Please use this identifier to cite or link to this item: https://doi.org/10.1186/cc10307
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dc.titleLevosimendan inhibits release of reactive oxygen species in polymorphonuclear leukocytes in vitro and in patients with acute heart failure and septic shock: A prospective observational study
dc.contributor.authorHasslacher, J
dc.contributor.authorBijuklic, K
dc.contributor.authorBertocchi, C
dc.contributor.authorKountchev, J
dc.contributor.authorBellmann, R
dc.contributor.authorDunzendorfer, S
dc.contributor.authorJoannidis, M
dc.date.accessioned2020-10-27T04:58:19Z
dc.date.available2020-10-27T04:58:19Z
dc.date.issued2011
dc.identifier.citationHasslacher, J, Bijuklic, K, Bertocchi, C, Kountchev, J, Bellmann, R, Dunzendorfer, S, Joannidis, M (2011). Levosimendan inhibits release of reactive oxygen species in polymorphonuclear leukocytes in vitro and in patients with acute heart failure and septic shock: A prospective observational study. Critical Care 15 (4) : R166. ScholarBank@NUS Repository. https://doi.org/10.1186/cc10307
dc.identifier.issn1364-8535
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/180856
dc.description.abstractIntroduction: Levosimendan is an extensively investigated inodilator showing also cardioprotective and antiinflammatory effects. The aim of our study was to explore the influence of levosimendan on polymorphonuclear leucocytes (PMN), a main source of reactive oxygen species, in vitro and in patients with acute heart failure or septic myocardial depression.Methods: PMN isolated from healthy volunteers were incubated with levosimendan in vitro. After stimulation with N-formyl-Met-Leu-Phe (fMLP) or phorbol 12-myristate 13-acetate (PMA) respiratory burst was quantified using a fluorescent dye. Apoptosis and expression of cell adhesion molecules of PMN were measured by flow cytometry. For determination of in vivo effects patients with acute heart failure (n = 16) or septic cardiac failure (n = 9) receiving levosimendan treatment were enrolled consecutively. PMN were isolated to measure respiratory burst activity before treatment as well as one and two hours after initiation of levosimendan administration. Furthermore inflammatory, hemodynamic and renal function parameters were obtained.Results: In vitro, levosimendan suppressed respiratory burst activity in fMLP or PMA stimulated PMN in a dose dependent manner by 30 ± 11% (P < 0.001) at 100 ng/mL and by 27 ± 17% (P < 0.001) at 1000 ng/mL respectively. Markers of apoptosis and PMN cell adhesion molecule expression remained unaffected by levosimendan treatment.In vivo, levosimendan treatment for two hours resulted in a significant reduction of PMA stimulated oxidative burst by 45% (P < 0.01) and fMLP stimulated oxidative burst by 49% (P < 0.05) in patients with acute heart failure. In patients suffering from septic shock levosimendan treatment decreased oxidative burst activity in unstimulated, fMLP and PMA stimulated PMN by 48% (P < 0.05), 46% (P < 0.01) and 43% (P < 0.01) respectively.Conclusions: Levosimendan appears to exert distinct immunomodulatory effects by decreasing oxidative burst activity of PMN. This property might contribute to the previously described cardioprotective effects of the drug. © 2011 Hasslacher et al.; licensee BioMed Central Ltd.
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.subjectdobutamine
dc.subjectformylmethionylleucylphenylalanine
dc.subjectlevosimendan
dc.subjectnoradrenalin
dc.subjectphorbol 13 acetate 12 myristate
dc.subjectreactive oxygen metabolite
dc.subjectcardiotonic agent
dc.subjecthydrazone derivative
dc.subjectpyridazine derivative
dc.subjectreactive oxygen metabolite
dc.subjectsimendan
dc.subjectacute heart failure
dc.subjectadult
dc.subjectaged
dc.subjectapoptosis
dc.subjectarticle
dc.subjectclinical article
dc.subjectcontinuous infusion
dc.subjectcontrolled study
dc.subjectdrug blood level
dc.subjectfemale
dc.subjectflow cytometry
dc.subjectheart hemodynamics
dc.subjecthuman
dc.subjecthuman cell
dc.subjectin vitro study
dc.subjectkidney function
dc.subjectmale
dc.subjectneutrophil
dc.subjectobservational study
dc.subjectpriority journal
dc.subjectprospective study
dc.subjectprotein expression
dc.subjectseptic shock
dc.subjectacute disease
dc.subjectAustria
dc.subjectdrug antagonism
dc.subjectdrug effect
dc.subjectheart failure
dc.subjectmiddle aged
dc.subjectpathophysiology
dc.subjectseptic shock
dc.subjectAcute Disease
dc.subjectAged
dc.subjectAged, 80 and over
dc.subjectAustria
dc.subjectCardiotonic Agents
dc.subjectFemale
dc.subjectFlow Cytometry
dc.subjectHeart Failure
dc.subjectHumans
dc.subjectHydrazones
dc.subjectMale
dc.subjectMiddle Aged
dc.subjectNeutrophils
dc.subjectProspective Studies
dc.subjectPyridazines
dc.subjectReactive Oxygen Species
dc.subjectShock, Septic
dc.typeArticle
dc.contributor.departmentMECHANOBIOLOGY INSTITUTE
dc.description.doi10.1186/cc10307
dc.description.sourcetitleCritical Care
dc.description.volume15
dc.description.issue4
dc.description.pageR166
dc.published.statePublished
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