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Respiratory allergy and pulmonary irritation to trimellitic anhydride in Brown Norway rats

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Author: Arts, J.H.E. · Bloksma, N. · Leusink-Muis, T. · Kuper, C.F.
Type:article
Date:2003
Source:Toxicology and Applied Pharmacology, 1, 187, 38-49
Identifier: 236966
doi: doi:10.1016/S0041-008X(02)00023-6
Keywords: Biology Nutrition · Toxicology and Applied Pharmacology · Airway irritation · Brown Norway rats · Nonspecific airway hyperresponsiveness · Respiratory allergy · Trimellitic anhydride · acetylglucosaminidase · immunoglobulin E · irritant agent · lactate dehydrogenase · methacholine · protein · trimellitic anhydride · animal experiment · animal tissue · article · female · histopathology · immunoglobulin blood level · leukocyte · lung injury · lung lavage · nonhuman · occupational asthma · rat · respiratory tract allergy · sensitization · Allergens · Animals · Body Weight · Bronchoalveolar Lavage Fluid · Female · Immunization · Immunoglobulin E · Lung · Organ Size · Phthalic Anhydrides · Rats · Rats, Inbred BN · Respiration · Respiratory Function Tests · Rattus norvegicus

Abstract

Occupational exposure to low-molecular-weight (LMW) allergens such as acid anhydrides can result in occupational asthma, an allergic disease characterized by episodic airway obstruction, airways inflammation, and non specific airways hyperresponsiveness. Since LMW irritants can provoke rather similar effects and since most, if not all, LMW allergens have irritant properties, this study addressed the distinction between allergenic and irritant effects of the respiratory allergen trimellitic anhydride (TMA). BN rats were sensitized by dermal application of TMA or vehicle alone and 3 weeks later were challenged by inhalation of a slightly irritating concentration of TMA or the vehicle. Lung function was measured before, during, and shortly after challenge. One day after challenge, in vivo and in vitro nonspecific airways hyperresponsiveness to methacholine was measured, and bronchoalveolar lavage was performed to measure total protein, lactate dehydrogenase, N-acetyl-glucosaminidase, and total and differential leukocyte numbers in the fluid. In addition, IgE measurements and histopathological examinations of the respiratory tract were carried out. TMA challenge of sensitized, but not sham-sensitized, BN rats reduced breathing frequency during challenge, elevated total and TMA-specific serum IgE levels, and caused a typical allergic asthma-associated airway pathology, as observed earlier. Vehicle challenge did not cause these effects, irrespective of sensitization. Hyperresponsiveness to methacholine was only seen in TMA-sensitized and -challenged rats. These rats also showed increased levels of the biochemical parameters and increased numbers of eosinophils and neutrophils in the lung lavage fluid; TMA challenge of sham-sensitized rats caused similar but markedly less pronounced effects. During TMA challenge of sham-sensitized rats, a breathing pattern typical of irritation was noticed but a clearly distinct pattern was seen upon TMA challenge of sensitized rats. In conclusion, TMA challenge of sensitized rats caused sensitization-dependent asthma-like early changes in breathing pattern that clearly could be distinguished from irritant-induced changes and non-specific airways hyperresponsiveness 24 h after challenge. Sensitization-dependent functional changes were accompanied by inflammatory changes characteristic of asthma and biochemical evidence of airway damage. © 2003 Elsevier Science (USA). All rights reserved.