Is myeloperoxidase a key component in the ROS-induced vascular damage related to nephropathy in type 2 diabetes?

Antioxid Redox Signal. 2013 Nov 1;19(13):1452-8. doi: 10.1089/ars.2013.5307. Epub 2013 May 19.

Abstract

It is still unclear whether microvascular complications of type 2 diabetes correlate with leukocyte-endothelium interactions and/or myeloperoxidase (MPO) levels. In the present study, we found that serum levels of glucose, the rate of ROS and MPO concentration were higher in type 2 diabetic patients. Patients with nephropathy (39.6%) presented higher MPO levels that correlate positively with the albumin/creatinine ratio (r = 0.59, p<0.05). In addition, nephropatic patients showed increased leukocyte-endothelium interactions due to an undermining of polymorphonuclear leukocytes (PMN) rolling velocity and increased rolling flux and adhesion, which was accompanied by a rise in levels of the proinflammatory cytokine tumour necrosis factor alpha (TNFα) and the adhesion molecule E-selectin. Furthermore, MPO levels were positively correlated with PMN rolling flux (r = 0.855, p < 0.01) and adhesion (r = 0.682, p<0.05). Our results lead to the hypothesis that type 2 diabetes induces oxidative stress and an increase in MPO levels and leukocyte-endothelium interactions, and that these effects correlate with the development of nephropathy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Adhesion
  • Cell Adhesion Molecules / analysis
  • Cell Adhesion Molecules / metabolism
  • Cells, Cultured
  • Cytokines / analysis
  • Cytokines / metabolism
  • Diabetes Mellitus, Type 2 / metabolism*
  • Diabetes Mellitus, Type 2 / pathology
  • Diabetic Nephropathies / metabolism*
  • Diabetic Nephropathies / pathology*
  • Human Umbilical Vein Endothelial Cells / metabolism*
  • Human Umbilical Vein Endothelial Cells / pathology
  • Humans
  • Leukocytes / cytology
  • Leukocytes / metabolism
  • Middle Aged
  • Peroxidase / metabolism*
  • Reactive Oxygen Species / metabolism*

Substances

  • Cell Adhesion Molecules
  • Cytokines
  • Reactive Oxygen Species
  • Peroxidase