ABSTRACT
During Chronic Obstructive Pulmonary Disease (COPD) progression, the intracellular antioxidant defence in RBCs must preserve the integrity of the plasmalemma through NADPH+ generation to obtain a sufficient number of reduced non-protein SH-groups. Here, we studied the activities of enzymes in RBCs that are related to glutathione metabolism under conditions of increasing oxidative stress, which are associated with COPD progression, by increasing cellular damage in vitro with PM2.5, a ROS generator. The study included 43 patients, who were separated according to their GOLD classification into moderate and severe groups, along with 11 healthy volunteers (HV). Blood samples were analysed for G6PD, GAPDH, GPx, and GR. The results showed significant decreases in the oxidation of the G6PD, GR and GPx proteins, resulting in decreased enzymatic activity. By contrast, an increase (p<0.05) in GAPDH was observed, suggesting a pool of ATP on the membrane. However, it is evident that RBCs are damaged during the progression of COPD, although their integrity is preserved, and they retain limited function, thus allowing patient survival without haemolysis.
Subject(s)
Erythrocytes/drug effects , Erythrocytes/enzymology , Glyceraldehyde-3-Phosphate Dehydrogenases/metabolism , Particulate Matter/toxicity , Pulmonary Disease, Chronic Obstructive/blood , Pulmonary Disease, Chronic Obstructive/enzymology , Case-Control Studies , Cohort Studies , Disease Progression , Enzyme Activation , Erythrocyte Membrane/drug effects , Erythrocyte Membrane/enzymology , Erythrocyte Membrane/metabolism , Erythrocytes/metabolism , Glutathione Peroxidase/blood , Glutathione Reductase/blood , Glyceraldehyde-3-Phosphate Dehydrogenases/blood , Hemolysis , Humans , Oxidation-Reduction , Oxidative Stress/drug effects , Particle Size , Particulate Matter/blood , Pulmonary Disease, Chronic Obstructive/metabolism , Reactive Oxygen Species/metabolism , Urban PopulationABSTRACT
Particulate matters (PM) produce adverse effects on the respiratory system and cause COPD. These effects are thought to involve intrinsic generation of ROS which are present in ambient PM (transition metals and aromatic organic compounds). Here, we examined the chemical composition and ultra-microscopic structure of PM2.5. The effect of this PM was studied in red blood cell (RBC) membranes (ghosts) from healthy volunteers (n = 11) and COPD patients (n = 43). These effects were compared with that produced by a Fenton metal-catalytic ROS generator. Oxidative biomarkers and cell damage were singificantly increased in presence of PM2.5 or ROS generator in RBC of COPD patients as compared with those in cells from healthy volunteers. In contrast, total SH groups, band 3 phospho-tyrosine phosphatase (PTPase) and glucose-6 phosphate dehydrogenase (G6PD) activities were all diminished in cells from COPD patients. In conclusion, PM2.5 increases damage to RBCs from COPD patients, decreases the activity of PTPase and G6PD, and alters the function of the anionic exchanger (AE1) and the antioxidant response by decreasing SH groups.