Vitamin C blocks vascular dysfunction and release of interleukin-6 induced by endothelin-1 in humans in vivo

Atherosclerosis. 2007 Feb;190(2):408-15. doi: 10.1016/j.atherosclerosis.2006.02.018. Epub 2006 Mar 9.

Abstract

Objective: Inflammation of the vessel wall is of importance in atherosclerosis. Endothelin-1 (ET-1) exerts pro-inflammatory effects and contributes to endothelial dysfunction. The objective was to test whether ET-1 impairs vascular function by increasing oxidative stress and release of pro-inflammatory cytokines in humans.

Methods: Forearm blood flow (FBF) was determined in 12 young healthy males with venous occlusion plethysmography.

Results: Intra-brachial infusion of ET-1 (20 pmol/min) decreased both endothelium-dependent and -independent vasodilatation (P<0.001). ET-1 also increased venous IL-6 levels (0.96+/-0.14-1.40+/-0.15 ng/ml; P<0.001). Administration of Vitamin C (24 mg/min) following the ET-1 infusion did not restore vascular function. However, pre-treatment with Vitamin C before ET-1 prevented the decrease in endothelium-dependent and -independent vasodilatation as well as the increase in IL-6 levels (1.20+/-0.28 versus 1.29+/-0.27 ng/ml; P=0.57). Infusion of a control vasoconstrictor substance, noradrenaline (80 ng/min) for 30 min did not affect IL-6 levels.

Conclusions: ET-1 impairs endothelium-dependent and -independent vasodilatation and stimulates release of IL-6 in humans in vivo. These effects are inhibited by pre-treatment with the antioxidant Vitamin C. This suggests that the mechanism by which ET-1 impairs vascular function and stimulates release of IL-6 involves increased oxidative stress.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylcholine / pharmacology
  • Adult
  • Ascorbic Acid / pharmacology*
  • Blood Flow Velocity / drug effects*
  • Blood Flow Velocity / physiology
  • Endothelin-1 / physiology*
  • Forearm / blood supply
  • Humans
  • Interleukin-6 / antagonists & inhibitors
  • Interleukin-6 / blood
  • Interleukin-6 / metabolism*
  • Male
  • Nitroprusside / pharmacology
  • Reference Values
  • Vasodilation / drug effects
  • Vasodilation / physiology*

Substances

  • Endothelin-1
  • Interleukin-6
  • Nitroprusside
  • Acetylcholine
  • Ascorbic Acid