Oxidative damages in erythrocytes of patients with metabolic syndrome

Mol Cell Biochem. 2013 Jun;378(1-2):267-73. doi: 10.1007/s11010-013-1617-7. Epub 2013 Mar 21.

Abstract

The aim of the study was to estimate the changes caused by oxidative stress in structure and function of membrane of erythrocytes from patients with metabolic syndrome (MS). The study involved 85 patients with MS before pharmacological treatment and 75 healthy volunteers as a control group. Cholesterol level, lipid peroxidation, glutathione level (GSH), and antioxidant enzyme activities in erythrocytes were investigated. The damage to erythrocyte proteins was also indicated by means of activity of ATPase (total and Na(+),K(+) ATPase) and thiol group level. The membrane fluidity of erythrocytes was estimated by the fluorescent method. The cholesterol concentration and the level of lipid peroxidation were significantly higher, whereas the concentration of proteins thiol groups decreased in the patient group. ATPase and GSH peroxidase activities diminished compared to those in the control group. There were no differences in either catalase or superoxide dismutase activities. The membrane fluidity was lower in erythrocytes from patients with MS than in the ones from control group. These results show changes in red blood cells of patients with MS as a consequence of a higher concentration of cholesterol in the membrane and an increased oxidative stress.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphatases / metabolism
  • Adult
  • Case-Control Studies
  • Catalase / metabolism
  • Cholesterol / metabolism
  • Erythrocytes / metabolism*
  • Female
  • Glutathione / metabolism
  • Glutathione Peroxidase / metabolism
  • Humans
  • Lipid Peroxidation
  • Male
  • Membrane Fluidity
  • Metabolic Syndrome / blood*
  • Middle Aged
  • Oxidative Stress*
  • Superoxide Dismutase / metabolism

Substances

  • Cholesterol
  • Catalase
  • Glutathione Peroxidase
  • Superoxide Dismutase
  • Adenosine Triphosphatases
  • Glutathione