Chronic sustained hypoxia-induced redox remodeling causes contractile dysfunction in mouse sternohyoid muscle

dc.contributor.authorLewis, Philip
dc.contributor.authorSheehan, David
dc.contributor.authorSoares, Renata
dc.contributor.authorCoelho, Ana Varela
dc.contributor.authorO'Halloran, Ken D.
dc.contributor.funderHealth Research Boarden
dc.contributor.funderUniversity College Corken
dc.date.accessioned2017-01-04T16:38:31Z
dc.date.available2017-01-04T16:38:31Z
dc.date.issued2015-04
dc.date.updated2017-01-04T16:32:17Z
dc.description.abstractChronic sustained hypoxia (CH) induces structural and functional adaptations in respiratory muscles of animal models, however the underlying molecular mechanisms are unclear. This study explores the putative role of CH-induced redox remodeling in a translational mouse model, with a focus on the sternohyoid—a representative upper airway dilator muscle involved in the control of pharyngeal airway caliber. We hypothesized that exposure to CH induces redox disturbance in mouse sternohyoid muscle in a time-dependent manner affecting metabolic capacity and contractile performance. C57Bl6/J mice were exposed to normoxia or normobaric CH (FiO2 = 0.1) for 1, 3, or 6 weeks. A second cohort of animals was exposed to CH for 6 weeks with and without antioxidant supplementation (tempol or N-acetyl cysteine in the drinking water). Following CH exposure, we performed 2D redox proteomics with mass spectrometry, metabolic enzyme activity assays, and cell-signaling assays. Additionally, we assessed isotonic contractile and endurance properties ex vivo. Temporal changes in protein oxidation and glycolytic enzyme activities were observed. Redox modulation of sternohyoid muscle proteins key to contraction, metabolism and cellular homeostasis was identified. There was no change in redox-sensitive proteasome activity or HIF-1α content, but CH decreased phospho-JNK content independent of antioxidant supplementation. CH was detrimental to sternohyoid force- and power-generating capacity and this was prevented by chronic antioxidant supplementation. We conclude that CH causes upper airway dilator muscle dysfunction due to redox modulation of proteins key to function and homeostasis. Such changes could serve to further disrupt respiratory homeostasis in diseases characterized by CH such as chronic obstructive pulmonary disease. Antioxidants may have potential use as an adjunctive therapy in hypoxic respiratory disease.en
dc.description.sponsorshipUniversity College Cork (Strategic Research Fund)en
dc.description.statusPeer revieweden
dc.description.versionPublished Versionen
dc.format.mimetypeapplication/pdfen
dc.identifier.citationLewis, P., Sheehan, D., Soares, R., Varela Coelho, A. and O'Halloran, K. D. (2015) 'Chronic sustained hypoxia-induced redox remodeling causes contractile dysfunction in mouse sternohyoid muscle', Frontiers in Physiology, 6,122 (12 pp). doi: 10.3389/fphys.2015.00122en
dc.identifier.doi10.3389/fphys.2015.00122
dc.identifier.endpage122-12en
dc.identifier.issn1664-042X
dc.identifier.journaltitleFrontiers in Physiologyen
dc.identifier.startpage122-1en
dc.identifier.urihttps://hdl.handle.net/10468/3427
dc.identifier.volume6en
dc.language.isoenen
dc.publisherFrontiers Mediaen
dc.rights© 2015 Lewis, Sheehan, Soares, Varela Coelho and O'Halloran. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.en
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en
dc.subjectHypoxiaen
dc.subjectOxidative stressen
dc.subjectAntioxidantsen
dc.subjectRespiratory muscleen
dc.subjectCOPDen
dc.titleChronic sustained hypoxia-induced redox remodeling causes contractile dysfunction in mouse sternohyoid muscleen
dc.typeArticle (peer-reviewed)en
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