Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2013 Jun;28(2):217-20.
doi: 10.1007/s11011-013-9377-3. Epub 2013 Jan 15.

Branched-chain amino acids and muscle ammonia detoxification in cirrhosis

Affiliations
Review

Branched-chain amino acids and muscle ammonia detoxification in cirrhosis

Gitte Dam et al. Metab Brain Dis. 2013 Jun.

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.

PubMed Disclaimer

References

    1. J Hepatol. 1990 Jul;11(1):92-101 - PubMed
    1. Gastroenterol Jpn. 1981;16(1):64-70 - PubMed
    1. Gut. 1978 Nov;19(11):1068-73 - PubMed
    1. Gastroenterology. 2003 Jun;124(7):1792-801 - PubMed
    1. Dig Dis Sci. 1979 Aug;24(8):594-601 - PubMed

MeSH terms