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1.
Int J Med Sci ; 14(11): 1065-1071, 2017.
Article in English | MEDLINE | ID: mdl-29104459

ABSTRACT

Background and Aims: Abdominal radiotherapy (RT) causes harm to the mid gastrointestinal mucosa by release of pro-inflammatory cytokines and promotes autophagic changes in tumor cells. This study was aimed to measure the effect of glutamine administration on markers of inflammation and autophagy in cancer patients treated with RT. Methods: In this double-blind, randomized, controlled pilot trial 43 patients under abdominal RT diagnosed of pelvic or abdominal malignancies receiving glutamine (30 g/d) or placebo (casein, 30 g/d). Patient recruitment took place in the Complejo Asistencial Universitario of León (CAULE), Spain. Patient evaluation took place at three different time points during the study: before RT (pre-treatment), in the middle of the RT period (mid-treatment), and after finishing RT (post-treatment). Data were compared by analysis of variance and the Newmann Keuls test. Significance was accepted at p < 0.05. Results Abdominal RT increased whole blood mRNA levels of inflammatory and autophagic markers, but glutamine administration showed significantly lower expression of toll-like receptor 4 (TLR4), CD36, interleukin-1ß (IL-1ß), tumor necrosis factor-alpha (TNF-α), cyclooxygenase-2 (COX-2), and matrix metalloproteinase-9 (MMP-9). Moreover, glutamine reduced the expression of the transcription factors nuclear factor kappa B (NF-κB) and activator protein 1 (AP-1). Glutamine also inhibited the autophagic response, with changes in expression of beclin-1, UV radiation resistance associated gene (UVRAG), autophagy-related protein-5 (Atg5), protein 1 light chain 3 (LC3), sequestosome 1 (p62/SQSTM1) and lysosome-associated membrane protein (LAMP)-1. Conclusions Findings provide evidence that glutamine decreases the inflammatory response and abolishes the changes of the autophagy machinery in patients receiving abdominal RT. The protective effect of glutamine must continue being investigated to disclose further molecular pathways.


Subject(s)
Glutamine/metabolism , Inflammation/metabolism , Neoplasms/metabolism , Autophagy/physiology , Cyclooxygenase 2/metabolism , Double-Blind Method , Humans , Interleukin-1beta/metabolism , Lysosomal-Associated Membrane Protein 1/metabolism , Toll-Like Receptor 4/metabolism , Transcription Factor AP-1/metabolism , Tumor Necrosis Factor-alpha/metabolism
2.
Contact Dermatitis ; 53(4): 240, 2005 Oct.
Article in English | MEDLINE | ID: mdl-16191029

ABSTRACT

Opium alkaloids can cause immunological reactions. Cross-sensitization among them must be considered in these situations.


Subject(s)
Analgesics, Opioid/adverse effects , Codeine/adverse effects , Drug Eruptions/etiology , Adult , Aged , Female , Humans , Male
3.
JPEN J Parenter Enteral Nutr ; 29(4): 262-5, 2005.
Article in English | MEDLINE | ID: mdl-15961682

ABSTRACT

BACKGROUND: Glutamine, a nonessential amino acid, has received increasing attention because it becomes essential during stress and catabolic conditions. Many investigations have shown that during severe stress, the consumption of glutamine exceeds glutamine synthesis, resulting in depletion of glutamine stores. The aim of this study was to evaluate the effects of supplementing parenteral diets with a glutamine-containing dipeptide, L-alanyl-L-glutamine, on rat nutrition status. METHODS: Male Wistar rats were used. Animals (n = 36) were centrally catheterized and randomly assigned to 1 of the following groups based on method of parenteral nutrition (PN): control group with oral nutrition and IV infusion of a saline solution; standard parenteral nutrition (SPN) group; or alanyl-glutamine-supplemented PN (ALA-GLN PN) group (20 g/L). Parenteral nutrition was isocaloric and isonitrogenous. Infusions were administered at a rate of 2.0 mL/h over 5 days. Nutrition status was assessed by body weight change, plasma proteins, accumulated urinary creatinine, and nitrogen balance. RESULTS: Accumulated urinary creatinine increased significantly after day 4 in the ALA-GLN PN group, compared with the SPN group and the controls. Body weight change significantly differed on day 5 between the ALA-GLN PN and SPN groups. After 3 days, nitrogen balance was significantly lower and nitrogen retention higher in the ALA-GLN PN group when compared with the SPN group. Albumin and transferrin concentrations decreased significantly in the SPN group, but did not differ from the controls in the ALA-GLN PN group. CONCLUSIONS: Weight, plasma proteins, urinary accumulated creatinine, and nitrogen retention showed a better evolution in the group supplemented with the glutamine dipeptide when compared with the SPN group. Our results suggest a more suitable nutrition support in animals receiving L-alanyl-L-glutamine.


Subject(s)
Dipeptides/pharmacology , Nutritional Status , Parenteral Nutrition , Animals , Blood Proteins , Body Weight/drug effects , Creatinine/urine , Dipeptides/metabolism , Male , Nitrogen/metabolism , Random Allocation , Rats , Rats, Wistar , Serum Albumin/metabolism , Transferrin/metabolism , Treatment Outcome
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