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1.
Biomed Pharmacother ; 2010 Sep 25.
Article in English | MEDLINE | ID: mdl-20951539

ABSTRACT

The Publisher regrets that this article is an accidental duplication of an article that has already been published, http://dx.doi.org/10.1016/j.biomag.2010.09.001. The duplicate article has therefore been withdrawn.

2.
Int J Vitam Nutr Res ; 75(1): 19-27, 2005 Jan.
Article in English | MEDLINE | ID: mdl-15830917

ABSTRACT

Several recent studies in human immunodeficiency virus (HIV) patients have identified micronutrient deficiencies as affecting progression to acquired immunodeficiency syndrome (AIDS) and death. Although the mechanisms are not known, micronutrient deficiencies may exacerbate the oxidative stress induced by HIV. In addition, infection and its evolution likely lead to an increased requirement for nutritional micronutrients, especially antioxidants. To evaluate this, 40 relatively healthy, institutionalized HIV-infected individuals were recruited for assessment before or three months after fresh fruit and vegetable supply were increased due to seasonal supply. Seven-day dietary records were recorded at the beginning (December) and end of the three-month study period (March). Oxidative stress indices and CD4+, CD38+/CD8+, and CD95+ T-lymphocyte subsets were also measured at these times. No significant differences were found in calorie or protein intake across the study period, but vitamin A, C, and E intakes all increased. A number of redox indicators were modified (increase: total antioxidant status, glutathione peroxidase, and glutathione; and decrease: superoxide dismutase) during the study period. However, no change in malondialdehyde, hydroperoxides, or DNA damage was noted but a significant reduction in CD38+/CD8+ relative count was seen. Within the context and limitations of this study, the increase of dietary fruits and vegetables intake for three months had some beneficial effects on nutrition, systemic redox balance, and immune parameters in HIV-infected persons.


Subject(s)
Diet/methods , HIV Infections/metabolism , Micronutrients/pharmacology , Oxidative Stress/drug effects , Adult , Antioxidants/analysis , DNA Damage/drug effects , Diet Records , Female , Flow Cytometry/methods , Fruit , Glutathione/blood , Glutathione/drug effects , Glutathione Peroxidase/blood , Glutathione Peroxidase/drug effects , Humans , Hydrogen Peroxide/blood , Male , Malondialdehyde/blood , Micronutrients/administration & dosage , Middle Aged , Superoxide Dismutase/blood , Superoxide Dismutase/drug effects , T-Lymphocytes/drug effects , Vegetables
3.
Pharmacol Res ; 47(3): 217-24, 2003 Mar.
Article in English | MEDLINE | ID: mdl-12591017

ABSTRACT

Infection by human immunodeficiency virus (HIV) causes persistent chronic inflammation. Viral Tat protein plays a role in the intracellular increase of reactive oxygen species (ROS) thus increasing apoptotic index, mostly the one mediated by FAS/CD95, and depleting CD4+ T lymphocytes. The aim of this study was to investigate whether there is a relationship between an extensive array of redox status indices (glutathione (GSH), malondialdehyde (MDA), peroxidation potential, total antioxidant status, glutathione peroxidase (GPx), superoxide dismutase (SOD), total hydroperoxide (TH), DNA fragmentation) and relative CD4, CD95, CD38/CD8 T lymphocyte counts in HIV/AIDS patients compared to healthy subjects. Blood samples from 85 HIV/AIDS patients and 40 healthy subjects were tested by spectrophotometric techniques in order to measure oxidative stress indices, and by flow cytometry to quantify T cell subsets. Patients were divided in two groups according to CDC 1993 guidelines. CD95 and CD38 increase paralleled the severity of HIV infection. Both a reduction of GSH levels and an increase in MDA and TH levels were detected in the plasma of HIV+ patients. These patients also showed an increase of DNA fragmentation in lymphocytes as well as a significant (P<0.05) reduction of GPx and an increase in SOD activity in erythrocytes. Relatively to the control group, HIV-infected patients had significantly differences in global indices of total antioxidant status. These results corroborate that substantial oxidative stress occurs during HIV infection. To our knowledge this study is the first relating oxidative stress indices with both CD38/CD8 and CD95 lymphocytes subsets.


Subject(s)
HIV Infections/blood , Oxidative Stress/physiology , Adult , Analysis of Variance , Biomarkers/blood , DNA Fragmentation , Enzyme-Linked Immunosorbent Assay , Female , Flow Cytometry , Glutathione/blood , Glutathione Peroxidase/blood , HIV Infections/immunology , Humans , Hydrogen Peroxide/blood , Lipid Peroxidation/physiology , Male , Malondialdehyde/blood , Middle Aged , Reference Values , Superoxide Dismutase/blood , T-Lymphocyte Subsets
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