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The influence of dexmedetomidine and propofol on circulating cytokine levels in healthy subjects

BACKGROUND: Surgery and diseases modify inflammatory responses and the immune system. Anesthetic agents also have effects on the human immune system but the responses they induce may be altered or masked by the surgical procedures or underlying illnesses. The aim of this study was to assess how sing...

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Autores principales: Kallioinen, Minna, Scheinin, Annalotta, Maksimow, Mikael, Långsjö, Jaakko, Kaisti, Kaike, Takala, Riikka, Vahlberg, Tero, Valli, Katja, Salmi, Marko, Scheinin, Harry, Maksimow, Anu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6894489/
https://www.ncbi.nlm.nih.gov/pubmed/31805854
http://dx.doi.org/10.1186/s12871-019-0895-3
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author Kallioinen, Minna
Scheinin, Annalotta
Maksimow, Mikael
Långsjö, Jaakko
Kaisti, Kaike
Takala, Riikka
Vahlberg, Tero
Valli, Katja
Salmi, Marko
Scheinin, Harry
Maksimow, Anu
author_facet Kallioinen, Minna
Scheinin, Annalotta
Maksimow, Mikael
Långsjö, Jaakko
Kaisti, Kaike
Takala, Riikka
Vahlberg, Tero
Valli, Katja
Salmi, Marko
Scheinin, Harry
Maksimow, Anu
author_sort Kallioinen, Minna
collection PubMed
description BACKGROUND: Surgery and diseases modify inflammatory responses and the immune system. Anesthetic agents also have effects on the human immune system but the responses they induce may be altered or masked by the surgical procedures or underlying illnesses. The aim of this study was to assess how single-drug dexmedetomidine and propofol anesthesia without any surgical intervention alter acute immunological biomarkers in healthy subjects. METHODS: Thirty-five healthy, young male subjects were anesthetized using increasing concentrations of dexmedetomidine (n = 18) or propofol (n = 17) until loss of responsiveness (LOR) was detected. The treatment allocation was randomized. Multi-parametric immunoassays for the detection of 48 cytokines, chemokines and growth factors were used. Concentrations were determined at baseline and at the highest drug concentration for each subject. RESULTS: The changes in the concentration of eotaxin (decrease after dexmedetomidine) and platelet-derived growth factor (PDGF, increase after propofol) were statistically significantly different between the groups. Significant changes were detected within both groups; the concentrations of monocyte chemotactic protein 1, chemokine ligand 27 and macrophage migration inhibitory factor were lower in both groups after the drug administration. Dexmedetomidine decreased the concentration of eotaxin, interleukin-18, interleukin-2Rα, stem cell factor, stem cell growth factor and vascular endothelial growth factor, and propofol decreased significantly the levels of hepatocyte growth factor, IFN-γ-induced protein 10 and monokine induced by IFN-γ, and increased the levels of interleukin-17, interleukin-5, interleukin-7 and PDGF. CONCLUSIONS: Dexmedetomidine seemed to have an immunosuppressive effect on the immune system whereas propofol seemed to induce mixed pro- and anti-inflammatory effects on the immune system. The choice of anesthetic agent could be relevant when treating patients with compromised immunological defense mechanisms. TRIAL REGISTRATION: Before subject enrollment, the study was registered in the European Clinical Trials database (EudraCT number 2013–001496-21, The Neural Mechanisms of Anesthesia and Human Consciousness) and in ClinicalTrials.gov (Principal Investigator: Harry Scheinin, number NCT01889004, The Neural Mechanisms of Anesthesia and Human Consciousness, Part 2, on the 23rd of June 2013).
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spelling pubmed-68944892019-12-11 The influence of dexmedetomidine and propofol on circulating cytokine levels in healthy subjects Kallioinen, Minna Scheinin, Annalotta Maksimow, Mikael Långsjö, Jaakko Kaisti, Kaike Takala, Riikka Vahlberg, Tero Valli, Katja Salmi, Marko Scheinin, Harry Maksimow, Anu BMC Anesthesiol Research Article BACKGROUND: Surgery and diseases modify inflammatory responses and the immune system. Anesthetic agents also have effects on the human immune system but the responses they induce may be altered or masked by the surgical procedures or underlying illnesses. The aim of this study was to assess how single-drug dexmedetomidine and propofol anesthesia without any surgical intervention alter acute immunological biomarkers in healthy subjects. METHODS: Thirty-five healthy, young male subjects were anesthetized using increasing concentrations of dexmedetomidine (n = 18) or propofol (n = 17) until loss of responsiveness (LOR) was detected. The treatment allocation was randomized. Multi-parametric immunoassays for the detection of 48 cytokines, chemokines and growth factors were used. Concentrations were determined at baseline and at the highest drug concentration for each subject. RESULTS: The changes in the concentration of eotaxin (decrease after dexmedetomidine) and platelet-derived growth factor (PDGF, increase after propofol) were statistically significantly different between the groups. Significant changes were detected within both groups; the concentrations of monocyte chemotactic protein 1, chemokine ligand 27 and macrophage migration inhibitory factor were lower in both groups after the drug administration. Dexmedetomidine decreased the concentration of eotaxin, interleukin-18, interleukin-2Rα, stem cell factor, stem cell growth factor and vascular endothelial growth factor, and propofol decreased significantly the levels of hepatocyte growth factor, IFN-γ-induced protein 10 and monokine induced by IFN-γ, and increased the levels of interleukin-17, interleukin-5, interleukin-7 and PDGF. CONCLUSIONS: Dexmedetomidine seemed to have an immunosuppressive effect on the immune system whereas propofol seemed to induce mixed pro- and anti-inflammatory effects on the immune system. The choice of anesthetic agent could be relevant when treating patients with compromised immunological defense mechanisms. TRIAL REGISTRATION: Before subject enrollment, the study was registered in the European Clinical Trials database (EudraCT number 2013–001496-21, The Neural Mechanisms of Anesthesia and Human Consciousness) and in ClinicalTrials.gov (Principal Investigator: Harry Scheinin, number NCT01889004, The Neural Mechanisms of Anesthesia and Human Consciousness, Part 2, on the 23rd of June 2013). BioMed Central 2019-12-05 /pmc/articles/PMC6894489/ /pubmed/31805854 http://dx.doi.org/10.1186/s12871-019-0895-3 Text en © The Author(s). 2019 Open AccessThis 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. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Kallioinen, Minna
Scheinin, Annalotta
Maksimow, Mikael
Långsjö, Jaakko
Kaisti, Kaike
Takala, Riikka
Vahlberg, Tero
Valli, Katja
Salmi, Marko
Scheinin, Harry
Maksimow, Anu
The influence of dexmedetomidine and propofol on circulating cytokine levels in healthy subjects
title The influence of dexmedetomidine and propofol on circulating cytokine levels in healthy subjects
title_full The influence of dexmedetomidine and propofol on circulating cytokine levels in healthy subjects
title_fullStr The influence of dexmedetomidine and propofol on circulating cytokine levels in healthy subjects
title_full_unstemmed The influence of dexmedetomidine and propofol on circulating cytokine levels in healthy subjects
title_short The influence of dexmedetomidine and propofol on circulating cytokine levels in healthy subjects
title_sort influence of dexmedetomidine and propofol on circulating cytokine levels in healthy subjects
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6894489/
https://www.ncbi.nlm.nih.gov/pubmed/31805854
http://dx.doi.org/10.1186/s12871-019-0895-3
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