Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/33470
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dc.contributor.authorBetrie, Ashenafi H-
dc.contributor.authorMa, Shuai-
dc.contributor.authorOw, Connie P C-
dc.contributor.authorPeiris, Rachel M-
dc.contributor.authorEvans, Roger G-
dc.contributor.authorAyton, Scott-
dc.contributor.authorLane, Darius J R-
dc.contributor.authorSouthon, Adam-
dc.contributor.authorBailey, Simon R-
dc.contributor.authorBellomo, Rinaldo-
dc.contributor.authorMay, Clive N-
dc.contributor.authorLankadeva, Yugeesh R-
dc.date2023-
dc.date.accessioned2023-08-09T04:43:07Z-
dc.date.available2023-08-09T04:43:07Z-
dc.date.issued2023-09-
dc.identifier.citationActa Physiologica (Oxford, England) 2023-09; 239(1)en_US
dc.identifier.issn1748-1716-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/33470-
dc.description.abstractRenal medullary hypoperfusion and hypoxia precede acute kidney injury (AKI) in ovine sepsis. Oxidative/nitrosative stress, inflammation, and impaired nitric oxide generation may contribute to such pathophysiology. We tested whether the antioxidant and anti-inflammatory drug, tempol, may modify these responses. Following unilateral nephrectomy, we inserted renal arterial catheters and laser-Doppler/oxygen-sensing probes in the renal cortex and medulla. Noanesthetized sheep were administered intravenous (IV) Escherichia coli and, at sepsis onset, IV tempol (IVT; 30 mg kg-1  h-1 ), renal arterial tempol (RAT; 3 mg kg-1  h-1 ), or vehicle. Septic sheep receiving vehicle developed renal medullary hypoperfusion (76 ± 16% decrease in perfusion), hypoxia (70 ± 13% decrease in oxygenation), and AKI (87 ± 8% decrease in creatinine clearance) with similar changes during IVT. However, RAT preserved medullary perfusion (1072 ± 307 to 1005 ± 271 units), oxygenation (46 ± 8 to 43 ± 6 mmHg), and creatinine clearance (61 ± 10 to 66 ± 20 mL min-1 ). Plasma, renal medullary, and cortical tissue malonaldehyde and medullary 3-nitrotyrosine decreased significantly with sepsis but were unaffected by IVT or RAT. Consistent with decreased oxidative/nitrosative stress markers, cortical and medullary nuclear factor-erythroid-related factor-2 increased significantly and were unaffected by IVT or RAT. However, RAT prevented sepsis-induced overexpression of cortical tissue tumor necrosis factor alpha (TNF-α; 51 ± 16% decrease; p = 0.003) and medullary Thr-495 phosphorylation of endothelial nitric oxide synthase (eNOS; 63 ± 18% decrease; p = 0.015). In ovine Gram-negative sepsis, renal arterial infusion of tempol prevented renal medullary hypoperfusion and hypoxia and AKI and decreased TNF-α expression and uncoupling of eNOS. However, it did not affect markers of oxidative/nitrosative stress, which were significantly decreased by Gram-negative sepsis.en_US
dc.language.isoeng-
dc.subjectacute kidney injuryen_US
dc.subjecthypoxiaen_US
dc.subjectinflammationen_US
dc.subjectnitric oxide synthaseen_US
dc.subjectrenal microcirculationen_US
dc.subjectsepsisen_US
dc.titleRenal arterial infusion of tempol prevents medullary hypoperfusion, hypoxia, and acute kidney injury in ovine Gram-negative sepsis.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleActa Physiologica (Oxford, England)en_US
dc.identifier.affiliationPreclinical Critical Care Unit, Florey Institute of Neuroscience and Mental Health, The University of Melbourne, Melbourne, Victoria, Australia.;Translational Neurodegeneration Laboratory, Florey Institute of Neuroscience and Mental Health, The University of Melbourne, Melbourne, Victoria, Australia.en_US
dc.identifier.affiliationPreclinical Critical Care Unit, Florey Institute of Neuroscience and Mental Health, The University of Melbourne, Melbourne, Victoria, Australia.;Division of Nephrology, Shanghai Ninth People's Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China.en_US
dc.identifier.affiliationTranslational Neurodegeneration Laboratory, Florey Institute of Neuroscience and Mental Health, The University of Melbourne, Melbourne, Victoria, Australia.en_US
dc.identifier.affiliationFaculty of Veterinary and Agricultural Sciences, The University of Melbourne, Melbourne, Victoria, Australia.en_US
dc.identifier.affiliationDepartment of Critical Care, Melbourne Medical School, The University of Melbourne, Melbourne, Victoria, Australia.;Australian and New Zealand Intensive Care Research Centre, Monash University, Melbourne, Victoria, Australia.;Department of Intensive Care, Austin Hospital, Melbourne, Victoria, Australia.;Department of Intensive Care, Royal Melbourne Hospital, Melbourne, Victoria, Australia.en_US
dc.identifier.affiliationPreclinical Critical Care Unit, Florey Institute of Neuroscience and Mental Health, The University of Melbourne, Melbourne, Victoria, Australia.;Department of Critical Care, Melbourne Medical School, The University of Melbourne, Melbourne, Victoria, Australia.en_US
dc.identifier.affiliationIntensive Careen_US
dc.identifier.doi10.1111/apha.14025en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0002-9241-0757en_US
dc.identifier.orcid0000-0001-8548-3846en_US
dc.identifier.orcid0000-0002-3589-9111en_US
dc.identifier.pubmedid37548350-
dc.description.startpagee14025-
item.openairetypeJournal Article-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
crisitem.author.deptIntensive Care-
crisitem.author.deptData Analytics Research and Evaluation (DARE) Centre-
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