation when the diet contained 500 or 2,500 ppm Zn (MAN x Zn interaction, P < 0.05). Although the magnitude of response to MAN was not equivalent to that of pharmacological concentrations of Zn, MAN may improve growth response when pharmacological Zn levels are restricted.]]></description><identifier>ISSN: 0021-8812</identifier><identifier>EISSN: 1525-3163</identifier><identifier>DOI: 10.1093/ansci/82.2.581</identifier><identifier>PMID: 14974558</identifier><language>eng</language><publisher>Savoy, IL: Am Soc Animal Sci</publisher><subject>Animal Feed ; Animal Nutritional Physiological Phenomena ; animal performance ; Animal productions ; Animals ; Biological and medical sciences ; Cell Division ; Dose-Response Relationship, Drug ; Female ; Fundamental and applied biological sciences. Psychology ; Hogs ; immune response ; Immunocompetence - drug effects ; immunostimulants ; liveweight gain ; lymphocyte proliferation ; Lymphocytes - immunology ; Lymphocytes - physiology ; Male ; mannans ; Mannans - administration &amp; dosage ; Mannans - pharmacology ; Oligosaccharides - administration &amp; dosage ; Oligosaccharides - pharmacology ; phosphorylated mannans ; Phosphorylation ; Physical growth ; piglet feeding ; Random Allocation ; swine ; Swine - growth &amp; development ; Swine - immunology ; swine feeding ; Terrestrial animal productions ; Vertebrates ; Weaning ; weanlings ; Weight Gain - drug effects ; Weight Gain - physiology ; Zinc ; zinc oxide ; Zinc Oxide - pharmacology</subject><ispartof>Journal of animal science, 2004-02, Vol.82 (2), p.581-587</ispartof><rights>2004 INIST-CNRS</rights><rights>Copyright American Society of Animal Science Feb 2004</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c334t-68dbab703f9f03715ccf0b6f02233a1039434eba35163bddbc68b314af8814fa3</citedby><cites>FETCH-LOGICAL-c334t-68dbab703f9f03715ccf0b6f02233a1039434eba35163bddbc68b314af8814fa3</cites></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=15590843$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/14974558$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Davis, M.E</creatorcontrib><creatorcontrib>Brown, D.C</creatorcontrib><creatorcontrib>Maxwell, C.V</creatorcontrib><creatorcontrib>Johnson, Z.B</creatorcontrib><creatorcontrib>Kegley, E.B</creatorcontrib><creatorcontrib>Dvorak, R.A</creatorcontrib><title>Effect of phosphorylated mannans and pharmacological additions of zinc oxide on growth and immunocompetence of weanling pigs</title><title>Journal of animal science</title><addtitle>J Anim Sci</addtitle><description><![CDATA[Three experiments were conducted to evaluate the efficacy of phosphorylated mannans (MAN) and pharmacological levels of ZnO on performance and immunity when added to nursery pig diets. Pigs (216 in each experiment), averaging 19 d of age and 6.2, 4.6, and 5.6 kg of BW in Exp. 1, 2, and 3, respectively, were blocked by BW in each experiment, and penned in groups of six. A lymphocyte blastogenesis assay was performed in each experiment to measure in vitro lymphocyte proliferation response. In Exp. 1, diets were arranged as a 2 x 2 factorial with two levels of Zn (200 and 2,500 ppm) and two levels of MAN (0 and 0.3% from d 0 to 10, and 0 and 0.2% from d 10 to 38). Zinc oxide increased (P < 0.05) ADG, ADFI, and G:F from d 0 to 10, and ADG and ADFI from d 10 to 24. In Exp. 2, diets were arranged as a 2 x 3 factorial with two levels of Zn (200 and 2,500 ppm) and three levels of MAN (0, 0.2, and 0.3%). Pigs fed 2,500 ppm Zn from d 0 to 10 had greater (P < 0.05) ADG, ADFI, and G:F than pigs fed 200 ppm Zn. From d 10 to 24, ADG was similar when pigs were fed 200 ppm Zn, regardless of MAN supplementation; however, ADG increased (P < 0.05) when 0.2% MAN was added to diets containing 2,500 ppm Zn (MAN x Zn interaction, P < 0.05). In Exp. 3, diets were arranged as a 2 x 3 factorial with two levels of MAN (0 and 0.3%) and three levels of Zn (200, 500, and 2,500 ppm). Zinc was maintained at 200 ppm from d 21 to 35, so only two dietary treatments (0 and 0.3% MAN) were fed during this period. Average daily gain was greater (P < 0.05) from d 7 to 21 when pigs were fed 2,500 ppm Zn compared with pigs fed 200 or 500 ppm Zn. The addition of MAN improved (P < 0.05) G:F from d 7 to 21 and d 0 to 35. Lymphocyte proliferation of unstimulated cells and phytohemagglutinin-stimulated cells was decreased (P < 0.05) in cells isolated from pigs fed MAN compared with cells isolated from pigs fed diets without MAN. Lymphocyte proliferation of pokeweed mitogen-stimulated cells isolated from pigs fed MAN was less (P < 0.05) than for pigs fed diets devoid of MAN when diets contained 200 ppm Zn; however, MAN had no effect on lymphocyte proliferation when the diet contained 500 or 2,500 ppm Zn (MAN x Zn interaction, P < 0.05). Although the magnitude of response to MAN was not equivalent to that of pharmacological concentrations of Zn, MAN may improve growth response when pharmacological Zn levels are restricted.]]