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ToxSci Advance Access published online on September 4, 2008

Toxicological Sciences, doi:10.1093/toxsci/kfn178
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© The Author 2008. Published by Oxford University Press on behalf of the Society of Toxicology. All rights reserved. For permissions, please email: journals.permissions@oxfordjournals.org

Ex vivo lung function measurements in precision cut lung slice (PCLS) from chemical allergen sensitized mice represent a suitable alternative to in vivo studies

Effect of TMA and DNCB on lung function (40 char.)

M. Henjakovic*,#, C. Martin**,#, H. G. Hoymann*, K. Sewald*, A. R. Ressmeyer**, C. Dassow**, G. Pohlmann*, N. Krug*, S. Uhlig** and A. Braun*

* Fraunhofer Institute of Toxicology and Experimental Medicine, Department of Immunology, Allergology and Immunotoxicology, Nikolai-Fuchs-Str. 1, 30625 Hannover, Germany ** Institute of Pharmacology and Toxicology, RWTH Aachen, Wendlingweg 2, 52074 Aachen, Germany, and Division of Pulmonary Pharmacology, Research Center Borstel, 23845 Borstel, Germany

Corresponding author and reprint requests: A. Braun, Fraunhofer Institute of Toxicology and Experimental Medicine, Department of Immunology, Allergology and Immunotoxicology, Nikolai-Fuchs-Str. 1, 30625 Hannover, Germany, phone +49 511 5350-263, fax +49 511 5350-155. E-mail: armin.braun{at}item.fraunhofer.de

Received June 23, 2008; revision received August 16, 2008; accepted August 18, 2008


   Abstract

A wide range of industrial chemicals can induce respiratory allergic reactions. Hence, there is an urgent need for methods identifying and characterizing the biological action of chemicals in the lung. Here, we present an easy, reliable alternative method to measure lung function changes ex vivo after exposure to chemical allergens and compare this to invasive in vivo measurements after sensitization with the industrial chemicals trimellitic anhydride (TMA) and 2,4-dinitrochlorobenzene (DNCB).

Female BALB/c mice were sensitized epicutaneously with the respiratory allergen TMA and the contact sensitizer DNCB. The early allergic response (EAR) to TMA and DNCB was registered in vivo and ex vivo on day 21 after inhalational challenge with dry standardized aerosols or after exposure of precision-cut lung slices (PCLS) to dissolved allergen. Airway hyperresponsiveness (AHR) to increasing doses of methacholine (MCh) was measured on the next day in vivo and ex vivo. Bronchoalveolar lavage (BAL) was performed for immunological characterization of local inflammation.

TMA-sensitized mice showed AHR to MCh in vivo (ED50: 0.06 µg MCh vs. 0.21 µg MCh in controls) and in PCLS (EC50: 0.24 µM MCh vs. 0.4 µM MCh). TMA-treated animals showed increased numbers of eosinophils (12.8•104 vs. 0.7•104) and elevated eotaxin-2 concentrations (994 pg/ml vs. 167 pg/ml) in BAL fluid 24 h after allergen challenge. In contrast, none of these parameters differed after sensitization with DNCB.

The present study suggests that the effects of low-molecular-weight (LMW) allergens, like TMA and DNCB, on ex vivo lung functions tested in PCLS reflect the in vivo situation.

Key Words: lung function; bronchoconstriction; PCLS; TMA; DNCB; methacholine.


# contributed equally


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