Increased lung resistance after diesel particulate and ozone co-exposure not associated with enhanced lung inflammation in allergic mice

Author： Farraj Aimen K. Boykin Elizabeth Ledbetter Allen Andrews Debora Gavett Stephen H.

Publisher： Informa Healthcare

ISSN： 1091-7691

Source： Inhalation Toxicology, Vol.22, Iss.1, 2010-01, pp. : 33-41

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Abstract

Exposure to diesel exhaust particulate matter (DEP) exacerbates asthma. Likewise, similar effects have been reported with exposure to the oxidizing air pollutant ozone (O₃). Since levels of both pollutants in ambient air tend to be simultaneously elevated, we investigated the possible synergistic effect of these agents on the exacerbation of allergic airways disease in mice. Male BALB/c mice were sensitized ip with ovalbumin (Ova) or vehicle only, then exposed once per week for 4 wk via nose-only inhalation (4 h) to the PM_2.5 fraction of DEP (2 mg/m³), O₃ (0.5 ppm), DEP and O₃, or filtered air, and then challenged with aerosolized ovalbumin. Ova sensitization in air-exposed mice enhanced pulmonary inflammatory cell infiltration, several indicators of injury in the lung (lactate dehydrogenase, albumin and total protein), and lung resistance (R_L) and elastance (E_L) in response to methacholine (MCh) aerosol challenge. DEP exposure did not enhance the Ova-induced increase in pulmonary cell infiltration, indicators of injury, or R_L and E_L. O₃ exposure enhanced the Ova-induced increase in inflammatory cell infiltration and N-acetylglucosaminidase (NAG) in the lung, but had no effect on R_L or E_L. DEP co-exposure significantly attenuated the O₃-induced increase in cell infiltration and indicators of injury; co-exposure had no effect on E_L relative to air-exposed Ova-sensitized mice. However, only DEP-O₃ co-exposure significantly increased the Ova-induced increase in R_L. Thus, O₃ and DEP co-exposure exacerbated airways hyperresponsiveness, a response that was not associated with parallel increases in pulmonary inflammation and one that may be mediated by a unique mechanism.