Cargando…

The effect of venovenous extra-corporeal membrane oxygenation (ECMO) therapy on immune inflammatory response of cerebral tissues in porcine model

BACKGROUND: Extra-Corporeal Membrane Oxygenation (ECMO) therapy is associated with high risk of neurologic injury. But the mechanism of neurologic injury during and/or after ECMO therapy is still unclear. Recent animal experiments confirmed that ECMO treatment increases the immune inflammatory respo...

Descripción completa

Detalles Bibliográficos
Autores principales: Chen, Qiyi, Yu, Wenkui, Shi, Jiangliang, Shen, Juanhong, Hu, Yimin, Gao, Tao, Zhang, Juanjuan, Xi, Fengchan, Gong, Jianfeng, Li, Jieshou, Li, Ning
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3766192/
https://www.ncbi.nlm.nih.gov/pubmed/23985062
http://dx.doi.org/10.1186/1749-8090-8-186
_version_ 1782283484283273216
author Chen, Qiyi
Yu, Wenkui
Shi, Jiangliang
Shen, Juanhong
Hu, Yimin
Gao, Tao
Zhang, Juanjuan
Xi, Fengchan
Gong, Jianfeng
Li, Jieshou
Li, Ning
author_facet Chen, Qiyi
Yu, Wenkui
Shi, Jiangliang
Shen, Juanhong
Hu, Yimin
Gao, Tao
Zhang, Juanjuan
Xi, Fengchan
Gong, Jianfeng
Li, Jieshou
Li, Ning
author_sort Chen, Qiyi
collection PubMed
description BACKGROUND: Extra-Corporeal Membrane Oxygenation (ECMO) therapy is associated with high risk of neurologic injury. But the mechanism of neurologic injury during and/or after ECMO therapy is still unclear. Recent animal experiments confirmed that ECMO treatment increases the immune inflammatory response. The aim of this study is to investigate the effect of VV- ECMO on immune inflammatory response of cerebral tissues and neurological impairment. METHODS: 18 porcine were randomly divided into control, sham and ECMO group (n = 6/group). ECMO was run 24 h in the ECMO group, and serum collected at 0, 2, 6, 12 and 24 h during ECMO treatment for the analysis of cytokine (IL-1β, IL-6, IL-10, TNF-a) and cerebral injury specific biomarker S100B and NSE. After 24 h ECMO treatment, all animals were euthanized and cerebral tissues (hypothalamus, hippocampus and cortex) were collected for measure of mRNA and protein levels of cytokine (IL-1β, IL-6, IL-10, TNF-a). RESULTS: The results during ECMO treatment showed that all the pro-inflammation cytokines were increased significantly after 2 h, and anti-inflammation IL-10 showed transient hoist in the first 2 h in serum. After 24 h ECMO therapy, the mRNA levels of pro-inflammation cytokines and anti-inflammation IL-10 were simultaneously up-regulated in cerebral tissues (hypothalamus, hippocampus and cortex). And protein concentrations also showed different increasing levels in cerebral tissues. However, during the ECMO treatment, S100B and NSE protein in serum did not change significantly. CONCLUSION: These findings suggest VV-ECMO treatment can not only lead to immune inflammatory response in blood, but can also produce immune and inflammatory response in cerebral tissues. However the extent of immune inflammation was not sufficient to cause significant neurological impairment in this study. But the correlation between cerebral inflammatory response and cerebral impairment need to further explore.
format Online
Article
Text
id pubmed-3766192
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-37661922013-09-08 The effect of venovenous extra-corporeal membrane oxygenation (ECMO) therapy on immune inflammatory response of cerebral tissues in porcine model Chen, Qiyi Yu, Wenkui Shi, Jiangliang Shen, Juanhong Hu, Yimin Gao, Tao Zhang, Juanjuan Xi, Fengchan Gong, Jianfeng Li, Jieshou Li, Ning J Cardiothorac Surg Research Article BACKGROUND: Extra-Corporeal Membrane Oxygenation (ECMO) therapy is associated with high risk of neurologic injury. But the mechanism of neurologic injury during and/or after ECMO therapy is still unclear. Recent animal experiments confirmed that ECMO treatment increases the immune inflammatory response. The aim of this study is to investigate the effect of VV- ECMO on immune inflammatory response of cerebral tissues and neurological impairment. METHODS: 18 porcine were randomly divided into control, sham and ECMO group (n = 6/group). ECMO was run 24 h in the ECMO group, and serum collected at 0, 2, 6, 12 and 24 h during ECMO treatment for the analysis of cytokine (IL-1β, IL-6, IL-10, TNF-a) and cerebral injury specific biomarker S100B and NSE. After 24 h ECMO treatment, all animals were euthanized and cerebral tissues (hypothalamus, hippocampus and cortex) were collected for measure of mRNA and protein levels of cytokine (IL-1β, IL-6, IL-10, TNF-a). RESULTS: The results during ECMO treatment showed that all the pro-inflammation cytokines were increased significantly after 2 h, and anti-inflammation IL-10 showed transient hoist in the first 2 h in serum. After 24 h ECMO therapy, the mRNA levels of pro-inflammation cytokines and anti-inflammation IL-10 were simultaneously up-regulated in cerebral tissues (hypothalamus, hippocampus and cortex). And protein concentrations also showed different increasing levels in cerebral tissues. However, during the ECMO treatment, S100B and NSE protein in serum did not change significantly. CONCLUSION: These findings suggest VV-ECMO treatment can not only lead to immune inflammatory response in blood, but can also produce immune and inflammatory response in cerebral tissues. However the extent of immune inflammation was not sufficient to cause significant neurological impairment in this study. But the correlation between cerebral inflammatory response and cerebral impairment need to further explore. BioMed Central 2013-08-29 /pmc/articles/PMC3766192/ /pubmed/23985062 http://dx.doi.org/10.1186/1749-8090-8-186 Text en Copyright © 2013 Chen et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Chen, Qiyi
