Source of the urinary maltose and maltotriose excreted during intravenous infusion of oligosaccharide solutions in young pigs
Pigs infused with preparations of glucose oligosaccharides excrete sizeable quantities of maltose in urine despite the absence of maltose in the infused solution. Maltose infused without other oligosaccharides is well utilized. Our studies examined possible sources of excreted maltose. We first exam...
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Veröffentlicht in: | Metabolism, clinical and experimental clinical and experimental, 1988-06, Vol.37 (6), p.562-567 |
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description | Pigs infused with preparations of glucose oligosaccharides excrete sizeable quantities of maltose in urine despite the absence of maltose in the infused solution. Maltose infused without other oligosaccharides is well utilized. Our studies examined possible sources of excreted maltose. We first examined whether simultaneous infusion of larger oligosaccharides with maltose inhibits maltose utilization. Four young pigs were infused for four days with 20 g/d of a maltose-free oligosaccharide preparation to which tracer quantities of U-
14C-maltose were added. Urinary excretion of maltose-plus-maltotriose increased significantly (
P < .05) from a mean ± SD baseline value of .01 ± .01 g/d to an overall four-day mean value of 1.33 ± 0.47 g/d. However, only 10.7 ± 0.78% of infused
14C-maltose was excreted, indicating that simultaneous infusion of larger oligosaccharides did not inhibit maltose utilization. The second study examined whether maltotriose present in the oligosaccharide mixture was the source of excreted maltose. Four young pigs were infused for three days with 20 g/d of a special preparation of oligosaccharides containing only frace quantities of maltose and maltotriose. Urinary maltose plus maltotriose excretion increased significantly (
P < .05) from a mean ± SD baseline value of .01 ± .01 g/d to 1.65 ± 0.41 g/d during oligosaccharide infusion. The data suggest that excreted maltose and maltotriose arise from the catabolism of larger oligosaccharides. |
doi_str_mv | 10.1016/0026-0495(88)90172-2 |
format | Article |
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14C-maltose were added. Urinary excretion of maltose-plus-maltotriose increased significantly (
P < .05) from a mean ± SD baseline value of .01 ± .01 g/d to an overall four-day mean value of 1.33 ± 0.47 g/d. However, only 10.7 ± 0.78% of infused
14C-maltose was excreted, indicating that simultaneous infusion of larger oligosaccharides did not inhibit maltose utilization. The second study examined whether maltotriose present in the oligosaccharide mixture was the source of excreted maltose. Four young pigs were infused for three days with 20 g/d of a special preparation of oligosaccharides containing only frace quantities of maltose and maltotriose. Urinary maltose plus maltotriose excretion increased significantly (
P < .05) from a mean ± SD baseline value of .01 ± .01 g/d to 1.65 ± 0.41 g/d during oligosaccharide infusion. The data suggest that excreted maltose and maltotriose arise from the catabolism of larger oligosaccharides.</description><identifier>ISSN: 0026-0495</identifier><identifier>EISSN: 1532-8600</identifier><identifier>DOI: 10.1016/0026-0495(88)90172-2</identifier><identifier>PMID: 3374322</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>alimentacion parenteral ; alimentation enterale ; Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy ; Animals ; azucares ; Biological and medical sciences ; cerdo ; Emergency and intensive care: metabolism and nutrition disorders. Enteral and parenteral nutrition ; Intensive care medicine ; maltosa ; maltose ; Maltose - urine ; maltotriosa ; maltotriose ; Medical sciences ; Oligosaccharides - administration & dosage ; Oligosaccharides - pharmacology ; orina ; parenteral feeding ; porcin ; sucres ; sugars ; Swine ; Trisaccharides - urine ; urine</subject><ispartof>Metabolism, clinical and experimental, 1988-06, Vol.37 (6), p.562-567</ispartof><rights>1988</rights><rights>1989 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c358t-bf2359933076971a60ad96de5cec5d2a36d6f70a1d62e3ab4258c3e67187991b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/0026-0495(88)90172-2$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3536,27903,27904,45974</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=6984511$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/3374322$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Andersen, Dean W.