Acute application of antioxidants protects against hyperoxia-induced reduction of plasma nitrite concentration

Clin Physiol Funct Imaging. 2015 Jan;35(1):76-80. doi: 10.1111/cpf.12169. Epub 2014 May 25.

Abstract

We investigated the effects of acute intake of antioxidants on hyperoxia-induced oxidative stress, reduction of plasma nitrite and change in arterial stiffness. Twelve healthy males randomly consumed either placebo or an oral antioxidant cocktail (vitamin C, 1000 mg; vitamin E, 600 IU; alpha-lipoic acid, 600 mg). Every therapy was consumed once, a week apart, in a cross-over design, 30 min before the experiment. The volunteers breathed 100% normobaric oxygen between 30th and 60th min of 1-h study protocol. Plasma levels of nitrite, lipid peroxides (LOOH) and vitamin C, arterial stiffness (indicated by augmentation index, AIx) and arterial oxygen (Ptc O2 ) pressure were measured before and after hyperoxia. Exposure to oxygen caused a similar increase of Ptc O2 in both placebo and antioxidants groups, confirming comparable exposure to hyperoxia (438 ± 100 versus 455 ± 83 mm Hg). Vitamin C was increased in the antioxidants group confirming successful application of antioxidants (69 ± 14 versus 57 ± 15 μm). Hyperoxia resulted in increased AIx and LOOH and decreased nitrite in placebo (-32 ± 11 versus -47 ± 13%, 72 ± 7 versus 62 ± 6 μm H2 O2 and 758 ± 184 versus 920 ± 191 nm, respectively), but not in the antioxidants group (-42 ± 13 versus -50 ± 13%, 64 ± 9 versus 61 ± 8 μm H2 O2 and 847 ± 156 versus 936 ± 201 nm, respectively). The acute intake of selected antioxidants was effective in preserving bioavailabity of ˙NO and vascular function, against hyperoxia-induced oxidative stress.

Keywords: arterial stiffness; nitric oxide; oxygen; vasoconstriction; vitamin C.

Publication types

  • Randomized Controlled Trial

MeSH terms

  • Administration, Oral
  • Adult
  • Antioxidants / administration & dosage*
  • Down-Regulation / drug effects
  • Humans
  • Hyperoxia / blood*
  • Hyperoxia / prevention & control*
  • Male
  • Nitrites / blood*
  • Oxidative Stress / drug effects*
  • Oxygen / blood
  • Reactive Oxygen Species / metabolism*
  • Reproducibility of Results
  • Sensitivity and Specificity

Substances

  • Antioxidants
  • Nitrites
  • Reactive Oxygen Species
  • Oxygen