The aim of the present work was to examine in pigs the effect of a dietary supplementation with the flavor enhancer monosodium glutamate (MSG) on intestinal amino acid metabolism. For this purpose, pigs weighing 60 ± 2 kg received a standard meal twice a day for 1 week, supplemented with either 10 g MSG per meal or, as control experiments, an isonitrogenous amount of glycine together with an equal amount of sodium in the form of NaCl, the animals being their own control in all experiments. At the end of this period, pigs received a MSG or glycine-NaCl-supplemented meal and samples of portal and arterial blood were collected for amino acid analysis in plasma. The results demonstrate after MSG supplementation rapid significant increases in glutamate concentration in the portal and arterial blood plasma after a test meal which resulted in a positive portoarterial difference. In comparison, after glycine-NaCl supplementation, glutamate concentrations were almost identical in portal and arterial plasma. Furthermore, significant increased aspartate concentration in the portal blood plasma was observed after MSG supplementation when compared with control experiments. When enterocytes were isolated at the end of the supplementation period from the jejunum and examined for their metabolic capacities towards L-glutamate and L-glutamine, it was found that metabolism did not differ according to the supplement used, with glutamate and glutamine being oxidized and transaminated at a similar level. It is concluded that the portal hyperglutamatemia observed shortly after the ingestion of a MSG- supplemented meal is likely due to the saturation of the intestinal capacity to metabolize glutamate with no measurable adaptation of the metabolic pathways controlling glutamate metabolism in enterocytes.

1.
Giacometti T: Free and bound glutamate in natural products; in Filer LJ, Garattini S, Kare MR, Reynolds WA, Wurtman RJ (eds): Glutamic Acid: Advances in Biochemistry and Physiology. New York, Raven Press, 1979, pp 25–34.
2.
Olney JW: Excitoxic amino acids: Research applications and safety implications; in Filer LJ, Garattini S, Kare MR, Reynolds WA, Wurtman RJ (eds): Glutamic Acid: Advances in Biochemistry and Physiology. New York, Raven Press, 1979, pp 287–319.
3.
Kerr GR, Wu-Lee M, El-Lozy M, McGandy R, Stare FJ: Food-symptomatology questionnaires: Risks of demand – bias questions and population – biased surveys; in Filer LJ, Garattini S, Kare MR, Reynolds WA, Wurtman RJ (eds): Glutamic Acid: Advances in Biochemistry and Physiology. New York, Raven Press, 1979, pp 375–387.
4.
Bogdanov MB, Tjurmina OA, Wurtman RJ: Consumption of a high dietary dose of monosodium glutamate fails to affect extracellular glutamate levels in the hypothalamic arcuate nucleus of adult rats. Brain Res 1996;736:76–81.
[PubMed]
5.
Matthews DE, Campbell RG: Splanchnic bed utilization of glutamine and glutamic acid in humans. Am J Physiol 1993;264:E848–E854.
[PubMed]
6.
Meister A: Glutamine metabolism in mammalian tissues; in Häussinger D, Sies S (eds): Enzymology of Glutamine. Berlin, Springer, 1984, pp 9–15.
7.
Dillon JC: L’acide glutamique. Cah Nutr Diet 1991;26:157–162.
8.
Windmueller HG, Spaeth AE: Uptake and metabolism of plasma glutamine by the small intestine. J Biol Chem 1974;249:5070–5079.
[PubMed]
9.
Windmueller HG, Spaeth AE: Intestinal metabolism of glutamine and glutamate from the lumen as compared to glutamine from blood. Arch Biochem Biophys 1975;171:662–672.
[PubMed]
10.
Watford M, Lund P, Krebs HA: Isolation and metabolic characteristics of rat and chicken enterocytes. Biochem J 1979;178:589–596.
[PubMed]
11.
Watford M: Glutamine metabolism in rat small intestine: Synthesis of three-carbon products in isolated enterocytes. Biochim Biophys Acta 1994;1200:73–78.
[PubMed]
12.
Blachier F, Darcy-Vrillon B, Sener A, Duée PH, Malaisse WJ: Arginine metabolism in rat enterocytes. Biochim Biophys Acta 1991;1092:304–310.
[PubMed]
13.
Dugan MER, Knabe DA, Wu G: The induction of citrulline synthesis from glutamine in enterocytes of weaned pigs is not due primarily to age or change in the diet. J Nutr 1995;125:2388–2393.
[PubMed]
14.
Henslee JG, Jones ME: Ornithine synthesis from glutamate in rat small intestinal mucosa. Arch Biochem Biophys 1982;219:186–197.
[PubMed]
15.
