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Novel Modification of Potassium Chloride Induced Cardiac Arrest Model for Aged Mice

Experimental cardiac arrest (CA) in aging research is infrequently studied in part due to the limitation of animal models. We aimed to develop an easily performed mouse CA model to meet this need. A standard mouse KCl-induced CA model using chest compressions and intravenous epinephrine for resuscit...

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Autores principales: Liu, Huaqin, Yu, Zhui, Li, Ying, Xu, Bin, Yan, Baihui, Paschen, Wulf, Warner, David S, Yang, Wei, Sheng, Huaxin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: JKL International LLC 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5772856/
https://www.ncbi.nlm.nih.gov/pubmed/29392079
http://dx.doi.org/10.14336/AD.2017.0221
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author Liu, Huaqin
Yu, Zhui
Li, Ying
Xu, Bin
Yan, Baihui
Paschen, Wulf
Warner, David S
Yang, Wei
Sheng, Huaxin
author_facet Liu, Huaqin
Yu, Zhui
Li, Ying
Xu, Bin
Yan, Baihui
Paschen, Wulf
Warner, David S
Yang, Wei
Sheng, Huaxin
author_sort Liu, Huaqin
collection PubMed
description Experimental cardiac arrest (CA) in aging research is infrequently studied in part due to the limitation of animal models. We aimed to develop an easily performed mouse CA model to meet this need. A standard mouse KCl-induced CA model using chest compressions and intravenous epinephrine for resuscitation was modified by blood withdrawal prior to CA onset, so as to decrease the requisite KCl dose to induce CA by decreasing the circulating blood volume. The modification was then compared to the standard model in young adult mice subjected to 8 min CA. 22-month old mice were then subjected to 8 min CA, resuscitated, and compared to young adult mice. Post-CA functional recovery was evaluated by measuring spontaneous locomotor activity pre-injury, and on post-CA days 1, 2, and 3. Neurological score and brain histology were examined on day 3. Brain elF2α phosphorylation levels were measured at 1 h to verify tissue stress. Compared to the standard model, the modification decreased cardiopulmonary resuscitation duration and increased 3-day survival in young mice. For aged mice, survival was 100 % at 24 h and 54% at 72 h. Neurological deficit was present 3 days post-CA, although more severe versus young mice. Mild neuronal necrosis was present in the cortex and hippocampus. The modified model markedly induced elF2α phosphorylation in both age groups. This modified procedure makes the CA model feasible in aged mice and provides a practical platform for understanding injury mechanisms and developing therapeutics for elderly patients.
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spelling pubmed-57728562018-02-02 Novel Modification of Potassium Chloride Induced Cardiac Arrest Model for Aged Mice Liu, Huaqin Yu, Zhui Li, Ying Xu, Bin Yan, Baihui Paschen, Wulf Warner, David S Yang, Wei Sheng, Huaxin Aging Dis Orginal Article Experimental cardiac arrest (CA) in aging research is infrequently studied in part due to the limitation of animal models. We aimed to develop an easily performed mouse CA model to meet this need. A standard mouse KCl-induced CA model using chest compressions and intravenous epinephrine for resuscitation was modified by blood withdrawal prior to CA onset, so as to decrease the requisite KCl dose to induce CA by decreasing the circulating blood volume. The modification was then compared to the standard model in young adult mice subjected to 8 min CA. 22-month old mice were then subjected to 8 min CA, resuscitated, and compared to young adult mice. Post-CA functional recovery was evaluated by measuring spontaneous locomotor activity pre-injury, and on post-CA days 1, 2, and 3. Neurological score and brain histology were examined on day 3. Brain elF2α phosphorylation levels were measured at 1 h to verify tissue stress. Compared to the standard model, the modification decreased cardiopulmonary resuscitation duration and increased 3-day survival in young mice. For aged mice, survival was 100 % at 24 h and 54% at 72 h. Neurological deficit was present 3 days post-CA, although more severe versus young mice. Mild neuronal necrosis was present in the cortex and hippocampus. The modified model markedly induced elF2α phosphorylation in both age groups. This modified procedure makes the CA model feasible in aged mice and provides a practical platform for understanding injury mechanisms and developing therapeutics for elderly patients. JKL International LLC 2018-02-01 /pmc/articles/PMC5772856/ /pubmed/29392079 http://dx.doi.org/10.14336/AD.2017.0221 Text en Copyright: © 2017 Liu et al. http://creativecommons.org/licenses/by/2.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Orginal Article
Liu, Huaqin
Yu, Zhui
Li, Ying
Xu, Bin
Yan, Baihui
Paschen, Wulf
Warner, David S
Yang, Wei
Sheng, Huaxin
Novel Modification of Potassium Chloride Induced Cardiac Arrest Model for Aged Mice
title Novel Modification of Potassium Chloride Induced Cardiac Arrest Model for Aged Mice
title_full Novel Modification of Potassium Chloride Induced Cardiac Arrest Model for Aged Mice
title_fullStr Novel Modification of Potassium Chloride Induced Cardiac Arrest Model for Aged Mice
title_full_unstemmed Novel Modification of Potassium Chloride Induced Cardiac Arrest Model for Aged Mice
title_short Novel Modification of Potassium Chloride Induced Cardiac Arrest Model for Aged Mice
title_sort novel modification of potassium chloride induced cardiac arrest model for aged mice
topic Orginal Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5772856/
https://www.ncbi.nlm.nih.gov/pubmed/29392079
http://dx.doi.org/10.14336/AD.2017.0221
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