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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
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.
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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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