Cigarette smoking blocks the protective expression of Nrf2/ARE pathway in peripheral mononuclear cells of young heavy smokers favouring inflammation

PLoS One. 2009 Dec 9;4(12):e8225. doi: 10.1371/journal.pone.0008225.

Abstract

Cigarette smoking is an important risk factor for atherosclerosis, a chronic inflammatory disease. However the underlying factors of this effect are unclear. It has been hypothesized that water-soluble components of cigarette smoke can directly promote oxidative stress in vasculature and blood cells. Aim of this study was to study the relationship between oxidative stress and inflammation in a group of young smokers. To do this we evaluated: 1) the oxidation products of phospholipids (oxPAPC) in peripheral blood mononuclear cells (PBMC); 2) their role in causing PBMC reactive oxygen species (ROS) generation and changes in GSH; 3) the expression of the transcription factor NF-E2-related factor 2 (Nrf2) and of related antioxidant genes (ARE); 4) the activation of NF-kB and C-reactive protein (CRP) values. We studied 90 healthy volunteers: 32 non-smokers, 32 moderate smokers (5-10 cigarettes/day) and 26 heavy smokers (25-40 cigarettes/day). OxPAPC and p47phox expression, that reasonably reflects NADPH oxidase activity, were higher in moderate smokers and heavy smokers than in non-smokers (p<0.01), the highest values being in heavy smokers (p<0.01). In in vitro studies oxPAPC increased ROS generation via NADPH oxidase activation. GSH in PBMC and plasma was lower in moderate smokers and heavy smokers than in non-smokers (p<0.01), the lowest values being in heavy smokers (p<0.01). Nrf2 expression in PBMC was higher in moderate smokers than in non-smokers (p<0.01), but not in heavy smokers, who had the highest levels of NF-kB and CRP (p<0.01). In in vitro studies oxPAPC dose-dependently increased NF-kB activation, whereas at the highest concentrations Nrf2 expression was repressed. The small interference (si) RNA-mediated knockdown of NF-kappaB/p65 increased about three times the expression of Nrf2 stimulated with oxPAPC. Cigarette smoke promotes oxPAPC formation and oxidative stress in PBMC. This may cause the activation of NF-kB that in turn may participate in the negative regulation of Nrf2/ARE pathway favouring inflammation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Antioxidants / metabolism*
  • Biomarkers / metabolism
  • Blood Donors
  • Cytoprotection*
  • Enzyme Activation
  • Female
  • Glutamate-Cysteine Ligase / metabolism
  • Glutathione / metabolism
  • Heme Oxygenase-1 / metabolism
  • Humans
  • I-kappa B Proteins / metabolism
  • Inflammation / enzymology
  • Inflammation / pathology*
  • Interleukin-6 / metabolism
  • Leukocytes, Mononuclear / enzymology
  • Leukocytes, Mononuclear / pathology*
  • Male
  • NADPH Oxidases / metabolism
  • NF-E2-Related Factor 2 / metabolism*
  • NF-KappaB Inhibitor alpha
  • NF-kappa B / metabolism
  • Phosphatidylcholines / blood
  • Reactive Oxygen Species / metabolism
  • Response Elements / genetics*
  • Smoking / adverse effects*
  • Smoking / blood
  • Young Adult

Substances

  • Antioxidants
  • Biomarkers
  • I-kappa B Proteins
  • Interleukin-6
  • NF-E2-Related Factor 2
  • NF-kappa B
  • NFE2L2 protein, human
  • NFKBIA protein, human
  • Phosphatidylcholines
  • Reactive Oxygen Species
  • oxidized-L-alpha-1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphorylcholine
  • NF-KappaB Inhibitor alpha
  • Heme Oxygenase-1
  • NADPH Oxidases
  • Glutamate-Cysteine Ligase
  • Glutathione