Document Detail


Protein synthesis is severely diminished following a simulated upper GI bleed in patients with cirrhosis.
MedLine Citation:
PMID:  18602715     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
BACKGROUND/AIMS: An upper gastrointestinal (GI) bleed in cirrhotic patients has been hypothesised to induce catabolism due to the absence of the essential branched chain amino acid (BCAA) isoleucine and an abundance of the BCAA leucine in haemoglobin. We tested whether an upper GI bleed produces hypoisoleucinemia via BCAA antagonism and impairs protein synthesis. METHODS: Isoleucine turnover and oxidation was studied in 5 metabolically stable patients with cirrhosis during a 4-h period of intragastric saline infusion followed by a 4-h period in which an upper GI bleed was simulated by an amino acid solution mimicking haemoglobin. RESULTS: The simulated upper GI bleed induced hypoisoleucinemia (26% of initial values) and an increase in leucine (400%) and valine (350%) concentrations. Isoleucine flux and isoleucine oxidation decreased to a third of initial values following a simulated bleed, but the fraction of isoleucine flux used for oxidation did not change. Consequently, the non-oxidative portion of isoleucine flux, representing protein synthesis, decreased similarly. CONCLUSIONS: The present study shows that a simulated upper GI bleed induces hypoisoleucinemia and decreases protein synthesis markedly. The fact that the percentage of isoleucine flux that was oxidized was not influenced by the hypoisoleucinemic state can only be explained by BCAA antagonism.
Authors:
Steven W M Olde Damink; Rajiv Jalan; Nicolaas E P Deutz; Peter C Hayes; Peter B Soeters
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't     Date:  2008-06-02
Journal Detail:
Title:  Journal of hepatology     Volume:  49     ISSN:  0168-8278     ISO Abbreviation:  J. Hepatol.     Publication Date:  2008 Nov 
Date Detail:
Created Date:  2008-10-20     Completed Date:  2009-01-07     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  8503886     Medline TA:  J Hepatol     Country:  England    
Other Details:
Languages:  eng     Pagination:  726-31     Citation Subset:  IM    
Affiliation:
Department of Surgery, University Hospital Maastricht, Maastricht, The Netherlands. steven.oldedanmink@ah.unimaas.nl
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MeSH Terms
Descriptor/Qualifier:
Adult
Amino Acids, Branched-Chain / antagonists & inhibitors,  metabolism
Female
Gastrointestinal Hemorrhage / complications,  metabolism*
Humans
Isoleucine / metabolism
Liver Cirrhosis / complications,  metabolism*
Liver Cirrhosis, Alcoholic / complications,  metabolism
Male
Middle Aged
Models, Biological
Oxidation-Reduction
Protein Biosynthesis*
Grant Support
ID/Acronym/Agency:
//Wellcome Trust
Chemical
Reg. No./Substance:
0/Amino Acids, Branched-Chain; 73-32-5/Isoleucine
Comments/Corrections
Comment In:
J Hepatol. 2008 Nov;49(5):686-7   [PMID:  18804308 ]

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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