Ionophores have limited effects on jejunal glucose absorption and energy metabolism in mice
Two experiments, Trial 1 (in vitro) and Trial 2 (in vivo), were conducted to examine the effects of ionophores, monensin, laidlomycin, and laidlomycin propionate on whole-animal O2 consumption, organ weights, jejunal glucose absorption, and O2 utilization, as well as growth, feed and water consumpti...
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description | Two experiments, Trial 1 (in vitro) and Trial 2 (in vivo), were conducted to examine the effects of ionophores, monensin, laidlomycin, and laidlomycin propionate on whole-animal O2 consumption, organ weights, jejunal glucose absorption, and O2 utilization, as well as growth, feed and water consumption, and feed efficiency. In Trial 1, 30 male Swiss-Webster mice, 8 wk old, were used to measure the in vitro effects of each of the ionophores at concentrations of 1.62 or 16.2 mM. Six combinations of three ionophores at two concentrations resulted in a total of eight treatments. All eight treatments were exposed to jejunal rings from a single mouse for a total of 30 observations per treatment. Jejunal rings were exposed to each ionophore treatment for 15 min. Laidlomycin propionate (16.2 mM) decreased (P < 0.02) glucose absorption, as estimated by H3-3-O-methyl glucose uptake compared with all other treatments, whereas laidlomycin propionate (1.62 mM) increased (P = 0.032) jejunal DM content compared with 16.2 mM laidlomycin propionate. In Trial 2, 40 5-wk-old mice were allotted into four treatments—control and 16.2 mM each of monensin, laidlomycin, and laidlomycin propionate—for a total of 10 observations per treatment. Ionophores were administered via the drinking water for 14 d. No ionophore treatment had any effect on whole-mouse O2 consumption. Monensin increased (P = 0.004) stomach size and decreased (P = 0.049) the efficiency of BW gain compared with controls. Laidlomycin propionate decreased (P = 0.032) the percentage of whole jejunum oxygen consumption due to oubain-sensitive respiration compared with control. The efficiency of intestinal glucose absorption was not changed due to treatment in either trial. Under the conditions of these studies, monensin, laidlomycin, and laidlomycin propionate had minimal and inconsistent effects on jejunal function and energy utilization in mice. This investigation suggests that changes in the energetic requirements of animals treated with ionophores are not an issue in animal production. |
doi_str_mv | 10.2527/2003.8182072x |
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In Trial 1, 30 male Swiss-Webster mice, 8 wk old, were used to measure the in vitro effects of each of the ionophores at concentrations of 1.62 or 16.2 mM. Six combinations of three ionophores at two concentrations resulted in a total of eight treatments. All eight treatments were exposed to jejunal rings from a single mouse for a total of 30 observations per treatment. Jejunal rings were exposed to each ionophore treatment for 15 min. Laidlomycin propionate (16.2 mM) decreased (P < 0.02) glucose absorption, as estimated by H3-3-O-methyl glucose uptake compared with all other treatments, whereas laidlomycin propionate (1.62 mM) increased (P = 0.032) jejunal DM content compared with 16.2 mM laidlomycin propionate. In Trial 2, 40 5-wk-old mice were allotted into four treatments—control and 16.2 mM each of monensin, laidlomycin, and laidlomycin propionate—for a total of 10 observations per treatment. Ionophores were administered via the drinking water for 14 d. No ionophore treatment had any effect on whole-mouse O2 consumption. Monensin increased (P = 0.004) stomach size and decreased (P = 0.049) the efficiency of BW gain compared with controls. Laidlomycin propionate decreased (P = 0.032) the percentage of whole jejunum oxygen consumption due to oubain-sensitive respiration compared with control. The efficiency of intestinal glucose absorption was not changed due to treatment in either trial. Under the conditions of these studies, monensin, laidlomycin, and laidlomycin propionate had minimal and inconsistent effects on jejunal function and energy utilization in mice. This investigation suggests that changes in the energetic requirements of animals treated with ionophores are not an issue in animal production.