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Permanent URL to this publication: http://dx.doi.org/10.5167/uzh-66745

Urner, M; Herrmann, I K; Booy, C; Roth-Z' Graggen, B; Maggiorini, M; Beck-Schimmer, B (2012). Effect of hypoxia and dexamethasone on inflammation and ion transporter function in pulmonary cells. Clinical and Experimental Immunology, 169(2):119-128.

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Abstract

Dexamethasone has been found to reduce the incidence of high-altitude pulmonary oedema. Mechanisms explaining this effect still remain unclear. We assessed the effect of dexamethasone using established cell lines, including rat alveolar epithelial cells (AEC), pulmonary artery endothelial cells (RPAEC) and alveolar macrophages (MAC), in an environment of low oxygen, simulating a condition of alveolar hypoxia as found at high altitude. Inflammatory mediators and ion transporter expression were quantified. Based on earlier results, we hypothesized that hypoxic conditions trigger inflammation. AEC, RPAEC and MAC, pre-incubated for 1 h with or without dexamethasone (10(-7) mol/l), were subsequently exposed to mild hypoxia (5% O(2), or normoxia as control) for 24 h. mRNA and protein levels of cytokine-induced neutrophil chemoattractant-1, monocyte chemoattractant protein-1 and interleukin-6 were analysed. mRNA expression and functional activity of the apical epithelial sodium channel and basolateral Na(+)/K(+)-ATPase were determined using radioactive marker ions. In all three types of pulmonary cells hypoxic conditions led to an attenuated secretion of inflammatory mediators, which was even more pronounced in dexamethasone pretreated samples. Function of Na(+)/K(+)-ATPase was not significantly influenced by hypoxia or dexamethasone, while activity of epithelial sodium channels was decreased under hypoxic conditions. When pre-incubated with dexamethasone, however, transporter activity was partially maintained. These findings illustrate that long-term hypoxia does not trigger an inflammatory response. The ion transport across apical epithelial sodium channels under hypoxic conditions is ameliorated in cells treated with dexamethasone.

Item Type:Journal Article, refereed, original work
Communities & Collections:04 Faculty of Medicine > Institute of Physiology
07 Faculty of Science > Institute of Physiology

04 Faculty of Medicine > Center for Integrative Human Physiology
04 Faculty of Medicine > University Hospital Zurich > Institute of Anesthesiology
DDC:570 Life sciences; biology
610 Medicine & health
Language:English
Date:2012
Deposited On:16 Nov 2012 16:39
Last Modified:03 Dec 2013 12:18
Publisher:Wiley-Blackwell
ISSN:0009-9104
Additional Information:The definitive version is available at www.blackwell-synergy.com
Free access at:Publisher DOI. An embargo period may apply.
Publisher DOI:10.1111/j.1365-2249.2012.04595.x
PubMed ID:22774986
Citations:Web of Science®. Times Cited: 2
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