Time course of nitric oxide synthases, nitrosative stress, and poly(ADP Ribosylation) in an ovine sepsis model

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dc.creatorLange, M.en
dc.creatorConnelly, R. L.en
dc.creatorTraber, D. L.en
dc.creatorHamahata, A.en
dc.creatorNakano, Y.en
dc.creatorEsechie, A.en
dc.creatorJonkam, C.en
dc.creatorBorzyskowski S. von, Traber, L. D.en
dc.creatorSchmalstieg, F. C.en
dc.creatorHerndon, D. N.en
dc.creatorEnkhbaatar, P.en
dc.date.accessioned2015-09-04T16:05:56Zen
dc.date.available2015-09-04T16:05:56Zen
dc.date.issued2010en
dc.description.abstractIntroduction: Different isoforms of nitric oxide synthases (NOS) and determinants of oxidative/nitrosative stress play important roles in the pathophysiology of pulmonary dysfunction induced by acute lung injury (ALI) and sepsis. However, the time changes of these pathogenic factors are largely undetermined. Methods: Twenty-four chronically instrumented sheep were subjected to inhalation of 48 breaths of cotton smoke and instillation of live Pseudomonas aeruginosa into both lungs and were euthanized at 4, 8, 12, 18, and 24 hours postinjury. Additional sheep received sham injury and were euthanized after 24 hrs (control). All animals were mechanically ventilated and fluid resuscitated. Lung tissue was obtained at the respective time points for the measurement of neuronal, endothelial, and inducible NOS (nNOS, eNOS, iNOS) mRNA and their protein expression, calcium-dependent and -independent NOS activity, 3-nitrotyrosine (3-NT), and poly(ADP-ribose) (PAR) protein expression. Results: The injury induced severe pulmonary dysfunction as indicated by a progressive decline in oxygenation index and concomitant increase in pulmonary shunt fraction. These changes were associated with an early and transient increase in eNOS and an early and profound increase in iNOS expression, while expression of nNOS remained unchanged. Both 3-NT, a marker of protein nitration, and PAR, an indicator of DNA damage, increased early but only transiently. Conclusions: Identification of the time course of the described pathogenetic factors provides important additional information on the pulmonary response to ALI and sepsis in the ovine model. This information may be crucial for future studies, especially when considering the timing of novel treatment strategies including selective inhibition of NOS isoforms, modulation of peroxynitrite, and PARP.en
dc.description.departmentCenter for Electromechanicsen
dc.identifierPR_510en
dc.identifier.citationM. Lange, R. Connelly, D.L Traber, A. Hamahata, Y. Nakano, A. Esechie, C. Jonkam, S. von Borzyskowski, L.D. Traber, F.C. Schmalstieg, D.N. Herndon, and P. Enkhbaatar, “Time Course of Nitric Oxide Synthases, Nitrosative Stress, and poly (ADP Ribosylation) in an Ovine Sepsis Model,” Critical Care, vol. 14, no. 4, 2010, p. R129.en
dc.identifier.urihttp://hdl.handle.net/2152/30752en
dc.language.isoenen
dc.publisherBioMed Centralen
dc.relation.ispartofCEM Publicationsen
dc.rights.restrictionopenen
dc.subjectBioproducts and Bioenergyen
dc.subjectnitric oxide synthasesen
dc.subjectacute lung injuryen
dc.titleTime course of nitric oxide synthases, nitrosative stress, and poly(ADP Ribosylation) in an ovine sepsis modelen
dc.typearticleen

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