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Morpho-Functional Characterisation of the Rat Ventral Caudal Nerve in a Model of Axonal Peripheral Neuropathy
Peripheral Neuropathies (PN) are common conditions whose treatment is still lacking in most cases. Animal models are crucial, but experimental procedures should be refined in some cases. We performed a detailed characterization of the ventral caudal nerve to contribute to a more effective assessment...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9863172/ https://www.ncbi.nlm.nih.gov/pubmed/36675203 http://dx.doi.org/10.3390/ijms24021687 |
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author | Pozzi, Eleonora Monza, Laura Ballarini, Elisa Bossi, Mario Rodriguez-Menendez, Virginia Canta, Annalisa Chiorazzi, Alessia Carozzi, Valentina Alda Crippa, Luca Marmiroli, Paola Cavaletti, Guido Alberti, Paola |
author_facet | Pozzi, Eleonora Monza, Laura Ballarini, Elisa Bossi, Mario Rodriguez-Menendez, Virginia Canta, Annalisa Chiorazzi, Alessia Carozzi, Valentina Alda Crippa, Luca Marmiroli, Paola Cavaletti, Guido Alberti, Paola |
author_sort | Pozzi, Eleonora |
collection | PubMed |
description | Peripheral Neuropathies (PN) are common conditions whose treatment is still lacking in most cases. Animal models are crucial, but experimental procedures should be refined in some cases. We performed a detailed characterization of the ventral caudal nerve to contribute to a more effective assessment of axonal damage in future PN studies. PN was induced via weekly systemic injection of a neurotoxic drug (paclitaxel); we compared the control and PN-affected rats, performing serial neurophysiological evaluations of the caudal nerve for its entire length. On the same nerve portions, we performed light microscopy and ultrastructural pathological observations to assess the severity of damage and verify the integrity of the surrounding structures. Neurophysiological and morphological analyses confirmed that a severe axonopathy had ensued in the PN group, with a length-dependent modality, matching morphological observations. The site of neurophysiological recording (e.g., distance from the base of the tail) was critical for achieving useful data. A flexible experimental paradigm should be considered in animal studies investigating axonal PN, particularly if the expected severity is relevant; the mid-portion of the tail might be the most appropriate site: there damage might be remarkable but neither as extreme as at the tip of the tail nor as mild as at the base of the tail. |
format | Online Article Text |
id | pubmed-9863172 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-98631722023-01-22 Morpho-Functional Characterisation of the Rat Ventral Caudal Nerve in a Model of Axonal Peripheral Neuropathy Pozzi, Eleonora Monza, Laura Ballarini, Elisa Bossi, Mario Rodriguez-Menendez, Virginia Canta, Annalisa Chiorazzi, Alessia Carozzi, Valentina Alda Crippa, Luca Marmiroli, Paola Cavaletti, Guido Alberti, Paola Int J Mol Sci Article Peripheral Neuropathies (PN) are common conditions whose treatment is still lacking in most cases. Animal models are crucial, but experimental procedures should be refined in some cases. We performed a detailed characterization of the ventral caudal nerve to contribute to a more effective assessment of axonal damage in future PN studies. PN was induced via weekly systemic injection of a neurotoxic drug (paclitaxel); we compared the control and PN-affected rats, performing serial neurophysiological evaluations of the caudal nerve for its entire length. On the same nerve portions, we performed light microscopy and ultrastructural pathological observations to assess the severity of damage and verify the integrity of the surrounding structures. Neurophysiological and morphological analyses confirmed that a severe axonopathy had ensued in the PN group, with a length-dependent modality, matching morphological observations. The site of neurophysiological recording (e.g., distance from the base of the tail) was critical for achieving useful data. A flexible experimental paradigm should be considered in animal studies investigating axonal PN, particularly if the expected severity is relevant; the mid-portion of the tail might be the most appropriate site: there damage might be remarkable but neither as extreme as at the tip of the tail nor as mild as at the base of the tail. MDPI 2023-01-14 /pmc/articles/PMC9863172/ /pubmed/36675203 http://dx.doi.org/10.3390/ijms24021687 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Pozzi, Eleonora Monza, Laura Ballarini, Elisa Bossi, Mario Rodriguez-Menendez, Virginia Canta, Annalisa Chiorazzi, Alessia Carozzi, Valentina Alda Crippa, Luca Marmiroli, Paola Cavaletti, Guido Alberti, Paola Morpho-Functional Characterisation of the Rat Ventral Caudal Nerve in a Model of Axonal Peripheral Neuropathy |
title | Morpho-Functional Characterisation of the Rat Ventral Caudal Nerve in a Model of Axonal Peripheral Neuropathy |
title_full | Morpho-Functional Characterisation of the Rat Ventral Caudal Nerve in a Model of Axonal Peripheral Neuropathy |
title_fullStr | Morpho-Functional Characterisation of the Rat Ventral Caudal Nerve in a Model of Axonal Peripheral Neuropathy |
title_full_unstemmed | Morpho-Functional Characterisation of the Rat Ventral Caudal Nerve in a Model of Axonal Peripheral Neuropathy |
title_short | Morpho-Functional Characterisation of the Rat Ventral Caudal Nerve in a Model of Axonal Peripheral Neuropathy |
title_sort | morpho-functional characterisation of the rat ventral caudal nerve in a model of axonal peripheral neuropathy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9863172/ https://www.ncbi.nlm.nih.gov/pubmed/36675203 http://dx.doi.org/10.3390/ijms24021687 |
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