Nitrogen in dietary glutamate is utilized exclusively for the synthesis of amino acids in the rat intestine

Am J Physiol Endocrinol Metab. 2013 Jan 1;304(1):E100-8. doi: 10.1152/ajpendo.00331.2012. Epub 2012 Oct 31.

Abstract

Although previous studies have shown that virtually the entire carbon skeleton of dietary glutamate (glutamate-C) is metabolized in the gut for energy production and amino acid synthesis, little is known regarding the fate of dietary glutamate nitrogen (glutamate-N). In this study, we hypothesized that dietary glutamate-N is an effective nitrogen source for amino acid synthesis and investigated the fate of dietary glutamate-N using [(15)N]glutamate. Fischer male rats were given hourly meals containing [U-(13)C]- or [(15)N]glutamate. The concentration and isotopic enrichment of several amino acids were measured after 0-9 h of feeding, and the net release of each amino acid into the portal vein was calculated. Most of the dietary glutamate-C was metabolized into CO(2), lactate, or alanine (56, 13, and 12% of the dietary input, respectively) in the portal drained viscera (PDV). Most of the glutamate-N was utilized for the synthesis of other amino acids such as alanine and citrulline (75 and 3% of dietary input, respectively) in the PDV, and only minor amounts were released into the portal vein in the form of ammonia and glutamate (2 and 3% of the dietary input, respectively). Substantial incorporation of (15)N into systemic amino acids such as alanine, glutamine, and proline, amino acids of the urea cycle, and branched-chain amino acids was also evident. These results provide quantitative evidence that dietary glutamate-N distributes extensively to amino acids synthesized in the PDV and, consequently, to circulating amino acids.

MeSH terms

  • Amino Acids / analysis
  • Amino Acids / biosynthesis*
  • Animals
  • Arteries / chemistry
  • Arteries / metabolism
  • Carbon / chemistry
  • Carbon / pharmacokinetics
  • Diet*
  • Eating / physiology
  • Glutamic Acid / chemistry*
  • Glutamic Acid / pharmacokinetics*
  • Intestinal Mucosa / metabolism*
  • Intestines / chemistry
  • Male
  • Nitrogen / pharmacokinetics*
  • Osmolar Concentration
  • Portal Vein / chemistry
  • Portal Vein / metabolism
  • Rats
  • Rats, Inbred F344
  • Time Factors

Substances

  • Amino Acids
  • Glutamic Acid
  • Carbon
  • Nitrogen