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A Method for Generate a Mouse Model of Stroke: Evaluation of Parameters for Blood Flow, Behavior, and Survival

Stroke is one of the common causes of death and disability. Despite extensive efforts in stroke research, therapeutic options for improving the functional recovery remain limited in clinical practice. Experimental stroke models using genetically modified mice could aid in unraveling the complex path...

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Autores principales: Park, Sin-Young, Marasini, Subash, Kim, Geu-Hee, Ku, Taeyun, Choi, Chulhee, Park, Min-Young, Kim, Eun-Hee, Lee, Young-Don, Suh-Kim, Haeyoung, Kim, Sung-Soo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society for Brain and Neural Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3984953/
https://www.ncbi.nlm.nih.gov/pubmed/24737945
http://dx.doi.org/10.5607/en.2014.23.1.104
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author Park, Sin-Young
Marasini, Subash
Kim, Geu-Hee
Ku, Taeyun
Choi, Chulhee
Park, Min-Young
Kim, Eun-Hee
Lee, Young-Don
Suh-Kim, Haeyoung
Kim, Sung-Soo
author_facet Park, Sin-Young
Marasini, Subash
Kim, Geu-Hee
Ku, Taeyun
Choi, Chulhee
Park, Min-Young
Kim, Eun-Hee
Lee, Young-Don
Suh-Kim, Haeyoung
Kim, Sung-Soo
author_sort Park, Sin-Young
collection PubMed
description Stroke is one of the common causes of death and disability. Despite extensive efforts in stroke research, therapeutic options for improving the functional recovery remain limited in clinical practice. Experimental stroke models using genetically modified mice could aid in unraveling the complex pathophysiology triggered by ischemic brain injury. Here, we optimized the procedure for generating mouse stroke model using an intraluminal suture in the middle cerebral artery and verified the blockage of blood flow using indocyanine green coupled with near infra-red radiation. The first week after the ischemic injury was critical for survivability. The survival rate of 11% in mice without any treatment but increased to 60% on administering prophylactic antibiotics. During this period, mice showed severe functional impairment but recovered spontaneously starting from the second week onward. Among the various behavioral tests, the pole tests and neurological severity score tests remained reliable up to 4 weeks after ischemia, whereas the rotarod and corner tests became less sensitive for assessing the severity of ischemic injury with time. Further, loss of body weight was also observed for up 4 weeks after ischemia induction. In conclusion, we have developed an improved approach which allows us to investigate the role of the cell death-related genes in the disease progression using genetically modified mice and to evaluate the modes of action of candidate drugs.
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spelling pubmed-39849532014-04-15 A Method for Generate a Mouse Model of Stroke: Evaluation of Parameters for Blood Flow, Behavior, and Survival Park, Sin-Young Marasini, Subash Kim, Geu-Hee Ku, Taeyun Choi, Chulhee Park, Min-Young Kim, Eun-Hee Lee, Young-Don Suh-Kim, Haeyoung Kim, Sung-Soo Exp Neurobiol Original Article Stroke is one of the common causes of death and disability. Despite extensive efforts in stroke research, therapeutic options for improving the functional recovery remain limited in clinical practice. Experimental stroke models using genetically modified mice could aid in unraveling the complex pathophysiology triggered by ischemic brain injury. Here, we optimized the procedure for generating mouse stroke model using an intraluminal suture in the middle cerebral artery and verified the blockage of blood flow using indocyanine green coupled with near infra-red radiation. The first week after the ischemic injury was critical for survivability. The survival rate of 11% in mice without any treatment but increased to 60% on administering prophylactic antibiotics. During this period, mice showed severe functional impairment but recovered spontaneously starting from the second week onward. Among the various behavioral tests, the pole tests and neurological severity score tests remained reliable up to 4 weeks after ischemia, whereas the rotarod and corner tests became less sensitive for assessing the severity of ischemic injury with time. Further, loss of body weight was also observed for up 4 weeks after ischemia induction. In conclusion, we have developed an improved approach which allows us to investigate the role of the cell death-related genes in the disease progression using genetically modified mice and to evaluate the modes of action of candidate drugs. The Korean Society for Brain and Neural Science 2014-03 2014-03-27 /pmc/articles/PMC3984953/ /pubmed/24737945 http://dx.doi.org/10.5607/en.2014.23.1.104 Text en Copyright © Experimental Neurobiology 2014. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Park, Sin-Young
Marasini, Subash
Kim, Geu-Hee
Ku, Taeyun
Choi, Chulhee
Park, Min-Young
Kim, Eun-Hee
Lee, Young-Don
Suh-Kim, Haeyoung
Kim, Sung-Soo
A Method for Generate a Mouse Model of Stroke: Evaluation of Parameters for Blood Flow, Behavior, and Survival
title A Method for Generate a Mouse Model of Stroke: Evaluation of Parameters for Blood Flow, Behavior, and Survival
title_full A Method for Generate a Mouse Model of Stroke: Evaluation of Parameters for Blood Flow, Behavior, and Survival
title_fullStr A Method for Generate a Mouse Model of Stroke: Evaluation of Parameters for Blood Flow, Behavior, and Survival
title_full_unstemmed A Method for Generate a Mouse Model of Stroke: Evaluation of Parameters for Blood Flow, Behavior, and Survival
title_short A Method for Generate a Mouse Model of Stroke: Evaluation of Parameters for Blood Flow, Behavior, and Survival
title_sort method for generate a mouse model of stroke: evaluation of parameters for blood flow, behavior, and survival
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3984953/
https://www.ncbi.nlm.nih.gov/pubmed/24737945
http://dx.doi.org/10.5607/en.2014.23.1.104
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