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Pathology of non-thermal irreversible electroporation (N-TIRE)-induced ablation of the canine brain
This study describes the neuropathologic features of normal canine brain ablated with non-thermal irreversible electroporation (N-TIRE). The parietal cerebral cortices of four dogs were treated with N-TIRE using a dose-escalation protocol with an additional dog receiving sham treatment. Animals were...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Society of Veterinary Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3885737/ https://www.ncbi.nlm.nih.gov/pubmed/23820168 http://dx.doi.org/10.4142/jvs.2013.14.4.433 |
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author | Rossmeisl, John H. Garcia, Paulo A. Roberston, John L. Ellis, Thomas L. Davalos, Rafael V. |
author_facet | Rossmeisl, John H. Garcia, Paulo A. Roberston, John L. Ellis, Thomas L. Davalos, Rafael V. |
author_sort | Rossmeisl, John H. |
collection | PubMed |
description | This study describes the neuropathologic features of normal canine brain ablated with non-thermal irreversible electroporation (N-TIRE). The parietal cerebral cortices of four dogs were treated with N-TIRE using a dose-escalation protocol with an additional dog receiving sham treatment. Animals were allowed to recover following N-TIRE ablation and the effects of treatment were monitored with clinical and magnetic resonance imaging examinations. Brains were subjected to histopathologic and ultrastructural assessment along with Bcl-2, caspase-3, and caspase-9 immunohistochemical staining following sacrifice 72 h post-treatment. Adverse clinical effects of N-TIRE were only observed in the dog treated at the upper energy tier. MRI and neuropathologic examinations indicated that N-TIRE ablation resulted in focal regions of severe cytoarchitectural and blood-brain-barrier disruption. Lesion size correlated to the intensity of the applied electrical field. N-TIRE-induced lesions were characterized by parenchymal necrosis and hemorrhage; however, large blood vessels were preserved. A transition zone containing parenchymal edema, perivascular inflammatory cuffs, and reactive gliosis was interspersed between the necrotic focus and normal neuropil. Apoptotic labeling indices were not different between the N-TIRE-treated and control brains. This study identified N-TIRE pulse parameters that can be used to safely create circumscribed foci of brain necrosis while selectively preserving major vascular structures. |
format | Online Article Text |
id | pubmed-3885737 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | The Korean Society of Veterinary Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-38857372014-01-13 Pathology of non-thermal irreversible electroporation (N-TIRE)-induced ablation of the canine brain Rossmeisl, John H. Garcia, Paulo A. Roberston, John L. Ellis, Thomas L. Davalos, Rafael V. J Vet Sci Original Article This study describes the neuropathologic features of normal canine brain ablated with non-thermal irreversible electroporation (N-TIRE). The parietal cerebral cortices of four dogs were treated with N-TIRE using a dose-escalation protocol with an additional dog receiving sham treatment. Animals were allowed to recover following N-TIRE ablation and the effects of treatment were monitored with clinical and magnetic resonance imaging examinations. Brains were subjected to histopathologic and ultrastructural assessment along with Bcl-2, caspase-3, and caspase-9 immunohistochemical staining following sacrifice 72 h post-treatment. Adverse clinical effects of N-TIRE were only observed in the dog treated at the upper energy tier. MRI and neuropathologic examinations indicated that N-TIRE ablation resulted in focal regions of severe cytoarchitectural and blood-brain-barrier disruption. Lesion size correlated to the intensity of the applied electrical field. N-TIRE-induced lesions were characterized by parenchymal necrosis and hemorrhage; however, large blood vessels were preserved. A transition zone containing parenchymal edema, perivascular inflammatory cuffs, and reactive gliosis was interspersed between the necrotic focus and normal neuropil. Apoptotic labeling indices were not different between the N-TIRE-treated and control brains. This study identified N-TIRE pulse parameters that can be used to safely create circumscribed foci of brain necrosis while selectively preserving major vascular structures. The Korean Society of Veterinary Science 2013-12 2013-12-19 /pmc/articles/PMC3885737/ /pubmed/23820168 http://dx.doi.org/10.4142/jvs.2013.14.4.433 Text en © 2013 The Korean Society of Veterinary Science. 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 Rossmeisl, John H. Garcia, Paulo A. Roberston, John L. Ellis, Thomas L. Davalos, Rafael V. Pathology of non-thermal irreversible electroporation (N-TIRE)-induced ablation of the canine brain |
title | Pathology of non-thermal irreversible electroporation (N-TIRE)-induced ablation of the canine brain |
title_full | Pathology of non-thermal irreversible electroporation (N-TIRE)-induced ablation of the canine brain |
title_fullStr | Pathology of non-thermal irreversible electroporation (N-TIRE)-induced ablation of the canine brain |
title_full_unstemmed | Pathology of non-thermal irreversible electroporation (N-TIRE)-induced ablation of the canine brain |
title_short | Pathology of non-thermal irreversible electroporation (N-TIRE)-induced ablation of the canine brain |
title_sort | pathology of non-thermal irreversible electroporation (n-tire)-induced ablation of the canine brain |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3885737/ https://www.ncbi.nlm.nih.gov/pubmed/23820168 http://dx.doi.org/10.4142/jvs.2013.14.4.433 |
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