Murphy JM, Murch SJ, Ball RO: Proline is synthesized from glutamate during intragastric infusion but not during intravenous infusion in neonatal piglets. J Nutr 1996;126:878–886.
[PubMed]
16.
Porteous JW: Glutamate, glutamine, aspartate, asparagine, glucose and ketone-body metabolism in chick intestinal brush-border cells. Biochem J 1980;188:619–632.
[PubMed]
17.
Reeds PJ, Burrin DG, Stoll B, Jahoor F, Wykes L, Henry J, Frazer ME: Enteral glutamate is the preferential source for mucosal glutathione synthesis in fed piglets. Am J Physiol 1997;273:E408–E415.
[PubMed]
18.
Uchiyama C, Mori M, Tatibana M: Subcellular localization and properties of N-acetylglutamate synthase in rat small intestinal mucosa. J Biochem 1981;89:1777–1786.
[PubMed]
19.
Battezzati A, Brillon DJ, Matthews DE: Oxidation of glutamic acid by the splanchnic bed in humans. Am J Physiol 1995;269:E269–E276.
[PubMed]
20.
Johnson AW, Berrington JM, Walker I, Manning A, Losowsky MS: Measurement of the transfer of the nitrogen moiety of intestinal lumen glutamic acid in man after oral ingestion of L-[15N] glutamic acid. Clin Sci 1988;75:499–502.
[PubMed]
21.
Reeds PJ, Burrin DG, Jahoor F, Wykes L, Henry J, Frazer EM: Enteral glutamate is almost completely metabolized in first pass by the gastrointestinal tract in infant pigs. Am J Physiol 1996;270:E413–E418.
[PubMed]
22.
Darcy-Vrillon B, Morel MT, Cherbuy C, Bernard F, Posho L, Blachier F, Meslin JC, Duée PH: Metabolic characteristics of pig colonocytes after adaptation to a high fiber diet. J Nutr 1993;123:234–243.
[PubMed]
23.
Rérat A, Chayvialle JA, Kandé J, Vaissade P, Vaugelade P, Bourrier T: Metabolic and hormonal effects of test meals with various protein contents in pigs. Can J Physiol Pharmacol 1985;63:1547–1559.
[PubMed]
24.
Blachier F, M’Rabet-Touil H, Posho L, Darcy-Vrillon B, Duée PH: Intestinal arginine metabolism during development. Evidence for de novo synthesis of L-arginine in newborn pig enterocytes. Eur J Biochem 1993;216:109–117.
[PubMed]
25.
Bergmeyer HU: Methods of Enzymatic Analysis, ed 3. New York, Academic Press, 1974, vol 1–4.
26.
Blachier F, Mignon A, Soubrane O: Polyamines inhibit lipopolysaccharide-induced nitric oxide synthase activity in rat liver cytosol. Nitric Oxide Biol Chem 1997;1:268–272.
27.
M’Rabet-Touil H, Blachier F, Hellio N, Robert V, Cherbuy C, Darcy-Vrillon B, Duée PH: Transglutaminase activity in enterocytes isolated from pig jejunum. Mol Cell Biochem 1995;146:49–54.
[PubMed]
28.
Vaugelade P, Posho L, Darcy-Vrillon B, Bernard F, Morel MT, Duée PH: Intestinal oxygen uptake and glucose metabolism during nutrient absorption in the pig. Proc Soc Exp Biol Med 1994;207:309–316.
[PubMed]
29.
Häussinger D: Nitrogen metabolism in liver: Structural and functional organization and physiological relevance. Biochem J 1990;267:281–290.
[PubMed]
30.
Fafournoux P, Remezy C, Demigne C: Fluxes and membrane transport of amino acids in rat liver under different protein diets. Am J Physiol 1990;259:E614–E625.
[PubMed]
31.
Stegink LD, Filer LJ, Baker GL: Effects of carbohydrate on plasma and erythrocyte glutamate levels in humans ingesting large doses of monosodium L-glutamate in water. Am J Clin Nutr 1983;37:961–968.
[PubMed]
32.
Stegink LD, Filler LJ, Baker GL, Bell EF: Effect of sucrose ingestion on plasma glutamate concentrations in humans administered monosodium L-glutamate. Am J Clin Nutr 1986;43:510–515.
[PubMed]
33.
Cynober L: Metabolic interaction between ornithine and α-ketoglutarate as a basis for the action of ornithine α-ketoglutarate. Clin Nutr 1993;12:54–56.
34.
Prior RL, Gross KL: Dietary arginine deficiency and gut ammonium infusion alter flux of urea cycle intermediates across the portal-drained viscera of pigs. J Nutr 1995;125:251–263.
[PubMed]
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