Advanced in vitro exposure systems.

Evaluation of an in vitro screening model to assess phosgene inhalation injury

27. Oct. 2016

DOI: 10.1080/15376516.2016.1243183

Dorian S. Olivera, Heidi Hoard-Fruchey & Alfred M. Sciuto
Analytical Toxicology Devision, US Army, Medical Research Institute of Chemical Defense, Aberdeen Proving Ground, MD, USA

In vitro studies have clearly shown that phosgene exposure can have overwhelming effects on cellular homeostasis with regard to mediator release, activation of inflammatory pathways and compromised lung function.
In this study an in vitro exposure model with which to evaluate potential therapeutics for edemagenic gas inhalation exposure was tested.
Human bronchial epithelial (16HBE) cell cultures were exposed in the Vitrocell System to phosgene.
Transepithelial electrical resistance (TEER), Cellular viability assay (XTT assay), [14C]-Glutamine oxidation assay, Glucose metabolism assays and Lactate production measurements were taken.

 

ABSTRACT
Therapeutic development against exposure to toxic gases is hindered by the lack of appropriate models to evaluate candidate compounds prior to animal efficacy studies. In this study, an in vitro, air-liquid interface exposure model has been tested to examine its potential application for screening treatments for phosgene (carbonyl chloride)-induced pulmonary injury. Epithelial cultures on Transwell® inserts, combined with a Vitrocell® exposure apparatus, provided a physiologically relevant exposure environment. Differentiated human bronchial epithelial (16HBE) cultures were exposed for 8 min to phosgene ranging from 0 to 64ppm and assessed for changes in transepithelial electrical resistance (TEER, epithelial barrier integrity), cellular viability (XTT) and post-exposure (PE) cellular metabolic energy status. Exposure to phosgene concentrations 8ppm caused dose-dependent and significant decreases in TEER and XTT which did not recover within 24-h PE. In addition, at 64ppm the rate of oxidative glutamine metabolism was significantly inhibited at 6 and 24 h after exposure. Glycolytic activities (glucose utilization and lactate production) were also inhibited, but to a lesser extent. Decreased glycolytic function can translate to insufficient energy sources to counteract barrier function failure. Consistent and sensitive markers of phosgene exposure were TEER, cell viability and decreased metabolism. As such, we have assessed an appropriate in vitro model of phosgene inhalation that produced quantifiable alterations in markers of lung cell metabolism and injury in human airway epithelial cells. Data indicate the suitability of this model for testing classes of anti-edemagenic compounds such as corticosteroids or phosphodiesterase inhibitors for evaluating phosgene therapeutics.

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