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A rabbit model for embolic infarct potentials of injectables using ultrasound-guided carotid artery puncture
In order to evaluate the in vivo thrombogenicity of injectable agents, a suitable animal model is needed. We introduce an ultrasound-guided non-selective cerebral artery occlusion model via the common carotid arteries of rabbits. A total of 30 rabbits were assigned to an experimental group (n = 20)...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9649683/ https://www.ncbi.nlm.nih.gov/pubmed/36357516 http://dx.doi.org/10.1038/s41598-022-21896-9 |
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author | Seo, Jiwoon Lee, Joon Woo Cho, Jungheum Lee, Eugene Kang, Heung Sik |
author_facet | Seo, Jiwoon Lee, Joon Woo Cho, Jungheum Lee, Eugene Kang, Heung Sik |
author_sort | Seo, Jiwoon |
collection | PubMed |
description | In order to evaluate the in vivo thrombogenicity of injectable agents, a suitable animal model is needed. We introduce an ultrasound-guided non-selective cerebral artery occlusion model via the common carotid arteries of rabbits. A total of 30 rabbits were assigned to an experimental group (n = 20) and a control group (n = 10). Each group received 2 mL suspension of embolic agent or 2 mL of normal saline, respectively, under ultrasound guidance. The animals were observed for immediate reaction and underwent magnetic resonance imaging (MRI) scan. Follow-up neurologic examination was conducted 24 h following the procedure. In 7 of the 30 rabbits, 2 in the control group and 5 in the experimental group, the administration of either normal saline or the embolic agent failed. Among the successfully injected 15 experimental animals, 14 showed neurologic impairment or deceased, whereas 1 animal did not show significant neurologic deficit. The MRI of 4 experimental animals showed detectable cerebral infarction on diffusion-weighted imaging. None of the 8 control animals showed neurologic abnormality and their brain MRI was normal. Our minimally invasive model is technically feasible and competent to show thrombogenecity of an injectable agent and consequent in vivo neurologic outcome. |
format | Online Article Text |
id | pubmed-9649683 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-96496832022-11-15 A rabbit model for embolic infarct potentials of injectables using ultrasound-guided carotid artery puncture Seo, Jiwoon Lee, Joon Woo Cho, Jungheum Lee, Eugene Kang, Heung Sik Sci Rep Article In order to evaluate the in vivo thrombogenicity of injectable agents, a suitable animal model is needed. We introduce an ultrasound-guided non-selective cerebral artery occlusion model via the common carotid arteries of rabbits. A total of 30 rabbits were assigned to an experimental group (n = 20) and a control group (n = 10). Each group received 2 mL suspension of embolic agent or 2 mL of normal saline, respectively, under ultrasound guidance. The animals were observed for immediate reaction and underwent magnetic resonance imaging (MRI) scan. Follow-up neurologic examination was conducted 24 h following the procedure. In 7 of the 30 rabbits, 2 in the control group and 5 in the experimental group, the administration of either normal saline or the embolic agent failed. Among the successfully injected 15 experimental animals, 14 showed neurologic impairment or deceased, whereas 1 animal did not show significant neurologic deficit. The MRI of 4 experimental animals showed detectable cerebral infarction on diffusion-weighted imaging. None of the 8 control animals showed neurologic abnormality and their brain MRI was normal. Our minimally invasive model is technically feasible and competent to show thrombogenecity of an injectable agent and consequent in vivo neurologic outcome. Nature Publishing Group UK 2022-11-10 /pmc/articles/PMC9649683/ /pubmed/36357516 http://dx.doi.org/10.1038/s41598-022-21896-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This 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/) . |
spellingShingle | Article Seo, Jiwoon Lee, Joon Woo Cho, Jungheum Lee, Eugene Kang, Heung Sik A rabbit model for embolic infarct potentials of injectables using ultrasound-guided carotid artery puncture |
title | A rabbit model for embolic infarct potentials of injectables using ultrasound-guided carotid artery puncture |
title_full | A rabbit model for embolic infarct potentials of injectables using ultrasound-guided carotid artery puncture |
title_fullStr | A rabbit model for embolic infarct potentials of injectables using ultrasound-guided carotid artery puncture |
title_full_unstemmed | A rabbit model for embolic infarct potentials of injectables using ultrasound-guided carotid artery puncture |
title_short | A rabbit model for embolic infarct potentials of injectables using ultrasound-guided carotid artery puncture |
title_sort | rabbit model for embolic infarct potentials of injectables using ultrasound-guided carotid artery puncture |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9649683/ https://www.ncbi.nlm.nih.gov/pubmed/36357516 http://dx.doi.org/10.1038/s41598-022-21896-9 |
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