Decreased vascular H2S production is associated with vascular oxidative stress in rats fed a high-fat western diet

Naunyn Schmiedebergs Arch Pharmacol. 2016 Jul;389(7):783-90. doi: 10.1007/s00210-016-1244-4. Epub 2016 Apr 18.

Abstract

A Western-style high-fat diet is known to cause vascular dysfunction and oxidative stress. H2S contributes to the regulation of vascular function and acts as a vasoprotective molecule; however, the effects of high-fat diet on vascular H2S production and function are not known. The aim of this study was to investigate the effects of high-fat diet on vascular function and H2S production. Wistar hooded rats were fed a western diet (WD, 21 % fat) or control rat chow (6 % fat) for 12 weeks. At the end of the experiment, the aorta was collected for assessing vascular function and NO and H2S bioavailability. Superoxide anion production was quantitated by lucigenin-enhanced chemiluminescence. The expression of NADPH oxidase subunit Nox2 and the H2S-producing protein cystathionine-γ-lyase (CSE) were examined by Western blotting. WD rats had significantly higher body weight and body fat than control (p < 0.001). Endothelial function and NO bioavailability were significantly reduced in the WD group (p < 0.05), but vascular smooth muscle cell function was unaffected. Vascular superoxide production and Nox2 expression were significantly increased in the aorta from WD rats. L-Cysteine-induced vasorelaxation was reduced in the WD group (p < 0.05) and insensitive to the inhibition of the CSE. In addition, vascular H2S bioavailability and CSE expression were significantly reduced in the aorta from WD rats (p < 0.01). These data show that fat feeding induces vascular oxidative stress and a reduction in endothelial function. Furthermore, there is a reduced capacity for both basal and stimulated vascular H2S production via CSE in fat fed rats.

Keywords: Cystathionine-γ-lyase; Endothelial dysfunction; Hyperlipidaemia; NADPH oxidase.

MeSH terms

  • Animals
  • Aorta / metabolism
  • Aorta / physiopathology
  • Cystathionine gamma-Lyase / metabolism
  • Diet, High-Fat*
  • Diet, Western*
  • Disease Models, Animal
  • Dose-Response Relationship, Drug
  • Down-Regulation
  • Hydrogen Sulfide / metabolism*
  • Membrane Glycoproteins / metabolism
  • Muscle, Smooth, Vascular / drug effects
  • Muscle, Smooth, Vascular / metabolism*
  • Muscle, Smooth, Vascular / physiopathology
  • NADPH Oxidase 2
  • NADPH Oxidases / metabolism
  • Nitric Oxide / metabolism
  • Obesity / etiology
  • Obesity / metabolism*
  • Obesity / physiopathology
  • Oxidative Stress*
  • Rats, Wistar
  • Superoxides / metabolism
  • Vascular Diseases / etiology
  • Vascular Diseases / metabolism*
  • Vascular Diseases / physiopathology
  • Vasodilation
  • Vasodilator Agents / pharmacology
  • Weight Gain

Substances

  • Membrane Glycoproteins
  • Vasodilator Agents
  • Superoxides
  • Nitric Oxide
  • Cybb protein, rat
  • NADPH Oxidase 2
  • NADPH Oxidases
  • Cystathionine gamma-Lyase
  • Hydrogen Sulfide