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Optimizing intraluminal monofilament model of ischemic stroke in middle-aged Sprague–Dawley rats

Intraluminal monofilament model of middle cerebral artery occlusion (MCAO) is widely adopted for ischemic stroke; and Sprague–Dawley (SD) rats are commonly used rodents for preclinical research. Due to the paucity of information on the appropriate monofilament size for inducing MCAO in SD rats and t...

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Autores principales: Biose, I. J., Chastain, W. H., Wang, H., Ouvrier, B., Bix, G. J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9733327/
https://www.ncbi.nlm.nih.gov/pubmed/36494808
http://dx.doi.org/10.1186/s12868-022-00764-2
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author Biose, I. J.
Chastain, W. H.
Wang, H.
Ouvrier, B.
Bix, G. J.
author_facet Biose, I. J.
Chastain, W. H.
Wang, H.
Ouvrier, B.
Bix, G. J.
author_sort Biose, I. J.
collection PubMed
description Intraluminal monofilament model of middle cerebral artery occlusion (MCAO) is widely adopted for ischemic stroke; and Sprague–Dawley (SD) rats are commonly used rodents for preclinical research. Due to the paucity of information on the appropriate monofilament size for inducing MCAO in SD rats and the importance of including middle-aged models in ischemic stroke studies, we aimed to: (i). determine an appropriate Doccol(®) monofilament size for middle-aged male SD rats which weighed > 500 g following 24-h transient MCAO survival as well as (ii). demonstrate the optimal Doccol(®) filament size for middle-aged males (≤ 500 g) and females (273–300 g) while using young adult male SD rats (372–472 g) as control for severity of infarct volume following 7-days post-MCAO. All rats were subjected to 90-min transient MCAO. We show that 0.43 mm Doccol(®) monofilament size is more appropriate to induce large infarct lesion and optimal functional deficit when compared to 0.45 mm and 0.47 mm at 24 h post-MCAO. Our data on infarct volumes at 7 days post-MCAO as well as the observed weight loss and functional deficits at post-MCAO days 1, 3 and 7 demonstrate that 0.41 mm, 0.37 mm and 0.39 mm are optimal Doccol(®) filament sizes for middle-aged male (477.3 ± 39.61 g) and female (302.6 ± 26.28 g) as well as young-adult male (362.2 ± 28.38 g) SD rats, respectively.
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spelling pubmed-97333272022-12-10 Optimizing intraluminal monofilament model of ischemic stroke in middle-aged Sprague–Dawley rats Biose, I. J. Chastain, W. H. Wang, H. Ouvrier, B. Bix, G. J. BMC Neurosci Research Intraluminal monofilament model of middle cerebral artery occlusion (MCAO) is widely adopted for ischemic stroke; and Sprague–Dawley (SD) rats are commonly used rodents for preclinical research. Due to the paucity of information on the appropriate monofilament size for inducing MCAO in SD rats and the importance of including middle-aged models in ischemic stroke studies, we aimed to: (i). determine an appropriate Doccol(®) monofilament size for middle-aged male SD rats which weighed > 500 g following 24-h transient MCAO survival as well as (ii). demonstrate the optimal Doccol(®) filament size for middle-aged males (≤ 500 g) and females (273–300 g) while using young adult male SD rats (372–472 g) as control for severity of infarct volume following 7-days post-MCAO. All rats were subjected to 90-min transient MCAO. We show that 0.43 mm Doccol(®) monofilament size is more appropriate to induce large infarct lesion and optimal functional deficit when compared to 0.45 mm and 0.47 mm at 24 h post-MCAO. Our data on infarct volumes at 7 days post-MCAO as well as the observed weight loss and functional deficits at post-MCAO days 1, 3 and 7 demonstrate that 0.41 mm, 0.37 mm and 0.39 mm are optimal Doccol(®) filament sizes for middle-aged male (477.3 ± 39.61 g) and female (302.6 ± 26.28 g) as well as young-adult male (362.2 ± 28.38 g) SD rats, respectively. BioMed Central 2022-12-09 /pmc/articles/PMC9733327/ /pubmed/36494808 http://dx.doi.org/10.1186/s12868-022-00764-2 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Biose, I. J.
Chastain, W. H.
Wang, H.
Ouvrier, B.
Bix, G. J.
Optimizing intraluminal monofilament model of ischemic stroke in middle-aged Sprague–Dawley rats
title Optimizing intraluminal monofilament model of ischemic stroke in middle-aged Sprague–Dawley rats
title_full Optimizing intraluminal monofilament model of ischemic stroke in middle-aged Sprague–Dawley rats
title_fullStr Optimizing intraluminal monofilament model of ischemic stroke in middle-aged Sprague–Dawley rats
title_full_unstemmed Optimizing intraluminal monofilament model of ischemic stroke in middle-aged Sprague–Dawley rats
title_short Optimizing intraluminal monofilament model of ischemic stroke in middle-aged Sprague–Dawley rats
title_sort optimizing intraluminal monofilament model of ischemic stroke in middle-aged sprague–dawley rats
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9733327/
https://www.ncbi.nlm.nih.gov/pubmed/36494808
http://dx.doi.org/10.1186/s12868-022-00764-2
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