Effects of inhaled nitric oxide on outcome after prolonged cardiac arrest in mild therapeutic hypothermia treated rats

Abstract Guidelines endorse targeted temperature management to reduce neurological sequelae and mortality after cardiac arrest (CA). Additional therapeutic approaches are lacking. Inhaled nitric oxide (iNO) given post systemic ischemia/reperfusion injury improves outcomes. Attenuated inflammation by...

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Autores principales: Anne Brücken, Christian Bleilevens, Philipp Berger, Kay Nolte, Nadine T. Gaisa, Rolf Rossaint, Gernot Marx, Matthias Derwall, Michael Fries
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Publicado: Nature Portfolio 2018
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Acceso en línea:https://doaj.org/article/133d2956de0f4dc6af449015ff033bd7
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spelling oai:doaj.org-article:133d2956de0f4dc6af449015ff033bd72021-12-02T16:07:51ZEffects of inhaled nitric oxide on outcome after prolonged cardiac arrest in mild therapeutic hypothermia treated rats10.1038/s41598-018-25213-12045-2322https://doaj.org/article/133d2956de0f4dc6af449015ff033bd72018-04-01T00:00:00Zhttps://doi.org/10.1038/s41598-018-25213-1https://doaj.org/toc/2045-2322Abstract Guidelines endorse targeted temperature management to reduce neurological sequelae and mortality after cardiac arrest (CA). Additional therapeutic approaches are lacking. Inhaled nitric oxide (iNO) given post systemic ischemia/reperfusion injury improves outcomes. Attenuated inflammation by iNO might be crucial in brain protection. iNO augmented mild therapeutic hypothermia (MTH) may improve outcome after CA exceeding the effect of MTH alone. Following ten minutes of CA and three minutes of cardiopulmonary resuscitation, 20 male Sprague-Dawley rats were randomized to receive MTH at 33 °C for 6hrs or MTH + 20ppm iNO for 5hrs; one group served as normothermic control. During the experiment blood was taken for biochemical evaluation. A neurological deficit score was calculated daily for seven days post CA. On day seven, brains and hearts were harvested for histological evaluation. Treatment groups showed a significant decrease in lactate levels six hours post resuscitation in comparison to controls. TNF-α release was significantly lower in MTH + iNO treated animals only at four hours post ROSC. While only the combination of MTH and iNO improved neurological function in a statistically significant manner in comparison to controls on days 4–7 after CA, there was no significant difference between groups treated with MTH and MTH + iNO.Anne BrückenChristian BleilevensPhilipp BergerKay NolteNadine T. GaisaRolf RossaintGernot MarxMatthias DerwallMichael FriesNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 8, Iss 1, Pp 1-9 (2018)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Anne Brücken
Christian Bleilevens
Philipp Berger
Kay Nolte
Nadine T. Gaisa
Rolf Rossaint
Gernot Marx
Matthias Derwall
Michael Fries
Effects of inhaled nitric oxide on outcome after prolonged cardiac arrest in mild therapeutic hypothermia treated rats
description Abstract Guidelines endorse targeted temperature management to reduce neurological sequelae and mortality after cardiac arrest (CA). Additional therapeutic approaches are lacking. Inhaled nitric oxide (iNO) given post systemic ischemia/reperfusion injury improves outcomes. Attenuated inflammation by iNO might be crucial in brain protection. iNO augmented mild therapeutic hypothermia (MTH) may improve outcome after CA exceeding the effect of MTH alone. Following ten minutes of CA and three minutes of cardiopulmonary resuscitation, 20 male Sprague-Dawley rats were randomized to receive MTH at 33 °C for 6hrs or MTH + 20ppm iNO for 5hrs; one group served as normothermic control. During the experiment blood was taken for biochemical evaluation. A neurological deficit score was calculated daily for seven days post CA. On day seven, brains and hearts were harvested for histological evaluation. Treatment groups showed a significant decrease in lactate levels six hours post resuscitation in comparison to controls. TNF-α release was significantly lower in MTH + iNO treated animals only at four hours post ROSC. While only the combination of MTH and iNO improved neurological function in a statistically significant manner in comparison to controls on days 4–7 after CA, there was no significant difference between groups treated with MTH and MTH + iNO.
format article
author Anne Brücken
Christian Bleilevens
Philipp Berger
Kay Nolte
Nadine T. Gaisa
Rolf Rossaint
Gernot Marx
Matthias Derwall
Michael Fries
author_facet Anne Brücken
Christian Bleilevens
Philipp Berger
Kay Nolte
Nadine T. Gaisa
Rolf Rossaint
Gernot Marx
Matthias Derwall
Michael Fries
author_sort Anne Brücken
title Effects of inhaled nitric oxide on outcome after prolonged cardiac arrest in mild therapeutic hypothermia treated rats
title_short Effects of inhaled nitric oxide on outcome after prolonged cardiac arrest in mild therapeutic hypothermia treated rats
title_full Effects of inhaled nitric oxide on outcome after prolonged cardiac arrest in mild therapeutic hypothermia treated rats
title_fullStr Effects of inhaled nitric oxide on outcome after prolonged cardiac arrest in mild therapeutic hypothermia treated rats
title_full_unstemmed Effects of inhaled nitric oxide on outcome after prolonged cardiac arrest in mild therapeutic hypothermia treated rats
title_sort effects of inhaled nitric oxide on outcome after prolonged cardiac arrest in mild therapeutic hypothermia treated rats
publisher Nature Portfolio
publishDate 2018
url https://doaj.org/article/133d2956de0f4dc6af449015ff033bd7
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