></description><subject>Animal Feed</subject><subject>Animal Nutritional Physiological Phenomena</subject><subject>animal performance</subject><subject>Animal productions</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Cell Division</subject><subject>Dose-Response Relationship, Drug</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Hogs</subject><subject>immune response</subject><subject>Immunocompetence - drug effects</subject><subject>immunostimulants</subject><subject>liveweight gain</subject><subject>lymphocyte proliferation</subject><subject>Lymphocytes - immunology</subject><subject>Lymphocytes - physiology</subject><subject>Male</subject><subject>mannans</subject><subject>Mannans - administration &amp; dosage</subject><subject>Mannans - pharmacology</subject><subject>Oligosaccharides - administration &amp; dosage</subject><subject>Oligosaccharides - pharmacology</subject><subject>phosphorylated mannans</subject><subject>Phosphorylation</subject><subject>Physical growth</subject><subject>piglet feeding</subject><subject>Random Allocation</subject><subject>swine</subject><subject>Swine - growth &amp; development</subject><subject>Swine - immunology</subject><subject>swine feeding</subject><subject>Terrestrial animal productions</subject><subject>Vertebrates</subject><subject>Weaning</subject><subject>weanlings</subject><subject>Weight Gain - drug effects</subject><subject>Weight Gain - physiology</subject><subject>Zinc</subject><subject>zinc oxide</subject><subject>Zinc Oxide - pharmacology</subject><issn>0021-8812</issn><issn>1525-3163</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNpdkUFv1DAQhS1ERZfClSNESHDLdmzHWeeIqgKVKnGAnq2JY2e9SuxgJ1qK-PG43ZW26sHyYb73PM-PkHcU1hQafok-aXcp2ZqthaQvyIoKJkpOa_6SrAAYLaWk7Jy8TmkHQJloxCtyTqtmUwkhV-TftbVGz0WwxbQNKZ94P-BsumJE77N7gb7LI4wj6jCE3mkcCuw6N7uQp1n313ldhD-uM0XwRR_Dft4-qtw4Lj7oME5mNl6bB3hv0A_O98Xk-vSGnFkcknl7vC_I3dfrX1ffy9sf326uvtyWmvNqLmvZtdhugNvGAt9QobWFtrbAGOdIgTcVr0yLXOTYbde1upYtpxXanL2yyC_I54PvFMPvxaRZjS5pMwzoTViSkkA3rAKZwY_PwF1Yos-7KUYl5VBzlqH1AdIxpBSNVVN0I8Z7RUE9lKIeS1GSKaZyKVnw_ui6tKPpTvixhQx8OgKY8vfaiF67dOKEaEBW_MRtXb_du2hUGnEYsi1VO0xPHvxw4CwGhX3MXnc_GeT9KUBOIPl_RzytgA</recordid><startdate>20040201</startdate><enddate>20040201</enddate><creator>Davis, M.E</creator><creator>Brown, D.C</creator><creator>Maxwell, C.V</creator><creator>Johnson, Z.B</creator><creator>Kegley, E.B</creator><creator>Dvorak, R.A</creator><general>Am Soc Animal Sci</general><general>American Society of Animal Science</general><general>Oxford University Press</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>3V.</scope><scope>7RQ</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M2P</scope><scope>M7P</scope><scope>M7S</scope><scope>MBDVC</scope><scope>PATMY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>Q9U</scope><scope>S0X</scope><scope>U9A</scope><scope>7X8</scope></search><sort><creationdate>20040201</creationdate><title>Effect of phosphorylated mannans and pharmacological additions of zinc oxide on growth and immunocompetence of weanling pigs</title><author>Davis, M.E ; Brown, D.C ; Maxwell, C.V ; Johnson, Z.B ; Kegley, E.B ; Dvorak, R.A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c334t-68dbab703f9f03715ccf0b6f02233a1039434eba35163bddbc68b314af8814fa3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Animal Feed</topic><topic>Animal Nutritional Physiological Phenomena</topic><topic>animal performance</topic><topic>Animal productions</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Cell Division</topic><topic>Dose-Response Relationship, Drug</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Hogs</topic><topic>immune response</topic><topic>Immunocompetence - drug effects</topic><topic>immunostimulants</topic><topic>liveweight gain</topic><topic>lymphocyte proliferation</topic><topic>Lymphocytes - immunology</topic><topic>Lymphocytes - physiology</topic><topic>Male</topic><topic>mannans</topic><topic>Mannans - administration &amp; dosage</topic><topic>Mannans - pharmacology</topic><topic>Oligosaccharides - administration &amp; dosage</topic><topic>Oligosaccharides - pharmacology</topic><topic>phosphorylated mannans</topic><topic>Phosphorylation</topic><topic>Physical