</description><identifier>ISSN: 0021-8812</identifier><identifier>EISSN: 1525-3163</identifier><identifier>DOI: 10.2527/2003.8182072x</identifier><identifier>PMID: 12926789</identifier><language>eng</language><publisher>Savoy, IL: Am Soc Animal Sci</publisher><subject>animal production ; Animal productions ; Animals ; Biological and medical sciences ; Biological Transport - drug effects ; Digestive system ; Dose-Response Relationship, Drug ; drinking water ; energy metabolism ; Energy Metabolism - drug effects ; Energy Metabolism - physiology ; feed conversion ; Feeding. Feeding behavior ; Fundamental and applied biological sciences. Psychology ; Glucose ; Glucose - pharmacokinetics ; In Vitro Techniques ; Intestinal Absorption - drug effects ; Ionophores - pharmacology ; jejunum ; Jejunum - drug effects ; Jejunum - metabolism ; Male ; Metabolism ; Mice ; monensin ; Monensin - analogs & derivatives ; Monensin - pharmacology ; Organ Size - drug effects ; oxygen ; oxygen consumption ; Oxygen Consumption - drug effects ; propionic acid ; Random Allocation ; Rodents ; stomach ; Terrestrial animal productions ; Vertebrates ; Vertebrates: anatomy and physiology, studies on body, several organs or systems</subject><ispartof>Journal of animal science, 2003-08, Vol.81 (8), p.2072-2079</ispartof><rights>2003 INIST-CNRS</rights><rights>Copyright American Society of Animal Science Aug 2003</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c401t-30d0b402016baafd63b267dbe4ec3c8968ff0e1e431cab1aa8c5219fae71183c3</citedby><cites>FETCH-LOGICAL-c401t-30d0b402016baafd63b267dbe4ec3c8968ff0e1e431cab1aa8c5219fae71183c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=15015247$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12926789$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fan, Y.K</creatorcontrib><creatorcontrib>Croom, J</creatorcontrib><creatorcontrib>Eisen, E.J</creatorcontrib><creatorcontrib>Spires, H.R</creatorcontrib><creatorcontrib>Daniel, L.R</creatorcontrib><title>Ionophores have limited effects on jejunal glucose absorption and energy metabolism in mice</title><title>Journal of animal science</title><addtitle>J Anim Sci</addtitle><description>Two experiments, Trial 1 (in vitro) and Trial 2 (in vivo), were conducted to examine the effects of ionophores, monensin, laidlomycin, and laidlomycin propionate on whole-animal O2 consumption, organ weights, jejunal glucose absorption, and O2 utilization, as well as growth, feed and water consumption, and feed efficiency. In Trial 1, 30 male Swiss-Webster mice, 8 wk old, were used to measure the in vitro effects of each of the ionophores at concentrations of 1.62 or 16.2 mM. Six combinations of three ionophores at two concentrations resulted in a total of eight treatments. All eight treatments were exposed to jejunal rings from a single mouse for a total of 30 observations per treatment. Jejunal rings were exposed to each ionophore treatment for 15 min. Laidlomycin propionate (16.2 mM) decreased (P < 0.02) glucose absorption, as estimated by H3-3-O-methyl glucose uptake compared with all other treatments, whereas laidlomycin propionate (1.62 mM) increased (P = 0.032) jejunal DM content compared with 16.2 mM laidlomycin propionate. In Trial 2, 40 5-wk-old mice were allotted into four treatments—control and 16.2 mM each of monensin, laidlomycin, and laidlomycin propionate—for a total of 10 observations per treatment. Ionophores were administered via the drinking water for 14 d. No ionophore treatment had any effect on whole-mouse O2 consumption. Monensin increased (P = 0.004) stomach size and decreased (P = 0.049) the efficiency of BW gain compared with controls. Laidlomycin propionate decreased (P = 0.032) the percentage of whole jejunum oxygen consumption due to oubain-sensitive respiration compared with control. The efficiency of intestinal glucose absorption was not changed due to treatment in either trial. Under the conditions of these studies, monensin, laidlomycin, and laidlomycin propionate had minimal and inconsistent effects on jejunal function and energy utilization in mice. This investigation suggests that changes in the energetic requirements of animals treated with ionophores are not an issue in animal production.