OBJECTIVES: Three series of studies investigated whether 1) glutamine defic
iency occurs in tumor-bearing rats, 2) glutamine supplementation improves p
rotein metabolism during chemotherapy in tumor-bearing rats, and 3) oral gl
utamine supplement improves systemic immune and gut-barrier function in pat
ients with esophageal cancer receiving radiochemotherapy.
METHODS: In the animal studies, AH109A hepatoma cells or Yoshida sarcoma ce
lls were inoculated into male Donryu rats to induce tumors. Glutamine produ
ction was measured by U-C-14-glutamine infusion and the conversion of argin
ine to glutamine was measured by infusion of U-C-14-arginine. The effect of
glutamine on protein metabolism was investigated by 1-C-14-leucine infusio
n. In the clinical study, 13 patients with esophageal cancer were randomize
d into two groups, control and glutamine supplemented (30 g/d), for 4 wk.
RESULTS: Glutamine levels in plasma and skeletal muscle were decreased in t
umor-bearing rats, although glutamine production and the conversion of argi
nine to glutamine were increased. Glutamine-supplemented total parenteral n
utrition reduced whole-body protein breakdown rate during chemotherapy in t
umor-bearing rats. Oral supplementation of glutamine to the patients with e
sophageal cancer enhanced lymphocyte mitogenic function and reduced permeab
ility of the gut during radiochemotherapy.
CONCLUSIONS: Glutamine depletion in host tissues occurs in tumor-bearing ra
ts. Glutamine supplementation can attenuate loss of protein in the muscle i
n tumor-bearing animals and protect immune and gut-barrier function during
radiochemotherapy in patients with advanced cancer. Nutrition 2001;17: 766-
768. (C) Elsevier Science Inc. 2001.