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Demyelination Lesions Do Not Correlate with Clinical Manifestations by Bordetella pertussis Toxin Concentrations

Multiple sclerosis (MS) is an autoimmune disease of the central nervous system, characterized as an inflammatory demyelinating disease. Given the need for improvements in MS treatment, many studies are mainly conducted through preclinical models such as experimental allergic encephalomyelitis (EAE)....

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Autores principales: Perussolo, Maiara Carolina, Mogharbel, Bassam Felipe, Saçaki, Claudia Sayuri, Dziedzic, Dilcele Silva Moreira, Nagashima, Seigo, de Meira, Leanderson Franco, Guarita-Souza, Luiz Cesar, de Noronha, Lúcia, Athayde Teixeira de Carvalho, Katherine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9316486/
https://www.ncbi.nlm.nih.gov/pubmed/35888052
http://dx.doi.org/10.3390/life12070962
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author Perussolo, Maiara Carolina
Mogharbel, Bassam Felipe
Saçaki, Claudia Sayuri
Dziedzic, Dilcele Silva Moreira
Nagashima, Seigo
de Meira, Leanderson Franco
Guarita-Souza, Luiz Cesar
de Noronha, Lúcia
Athayde Teixeira de Carvalho, Katherine
author_facet Perussolo, Maiara Carolina
Mogharbel, Bassam Felipe
Saçaki, Claudia Sayuri
Dziedzic, Dilcele Silva Moreira
Nagashima, Seigo
de Meira, Leanderson Franco
Guarita-Souza, Luiz Cesar
de Noronha, Lúcia
Athayde Teixeira de Carvalho, Katherine
author_sort Perussolo, Maiara Carolina
collection PubMed
description Multiple sclerosis (MS) is an autoimmune disease of the central nervous system, characterized as an inflammatory demyelinating disease. Given the need for improvements in MS treatment, many studies are mainly conducted through preclinical models such as experimental allergic encephalomyelitis (EAE). This study analyzes the relationships between histopathological and clinical score findings at EAE. Twenty-three female Rattus norvegicus Lewis rats from 6 to 8 weeks were induced to EAE. Nineteen rats underwent EAE induction distributed in six groups to establish the evolution of clinical signs, and four animals were in the control group. Bordetella pertussis toxin (PTX) doses were 200, 250, 300, 350 and 400 ng. The clinical scores of the animals were analyzed daily, from seven to 24 days after induction. The brains and spinal cords were collected for histopathological analyses. The results demonstrated that the dose of 250 ng of PTX induced a higher clinical score and reduction in weight. All induced groups demonstrated leukocyte infiltration, activation of microglia and astrocytes, and demyelinated plaques in the brains in histopathology. It was concluded that the dose of 250 ng and 350 ng of PTX were the best choices to trigger the brain and spinal cord demyelination lesions and did not correlate with clinical scores.
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spelling pubmed-93164862022-07-27 Demyelination Lesions Do Not Correlate with Clinical Manifestations by Bordetella pertussis Toxin Concentrations Perussolo, Maiara Carolina Mogharbel, Bassam Felipe Saçaki, Claudia Sayuri Dziedzic, Dilcele Silva Moreira Nagashima, Seigo de Meira, Leanderson Franco Guarita-Souza, Luiz Cesar de Noronha, Lúcia Athayde Teixeira de Carvalho, Katherine Life (Basel) Article Multiple sclerosis (MS) is an autoimmune disease of the central nervous system, characterized as an inflammatory demyelinating disease. Given the need for improvements in MS treatment, many studies are mainly conducted through preclinical models such as experimental allergic encephalomyelitis (EAE). This study analyzes the relationships between histopathological and clinical score findings at EAE. Twenty-three female Rattus norvegicus Lewis rats from 6 to 8 weeks were induced to EAE. Nineteen rats underwent EAE induction distributed in six groups to establish the evolution of clinical signs, and four animals were in the control group. Bordetella pertussis toxin (PTX) doses were 200, 250, 300, 350 and 400 ng. The clinical scores of the animals were analyzed daily, from seven to 24 days after induction. The brains and spinal cords were collected for histopathological analyses. The results demonstrated that the dose of 250 ng of PTX induced a higher clinical score and reduction in weight. All induced groups demonstrated leukocyte infiltration, activation of microglia and astrocytes, and demyelinated plaques in the brains in histopathology. It was concluded that the dose of 250 ng and 350 ng of PTX were the best choices to trigger the brain and spinal cord demyelination lesions and did not correlate with clinical scores. MDPI 2022-06-27 /pmc/articles/PMC9316486/ /pubmed/35888052 http://dx.doi.org/10.3390/life12070962 Text en © 2022 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
Perussolo, Maiara Carolina
Mogharbel, Bassam Felipe
Saçaki, Claudia Sayuri
Dziedzic, Dilcele Silva Moreira
Nagashima, Seigo
de Meira, Leanderson Franco
Guarita-Souza, Luiz Cesar
de Noronha, Lúcia
Athayde Teixeira de Carvalho, Katherine
Demyelination Lesions Do Not Correlate with Clinical Manifestations by Bordetella pertussis Toxin Concentrations
title Demyelination Lesions Do Not Correlate with Clinical Manifestations by Bordetella pertussis Toxin Concentrations
title_full Demyelination Lesions Do Not Correlate with Clinical Manifestations by Bordetella pertussis Toxin Concentrations
title_fullStr Demyelination Lesions Do Not Correlate with Clinical Manifestations by Bordetella pertussis Toxin Concentrations
title_full_unstemmed Demyelination Lesions Do Not Correlate with Clinical Manifestations by Bordetella pertussis Toxin Concentrations
title_short Demyelination Lesions Do Not Correlate with Clinical Manifestations by Bordetella pertussis Toxin Concentrations
title_sort demyelination lesions do not correlate with clinical manifestations by bordetella pertussis toxin concentrations
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9316486/
https://www.ncbi.nlm.nih.gov/pubmed/35888052
http://dx.doi.org/10.3390/life12070962
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