Levosimendan increases brain tissue oxygen levels after cardiopulmonary resuscitation independent of cardiac function and cerebral perfusion

Abstract Prompt reperfusion is important to rescue ischemic tissue; however, the process itself presents a key pathomechanism that contributes to a poor outcome following cardiac arrest. Experimental data have suggested the use of levosimendan to limit ischemia–reperfusion injury by improving cerebr...

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Autores principales: Andreas García-Bardon, Jens Kamuf, Alexander Ziebart, Tanghua Liu, Nadia Krebs, Bastian Dünges, Robert F. Kelm, Svenja Morsbach, Kristin Mohr, Axel Heimann, Erik K. Hartmann, Serge C. Thal
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Publicado: Nature Portfolio 2021
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spelling oai:doaj.org-article:0b3024ea80bb40e587483fa6b521fe732021-12-02T15:23:07ZLevosimendan increases brain tissue oxygen levels after cardiopulmonary resuscitation independent of cardiac function and cerebral perfusion10.1038/s41598-021-93621-x2045-2322https://doaj.org/article/0b3024ea80bb40e587483fa6b521fe732021-07-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-93621-xhttps://doaj.org/toc/2045-2322Abstract Prompt reperfusion is important to rescue ischemic tissue; however, the process itself presents a key pathomechanism that contributes to a poor outcome following cardiac arrest. Experimental data have suggested the use of levosimendan to limit ischemia–reperfusion injury by improving cerebral microcirculation. However, recent studies have questioned this effect. The present study aimed to investigate the influence on hemodynamic parameters, cerebral perfusion and oxygenation following cardiac arrest by ventricular fibrillation in juvenile male pigs. Following the return of spontaneous circulation (ROSC), animals were randomly assigned to levosimendan (12 µg/kg, followed by 0.3 µg/kg/min) or vehicle treatment for 6 h. Levosimendan-treated animals showed significantly higher brain PbtO2 levels. This effect was not accompanied by changes in cardiac output, preload and afterload, arterial blood pressure, or cerebral microcirculation indicating a local effect. Cerebral oxygenation is key to minimizing damage, and thus, current concepts are aimed at improving impaired cardiac output or cerebral perfusion. In the present study, we showed that NIRS does not reliably detect low PbtO2 levels and that levosimendan increases brain oxygen content. Thus, levosimendan may present a promising therapeutic approach to rescue brain tissue at risk following cardiac arrest or ischemic events such as stroke or traumatic brain injury.Andreas García-BardonJens KamufAlexander ZiebartTanghua LiuNadia KrebsBastian DüngesRobert F. KelmSvenja MorsbachKristin MohrAxel HeimannErik K. HartmannSerge C. ThalNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-10 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Andreas García-Bardon
Jens Kamuf
Alexander Ziebart
Tanghua Liu
Nadia Krebs
Bastian Dünges
Robert F. Kelm
Svenja Morsbach
Kristin Mohr
Axel Heimann
Erik K. Hartmann
Serge C. Thal
Levosimendan increases brain tissue oxygen levels after cardiopulmonary resuscitation independent of cardiac function and cerebral perfusion
description Abstract Prompt reperfusion is important to rescue ischemic tissue; however, the process itself presents a key pathomechanism that contributes to a poor outcome following cardiac arrest. Experimental data have suggested the use of levosimendan to limit ischemia–reperfusion injury by improving cerebral microcirculation. However, recent studies have questioned this effect. The present study aimed to investigate the influence on hemodynamic parameters, cerebral perfusion and oxygenation following cardiac arrest by ventricular fibrillation in juvenile male pigs. Following the return of spontaneous circulation (ROSC), animals were randomly assigned to levosimendan (12 µg/kg, followed by 0.3 µg/kg/min) or vehicle treatment for 6 h. Levosimendan-treated animals showed significantly higher brain PbtO2 levels. This effect was not accompanied by changes in cardiac output, preload and afterload, arterial blood pressure, or cerebral microcirculation indicating a local effect. Cerebral oxygenation is key to minimizing damage, and thus, current concepts are aimed at improving impaired cardiac output or cerebral perfusion. In the present study, we showed that NIRS does not reliably detect low PbtO2 levels and that levosimendan increases brain oxygen content. Thus, levosimendan may present a promising therapeutic approach to rescue brain tissue at risk following cardiac arrest or ischemic events such as stroke or traumatic brain injury.
format article
author Andreas García-Bardon
Jens Kamuf
Alexander Ziebart
Tanghua Liu
Nadia Krebs
Bastian Dünges
Robert F. Kelm
Svenja Morsbach
Kristin Mohr
Axel Heimann
Erik K. Hartmann
Serge C. Thal
author_facet Andreas García-Bardon
Jens Kamuf
Alexander Ziebart
Tanghua Liu
Nadia Krebs
Bastian Dünges
Robert F. Kelm
Svenja Morsbach
Kristin Mohr
Axel Heimann
Erik K. Hartmann
Serge C. Thal
author_sort Andreas García-Bardon
title Levosimendan increases brain tissue oxygen levels after cardiopulmonary resuscitation independent of cardiac function and cerebral perfusion
title_short Levosimendan increases brain tissue oxygen levels after cardiopulmonary resuscitation independent of cardiac function and cerebral perfusion
title_full Levosimendan increases brain tissue oxygen levels after cardiopulmonary resuscitation independent of cardiac function and cerebral perfusion
title_fullStr Levosimendan increases brain tissue oxygen levels after cardiopulmonary resuscitation independent of cardiac function and cerebral perfusion
title_full_unstemmed Levosimendan increases brain tissue oxygen levels after cardiopulmonary resuscitation independent of cardiac function and cerebral perfusion
title_sort levosimendan increases brain tissue oxygen levels after cardiopulmonary resuscitation independent of cardiac function and cerebral perfusion
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/0b3024ea80bb40e587483fa6b521fe73
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