</description><subject>animal production</subject><subject>Animal productions</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Biological Transport - drug effects</subject><subject>Digestive system</subject><subject>Dose-Response Relationship, Drug</subject><subject>drinking water</subject><subject>energy metabolism</subject><subject>Energy Metabolism - drug effects</subject><subject>Energy Metabolism - physiology</subject><subject>feed conversion</subject><subject>Feeding. Feeding behavior</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Glucose</subject><subject>Glucose - pharmacokinetics</subject><subject>In Vitro Techniques</subject><subject>Intestinal Absorption - drug effects</subject><subject>Ionophores - pharmacology</subject><subject>jejunum</subject><subject>Jejunum - drug effects</subject><subject>Jejunum - metabolism</subject><subject>Male</subject><subject>Metabolism</subject><subject>Mice</subject><subject>monensin</subject><subject>Monensin - analogs & derivatives</subject><subject>Monensin - pharmacology</subject><subject>Organ Size - drug effects</subject><subject>oxygen</subject><subject>oxygen consumption</subject><subject>Oxygen Consumption - drug effects</subject><subject>propionic acid</subject><subject>Random Allocation</subject><subject>Rodents</subject><subject>stomach</subject><subject>Terrestrial animal productions</subject><subject>Vertebrates</subject><subject>Vertebrates: anatomy and physiology, studies on body, several organs or systems</subject><issn>0021-8812</issn><issn>1525-3163</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNpd0U1v1DAQBmALgei2cOQKERLcUjy2kzhHVPFRqRIH6ImDNXHGu46SeLGTQv89Xu2ilTj54EevPe8w9gr4tahE80FwLq81aMEb8ecJ20AlqlJCLZ-yDecCSq1BXLDLlAbOQVRt9ZxdgGhF3eh2w37ehjnsdyFSKnb4QMXoJ79QX5BzZJdUhLkYaFhnHIvtuNqQqMAuhbhffL7COcuZ4vaxmGjBLow-TYWfi8lbesGeORwTvTydV-z-86cfN1_Lu29fbm8-3pVWcVhKyXveKS441B2i62vZ5c_1HSmy0uq21s5xAlISLHaAqG0loHVIDYCWVl6x98fcfQy_VkqLmXyyNI44U1iTaWSloVYqw7f_wSGsMY-WjIBck6yUyKg8IhtDSpGc2Uc_YXw0wM2hcnOo3PyrPPvXp9C1m6g_61PHGbw7AUwWRxdxtj6dXcXzzlRzHmPnt7vfPpJJE45jjgUzYNJgtDk8meGbI3QYDG5jDrv_nutTnPO2qSsl_wJQhp8_</recordid><startdate>20030801</startdate><enddate>20030801</enddate><creator>Fan, Y.K</creator><creator>Croom, J</creator><creator>Eisen, E.J</creator><creator>Spires, H.R</creator><creator>Daniel, L.R</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>PTHSS</scope><scope>PYCSY</scope><scope>Q9U</scope><scope>S0X</scope><scope>U9A</scope><scope>7X8</scope></search><sort><creationdate>20030801</creationdate><title>Ionophores have limited effects on jejunal glucose absorption and energy metabolism in mice</title><author>Fan, Y.K ; Croom, J ; Eisen, E.J ; Spires, H.R ; Daniel, L.R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c401t-30d0b402016baafd63b267dbe4ec3c8968ff0e1e431cab1aa8c5219fae71183c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>animal production</topic><topic>Animal productions</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Biological Transport - drug effects</topic><topic>Digestive system</topic><topic>Dose-Response Relationship, Drug</topic><topic>drinking water</topic><topic>energy metabolism</topic><topic>Energy Metabolism - drug effects</topic><topic>Energy Metabolism - physiology</topic><topic>feed conversion</topic><topic>Feeding. Feeding behavior</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Glucose</topic><topic>Glucose - pharmacokinetics</topic><topic>In Vitro Techniques</topic><topic>Intestinal Absorption - drug effects</topic><topic>Ionophores - pharmacology</topic><topic>jejunum</topic><topic>Jejunum - drug effects</topic><topic>Jejunum - metabolism</topic><topic>Male</topic><topic>Metabolism</topic><topic>Mice</topic><topic>monensin</topic><topic>Monensin - analogs & derivatives</topic><topic>Monensin - pharmacology</topic><topic>Organ Size - drug effects</topic><topic>oxygen</topic><topic>oxygen consumption</topic><topic>Oxygen Consumption - drug effects</topic><topic>propionic acid</topic><topic>Random Allocation</topic><topic>Rodents</topic><topic>stomach</topic><topic>Terrestrial animal productions</topic><topic>Vertebrates</topic><topic>Vertebrates: anatomy and physiology, studies on body, several organs or systems</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fan, Y.K</creatorcontrib><creatorcontrib>Croom, J</creatorcontrib><creatorcontrib>Eisen, E.J</creatorcontrib><creatorcontrib>Spires, H.R</creatorcontrib><creatorcontrib>Daniel, L.R</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 & Technical Education Database</collection><collection>Agricultural Science