Source:http://linkedlifedata.com/resource/pubmed/id/15933220
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2005-9-14
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pubmed:abstractText |
Previously, we observed increased plasma arginine (ARG) concentrations after glutamine (GLN)-enriched diets, in combination with clinical benefits. GLN delivers nitrogen for ARG synthesis, and the present study was designed to quantify the interorgan relationship of exogenous L-GLN or GLN dipeptide, by enteral or parenteral route, contributing to intestinal citrulline (CIT) and renal de novo ARG synthesis in mice. To study this, we used a multicatheterized mouse model with Swiss mice (n = 43) in the postabsorptive state. Stable isotopes were infused into the jugular vein or into the duodenum {per group either free L-[2,(15)N]GLN or dipeptide L-ALA-L-[2,(15)N]GLN, all with L-[ureido-(13)C-(2)H(2)]CIT and L-[guanidino-(15)N(2)-(2)H(2)]ARG} to establish renal and intestinal ARG and CIT metabolism. Blood flow was measured using (14)C-para-aminohippuric acid. Net intestinal CIT release, renal uptake of CIT, and net renal ARG efflux was found, as assessed by arteriovenous flux measurements. Quantitatively, more de novo L-[2,(15)N]CIT was produced when free L-[2,(15)N]GLN was given than when L-ALA-L-[2,(15)N]GLN was given, whereas renal de novo L-[2,(15)N]ARG was similar in all groups. In conclusion, the intestinal-renal axis is hereby proven in mice in that L-[2,(15)N]GLN or dipeptide were both converted into de novo renal L-[2,(15)N]ARG; however, not all was derived from intestinal L-[2,(15)N]CIT production. In this model, the feeding route and form of GLN did not influence de novo renal ARG production derived from GLN.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Arginine,
http://linkedlifedata.com/resource/pubmed/chemical/Citrulline,
http://linkedlifedata.com/resource/pubmed/chemical/Dipeptides,
http://linkedlifedata.com/resource/pubmed/chemical/Glutamine,
http://linkedlifedata.com/resource/pubmed/chemical/alanylglutamine,
http://linkedlifedata.com/resource/pubmed/chemical/p-Aminohippuric Acid
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
0193-1857
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
289
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
G679-85
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:15933220-Algorithms,
pubmed-meshheading:15933220-Animals,
pubmed-meshheading:15933220-Arginine,
pubmed-meshheading:15933220-Citrulline,
pubmed-meshheading:15933220-Dipeptides,
pubmed-meshheading:15933220-Glutamine,
pubmed-meshheading:15933220-Hematocrit,
pubmed-meshheading:15933220-Intestines,
pubmed-meshheading:15933220-Kidney,
pubmed-meshheading:15933220-Kinetics,
pubmed-meshheading:15933220-Male,
pubmed-meshheading:15933220-Mice,
pubmed-meshheading:15933220-Regional Blood Flow,
pubmed-meshheading:15933220-Renal Plasma Flow,
pubmed-meshheading:15933220-p-Aminohippuric Acid
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pubmed:year |
2005
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pubmed:articleTitle |
Intestinal renal metabolism of L-citrulline and L-arginine following enteral or parenteral infusion of L-alanyl-L-[2,15N]glutamine or L-[2,15N]glutamine in mice.
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pubmed:affiliation |
Dept. of Surgery, Vrije Universiteit University Medical Center, 1007 MB Amsterdam, The Netherlands.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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