Aspirin Intolerance: Experimental Models for Bed-to-Bench

Author(s): Masamichi Yamashita.

Journal Name: Current Drug Targets

Volume 17 , Issue 16 , 2016

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Abstract:

Aspirin is the oldest non-steroidal anti-inflammatory drug (NSAID), and it sometimes causes asthma-like symptoms known as aspirin-exacerbated respiratory disease (AERD), which can be serious. Unwanted effects of aspirin (aspirin intolerance) are also observed in patients with food-dependent exercise-induced anaphylaxis, a type I allergy disease, and aspirin-induced urticaria (AIU). However the target and the mechanism of the aspirin intolerance are still unknown. There is no animal or cellular model of AERD, because its pathophysiological mechanism is still unknown, but it is thought that inhibition of cyclooxygenase by causative agents leads to an increase of free arachidonic acid, which is metabolized into cysteinyl leukotrienes (cysLTs) that provoke airway smooth muscle constriction and asthma symptoms. As the bed-tobench approach, to confirm the clinical discussion in experimental cellular models, we have tried to develop a cellular model of AERD using activated RBL-2H3 cells, a rat mast cell like cell line. Indomethacin (another NSAID and also causes AERD), enhances in vitro cysLTs production by RBL-2H3 cells, while there is no induction of cysLTs production in the absence of inflammatory activation. Since this suggests that all inflammatory cells with activation of prostaglandin and cysLT metabolism should respond to NSAIDs, and then I have concluded that aspirin intolerance should be separated from subsequent bronchoconstriction. Evidence about the cellular mechanisms of NSAIDs may be employed for development of in vitro AERD models as the approach from bench-to-bed.

Keywords: Arachidonic acid metabolism, aspirin intolerance, aspirin-exacerbated respiratory disease, aspirin-induced urticaria, cysteinyl leukotrienes, food-dependent exercise-induced anaphylaxis, prostaglandins, mast cells.

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Article Details

VOLUME: 17
ISSUE: 16
Year: 2016
Page: [1963 - 1970]
Pages: 8
DOI: 10.2174/1389450117666161005152327

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