Literature DB >> 23315357

Branched-chain amino acids and muscle ammonia detoxification in cirrhosis.

Gitte Dam1, Peter Ott, Niels Kristian Aagaard, Hendrik Vilstrup.   

Abstract

Branched-chain amino acids (BCAA) are used as a therapeutic nutritional supplement in patients with cirrhosis and hepatic encephalopathy (HE). During liver disease, the decreased capacity for urea synthesis and porto-systemic shunting reduce the hepatic clearance of ammonia and skeletal muscle may become the main alternative organ for ammonia detoxification. We here summarize current knowledge of muscle BCAA and ammonia metabolism with a focus on liver cirrhosis and HE. Plasma levels of BCAA are lower and muscle uptake of BCAA seems to be higher in patients with cirrhosis and hyperammonemia. BCAA metabolism may improve muscle net ammonia removal by supplying carbon skeletons for formation of alfa-ketoglutarate that combines with two ammonia molecules to become glutamine. An oral dose of BCAA enhances muscle ammonia metabolism but also transiently increases the arterial ammonia concentration, likely due to extramuscular metabolism of glutamine. We, therefore, speculate that the beneficial effect of long term intake of BCAA on HE demonstrated in clinical studies may be related to an improved muscle mass and nutritional status rather than to an ammonia lowering effect of BCAA themselves.

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Year:  2013        PMID: 23315357     DOI: 10.1007/s11011-013-9377-3

Source DB:  PubMed          Journal:  Metab Brain Dis        ISSN: 0885-7490            Impact factor:   3.584


  25 in total

1.  Branched-chain amino acids increase arterial blood ammonia in spite of enhanced intrinsic muscle ammonia metabolism in patients with cirrhosis and healthy subjects.

Authors:  Gitte Dam; Susanne Keiding; Ole Lajord Munk; Peter Ott; Mads Buhl; Hendrik Vilstrup; Lasse Kristoffer Bak; Helle Sønderby Waagepetersen; Arne Schousboe; Niels Møller; Michael Sørensen
Journal:  Am J Physiol Gastrointest Liver Physiol       Date:  2011-06-02       Impact factor: 4.052

2.  Effects of oral branched-chain amino acid granules on event-free survival in patients with liver cirrhosis.

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Journal:  Clin Gastroenterol Hepatol       Date:  2005-07       Impact factor: 11.382

3.  Uptake and metabolism of plasma glutamine by the small intestine.

Authors:  H G Windmueller; A E Spaeth
Journal:  J Biol Chem       Date:  1974-08-25       Impact factor: 5.157

4.  Does leucine, leucyl-tRNA, or some metabolite of leucine regulate protein synthesis and degradation in skeletal and cardiac muscle?

Authors:  M E Tischler; M Desautels; A L Goldberg
Journal:  J Biol Chem       Date:  1982-02-25       Impact factor: 5.157

5.  Leucine stimulates the secretion of hepatocyte growth factor by hepatic stellate cells.

Authors:  Tomoaki Tomiya; Yukiko Inoue; Mikio Yanase; Masahiro Arai; Hitoshi Ikeda; Kazuaki Tejima; Kayo Nagashima; Takako Nishikawa; Kenji Fujiwara
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6.  Branched-chain amino acid oxidation by isolated rat tissue preparations.

Authors:  F L Shinnick; A E Harper
Journal:  Biochim Biophys Acta       Date:  1976-07-21

7.  Hyperammonemia-induced depletion of glutamate and branched-chain amino acids in muscle and plasma.

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Journal:  J Hepatol       Date:  1996-11       Impact factor: 25.083

8.  Direct molecular and spectroscopic evidence for increased ammonia removal capacity of skeletal muscle in acute liver failure.

Authors:  Nicolas Chatauret; Paul Desjardins; Claudia Zwingmann; Christopher Rose; K V Rama Rao; Roger F Butterworth
Journal:  J Hepatol       Date:  2006-01-04       Impact factor: 25.083

9.  Insulin and glucagon levels in liver cirrhosis. Relationship with plasma amino acid imbalance of chronic hepatic encephalopathy.

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Journal:  Dig Dis Sci       Date:  1979-08       Impact factor: 3.199

10.  Plasma clearances of branched-chain amino acids in control subjects and in patients with cirrhosis.

Authors:  G Marchesini; G P Bianchi; H Vilstrup; G A Checchia; D Patrono; M Zoli
Journal:  J Hepatol       Date:  1987-02       Impact factor: 25.083

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  23 in total

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Authors:  Natalia Qvartskhava; Philipp A Lang; Boris Görg; Vitaly I Pozdeev; Marina Pascual Ortiz; Karl S Lang; Hans J Bidmon; Elisabeth Lang; Christina B Leibrock; Diran Herebian; Johannes G Bode; Florian Lang; Dieter Häussinger
Journal:  Proc Natl Acad Sci U S A       Date:  2015-04-13       Impact factor: 11.205

Review 2.  When can nutritional therapy impact liver disease?

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3.  Practical Issues in the Management of Overt Hepatic Encephalopathy.

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Review 4.  Nutrition and Muscle in Cirrhosis.

Authors:  Anil C Anand
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Review 5.  Interactions in the Metabolism of Glutamate and the Branched-Chain Amino Acids and Ketoacids in the CNS.

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Review 6.  EASL Clinical Practice Guidelines on nutrition in chronic liver disease.

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Review 7.  The metabolomic window into hepatobiliary disease.

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Review 8.  Cause and management of muscle wasting in chronic liver disease.

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Review 9.  Sarcopenia from mechanism to diagnosis and treatment in liver disease.

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10.  Valproate disturbs the balance between branched and aromatic amino acids in rats.

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