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Inhalation Toxicology
International Forum for Respiratory Research
Volume 28, 2016 - Issue 11
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Review Article

Evaluation of neural reflex activation as a mode of action for the acute respiratory effects of ozone

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Pages 484-499 | Received 17 Feb 2016, Accepted 11 Jul 2016, Published online: 28 Aug 2016
 

Abstract

Exposure to elevated levels of ozone has been associated with a variety of respiratory-related health endpoints in both epidemiology and controlled human exposure studies, including lung function decrements and airway inflammation. A mode of action (MoA) for these effects has not been established, but it has been proposed that they may occur through ozone-induced activation of neural reflexes. We critically reviewed experimental studies of ozone exposure and neural reflex activation and applied the International Programme on Chemical Safety (IPCS) mode-of-action/human relevance framework to evaluate the biological plausibility and human relevance of this proposed MoA. Based on the currently available experimental data, we found that the proposed MoA of neural reflex activation is biologically plausible for the endpoint of ozone-induced lung function decrements at high ozone exposures, but further studies are needed to fill important data gaps regarding the relevance of this MoA at lower exposures. A role for the proposed MoA in ozone-induced airway inflammation is less plausible, as the evidence is conflicting and is also of unclear relevance given the lack of studies conducted at lower exposures. The evidence suggests a different MoA for ozone-induced inflammation that may still be linked to the key events in the proposed MoA, such that neural reflex activation may have some degree of involvement in modulating ozone-induced neutrophil influx, even if it is not a direct role.

Declaration of interest

The authors are employed by Gradient, a private environmental consulting firm. The work reported in this paper was conducted during the normal course of employment. This paper was prepared with financial support from ExxonMobil Biomedical Sciences, Inc. (EMBSI). The authors have the sole responsibility for the writing and contents of this paper.

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