Seasonal superoxide overproduction and endothelial activation in guinea-pig heart; seasonal oxidative stress in rats and humans

J Mol Cell Cardiol. 2011 Apr;50(4):686-94. doi: 10.1016/j.yjmcc.2010.11.010. Epub 2010 Nov 26.

Abstract

Seasonality in endothelial dysfunction and oxidative stress was noted in humans and rats, suggesting it is a common phenomenon of a potential clinical relevance. We aimed at studying (i) seasonal variations in cardiac superoxide (O(2)(-)) production in rodents and in 8-isoprostane urinary excretion in humans, (ii) the mechanism of cardiac O(2)(-) overproduction occurring in late spring/summer months in rodents, (iii) whether this seasonal O(2)(-)-overproduction is associated with a pro-inflammatory endothelial activation, and (iv) how the summer-associated changes compare to those caused by diabetes, a classical cardiovascular risk factor. Langendorff-perfused guinea-pig and rat hearts generated ~100% more O(2)(-), and human subjects excreted 65% more 8-isoprostane in the summer vs. other seasons. Inhibitors of NADPH oxidase, xanthine oxidase, and NO synthase inhibited the seasonal O(2)(-)-overproduction. In the summer vs. other seasons, cardiac NADPH oxidase and xanthine oxidase activity, and protein expression were increased, the endothelial NO synthase and superoxide dismutases were downregulated, and, in guinea-pig hearts, adhesion molecules upregulation and the endothelial glycocalyx destruction associated these changes. In guinea-pig hearts, the summer and a streptozotocin-induced diabetes mediated similar changes, yet, more severe endothelial activation associated the diabetes. These findings suggest that the seasonal oxidative stress is a common phenomenon, associated, at least in guinea-pigs, with the endothelial activation. Nonetheless, its biological meaning (regulatory vs. deleterious) remains unclear. Upregulated NADPH oxidase and xanthine oxidase and uncoupled NO synthase are the sources of the seasonal O(2)(-)-overproduction.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blotting, Western
  • Dinoprost / analogs & derivatives
  • Dinoprost / metabolism
  • Endothelium, Vascular / metabolism*
  • Female
  • Glycocalyx / metabolism
  • Guinea Pigs
  • Heart / physiology*
  • Humans
  • Male
  • NADPH Oxidases / metabolism
  • Oxidative Stress / physiology
  • Rats
  • Rats, Wistar
  • Seasons
  • Superoxides / metabolism*
  • Vasodilation / physiology
  • Xanthine Oxidase / metabolism

Substances

  • Superoxides
  • 8-epi-prostaglandin F2alpha
  • Dinoprost
  • Xanthine Oxidase
  • NADPH Oxidases