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Characterization of Brain–Heart Interactions in a Rodent Model of Sepsis

Loss of heart rate variability (HRV) and autonomic dysfunction are associated with poor outcomes in critically ill patients. Neuronal networks comprising brainstem and hypothalamus are involved in the “flight-or-fight” response via control over the autonomic nervous system and circulation. We hypoth...

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Autores principales: Pinto, Bernardo Bollen, Ritter, Cristiane, Michels, Monique, Gambarotta, Nicolò, Ferrario, Manuela, Dal-Pizzol, Felipe, Singer, Mervyn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5443875/
https://www.ncbi.nlm.nih.gov/pubmed/27229490
http://dx.doi.org/10.1007/s12035-016-9941-z
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author Pinto, Bernardo Bollen
Ritter, Cristiane
Michels, Monique
Gambarotta, Nicolò
Ferrario, Manuela
Dal-Pizzol, Felipe
Singer, Mervyn
author_facet Pinto, Bernardo Bollen
Ritter, Cristiane
Michels, Monique
Gambarotta, Nicolò
Ferrario, Manuela
Dal-Pizzol, Felipe
Singer, Mervyn
author_sort Pinto, Bernardo Bollen
collection PubMed
description Loss of heart rate variability (HRV) and autonomic dysfunction are associated with poor outcomes in critically ill patients. Neuronal networks comprising brainstem and hypothalamus are involved in the “flight-or-fight” response via control over the autonomic nervous system and circulation. We hypothesized that sepsis-induced inflammation in brain regions responsible for autonomic control is associated with sympathovagal imbalance and depressed contractility. Sepsis was induced by fecal slurry injection in fluid-resuscitated rats. Sham-operated animals served as controls. Echocardiography-derived peak velocity (PV) was used to separate septic animals into good (PV ≥0.93 m/s, low 72-h mortality) and bad (PV <0.93, high 72-h mortality) prognosis. Cytokine protein levels were assessed by ELISA. All experiments were performed at 24 h post-insult. Increased levels of inflammation and oxidative injury were observed in the hypothalamus (TNF-α, IL-10, nitrite and nitrate and carbonyl groups) and brainstem (IL-1, IL-6, IL-10, nitrite and nitrate and carbonyl groups) of the septic animals (p < 0.05 vs. sham), but not in the pre-frontal cortex, an area not directly implicated in control of the autonomic nervous system. Good prognosis septic animals had increased sympathetic output and increased left ventricular contractility (p < 0.05 vs. sham). There was a significant inverse correlation between high frequency power (a marker of parasympathetic outflow) and contractility (r = −0.73, p < 0.05). We found no correlation between the degree of inflammation or injury to autonomic centers and cardiovascular function. In conclusion, control of autonomic centers and cardiac function in our long-term rodent model of sepsis was related to clinical severity but not directly to the degree of inflammation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s12035-016-9941-z) contains supplementary material, which is available to authorized users.
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spelling pubmed-54438752017-06-09 Characterization of Brain–Heart Interactions in a Rodent Model of Sepsis Pinto, Bernardo Bollen Ritter, Cristiane Michels, Monique Gambarotta, Nicolò Ferrario, Manuela Dal-Pizzol, Felipe Singer, Mervyn Mol Neurobiol Article Loss of heart rate variability (HRV) and autonomic dysfunction are associated with poor outcomes in critically ill patients. Neuronal networks comprising brainstem and hypothalamus are involved in the “flight-or-fight” response via control over the autonomic nervous system and circulation. We hypothesized that sepsis-induced inflammation in brain regions responsible for autonomic control is associated with sympathovagal imbalance and depressed contractility. Sepsis was induced by fecal slurry injection in fluid-resuscitated rats. Sham-operated animals served as controls. Echocardiography-derived peak velocity (PV) was used to separate septic animals into good (PV ≥0.93 m/s, low 72-h mortality) and bad (PV <0.93, high 72-h mortality) prognosis. Cytokine protein levels were assessed by ELISA. All experiments were performed at 24 h post-insult. Increased levels of inflammation and oxidative injury were observed in the hypothalamus (TNF-α, IL-10, nitrite and nitrate and carbonyl groups) and brainstem (IL-1, IL-6, IL-10, nitrite and nitrate and carbonyl groups) of the septic animals (p < 0.05 vs. sham), but not in the pre-frontal cortex, an area not directly implicated in control of the autonomic nervous system. Good prognosis septic animals had increased sympathetic output and increased left ventricular contractility (p < 0.05 vs. sham). There was a significant inverse correlation between high frequency power (a marker of parasympathetic outflow) and contractility (r = −0.73, p < 0.05). We found no correlation between the degree of inflammation or injury to autonomic centers and cardiovascular function. In conclusion, control of autonomic centers and cardiac function in our long-term rodent model of sepsis was related to clinical severity but not directly to the degree of inflammation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s12035-016-9941-z) contains supplementary material, which is available to authorized users. Springer US 2016-05-26 2017 /pmc/articles/PMC5443875/ /pubmed/27229490 http://dx.doi.org/10.1007/s12035-016-9941-z Text en © The Author(s) 2016 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Article
Pinto, Bernardo Bollen
Ritter, Cristiane
Michels, Monique
Gambarotta, Nicolò
Ferrario, Manuela
Dal-Pizzol, Felipe
Singer, Mervyn
Characterization of Brain–Heart Interactions in a Rodent Model of Sepsis
title Characterization of Brain–Heart Interactions in a Rodent Model of Sepsis
title_full Characterization of Brain–Heart Interactions in a Rodent Model of Sepsis
title_fullStr Characterization of Brain–Heart Interactions in a Rodent Model of Sepsis
title_full_unstemmed Characterization of Brain–Heart Interactions in a Rodent Model of Sepsis
title_short Characterization of Brain–Heart Interactions in a Rodent Model of Sepsis
title_sort characterization of brain–heart interactions in a rodent model of sepsis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5443875/
https://www.ncbi.nlm.nih.gov/pubmed/27229490
http://dx.doi.org/10.1007/s12035-016-9941-z
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