Collection</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Engineering Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Agricultural Science Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Engineering Database</collection><collection>Research Library (Corporate)</collection><collection>Environmental Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Engineering Collection</collection><collection>Environmental Science Collection</collection><collection>ProQuest Central Basic</collection><collection>SIRS Editorial</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of animal science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fan, Y.K</au><au>Croom, J</au><au>Eisen, E.J</au><au>Spires, H.R</au><au>Daniel, L.R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ionophores have limited effects on jejunal glucose absorption and energy metabolism in mice</atitle><jtitle>Journal of animal science</jtitle><addtitle>J Anim Sci</addtitle><date>2003-08-01</date><risdate>2003</risdate><volume>81</volume><issue>8</issue><spage>2072</spage><epage>2079</epage><pages>2072-2079</pages><issn>0021-8812</issn><eissn>1525-3163</eissn><abstract>Two experiments, Trial 1 (in vitro) and Trial 2 (in vivo), were conducted to examine the effects of ionophores, monensin, laidlomycin, and laidlomycin propionate on whole-animal O2 consumption, organ weights, jejunal glucose absorption, and O2 utilization, as well as growth, feed and water consumption, and feed efficiency. In Trial 1, 30 male Swiss-Webster mice, 8 wk old, were used to measure the in vitro effects of each of the ionophores at concentrations of 1.62 or 16.2 mM. Six combinations of three ionophores at two concentrations resulted in a total of eight treatments. All eight treatments were exposed to jejunal rings from a single mouse for a total of 30 observations per treatment. Jejunal rings were exposed to each ionophore treatment for 15 min. Laidlomycin propionate (16.2 mM) decreased (P < 0.02) glucose absorption, as estimated by H3-3-O-methyl glucose uptake compared with all other treatments, whereas laidlomycin propionate (1.62 mM) increased (P = 0.032) jejunal DM content compared with 16.2 mM laidlomycin propionate. In Trial 2, 40 5-wk-old mice were allotted into four treatments—control and 16.2 mM each of monensin, laidlomycin, and laidlomycin propionate—for a total of 10 observations per treatment. Ionophores were administered via the drinking water for 14 d. No ionophore treatment had any effect on whole-mouse O2 consumption. Monensin increased (P = 0.004) stomach size and decreased (P = 0.049) the efficiency of BW gain compared with controls. Laidlomycin propionate decreased (P = 0.032) the percentage of whole jejunum oxygen consumption due to oubain-sensitive respiration compared with control. The efficiency of intestinal glucose absorption was not changed due to treatment in either trial. Under the conditions of these studies, monensin, laidlomycin, and laidlomycin propionate had minimal and inconsistent effects on jejunal function and energy utilization in mice. This investigation suggests that changes in the energetic requirements of animals treated with ionophores are not an issue in animal production.</abstract><cop>Savoy, IL</cop><pub>Am Soc Animal Sci</pub><pmid>12926789</pmid><doi>10.2527/2003.8182072x</doi><tpages>8</tpages></addata></record> |
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subjects | animal production Animal productions Animals Biological and medical sciences Biological Transport - drug effects Digestive system Dose-Response Relationship, Drug drinking water energy metabolism Energy Metabolism - drug effects Energy Metabolism - physiology feed conversion Feeding. Feeding behavior Fundamental and applied biological sciences. Psychology Glucose Glucose - pharmacokinetics In Vitro Techniques Intestinal Absorption - drug effects Ionophores - pharmacology jejunum Jejunum - drug effects Jejunum - metabolism Male Metabolism Mice monensin Monensin - analogs & derivatives Monensin - pharmacology Organ Size - drug effects oxygen oxygen consumption Oxygen Consumption - drug effects propionic acid Random Allocation Rodents stomach Terrestrial animal productions Vertebrates Vertebrates: anatomy and physiology, studies on body, several organs or systems |
title | Ionophores have limited effects on jejunal glucose absorption and energy metabolism in mice |
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