Amino-acid-based peritoneal dialysis solution improves amino-acid transport into skeletal muscle View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2008-04

AUTHORS

M Asola, K Virtanen, K Någren, S Helin, M Taittonen, H Kastarinen, B Anderstam, J Knuuti, K Metsärinne, P Nuutila

ABSTRACT

Abnormalities of amino-acid (AA) and protein metabolism are known to occur in chronic kidney disease (CKD). Protein malnutrition may contribute to impaired prognosis of dialysis patients. A crucial step in protein metabolism is AA transport into the cells. We compared the effects of an AA-containing peritoneal dialysis (PD) solution to glucose-based solutions on skeletal muscle AA uptake. Thirteen nondiabetic PD patients were studied twice in a random order and in a crossover manner both in the fasting state and during euglycemic insulin stimulation using [(11)C]methylaminoisobutyrate ([(11)C]MeAIB) and positron emission tomography (PET). Before both PET study days, patients had been using either glucose-based PD solutions only or one daily bag of AA solution in addition to glucose-based PD solutions for at least 6 weeks. Skeletal muscle AA uptake was calculated with graphical analysis. AA-containing PD solution increased plasma AA concentrations from 2.18+/-0.34 to 3.08+/-0.55 mmol l(-1) in the fasting state (P=0.0002) and from 1.88+/-0.15 to 2.42+/-0.30 mmol l(-1) during insulin stimulation (P<0.0001). As compared to PD treatment using glucose-based solutions only, skeletal muscle AA uptake was significantly higher during treatment containing AA solution both in the fasting state (15.2+/-5.8 vs 20.0+/-5.6 micromol kg(-1) min(-1), respectively, P=0.0057) and during insulin stimulation (16.8+/-4.5 vs 21.1+/-4.9 micromol kg(-1) min(-1), respectively, P=0.0046). In conclusion, PD treatment with an AA-containing PD solution is associated with a significant increase in skeletal muscle AA uptake both in the fasting state and during insulin stimulation. More... »

PAGES

s131-s136

Identifiers

URI

http://scigraph.springernature.com/pub.10.1038/sj.ki.5002614

DOI

http://dx.doi.org/10.1038/sj.ki.5002614

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1051474687

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/18379536


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Download the RDF metadata as:  json-ld nt turtle xml License info

HOW TO GET THIS DATA PROGRAMMATICALLY:

JSON-LD is a popular format for linked data which is fully compatible with JSON.

curl -H 'Accept: application/ld+json' 'https://scigraph.springernature.com/pub.10.1038/sj.ki.5002614'

N-Triples is a line-based linked data format ideal for batch operations.

curl -H 'Accept: application/n-triples' 'https://scigraph.springernature.com/pub.10.1038/sj.ki.5002614'

Turtle is a human-readable linked data format.

curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/pub.10.1038/sj.ki.5002614'

RDF/XML is a standard XML format for linked data.

curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/pub.10.1038/sj.ki.5002614'


 

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308 schema:name Department of Anaesthesiology, Turku University Central Hospital, Turku, Finland
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313 https://www.grid.ac/institutes/grid.470895.7 schema:alternateName Turku PET Centre
314 schema:name Baxter Nordic Renal, Stockholm, Sweden
315 Department of Medicine, Satakunta Central Hospital, Pori, Finland
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318 https://www.grid.ac/institutes/grid.4714.6 schema:alternateName Karolinska Institute
319 schema:name Department of Renal Medicine, Karolinska Institute, Stockholm, Sweden
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