{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,12,25]],"date-time":"2025-12-25T01:49:28Z","timestamp":1766627368006,"version":"build-2065373602"},"reference-count":25,"publisher":"Wiley","issue":"5S","license":[{"start":{"date-parts":[[1999,9,1]],"date-time":"1999-09-01T00:00:00Z","timestamp":936144000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J Parenter Enteral Nutr"],"published-print":{"date-parts":[[1999,9]]},"abstract":"<jats:p>Bacterial translocation (BT) is a well\u2010known insult during total parenteral nutrition (TPN) and a high incidence of morbidity has been reported in septic patients receiving TPN. Inflammatory cytokines were shown to play an important role in the pathogenesis of critical complications following sepsis. Previous studies have indicated that supplementation of TPN with glutamine is effective in preventing BT in animals, but its effectiveness in humans is unclear. The aim of this study was to determine the effectiveness of oral glutamine supplementation to patients receiving TPN in suppressing cytokine production of mesenteric blood mononuclear cells (M\u2010MNC). Fifteen colorectal cancer patients were divided into 3 groups according to preoperative nutrition management. (1) TPN group: TPN with conventional glutamine\u2010free amino acid solution. (2) Gln group: TPN with oral glutamine supplementation of 30 g\/d. (3) Control group: oral intake of normal food. M\u2010MNC were obtained immediately after laparotomy and tumor necrosis factor\u2010alpha (TNF\u2010\u03b1) and interleukin\u201010 (IL\u201010) production of M\u2010MNC was evaluated with or without lipopolysaccharide (LPS) stimulation. TNF\u2010\u03b1 and IL\u201010 production by LPS\u2010stimulated M\u2010MNC was increased in the TPN group and suppressed in the Gln group. In conclusion, oral glutamine supplementation to patients with TPN was shown to be effective for the prevention of M\u2010MNC activation to avoid excessive production of cytokines. 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