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© 2003 The American Society for Nutritional Sciences J. Nutr. 133:2068S-2072S, June 2003


Supplement: 2nd Amino Acid Workshop

Interorgan Amino Acid Transport and its Regulation1,2

John T. Brosnan3

Department of Biochemistry, Memorial University of Newfoundland, St. John's, NF Canada A1B 3X9

3 To whom correspondence should be addressed. E-mail: jbrosnan{at}mun.ca.

Interorgan amino acid transport is a highly active and regulated process that provides amino acids to all tissues of the body, both for protein synthesis and to enable amino acids to be used for specific metabolic functions. It is also an important component of plasma amino acid homeostasis. Net movement of amino acids depends on the physiological and nutritional state. For example, in the fed state the dominant flux is from the intestine to the other tissues. In starvation the dominant flux is from muscle to the liver and kidney. A number of general principles underlie many amino acid fluxes: i) The body does not have a store for amino acids. This means that dietary amino acids, in excess of those required for protein synthesis, are rapidly catabolized; ii) Amino acid catabolism must occur in a manner that does not elevate blood ammonia. Thus, extrasplanchnic amino acid metabolism often involves an innocuous means of transporting nitrogen to the liver; iii) Because most amino acids are glucogenic, there will be a considerable flux of amino acids to the gluconeogenic organs when there is a need to produce glucose. In addition to these bulk flows, fluxes of many specific amino acids underlie specific organ function. These include intestinal oxidation of enteral amino acids, the intestinal/renal axis for arginine production, the brain uptake of neurotransmitter precursors and renal glutamine metabolism. There is no single means of regulating amino acid fluxes; rather, such varied mechanisms as substrate supply, enzyme activity, transporter activity and competitive inhibition of transport are all found.


KEY WORDS: • arteriovenous differences • intestinal metabolism • perivenous and periportal hepatocytes • glutamine • arginine




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