Comparison of Airway Responses Induced in a Mouse Model by the Gas and Particulate Fractions of Gasoline Direct Injection Engine Exhaust

Int J Environ Res Public Health. 2018 Mar 1;15(3):429. doi: 10.3390/ijerph15030429.

Abstract

Diesel exhaust has been associated with asthma, but its response to other engine emissions is not clear. The increasing prevalence of vehicles with gasoline direct injection (GDI) engines motivated this study, and the objective was to evaluate pulmonary responses induced by acute exposure to GDI engine exhaust in an allergic asthma murine model. Mice were sensitized with an allergen to induce airway hyperresponsiveness or treated with saline (non-allergic group). Animals were challenged for 2-h to exhaust from a laboratory GDI engine operated at conditions equivalent to a highway cruise. Exhaust was filtered to assess responses induced by the particulate and gas fractions. Short-term exposure to particulate matter from GDI engine exhaust induced upregulation of genes related to polycyclic aromatic hydrocarbon (PAH) metabolism (Cyp1b1) and inflammation (TNFα) in the lungs of non-allergic mice. High molecular weight PAHs dominated the particulate fraction of the exhaust, and this response was therefore likely attributable to the presence of these PAHs. The particle fraction of GDI engine exhaust further contributed to enhanced methacholine responsiveness in the central and peripheral tissues in animals with airway hyperresponsiveness. As GDI engines gain prevalence in the vehicle fleet, understanding the health impacts of their emissions becomes increasingly important.

Keywords: Cyp1b1; TNFα; gasoline direct injection engine exhaust; in vivo; inflammation; polycyclic aromatic hydrocarbons.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Air Pollutants / toxicity*
  • Animals
  • Antigens, Dermatophagoides
  • Asthma / metabolism*
  • Asthma / physiopathology
  • Cytochrome P-450 CYP1B1 / metabolism
  • Female
  • Gasoline
  • Mice, Inbred BALB C
  • Particulate Matter / toxicity*
  • Polycyclic Aromatic Hydrocarbons / toxicity*
  • Tumor Necrosis Factor-alpha / metabolism
  • Vehicle Emissions / toxicity*

Substances

  • Air Pollutants
  • Antigens, Dermatophagoides
  • Gasoline
  • Particulate Matter
  • Polycyclic Aromatic Hydrocarbons
  • Tumor Necrosis Factor-alpha
  • Vehicle Emissions
  • Cyp1b1 protein, mouse
  • Cytochrome P-450 CYP1B1