</creatorcontrib><creatorcontrib>Filer, Lloyd J.</creatorcontrib><creatorcontrib>Stegink, Lewis D.</creatorcontrib><title>Source of the urinary maltose and maltotriose excreted during intravenous infusion of oligosaccharide solutions in young pigs</title><title>Metabolism, clinical and experimental</title><addtitle>Metabolism</addtitle><description>Pigs infused with preparations of glucose oligosaccharides excrete sizeable quantities of maltose in urine despite the absence of maltose in the infused solution. Maltose infused without other oligosaccharides is well utilized. Our studies examined possible sources of excreted maltose. We first examined whether simultaneous infusion of larger oligosaccharides with maltose inhibits maltose utilization. Four young pigs were infused for four days with 20 g/d of a maltose-free oligosaccharide preparation to which tracer quantities of U-
14C-maltose were added. Urinary excretion of maltose-plus-maltotriose increased significantly (
P < .05) from a mean ± SD baseline value of .01 ± .01 g/d to an overall four-day mean value of 1.33 ± 0.47 g/d. However, only 10.7 ± 0.78% of infused
14C-maltose was excreted, indicating that simultaneous infusion of larger oligosaccharides did not inhibit maltose utilization. The second study examined whether maltotriose present in the oligosaccharide mixture was the source of excreted maltose. Four young pigs were infused for three days with 20 g/d of a special preparation of oligosaccharides containing only frace quantities of maltose and maltotriose. Urinary maltose plus maltotriose excretion increased significantly (
P < .05) from a mean ± SD baseline value of .01 ± .01 g/d to 1.65 ± 0.41 g/d during oligosaccharide infusion. The data suggest that excreted maltose and maltotriose arise from the catabolism of larger oligosaccharides.</description><subject>alimentacion parenteral</subject><subject>alimentation enterale</subject><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</subject><subject>Animals</subject><subject>azucares</subject><subject>Biological and medical sciences</subject><subject>cerdo</subject><subject>Emergency and intensive care: metabolism and nutrition disorders. Enteral and parenteral nutrition</subject><subject>Intensive care medicine</subject><subject>maltosa</subject><subject>maltose</subject><subject>Maltose - urine</subject><subject>maltotriosa</subject><subject>maltotriose</subject><subject>Medical sciences</subject><subject>Oligosaccharides - administration & dosage</subject><subject>Oligosaccharides - pharmacology</subject><subject>orina</subject><subject>parenteral feeding</subject><subject>porcin</subject><subject>sucres</subject><subject>sugars</subject><subject>Swine</subject><subject>Trisaccharides - urine</subject><subject>urine</subject><issn>0026-0495</issn><issn>1532-8600</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1988</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE2LFDEQhoMo6zj6D1T6IKKH1nx05-MiyOIXLHhY9xxqkurZSE9nTNKLe_C_m7aHOXpKhXrqreIh5Dmj7xhl8j2lXLa0M_0brd8ayhRv-QOyYb3grZaUPiSbM_KYPMn5J6VUKS0vyIUQqhOcb8if6zgnh00cmnKLzZzCBOm-OcBYYsYGJr_WJYXlj79dwoK-8Qu5b8JUEtzhFOdc62HOIU5LVhzDPmZw7hZS8NjkOM6l9haquY9zHT2GfX5KHg0wZnx2erfk5vOnH5df26vvX75dfrxqneh1aXcDF70xQlAljWIgKXgjPfYOXe85COnloCgwLzkK2HW8106gVEwrY9hObMnrNfeY4q8Zc7GHkB2OI0xYT7dK8451VcmWdCvoUsw54WCPKRyqEcuoXazbRaldlFqt7T_rltexF6f8eXdAfx46aa79V6c-ZAfjkGByIZ8xaXTXM1axlys2QLSwTxW5uWZG1zWUsm7J-bACWGXdBUw2u4CTQx8SumJ9DP8_9C8yvqlT</recordid><startdate>19880601</startdate><enddate>19880601</enddate><creator>Andersen, Dean W.</creator><creator>Filer, Lloyd J.</creator><creator>Stegink, Lewis D.</creator><general>Elsevier Inc</general><general>Elsevier</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>19880601</creationdate><title>Source of the urinary maltose and maltotriose excreted during intravenous infusion of oligosaccharide solutions in young pigs</title><author>Andersen, Dean W. ; Filer, Lloyd J. ; Stegink, Lewis D.