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
Hauptverfasser: Andersen, Dean W., Filer, Lloyd J., Stegink, Lewis D.
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container_title Metabolism, clinical and experimental
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creator Andersen, Dean W.
Filer, Lloyd J.
Stegink, Lewis D.
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.
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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 &lt; .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. 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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 &lt; .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 &lt; .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. 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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 &amp; 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 &lt; .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. 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source MEDLINE; Elsevier ScienceDirect Journals
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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