The effect of in-utero-through-postnatal exposure of mice to perfluorinated compounds on airway inflammation and function

Perfluorinated compounds, non-degradable xenobiotics in many consumer products, can cause developmental toxicity in animals, and human exposure is associated with asthma symptoms. We tested the hypothesis that sustained chronic exposure to perfluorooctanoic acid (PFOA), fluorotelomer alcohol (FTOH)...

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Main Author: Ryu, Min Hyung
Other Authors: Halayko, Andrew (Physiology and Pathophysiology)
Published: The American Physiological Society 2015
Subjects:
Online Access:http://hdl.handle.net/1993/30195
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spelling ndltd-MANITOBA-oai-mspace.lib.umanitoba.ca-1993-301952015-01-24T03:48:11Z The effect of in-utero-through-postnatal exposure of mice to perfluorinated compounds on airway inflammation and function Ryu, Min Hyung Halayko, Andrew (Physiology and Pathophysiology) Keijzer, Richard (Physiology and Pathophysiology) Kroeger, Edwin (Physiology and Pathophysiology) HayGlass, Kent (Immunology) airway hyperresponsiveness perfluorinated compounds environmental pollution airway inflammation Perfluorinated compounds, non-degradable xenobiotics in many consumer products, can cause developmental toxicity in animals, and human exposure is associated with asthma symptoms. We tested the hypothesis that sustained chronic exposure to perfluorooctanoic acid (PFOA), fluorotelomer alcohol (FTOH) or perfluorooctanesulfonic acid (PFOS) induces lung dysfunction that exacerbates allergen-induced airway hyperresponsiveness (AHR) and inflammation. Mice were exposed to the chemicals from early gestation day to adulthood. Some pups were sensitized and challenged with ovalbumin. Serum PFOA was analyzed by liquid chromatograph-tandem mass spectrometry. Lung function was measured using a small animal ventilator. We assayed inflammatory cells in the lung, performed PCR for lung cytokines, and examined bronchial goblet cell hyperplasia by histology. Here we show that either PFOA or FTOH exposure can induce AHR, but neither one predisposes for exaggerated allergic lung inflammation or AHR. FTOH or PFOS exposure appears to suppress allergic lung inflammation, but does not affect allergic lung dysfunction. 2015-01-12T19:49:29Z 2015-01-12T19:49:29Z 2014-11-15 Ryu MH, Jha A, Ojo OO, Mahood TH, Basu S, Detillieux KA, Nikoobakht N, Wong CS, Loewen M, Becker AB, Halayko AJ. Chronic exposure to perfluorinated compounds: Impact on airway hyperresponsiveness and inflammation. Am J Physiol - Lung Cell Mol Physiol 2014; 307(10):L765-774. http://hdl.handle.net/1993/30195 The American Physiological Society
collection NDLTD
sources NDLTD
topic airway hyperresponsiveness
perfluorinated compounds
environmental pollution
airway inflammation
spellingShingle airway hyperresponsiveness
perfluorinated compounds
environmental pollution
airway inflammation
Ryu, Min Hyung
The effect of in-utero-through-postnatal exposure of mice to perfluorinated compounds on airway inflammation and function
description Perfluorinated compounds, non-degradable xenobiotics in many consumer products, can cause developmental toxicity in animals, and human exposure is associated with asthma symptoms. We tested the hypothesis that sustained chronic exposure to perfluorooctanoic acid (PFOA), fluorotelomer alcohol (FTOH) or perfluorooctanesulfonic acid (PFOS) induces lung dysfunction that exacerbates allergen-induced airway hyperresponsiveness (AHR) and inflammation. Mice were exposed to the chemicals from early gestation day to adulthood. Some pups were sensitized and challenged with ovalbumin. Serum PFOA was analyzed by liquid chromatograph-tandem mass spectrometry. Lung function was measured using a small animal ventilator. We assayed inflammatory cells in the lung, performed PCR for lung cytokines, and examined bronchial goblet cell hyperplasia by histology. Here we show that either PFOA or FTOH exposure can induce AHR, but neither one predisposes for exaggerated allergic lung inflammation or AHR. FTOH or PFOS exposure appears to suppress allergic lung inflammation, but does not affect allergic lung dysfunction.
author2 Halayko, Andrew (Physiology and Pathophysiology)
author_facet Halayko, Andrew (Physiology and Pathophysiology)
Ryu, Min Hyung
author Ryu, Min Hyung
author_sort Ryu, Min Hyung
title The effect of in-utero-through-postnatal exposure of mice to perfluorinated compounds on airway inflammation and function
title_short The effect of in-utero-through-postnatal exposure of mice to perfluorinated compounds on airway inflammation and function
title_full The effect of in-utero-through-postnatal exposure of mice to perfluorinated compounds on airway inflammation and function
title_fullStr The effect of in-utero-through-postnatal exposure of mice to perfluorinated compounds on airway inflammation and function
title_full_unstemmed The effect of in-utero-through-postnatal exposure of mice to perfluorinated compounds on airway inflammation and function
title_sort effect of in-utero-through-postnatal exposure of mice to perfluorinated compounds on airway inflammation and function
publisher The American Physiological Society
publishDate 2015
url http://hdl.handle.net/1993/30195
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