growth</topic><topic>piglet feeding</topic><topic>Random Allocation</topic><topic>swine</topic><topic>Swine - growth &amp; development</topic><topic>Swine - immunology</topic><topic>swine feeding</topic><topic>Terrestrial animal productions</topic><topic>Vertebrates</topic><topic>Weaning</topic><topic>weanlings</topic><topic>Weight Gain - drug effects</topic><topic>Weight Gain - physiology</topic><topic>Zinc</topic><topic>zinc oxide</topic><topic>Zinc Oxide - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Davis, M.E</creatorcontrib><creatorcontrib>Brown, D.C</creatorcontrib><creatorcontrib>Maxwell, C.V</creatorcontrib><creatorcontrib>Johnson, Z.B</creatorcontrib><creatorcontrib>Kegley, E.B</creatorcontrib><creatorcontrib>Dvorak, R.A</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>ProQuest Central (Corporate)</collection><collection>Career &amp; 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Pigs (216 in each experiment), averaging 19 d of age and 6.2, 4.6, and 5.6 kg of BW in Exp. 1, 2, and 3, respectively, were blocked by BW in each experiment, and penned in groups of six. A lymphocyte blastogenesis assay was performed in each experiment to measure in vitro lymphocyte proliferation response. In Exp. 1, diets were arranged as a 2 x 2 factorial with two levels of Zn (200 and 2,500 ppm) and two levels of MAN (0 and 0.3% from d 0 to 10, and 0 and 0.2% from d 10 to 38). Zinc oxide increased (P < 0.05) ADG, ADFI, and G:F from d 0 to 10, and ADG and ADFI from d 10 to 24. In Exp. 2, diets were arranged as a 2 x 3 factorial with two levels of Zn (200 and 2,500 ppm) and three levels of MAN (0, 0.2, and 0.3%). Pigs fed 2,500 ppm Zn from d 0 to 10 had greater (P < 0.05) ADG, ADFI, and G:F than pigs fed 200 ppm Zn. From d 10 to 24, ADG was similar when pigs were fed 200 ppm Zn, regardless of MAN supplementation; however, ADG increased (P < 0.05) when 0.2% MAN was added to diets containing 2,500 ppm Zn (MAN x Zn interaction, P < 0.05). In Exp. 3, diets were arranged as a 2 x 3 factorial with two levels of MAN (0 and 0.3%) and three levels of Zn (200, 500, and 2,500 ppm). Zinc was maintained at 200 ppm from d 21 to 35, so only two dietary treatments (0 and 0.3% MAN) were fed during this period. Average daily gain was greater (P < 0.05) from d 7 to 21 when pigs were fed 2,500 ppm Zn compared with pigs fed 200 or 500 ppm Zn. The addition of MAN improved (P < 0.05) G:F from d 7 to 21 and d 0 to 35. Lymphocyte proliferation of unstimulated cells and phytohemagglutinin-stimulated cells was decreased (P < 0.05) in cells isolated from pigs fed MAN compared with cells isolated from pigs fed diets without MAN. Lymphocyte proliferation of pokeweed mitogen-stimulated cells isolated from pigs fed MAN was less (P < 0.05) than for pigs fed diets devoid of MAN when diets contained 200 ppm Zn; however, MAN had no effect on lymphocyte proliferation when the diet contained 500 or 2,500 ppm Zn (MAN x Zn interaction, P < 0.05). Although the magnitude of response to MAN was not equivalent to that of pharmacological concentrations of Zn, MAN may improve growth response when pharmacological Zn levels are restricted.]]></abstract><cop>Savoy, IL</cop><pub>Am Soc Animal Sci</pub><pmid>14974558</pmid><doi>10.1093/ansci/82.2.581</doi><tpages>7</tpages></addata></record>
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identifier ISSN: 0021-8812
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source Oxford University Press Journals All Titles (1996-Current); MEDLINE
subjects Animal Feed
Animal Nutritional Physiological Phenomena
animal performance
Animal productions
Animals
Biological and medical sciences
Cell Division
Dose-Response Relationship, Drug
Female
Fundamental and applied biological sciences. Psychology
Hogs
immune response
Immunocompetence - drug effects
immunostimulants
liveweight gain
lymphocyte proliferation
Lymphocytes - immunology
Lymphocytes - physiology
Male
mannans
Mannans - administration & dosage
Mannans - pharmacology
Oligosaccharides - administration & dosage
Oligosaccharides - pharmacology
phosphorylated mannans
Phosphorylation
Physical growth
piglet feeding
Random Allocation
swine
Swine - growth & development
Swine - immunology
swine feeding
Terrestrial animal productions
Vertebrates
Weaning
weanlings
Weight Gain - drug effects
Weight Gain - physiology
Zinc
zinc oxide
Zinc Oxide - pharmacology
title Effect of phosphorylated mannans and pharmacological additions of zinc oxide on growth and immunocompetence of weanling pigs
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