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Glutamine Facilitates Chemotherapy While Reducing Toxicity

Department of Surgery, University of Arkansas for Medical Sciences, Little Rock, The John L. McClellan Memorial Veteran's Administration Hospital, Little Rock, Arkansas

Emmanuel Nwokedi, BS

Department of Surgery, University of Arkansas for Medical Sciences, Little Rock, The John L. McClellan Memorial Veteran's Administration Hospital, Little Rock, Arkansas

Laura F. Hutchins, MD

Department of Medicine, University of Arkansas for Medical Sciences, Little Rock, The John L. McClellan Memorial Veteran's Administration Hospital, Little Rock, Arkansas

Alex A. Pappas, MD

Department of Pathology, University of Arkansas for Medical Sciences, Little Rock, The John L. McClellan Memorial Veteran's Administration Hospital, Little Rock, Arkansas

Nicholas P. Lang, MD

Department of Surgery, University of Arkansas for Medical Sciences, Little Rock, The John L. McClellan Memorial Veteran's Administration Hospital, Little Rock, Arkansas

J. Ralph Btoadwater, MD

Department of Surgery, University of Arkansas for Medical Sciences, Little Rock, The John L. McClellan Memorial Veteran's Administration Hospital, Little Rock, Arkansas

Raymond C. Read, MD

Department of Surgery, University of Arkansas for Medical Sciences, Little Rock, The John L. McClellan Memorial Veteran's Administration Hospital, Little Rock, Arkansas

Kent C. Westbrook, MD

Department of Surgery, University of Arkansas for Medical Sciences, Little Rock, The John L. McClellan Memorial Veteran's Administration Hospital, Little Rock, Arkansas

Dose intensification of chemotherapy is thought to increase survival. With recent advances in hemopoietic cell modulators such as granulocyte colony stimulating factor, the limiting toxicity of intensifying chemotherapeutic regimens has become the severity of the associated enterocolitis. In animal models, glutamine protects the host from methotrexate-induced enterocolitis. This study evaluates the effects of a glutamine-supplemented diet on the tumoricidal effectiveness of methotrexate. Sarcoma-bearing Fisher 344 rats (n = 30) were pair-fed an isocaloric elemental diet containing 1% glutamine or an isonitrogenous amount of glycine beginning on day 25 of the study. Rats from each group received two intraperitoneal injections of methotrexate (5 mg/kg) or saline on days 26 and 33 of the study. On day 40, rats were killed, tumor volume and weight were recorded, and tumor glutaminase activity and tumor morphometrics were measured. Blood was taken for arterial glutamine content, complete blood count, and blood culture. The gut was processed for glutaminase activity and synthesis phase of the deoxyribonucleic acid. In rats receiving methotrexate, the tumor volume loss was nearly doubled when glutamine was added to the diet. Significant differences in tumor glutaminase activity and morphometrics were not detected. The toxicity to the host was ameliorated. Significantly increased synthesis phase of deoxyribonucleic acid of the whole jejunum, decreased bacteremia, "sepsis," and mortality were demonstrated. Glutamine supplementation enhances the tumoricidal effectiveness of methotrexate while reducing its morbidity and mortality in this sarcoma rat model. (Journal of Parenteral and Enteral Nutrition 16:83S-87S, 1992)

Journal of Parenteral and Enteral Nutrition, Vol. 16, No. 6 Suppl, 83S-87S (1992)
DOI: 10.1177/014860719201600609


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