Therapeutic Effects of Dimethyl Fumarate on the Rat Model of Brain Ischemia
Autor(a) principal: | |
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Data de Publicação: | 2022 |
Outros Autores: | , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Brazilian Journal of Pharmaceutical Sciences |
DOI: | 10.1590/s2175-97902022e19677 |
Texto Completo: | https://www.revistas.usp.br/bjps/article/view/204609 |
Resumo: | Blood-brain barrier (BBB) disruption, inflammation, and cell death are major pathogenic mechanisms in ischemic stroke. Dimethyl fumarate (DMF) has anti-inflammatory and immune-modulatory effects. So, this study aimed to elucidate the effects of DMF on brain ischemia in the middle cerebral artery occlusion (MCAO) model. 69 Sprague-Dawley male rats were allocated into a sham group that was just subjected to surgery stress; vehicle and DMF groups, after MCAO, received vehicle or 30 mg/kg DMF for three days. Neurological scores were evaluated every day. BBB disruption was evaluated by the extravasation of Evans blue. In addition to the measurement of brain water content, the total and infarct volume, numerical density, and the total number of neurons, non-neurons, and dead neurons in the right cortex were estimated by stereological methods. RT-PCR was done to analyze the expression levels of NF-κB and Nrf2. Although brain ischemia treatment with DMF did not have a significant effect on the infarction size, it improved neurobehavioral function, BBB disruption, cerebral edema, increased number of neurons, and expression of Nrf2. It also decreased the number of dead neurons and the expression of NF-κB. DMF beneficial effects on stroke may be mediated through both increase of the Nrf2 and decrease of NF-κB expression. |
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Brazilian Journal of Pharmaceutical Sciences |
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Therapeutic Effects of Dimethyl Fumarate on the Rat Model of Brain IschemiaDimethyl fumarateBrain ischemia;Brain edemacell deathNrf2NF-κBBlood-brain barrier (BBB) disruption, inflammation, and cell death are major pathogenic mechanisms in ischemic stroke. Dimethyl fumarate (DMF) has anti-inflammatory and immune-modulatory effects. So, this study aimed to elucidate the effects of DMF on brain ischemia in the middle cerebral artery occlusion (MCAO) model. 69 Sprague-Dawley male rats were allocated into a sham group that was just subjected to surgery stress; vehicle and DMF groups, after MCAO, received vehicle or 30 mg/kg DMF for three days. Neurological scores were evaluated every day. BBB disruption was evaluated by the extravasation of Evans blue. In addition to the measurement of brain water content, the total and infarct volume, numerical density, and the total number of neurons, non-neurons, and dead neurons in the right cortex were estimated by stereological methods. RT-PCR was done to analyze the expression levels of NF-κB and Nrf2. Although brain ischemia treatment with DMF did not have a significant effect on the infarction size, it improved neurobehavioral function, BBB disruption, cerebral edema, increased number of neurons, and expression of Nrf2. It also decreased the number of dead neurons and the expression of NF-κB. DMF beneficial effects on stroke may be mediated through both increase of the Nrf2 and decrease of NF-κB expression.Universidade de São Paulo. Faculdade de Ciências Farmacêuticas2022-11-23info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://www.revistas.usp.br/bjps/article/view/20460910.1590/s2175-97902022e19677Brazilian Journal of Pharmaceutical Sciences; Vol. 58 (2022)Brazilian Journal of Pharmaceutical Sciences; v. 58 (2022)Brazilian Journal of Pharmaceutical Sciences; Vol. 58 (2022)2175-97901984-8250reponame:Brazilian Journal of Pharmaceutical Sciencesinstname:Universidade de São Paulo (USP)instacron:USPenghttps://www.revistas.usp.br/bjps/article/view/204609/194548Copyright (c) 2022 Brazilian Journal of Pharmaceutical Scienceshttps://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessOwjfard, MaryamBigdeli, Mohammad Reza Safari, AnahidNamavar, Mohammad Reza2023-05-29T14:33:23Zoai:revistas.usp.br:article/204609Revistahttps://www.revistas.usp.br/bjps/indexPUBhttps://old.scielo.br/oai/scielo-oai.phpbjps@usp.br||elizabeth.igne@gmail.com2175-97901984-8250opendoar:2023-05-29T14:33:23Brazilian Journal of Pharmaceutical Sciences - Universidade de São Paulo (USP)false |
dc.title.none.fl_str_mv |
Therapeutic Effects of Dimethyl Fumarate on the Rat Model of Brain Ischemia |
title |
Therapeutic Effects of Dimethyl Fumarate on the Rat Model of Brain Ischemia |
spellingShingle |
