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1.
Mol Nutr Food Res ; 54(12): 1722-33, 2010 Dec.
Article in English | MEDLINE | ID: mdl-20589860

ABSTRACT

SCOPE: Coffee is among the most frequently consumed beverages. Its consumption is inversely associated to the incidence of diseases related to reactive oxygen species; the phenomenon may be due to its antioxidant properties. Our primary objective was to investigate the impact of consumption of a coffee containing high levels of chlorogenic acids on the oxidation of proteins, DNA and membrane lipids; additionally, other redox biomarkers were monitored in an intervention trial. METHODS AND RESULTS: The treatment group (n=36) consumed instant coffee co-extracted from green and roasted beans, whereas the control consumed water (800 mL/P/day, 5 days). A global statistical analysis of four main biomarkers selected as primary outcomes showed that the overall changes are significant. 8-Isoprostaglandin F2α in urine declined by 15.3%, 3-nitrotyrosine was decreased by 16.1%, DNA migration due to oxidized purines and pyrimidines was (not significantly) reduced in lymphocytes by 12.5 and 14.1%. Other markers such as the total antioxidant capacity were moderately increased; e.g. LDL and malondialdehyde were shifted towards a non-significant reduction. CONCLUSION: The oxidation of DNA, lipids and proteins associated with the incidence of various diseases and the protection against their oxidative damage may be indicative for beneficial health effects of coffee.


Subject(s)
Chlorogenic Acid/analysis , Coffee/chemistry , DNA Damage , Macromolecular Substances/toxicity , Oxidative Stress , Adult , Antioxidants/metabolism , Comet Assay , Dinoprost/analogs & derivatives , Dinoprost/urine , Female , Humans , Lipid Peroxidation , Lymphocytes/metabolism , Male , Malondialdehyde/analysis , Middle Aged , Oxidation-Reduction , Reactive Oxygen Species/metabolism , Tyrosine/analogs & derivatives , Tyrosine/analysis , Young Adult
2.
Eur J Nutr ; 42(3): 171-9, 2003 Jun.
Article in English | MEDLINE | ID: mdl-12811475

ABSTRACT

BACKGROUND: Conjugated linoleic acid (CLA) has been reported to decrease fat deposition, and increase lean body mass. This has been broadly inferred to mean that CLA alters protein turnover. However, data to test the effects of CLA on protein turnover are lacking. An enhancement in immune responses by CLA has also been demonstrated. AIM OF THE STUDY: The objective of this study was to determine the potential for dietary CLA and protein intervention to improve nutritional and functional recovery in an animal model of catabolic stress and immunodepletion. METHODS: Diets varying in their protein levels in the presence or absence of CLA were tested for their effects on the recovery of glucocorticoid (intraperitoneal injection of dexamethasone, 120 mg/kg) treated rats. Following steroid injection, rats were fed 4 dietary treatments for 4 d. The diets contained 10 or 20 g/100 g protein with or without 0.5 g/100 g CLA. RESULTS: Dexamethasone treatment resulted in a decreased food intake and loss of weight, independent of dietary treatment. A higher number of blood monocytes occurred in rats fed the high CLA diets. The protein fractional synthesis rate in spleens of rats fed the diets containing either high proteins or CLA were higher compared to those fed diets with low protein content or without CLA, respectively. CLA, consumed post-dexamethasone treatment, did not improve protein turnover in the other tissues studied, including gut mucosa, liver, muscle and thymus. CONCLUSIONS: The present study was performed to determine the effect of CLA in acute conditions, as opposed to a preventive approach, on the recovery from a catabolic stress with immunodepletion. Overall, no effect of short-term feeding CLA on the recovery from dexamethasone-mediated immunodepletion was observed.


Subject(s)
Dexamethasone/pharmacology , Dietary Proteins/administration & dosage , Glucocorticoids/pharmacology , Immunity, Cellular/drug effects , Linoleic Acids/administration & dosage , Animals , Blood Cell Count , Dietary Proteins/metabolism , Dietary Supplements , Disease Models, Animal , Dose-Response Relationship, Drug , Glutathione/analysis , Injections, Intraperitoneal/veterinary , Linoleic Acids/pharmacology , Liver/chemistry , Liver/drug effects , Lymphocyte Activation/drug effects , Muscle, Skeletal/chemistry , Muscle, Skeletal/drug effects , Organ Size/drug effects , Random Allocation , Rats , Rats, Sprague-Dawley , Thymus Gland/drug effects
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