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Comparison of humoral neuroinflammation and adhesion molecule expression in two models of experimental intracerebral hemorrhage

BACKGROUND: Inflammatory cascades contribute to secondary injury after intracerebral hemorrhage (ICH) via humoral factors and cell-mediated cytotoxicity. Several experimental models were previously developed to analyze post-hemorrhagic neuroinflammation. However, neuroinflammatory markers have not b...

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Autores principales: Liesz, Arthur, Middelhoff, Moritz, Zhou, Wei, Karcher, Simone, Illanes, Sergio, Veltkamp, Roland
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3195108/
https://www.ncbi.nlm.nih.gov/pubmed/21967730
http://dx.doi.org/10.1186/2040-7378-3-11
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author Liesz, Arthur
Middelhoff, Moritz
Zhou, Wei
Karcher, Simone
Illanes, Sergio
Veltkamp, Roland
author_facet Liesz, Arthur
Middelhoff, Moritz
Zhou, Wei
Karcher, Simone
Illanes, Sergio
Veltkamp, Roland
author_sort Liesz, Arthur
collection PubMed
description BACKGROUND: Inflammatory cascades contribute to secondary injury after intracerebral hemorrhage (ICH) via humoral factors and cell-mediated cytotoxicity. Several experimental models were previously developed to analyze post-hemorrhagic neuroinflammation. However, neuroinflammatory markers have not been compared face-to-face between these models so far, and therefore, pathophysiological conclusions drawn from only one individual model may not be valid. METHODS: We compared neuroinflammatory pathways in the two most common murine models: striatal injection of autologous blood or collagenase. Expression of pro- and anti-inflammatory cytokines (IL-1, TNF-α, IFN-γ, IL-6, TGF-β and IL-10) as well adhesion molecule expression (VCAM-1, ICAM-1) was analyzed by RT-PCR at several time points after ICH induction. Outcome and physiological parameters were compared between the models. RESULTS: Both models induced a profound and dynamic increase in the expression of pro-inflammatory cytokines and adhesion molecules. However, blood injection resulted in significantly more pronounced alteration of these markers than collagenase injection. This difference was associated with worse outcome after blood injection compared to the collagenase model despite equal ICH volumes. CONCLUSIONS: This is the first study performing a face-to-face comparison of neuroinflammatory pathways in the two most widely used murine ICH models, revealing substantial differences between the models. This discrepancies need to be taken into account in designing future studies employing experimental ICH models, especially when analyzing neuroinflammatory pathways and therapies.
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spelling pubmed-31951082011-10-18 Comparison of humoral neuroinflammation and adhesion molecule expression in two models of experimental intracerebral hemorrhage Liesz, Arthur Middelhoff, Moritz Zhou, Wei Karcher, Simone Illanes, Sergio Veltkamp, Roland Exp Transl Stroke Med Research BACKGROUND: Inflammatory cascades contribute to secondary injury after intracerebral hemorrhage (ICH) via humoral factors and cell-mediated cytotoxicity. Several experimental models were previously developed to analyze post-hemorrhagic neuroinflammation. However, neuroinflammatory markers have not been compared face-to-face between these models so far, and therefore, pathophysiological conclusions drawn from only one individual model may not be valid. METHODS: We compared neuroinflammatory pathways in the two most common murine models: striatal injection of autologous blood or collagenase. Expression of pro- and anti-inflammatory cytokines (IL-1, TNF-α, IFN-γ, IL-6, TGF-β and IL-10) as well adhesion molecule expression (VCAM-1, ICAM-1) was analyzed by RT-PCR at several time points after ICH induction. Outcome and physiological parameters were compared between the models. RESULTS: Both models induced a profound and dynamic increase in the expression of pro-inflammatory cytokines and adhesion molecules. However, blood injection resulted in significantly more pronounced alteration of these markers than collagenase injection. This difference was associated with worse outcome after blood injection compared to the collagenase model despite equal ICH volumes. CONCLUSIONS: This is the first study performing a face-to-face comparison of neuroinflammatory pathways in the two most widely used murine ICH models, revealing substantial differences between the models. This discrepancies need to be taken into account in designing future studies employing experimental ICH models, especially when analyzing neuroinflammatory pathways and therapies. BioMed Central 2011-10-03 /pmc/articles/PMC3195108/ /pubmed/21967730 http://dx.doi.org/10.1186/2040-7378-3-11 Text en Copyright ©2011 Liesz 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
Liesz, Arthur
Middelhoff, Moritz
Zhou, Wei
Karcher, Simone
Illanes, Sergio
Veltkamp, Roland
Comparison of humoral neuroinflammation and adhesion molecule expression in two models of experimental intracerebral hemorrhage
title Comparison of humoral neuroinflammation and adhesion molecule expression in two models of experimental intracerebral hemorrhage
title_full Comparison of humoral neuroinflammation and adhesion molecule expression in two models of experimental intracerebral hemorrhage
title_fullStr Comparison of humoral neuroinflammation and adhesion molecule expression in two models of experimental intracerebral hemorrhage
title_full_unstemmed Comparison of humoral neuroinflammation and adhesion molecule expression in two models of experimental intracerebral hemorrhage
title_short Comparison of humoral neuroinflammation and adhesion molecule expression in two models of experimental intracerebral hemorrhage
title_sort comparison of humoral neuroinflammation and adhesion molecule expression in two models of experimental intracerebral hemorrhage
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3195108/
https://www.ncbi.nlm.nih.gov/pubmed/21967730
http://dx.doi.org/10.1186/2040-7378-3-11
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