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Institute of Human Nutrition, University of Southampton, Bassett Crescent East, Southampton SO16 7PX, United Kingdom
2To whom correspondence and reprint requests should be addressed.
To examine the effects of dietary glutamine on lymphocyte function,
male mice aged 6 wk were fed for 2 wk one of three isonitrogenous,
isocaloric diets, which varied in glutamine concentration. The control
diet included 200 g casein/kg, providing 19.6 g glutamine/kg;
the glutamine-enriched diet provided 54.8 g glutamine/kg
partly at the expense of casein; and the alanine + glycine-enriched
diet provided 13.3 g glutamine/kg. The plasma concentrations of a
number of amino acids varied because of the diet fed. The plasma
glycine concentration was greater in mice fed the alanine +
glycine-enriched diet (380 ± 22 µmol/L) than in mice fed
the control (177 ± 17 µmol/L) or the glutamine-enriched (115
± 18 µmol/L) diets. The plasma glutamine concentration was
greater in mice fed the glutamine-enriched diet (945 ± 117
µmol/L) than in those fed the diet enriched with alanine + glycine
(561 ± 127 µmol/L), but was not different from that in mice fed
the control diet (791 ± 35 µmol/L). There was a significant
linear relationship between the amount of glutamine in the diet and
plasma glutamine concentration (r = 0.655,
P = 0.015). Plasma alanine concentration was
unaffected by diet. The reason for the lack of effect of
increasing the amount of alanine in the diet upon its concentration in
the circulation may relate to its use by the liver. Thymidine
incorporation (56 ± 18 kBq/well versus <10 kBq/well), expression
of the
-subunit of the interleukin-2 receptor (62 versus 30%
receptor positive cells) and interleukin-2 production [189 ± 28 versus 106 ± 5 (control) or 61 ± 13 (alanine +
glycine enriched) ng/L] were greater for concanavalin A-stimulated spleen lymphocytes from mice fed the
glutamine-enriched diet compared to those from mice fed the other
two diets. Thus, increasing the amount of glutamine in the murine diet
enhances the ability of T lymphocytes to respond to mitogenic
stimulation. Taken together, these observations suggest that increasing
the oral availability of glutamine could promote the T-cell driven,
cell-mediated immune response.
KEY WORDS: lymphocyte glutamine cytokine interleukin-2 mice
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