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c358t-bf2359933076971a60ad96de5cec5d2a36d6f70a1d62e3ab4258c3e67187991b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1988</creationdate><topic>alimentacion parenteral</topic><topic>alimentation enterale</topic><topic>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</topic><topic>Animals</topic><topic>azucares</topic><topic>Biological and medical sciences</topic><topic>cerdo</topic><topic>Emergency and intensive care: metabolism and nutrition disorders. Enteral and parenteral nutrition</topic><topic>Intensive care medicine</topic><topic>maltosa</topic><topic>maltose</topic><topic>Maltose - urine</topic><topic>maltotriosa</topic><topic>maltotriose</topic><topic>Medical sciences</topic><topic>Oligosaccharides - administration & dosage</topic><topic>Oligosaccharides - pharmacology</topic><topic>orina</topic><topic>parenteral feeding</topic><topic>porcin</topic><topic>sucres</topic><topic>sugars</topic><topic>Swine</topic><topic>Trisaccharides - urine</topic><topic>urine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Andersen, Dean W.</creatorcontrib><creatorcontrib>Filer, Lloyd J.</creatorcontrib><creatorcontrib>Stegink, Lewis 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>Metabolism, clinical and experimental</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Andersen, Dean W.</au><au>Filer, Lloyd J.</au><au>Stegink, Lewis D.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Source of the urinary maltose and maltotriose excreted during intravenous infusion of oligosaccharide solutions in young pigs</atitle><jtitle>Metabolism, clinical and experimental</jtitle><addtitle>Metabolism</addtitle><date>1988-06-01</date><risdate>1988</risdate><volume>37</volume><issue>6</issue><spage>562</spage><epage>567</epage><pages>562-567</pages><issn>0026-0495</issn><eissn>1532-8600</eissn><abstract>Pigs infused with preparations of glucose oligosaccharides excrete sizeable quantities of maltose in urine despite the absence of maltose in the infused solution. Maltose infused without other oligosaccharides is well utilized. Our studies examined possible sources of excreted maltose. We first examined whether simultaneous infusion of larger oligosaccharides with maltose inhibits maltose utilization. Four young pigs were infused for four days with 20 g/d of a maltose-free oligosaccharide preparation to which tracer quantities of U-
14C-maltose were added. Urinary excretion of maltose-plus-maltotriose increased significantly (
P < .05) from a mean ± SD baseline value of .01 ± .01 g/d to an overall four-day mean value of 1.33 ± 0.47 g/d. However, only 10.7 ± 0.78% of infused
14C-maltose was excreted, indicating that simultaneous infusion of larger oligosaccharides did not inhibit maltose utilization. The second study examined whether maltotriose present in the oligosaccharide mixture was the source of excreted maltose. Four young pigs were infused for three days with 20 g/d of a special preparation of oligosaccharides containing only frace quantities of maltose and maltotriose. Urinary maltose plus maltotriose excretion increased significantly (
P < .05) from a mean ± SD baseline value of .01 ± .01 g/d to 1.65 ± 0.41 g/d during oligosaccharide infusion. The data suggest that excreted maltose and maltotriose arise from the catabolism of larger oligosaccharides.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>3374322</pmid><doi>10.1016/0026-0495(88)90172-2</doi><tpages>6</tpages></addata></record> |
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subjects | alimentacion parenteral alimentation enterale Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy Animals azucares Biological and medical sciences cerdo Emergency and intensive care: metabolism and nutrition disorders. Enteral and parenteral nutrition Intensive care medicine maltosa maltose Maltose - urine maltotriosa maltotriose Medical sciences Oligosaccharides - administration & dosage Oligosaccharides - pharmacology orina parenteral feeding porcin sucres sugars Swine Trisaccharides - urine urine |
title | Source of the urinary maltose and maltotriose excreted during intravenous infusion of oligosaccharide solutions in young pigs |
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