Relationship between serum levels of triglycerides and vascular inflammation, measured as COX-2, in arteries from diabetic patients: a translational study

Lipids Health Dis. 2013 May 3:12:62. doi: 10.1186/1476-511X-12-62.

Abstract

Background: Inflammation is a common feature in the majority of cardiovascular disease, including Diabetes Mellitus (DM). Levels of pro-inflammatory markers have been found in increasing levels in serum from diabetic patients (DP). Moreover, levels of Cyclooxygenase-2 (COX-2) are increased in coronary arteries from DP.

Methods: Through a cross-sectional design, patients who underwent CABG were recruited. Vascular smooth muscle cells (VSMC) were cultured and COX-2 was measured by western blot. Biochemical and clinical data were collected from the medical record and by blood testing. COX-2 expression was analyzed in internal mammary artery cross-sections by confocal microscopy. Eventually, PGI2 and PGE2 were assessed from VSMC conditioned media by ELISA.

Results: Only a high glucose concentration, but a physiological concentration of triglycerides exposure of cultured human VSMC derived from non-diabetic patients increased COX-2 expression .Diabetic patients showed increasing serum levels of glucose, Hb1ac and triglycerides. The bivariate analysis of the variables showed that triglycerides was positively correlated with the expression of COX-2 in internal mammary arteries from patients (r(2) = 0.214, P < 0.04).

Conclusions: We conclude that is not the glucose blood levels but the triglycerides levels what increases the expression of COX-2 in arteries from DP.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Blood Glucose
  • Coronary Vessels / metabolism
  • Cyclooxygenase 2 / blood*
  • Diabetes Mellitus / blood*
  • Diabetes Mellitus / physiopathology
  • Female
  • Gene Expression Regulation
  • Humans
  • Inflammation / blood*
  • Inflammation / physiopathology
  • Male
  • Middle Aged
  • Triglycerides / blood*
  • Tunica Media / metabolism
  • Tunica Media / pathology

Substances

  • Blood Glucose
  • Triglycerides
  • Cyclooxygenase 2
  • PTGS2 protein, human