Comparative effects of dexmedetomidine and propofol on brain and lung damage in experimental acute ischemic stroke

Abstract Acute ischemic stroke is associated with pulmonary complications, and often dexmedetomidine and propofol are used to decrease cerebral metabolic rate. However, it is unknown the immunomodulatory actions of dexmedetomidine and propofol on brain and lungs during acute ischemic stroke. The eff...

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Autores principales: Giselle C. Sousa, Marcos Vinicius Fernandes, Fernanda F. Cruz, Mariana A. Antunes, Carla M. da Silva, Christina Takyia, Denise Battaglini, Cynthia S. Samary, Chiara Robba, Paolo Pelosi, Patricia R. M. Rocco, Pedro L. Silva
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Publicado: Nature Portfolio 2021
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spelling oai:doaj.org-article:3ab2bbadb21745a5b4c23dc621e4e38b2021-12-05T12:14:51ZComparative effects of dexmedetomidine and propofol on brain and lung damage in experimental acute ischemic stroke10.1038/s41598-021-02608-12045-2322https://doaj.org/article/3ab2bbadb21745a5b4c23dc621e4e38b2021-11-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-02608-1https://doaj.org/toc/2045-2322Abstract Acute ischemic stroke is associated with pulmonary complications, and often dexmedetomidine and propofol are used to decrease cerebral metabolic rate. However, it is unknown the immunomodulatory actions of dexmedetomidine and propofol on brain and lungs during acute ischemic stroke. The effects of dexmedetomidine and propofol were compared on perilesional brain tissue and lung damage after acute ischemic stroke in rats. Further, the mean amount of both sedatives was directly evaluated on alveolar macrophages and lung endothelial cells primarily extracted 24-h after acute ischemic stroke. In twenty-five Wistar rats, ischemic stroke was induced and after 24-h treated with sodium thiopental (STROKE), dexmedetomidine and propofol. Dexmedetomidine, compared to STROKE, reduced diffuse alveolar damage score [median(interquartile range); 12(7.8–15.3) vs. 19.5(18–24), p = 0.007)], bronchoconstriction index [2.28(2.08–2.36) vs. 2.64(2.53–2.77), p = 0.006], and TNF-α expression (p = 0.0003), while propofol increased VCAM-1 expression compared to STROKE (p = 0.0004). In perilesional brain tissue, dexmedetomidine, compared to STROKE, decreased TNF-α (p = 0.010), while propofol increased VCAM-1 compared to STROKE (p = 0.024). In alveolar macrophages and endothelial cells, dexmedetomidine decreased IL-6 and IL-1β compared to STROKE (p = 0.002, and p = 0.040, respectively), and reduced IL-1β compared to propofol (p = 0.014). Dexmedetomidine, but not propofol, induced brain and lung protection in experimental acute ischemic stroke.Giselle C. SousaMarcos Vinicius FernandesFernanda F. CruzMariana A. AntunesCarla M. da SilvaChristina TakyiaDenise BattagliniCynthia S. SamaryChiara RobbaPaolo PelosiPatricia R. M. RoccoPedro L. SilvaNature 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
Giselle C. Sousa
Marcos Vinicius Fernandes
Fernanda F. Cruz
Mariana A. Antunes
Carla M. da Silva
Christina Takyia
Denise Battaglini
Cynthia S. Samary
Chiara Robba
Paolo Pelosi
Patricia R. M. Rocco
Pedro L. Silva
Comparative effects of dexmedetomidine and propofol on brain and lung damage in experimental acute ischemic stroke
description Abstract Acute ischemic stroke is associated with pulmonary complications, and often dexmedetomidine and propofol are used to decrease cerebral metabolic rate. However, it is unknown the immunomodulatory actions of dexmedetomidine and propofol on brain and lungs during acute ischemic stroke. The effects of dexmedetomidine and propofol were compared on perilesional brain tissue and lung damage after acute ischemic stroke in rats. Further, the mean amount of both sedatives was directly evaluated on alveolar macrophages and lung endothelial cells primarily extracted 24-h after acute ischemic stroke. In twenty-five Wistar rats, ischemic stroke was induced and after 24-h treated with sodium thiopental (STROKE), dexmedetomidine and propofol. Dexmedetomidine, compared to STROKE, reduced diffuse alveolar damage score [median(interquartile range); 12(7.8–15.3) vs. 19.5(18–24), p = 0.007)], bronchoconstriction index [2.28(2.08–2.36) vs. 2.64(2.53–2.77), p = 0.006], and TNF-α expression (p = 0.0003), while propofol increased VCAM-1 expression compared to STROKE (p = 0.0004). In perilesional brain tissue, dexmedetomidine, compared to STROKE, decreased TNF-α (p = 0.010), while propofol increased VCAM-1 compared to STROKE (p = 0.024). In alveolar macrophages and endothelial cells, dexmedetomidine decreased IL-6 and IL-1β compared to STROKE (p = 0.002, and p = 0.040, respectively), and reduced IL-1β compared to propofol (p = 0.014). Dexmedetomidine, but not propofol, induced brain and lung protection in experimental acute ischemic stroke.
format article
author Giselle C. Sousa
Marcos Vinicius Fernandes
Fernanda F. Cruz
Mariana A. Antunes
Carla M. da Silva
Christina Takyia
Denise Battaglini
Cynthia S. Samary
Chiara Robba
Paolo Pelosi
Patricia R. M. Rocco
Pedro L. Silva
author_facet Giselle C. Sousa
Marcos Vinicius Fernandes
Fernanda F. Cruz
Mariana A. Antunes
Carla M. da Silva
Christina Takyia
Denise Battaglini
Cynthia S. Samary
Chiara Robba
Paolo Pelosi
Patricia R. M. Rocco
Pedro L. Silva
author_sort Giselle C. Sousa
title Comparative effects of dexmedetomidine and propofol on brain and lung damage in experimental acute ischemic stroke
title_short Comparative effects of dexmedetomidine and propofol on brain and lung damage in experimental acute ischemic stroke
title_full Comparative effects of dexmedetomidine and propofol on brain and lung damage in experimental acute ischemic stroke
title_fullStr Comparative effects of dexmedetomidine and propofol on brain and lung damage in experimental acute ischemic stroke
title_full_unstemmed Comparative effects of dexmedetomidine and propofol on brain and lung damage in experimental acute ischemic stroke
title_sort comparative effects of dexmedetomidine and propofol on brain and lung damage in experimental acute ischemic stroke
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/3ab2bbadb21745a5b4c23dc621e4e38b
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