Yu, Wenkui
Shi, Jiangliang
Shen, Juanhong
Hu, Yimin
Gao, Tao
Zhang, Juanjuan
Xi, Fengchan
Gong, Jianfeng
Li, Jieshou
Li, Ning
The effect of venovenous extra-corporeal membrane oxygenation (ECMO) therapy on immune inflammatory response of cerebral tissues in porcine model
title The effect of venovenous extra-corporeal membrane oxygenation (ECMO) therapy on immune inflammatory response of cerebral tissues in porcine model
title_full The effect of venovenous extra-corporeal membrane oxygenation (ECMO) therapy on immune inflammatory response of cerebral tissues in porcine model
title_fullStr The effect of venovenous extra-corporeal membrane oxygenation (ECMO) therapy on immune inflammatory response of cerebral tissues in porcine model
title_full_unstemmed The effect of venovenous extra-corporeal membrane oxygenation (ECMO) therapy on immune inflammatory response of cerebral tissues in porcine model
title_short The effect of venovenous extra-corporeal membrane oxygenation (ECMO) therapy on immune inflammatory response of cerebral tissues in porcine model
title_sort effect of venovenous extra-corporeal membrane oxygenation (ecmo) therapy on immune inflammatory response of cerebral tissues in porcine model
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3766192/
https://www.ncbi.nlm.nih.gov/pubmed/23985062
http://dx.doi.org/10.1186/1749-8090-8-186
work_keys_str_mv AT chenqiyi theeffectofvenovenousextracorporealmembraneoxygenationecmotherapyonimmuneinflammatoryresponseofcerebraltissuesinporcinemodel
AT yuwenkui theeffectofvenovenousextracorporealmembraneoxygenationecmotherapyonimmuneinflammatoryresponseofcerebraltissuesinporcinemodel
AT shijiangliang theeffectofvenovenousextracorporealmembraneoxygenationecmotherapyonimmuneinflammatoryresponseofcerebraltissuesinporcinemodel
AT shenjuanhong theeffectofvenovenousextracorporealmembraneoxygenationecmotherapyonimmuneinflammatoryresponseofcerebraltissuesinporcinemodel
AT huyimin theeffectofvenovenousextracorporealmembraneoxygenationecmotherapyonimmuneinflammatoryresponseofcerebraltissuesinporcinemodel
AT gaotao theeffectofvenovenousextracorporealmembraneoxygenationecmotherapyonimmuneinflammatoryresponseofcerebraltissuesinporcinemodel
AT zhangjuanjuan theeffectofvenovenousextracorporealmembraneoxygenationecmotherapyonimmuneinflammatoryresponseofcerebraltissuesinporcinemodel
AT xifengchan theeffectofvenovenousextracorporealmembraneoxygenationecmotherapyonimmuneinflammatoryresponseofcerebraltissuesinporcinemodel
AT gongjianfeng theeffectofvenovenousextracorporealmembraneoxygenationecmotherapyonimmuneinflammatoryresponseofcerebraltissuesinporcinemodel
AT lijieshou theeffectofvenovenousextracorporealmembraneoxygenationecmotherapyonimmuneinflammatoryresponseofcerebraltissuesinporcinemodel
AT lining theeffectofvenovenousextracorporealmembraneoxygenationecmotherapyonimmuneinflammatoryresponseofcerebraltissuesinporcinemodel
AT chenqiyi effectofvenovenousextracorporealmembraneoxygenationecmotherapyonimmuneinflammatoryresponseofcerebraltissuesinporcinemodel
AT yuwenkui effectofvenovenousextracorporealmembraneoxygenationecmotherapyonimmuneinflammatoryresponseofcerebraltissuesinporcinemodel
AT shijiangliang effectofvenovenousextracorporealmembraneoxygenationecmotherapyonimmuneinflammatoryresponseofcerebraltissuesinporcinemodel
AT shenjuanhong effectofvenovenousextracorporealmembraneoxygenationecmotherapyonimmuneinflammatoryresponseofcerebraltissuesinporcinemodel
AT huyimin effectofvenovenousextracorporealmembraneoxygenationecmotherapyonimmuneinflammatoryresponseofcerebraltissuesinporcinemodel
AT gaotao effectofvenovenousextracorporealmembraneoxygenationecmotherapyonimmuneinflammatoryresponseofcerebraltissuesinporcinemodel
AT zhangjuanjuan effectofvenovenousextracorporealmembraneoxygenationecmotherapyonimmuneinflammatoryresponseofcerebraltissuesinporcinemodel
AT xifengchan effectofvenovenousextracorporealmembraneoxygenationecmotherapyonimmuneinflammatoryresponseofcerebraltissuesinporcinemodel
AT gongjianfeng effectofvenovenousextracorporealmembraneoxygenationecmotherapyonimmuneinflammatoryresponseofcerebraltissuesinporcinemodel
AT lijieshou effectofvenovenousextracorporealmembraneoxygenationecmotherapyonimmuneinflammatoryresponseofcerebraltissuesinporcinemodel
AT lining effectofvenovenousextracorporealmembraneoxygenationecmotherapyonimmuneinflammatoryresponseofcerebraltissuesinporcinemodel