Effects of cyclooxygenase-2 gene inactivation on cardiac autonomic and left ventricular function in experimental diabetes

Am J Physiol Heart Circ Physiol. 2009 Feb;296(2):H453-61. doi: 10.1152/ajpheart.00678.2008. Epub 2008 Dec 5.

Abstract

Glucose-mediated oxidative stress and the upregulation of cyclooxygenase (COX)-2 pathway activity have been implicated in the pathogenesis of several vascular complications of diabetes including diabetic neuropathy. However, in nondiabetic subjects, the cardiovascular safety of selective COX-2 inhibition is controversial. The aim of this study was to explore the links between hyperglycemia, oxidative stress, activation of the COX-2 pathway, cardiac sympathetic integrity, and the development of left ventricular (LV) dysfunction in experimental diabetes. R wave-to-R wave interval (R-R interval) and parameters of LV function measured by echocardiography using 1% isoflurane, LV sympathetic nerve fiber density, LV collagen content, and markers of myocardial oxidative stress, inflammation, and PG content were assessed after 6 mo in control and diabetic COX-2-deficient (COX-2(-/-)) and littermate, wild-type (COX-2(+/+)) mice. There were no differences in blood glucose, LV echocardiographic measures, collagen content, sympathetic nerve fiber density, and markers of oxidative stress and inflammation between nondiabetic (ND) COX-2(+/+) and COX-2(-/-) mice at baseline and thereafter. After 6 mo, diabetic COX-2(+/+) mice developed significant deteriorations in the R-R interval and signs of LV dysfunction. These were associated with a loss of LV sympathetic nerve fiber density, increased LV collagen content, and a significant increase in myocardial oxidative stress and inflammation compared with those of ND mice. Diabetic COX-2(-/-) mice were protected against all these biochemical, structural, and functional deficits. These data suggest that in experimental diabetes, selective COX-2 inactivation confers protection against sympathetic denervation and LV dysfunction by reducing intramyocardial oxidative stress, inflammation, and myocardial fibrosis.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blood Glucose / metabolism
  • Body Weight
  • Collagen / metabolism
  • Cyclooxygenase 2 / deficiency*
  • Cyclooxygenase 2 / genetics
  • Diabetes Mellitus, Experimental / complications
  • Diabetes Mellitus, Experimental / enzymology
  • Diabetes Mellitus, Experimental / genetics
  • Diabetes Mellitus, Experimental / physiopathology*
  • Echocardiography, Doppler
  • Gene Silencing*
  • Glutathione / metabolism
  • Heart / innervation*
  • Heart Rate
  • Inflammation Mediators / metabolism
  • Male
  • Malondialdehyde / metabolism
  • Mice
  • Mice, Knockout
  • Myocardial Contraction
  • Myocardium / enzymology*
  • Myocardium / pathology
  • Oxidative Stress
  • Prostaglandins / metabolism
  • Stroke Volume
  • Sympathetic Nervous System / physiopathology*
  • Time Factors
  • Tumor Necrosis Factor-alpha / metabolism
  • Ventricular Dysfunction, Left / enzymology
  • Ventricular Dysfunction, Left / genetics
  • Ventricular Dysfunction, Left / physiopathology
  • Ventricular Dysfunction, Left / prevention & control*
  • Ventricular Function, Left*

Substances

  • Blood Glucose
  • Inflammation Mediators
  • Prostaglandins
  • Tumor Necrosis Factor-alpha
  • Malondialdehyde
  • Collagen
  • Ptgs2 protein, mouse
  • Cyclooxygenase 2
  • Glutathione