The endogenous cannabinoid anandamide increases human airway epithelial cell permeability through an arachidonic acid metabolite

Injury to the bronchial epithelium in respiratory diseases such as asthma and COPD results in the lossof barrier function and an elevated sensitivity to environmental insults. An increased release of theendogenous cannabinoid, anandamide in response to inhalation of allergen in asthmatic patients ha...

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Main Authors: Shang, V.C.M., O'Sullivan, Saoirse, Kendall, D.A., Roberts, Richard E.
Format: Article
Published: Elsevier 2016
Subjects:
Online Access:https://eprints.nottingham.ac.uk/35682/
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author Shang, V.C.M.
O'Sullivan, Saoirse
Kendall, D.A.
Roberts, Richard E.
author_facet Shang, V.C.M.
O'Sullivan, Saoirse
Kendall, D.A.
Roberts, Richard E.
author_sort Shang, V.C.M.
building Nottingham Research Data Repository
collection Online Access
description Injury to the bronchial epithelium in respiratory diseases such as asthma and COPD results in the lossof barrier function and an elevated sensitivity to environmental insults. An increased release of theendogenous cannabinoid, anandamide in response to inhalation of allergen in asthmatic patients hasbeen reported. The aim of this study was, therefore, to determine the effects of endocannabinoids onbronchial epithelial cell permeability and to investigate the mechanisms involved.Calu-3 human bronchial epithelial cells were cultured at air–liquid interface to allow developmentof tight junctions. Changes in Transepithelial Electrical Resistance (TEER), a reflection of epithelial per-meability, were measured at various time points post-treatment, and expression of the tight junctionproteins, occludin and ZO-1, were determined using Western immunoblotting.Anandamide produced a significant reduction in TEER, which was unaffected by cannabinoid receptorantagonists, but attenuated by URB597, an inhibitor of fatty acid amide hydrolase, and by a combinationof cyclooxygenase (COX) and lipoxygenase (LOX) blockade. The anandamide metabolite, arachidonicacid, showed similar TEER decrease that was also prevented in the presence of COX and LOX inhibitor.Expression of occludin and ZO-1 were also reduced by anandamide.These findings indicate a pro-inflammatory-like effect of anandamide on bronchial epithelial per-meability, mediated by cyclooxygenase and lipoxygenase metabolites, and suggest that inhibition ofanandamide degradation might provide a novel approach to treat airway inflammation.
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spelling nottingham-356822020-05-04T17:43:13Z https://eprints.nottingham.ac.uk/35682/ The endogenous cannabinoid anandamide increases human airway epithelial cell permeability through an arachidonic acid metabolite Shang, V.C.M. O'Sullivan, Saoirse Kendall, D.A. Roberts, Richard E. Injury to the bronchial epithelium in respiratory diseases such as asthma and COPD results in the lossof barrier function and an elevated sensitivity to environmental insults. An increased release of theendogenous cannabinoid, anandamide in response to inhalation of allergen in asthmatic patients hasbeen reported. The aim of this study was, therefore, to determine the effects of endocannabinoids onbronchial epithelial cell permeability and to investigate the mechanisms involved.Calu-3 human bronchial epithelial cells were cultured at air–liquid interface to allow developmentof tight junctions. Changes in Transepithelial Electrical Resistance (TEER), a reflection of epithelial per-meability, were measured at various time points post-treatment, and expression of the tight junctionproteins, occludin and ZO-1, were determined using Western immunoblotting.Anandamide produced a significant reduction in TEER, which was unaffected by cannabinoid receptorantagonists, but attenuated by URB597, an inhibitor of fatty acid amide hydrolase, and by a combinationof cyclooxygenase (COX) and lipoxygenase (LOX) blockade. The anandamide metabolite, arachidonicacid, showed similar TEER decrease that was also prevented in the presence of COX and LOX inhibitor.Expression of occludin and ZO-1 were also reduced by anandamide.These findings indicate a pro-inflammatory-like effect of anandamide on bronchial epithelial per-meability, mediated by cyclooxygenase and lipoxygenase metabolites, and suggest that inhibition ofanandamide degradation might provide a novel approach to treat airway inflammation. Elsevier 2016-03-02 Article PeerReviewed Shang, V.C.M., O'Sullivan, Saoirse, Kendall, D.A. and Roberts, Richard E. (2016) The endogenous cannabinoid anandamide increases human airway epithelial cell permeability through an arachidonic acid metabolite. Pharmacological Research, 105 . pp. 152-163. ISSN 1043-6618 Anandamide; Bronchial epithelium; Chronic airway inflammation; Endocannabinoid; Permeability; Tight junction http://www.sciencedirect.com/science/article/pii/S1043661816000256 doi:10.1016/j.phrs.2016.01.023 doi:10.1016/j.phrs.2016.01.023
spellingShingle Anandamide; Bronchial epithelium; Chronic airway inflammation; Endocannabinoid; Permeability; Tight junction
Shang, V.C.M.
O'Sullivan, Saoirse
Kendall, D.A.
Roberts, Richard E.
The endogenous cannabinoid anandamide increases human airway epithelial cell permeability through an arachidonic acid metabolite
title The endogenous cannabinoid anandamide increases human airway epithelial cell permeability through an arachidonic acid metabolite
title_full The endogenous cannabinoid anandamide increases human airway epithelial cell permeability through an arachidonic acid metabolite
title_fullStr The endogenous cannabinoid anandamide increases human airway epithelial cell permeability through an arachidonic acid metabolite
title_full_unstemmed The endogenous cannabinoid anandamide increases human airway epithelial cell permeability through an arachidonic acid metabolite
title_short The endogenous cannabinoid anandamide increases human airway epithelial cell permeability through an arachidonic acid metabolite
title_sort endogenous cannabinoid anandamide increases human airway epithelial cell permeability through an arachidonic acid metabolite
topic Anandamide; Bronchial epithelium; Chronic airway inflammation; Endocannabinoid; Permeability; Tight junction
url https://eprints.nottingham.ac.uk/35682/
https://eprints.nottingham.ac.uk/35682/
https://eprints.nottingham.ac.uk/35682/