The effects of pycnogenol on antioxidant enzymes in a mouse model of ozone exposure

Korean J Intern Med. 2013 Mar;28(2):216-23. doi: 10.3904/kjim.2013.28.2.216. Epub 2013 Feb 27.

Abstract

Background/aims: Ozone is an environmentally reactive oxidant, and pycnogenol is a mixture of flavonoid compounds extracted from pine tree bark that have antioxidant activity. We investigated the effects of pycnogenol on reactive nitrogen species, antioxidant responses, and airway responsiveness in BALB/c mice exposed to ozone.

Methods: Antioxidant levels were determined using high performance liquid chromatography with electrochemical detection. Nitric oxide (NO) metabolites in bronchoalveolar lavage (BAL) fluid from BALB/c mice in filtered air and 2 ppm ozone with pycnogenol pretreatment before ozone exposure (n = 6) were quantified colorimetrically using the Griess reaction.

Results: Uric acid and ascorbic acid concentrations were significantly higher in BAL fluid following pretreatment with pycnogenol, whereas γ-tocopherol concentrations were higher in the ozone exposed group but were similar in the ozone and pycnogenol pretreatment groups. Retinol and γ-tocopherol concentrations tended to increase in the ozone exposure group but were similar in the ozone and pycnogenol pretreatment groups following ozone exposure. Malonylaldehyde concentrations increased in the ozone exposure group but were similar in the ozone and pycnogenol plus ozone groups. The nitrite and total NO metabolite concentrations in BAL fluid, which parallel the in vivo generation of NO in the airways, were significantly greater in the ozone exposed group than the group exposed to filtered air, but decreased with pycnogenol pretreatment.

Conclusions: Pycnogenol may increase levels of antioxidant enzymes and decrease levels of nitrogen species, suggesting that antioxidants minimize the effects of acute ozone exposure via a protective mechanism.

Keywords: Antioxidants; Nitric oxide; Ozone; Reactive nitrogen species.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antioxidants / pharmacology*
  • Ascorbic Acid / metabolism
  • Bronchial Hyperreactivity / chemically induced
  • Bronchial Hyperreactivity / metabolism
  • Bronchial Hyperreactivity / prevention & control*
  • Bronchoalveolar Lavage Fluid / chemistry
  • Bronchoconstriction / drug effects
  • Disease Models, Animal
  • Female
  • Flavonoids / pharmacology*
  • Inhalation Exposure
  • Lung / drug effects*
  • Lung / enzymology
  • Lung / physiopathology
  • Malondialdehyde / metabolism
  • Mice
  • Mice, Inbred BALB C
  • Nitric Oxide / metabolism
  • Oxidative Stress / drug effects*
  • Ozone*
  • Plant Extracts
  • Uric Acid / metabolism
  • Vitamin A / metabolism
  • alpha-Tocopherol / metabolism

Substances

  • Antioxidants
  • Flavonoids
  • Plant Extracts
  • Vitamin A
  • Uric Acid
  • Nitric Oxide
  • Malondialdehyde
  • pycnogenols
  • Ozone
  • alpha-Tocopherol
  • Ascorbic Acid