Therapeutic Effects of Dimethyl Fumarate on the Rat Model of Brain Ischemia Therapeutic Effects of Dimethyl Fumarate on the Rat Model of Brain Ischemia Owjfard, Maryam Dimethyl fumarate Brain ischemia; Brain edema cell death Nrf2 NF-κB Owjfard, Maryam Dimethyl fumarate Brain ischemia; Brain edema cell death Nrf2 NF-κB |
title_short |
Therapeutic Effects of Dimethyl Fumarate on the Rat Model of Brain Ischemia |
title_full |
Therapeutic Effects of Dimethyl Fumarate on the Rat Model of Brain Ischemia |
title_fullStr |
Therapeutic Effects of Dimethyl Fumarate on the Rat Model of Brain Ischemia Therapeutic Effects of Dimethyl Fumarate on the Rat Model of Brain Ischemia |
title_full_unstemmed |
Therapeutic Effects of Dimethyl Fumarate on the Rat Model of Brain Ischemia Therapeutic Effects of Dimethyl Fumarate on the Rat Model of Brain Ischemia |
title_sort |
Therapeutic Effects of Dimethyl Fumarate on the Rat Model of Brain Ischemia |
author |
Owjfard, Maryam |
author_facet |
Owjfard, Maryam Owjfard, Maryam Bigdeli, Mohammad Reza Safari, Anahid Namavar, Mohammad Reza Bigdeli, Mohammad Reza Safari, Anahid Namavar, Mohammad Reza |
author_role |
author |
author2 |
Bigdeli, Mohammad Reza Safari, Anahid Namavar, Mohammad Reza |
author2_role |
author author author |
dc.contributor.author.fl_str_mv |
Owjfard, Maryam Bigdeli, Mohammad Reza Safari, Anahid Namavar, Mohammad Reza |
dc.subject.por.fl_str_mv |
Dimethyl fumarate Brain ischemia; Brain edema cell death Nrf2 NF-κB |
topic |
Dimethyl fumarate Brain ischemia; Brain edema cell death Nrf2 NF-κB |
description |
Blood-brain barrier (BBB) disruption, inflammation, and cell death are major pathogenic mechanisms in ischemic stroke. Dimethyl fumarate (DMF) has anti-inflammatory and immune-modulatory effects. So, this study aimed to elucidate the effects of DMF on brain ischemia in the middle cerebral artery occlusion (MCAO) model. 69 Sprague-Dawley male rats were allocated into a sham group that was just subjected to surgery stress; vehicle and DMF groups, after MCAO, received vehicle or 30 mg/kg DMF for three days. Neurological scores were evaluated every day. BBB disruption was evaluated by the extravasation of Evans blue. In addition to the measurement of brain water content, the total and infarct volume, numerical density, and the total number of neurons, non-neurons, and dead neurons in the right cortex were estimated by stereological methods. RT-PCR was done to analyze the expression levels of NF-κB and Nrf2. Although brain ischemia treatment with DMF did not have a significant effect on the infarction size, it improved neurobehavioral function, BBB disruption, cerebral edema, increased number of neurons, and expression of Nrf2. It also decreased the number of dead neurons and the expression of NF-κB. DMF beneficial effects on stroke may be mediated through both increase of the Nrf2 and decrease of NF-κB expression. |
publishDate |
2022 |
dc.date.none.fl_str_mv |
2022-11-23 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://www.revistas.usp.br/bjps/article/view/204609 10.1590/s2175-97902022e19677 |
url |
https://www.revistas.usp.br/bjps/article/view/204609 |
identifier_str_mv |
10.1590/s2175-97902022e19677 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
https://www.revistas.usp.br/bjps/article/view/204609/194548 |
dc.rights.driver.fl_str_mv |
Copyright (c) 2022 Brazilian Journal of Pharmaceutical Sciences https://creativecommons.org/licenses/by/4.0 info:eu-repo/semantics/openAccess |
rights_invalid_str_mv |
Copyright (c) 2022 Brazilian Journal of Pharmaceutical Sciences https://creativecommons.org/licenses/by/4.0 |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Universidade de São Paulo. Faculdade de Ciências Farmacêuticas |
publisher.none.fl_str_mv |
Universidade de São Paulo. Faculdade de Ciências Farmacêuticas |
dc.source.none.fl_str_mv |
Brazilian Journal of Pharmaceutical Sciences; Vol. 58 (2022) Brazilian Journal of Pharmaceutical Sciences; v. 58 (2022) Brazilian Journal of Pharmaceutical Sciences; Vol. 58 (2022) 2175-9790 1984-8250 reponame:Brazilian Journal of Pharmaceutical Sciences instname:Universidade de São Paulo (USP) instacron:USP |
instname_str |
Universidade de São Paulo (USP) |
instacron_str |
USP |
institution |
USP |
reponame_str |
Brazilian Journal of Pharmaceutical Sciences |
collection |
Brazilian Journal of Pharmaceutical Sciences |
repository.name.fl_str_mv |
Brazilian Journal of Pharmaceutical Sciences - Universidade de São Paulo (USP) |
repository.mail.fl_str_mv |
bjps@usp.br||elizabeth.igne@gmail.com |
_version_ |
1822179249607409664 |
dc.identifier.doi.none.fl_str_mv |
10.1590/s2175-97902022e19677 |