Neuroprotective effects of taurine on SH-SY5Y cells under hydrocortisone induced stress
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Data de Publicação: | 2021 |
Outros Autores: | , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Research, Society and Development |
Texto Completo: | https://rsdjournal.org/index.php/rsd/article/view/18426 |
Resumo: | Alzheimer's disease (AD) is the most common, progressive and irreversible neurodegenerative disorder, characterized by memory loss, cognitive impairment and behavioral abnormalities. Although there is no cure, several study strategies seek to elucidate mechanisms of the disease. Recent studies address the benefits of taurine. Thus, the present study aims to analyze neuroprotective effects of taurine in human neuroblastoma (SH-SY5Y), using an in vitro experimental model of oxidative stress induced by hydrocortisone. This work showed for the first time that taurine can promote neuroprotection in SH-SY5Y under oxidative stress caused by hydrocortisone. Cell viability was evaluated using crystal violet and the evaluation of cell morphology was performed by scanning electron microscopy (SEM). The viability of SH-SY5Y pre-treated with taurine and stressed with hydrocortisone was preserved, compared to the stressed only group, which was also morphologically observed. Therefore, taurine can represent a considerable therapeutic candidate in the prevention of neurodegenerative diseases, such as AD. |
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Neuroprotective effects of taurine on SH-SY5Y cells under hydrocortisone induced stressEfectos neuroprotectivos de la taurina en células SH-SY5Y bajo estrés por hidrocortisonaEfeitos neuroprotetores da taurina em células SH-SY5Y sob estresse induzido por hidrocortisonaDoença de AlzheimerEstresse OxidativoNeuroproteçãoHidrocortisona.Enfermedad de AlzheimerEstrés oxidativoNeuroprotecciónHidrocortisona.Alzheimer's DiseaseOxidative StressNeuroprotectionHydrocortisone.Alzheimer's disease (AD) is the most common, progressive and irreversible neurodegenerative disorder, characterized by memory loss, cognitive impairment and behavioral abnormalities. Although there is no cure, several study strategies seek to elucidate mechanisms of the disease. Recent studies address the benefits of taurine. Thus, the present study aims to analyze neuroprotective effects of taurine in human neuroblastoma (SH-SY5Y), using an in vitro experimental model of oxidative stress induced by hydrocortisone. This work showed for the first time that taurine can promote neuroprotection in SH-SY5Y under oxidative stress caused by hydrocortisone. Cell viability was evaluated using crystal violet and the evaluation of cell morphology was performed by scanning electron microscopy (SEM). The viability of SH-SY5Y pre-treated with taurine and stressed with hydrocortisone was preserved, compared to the stressed only group, which was also morphologically observed. Therefore, taurine can represent a considerable therapeutic candidate in the prevention of neurodegenerative diseases, such as AD.La enfermedad de Alzheimer (EA) es el trastorno neurodegenerativo más común, progresivo e irreversible, caracterizado por pérdida de memoria, deterioro cognitivo y alteraciones del comportamiento. Aunque no existe cura, varias estrategias de estudio buscan dilucidar los mecanismos de la enfermedad. Estudios recientes abordan los beneficios de la taurina. Así, el presente estudio tiene como objetivo analizar el efecto neuroprotector de la taurina en el neuroblastoma humano (SH-SY5Y), utilizando un modelo experimental in vitro de estrés oxidativo inducido por hidrocortisona. Este trabajo demostró por primera vez que la taurina puede promover la neuroprotección en las células SH-SY5Y bajo el estrés oxidativo causado por la hidrocortisona. La viabilidad celular se evaluó utilizando cristal violeta y la evaluación de la morfología celular se realizó mediante microscopía electrónica de barrido (MEB). Se conservó la viabilidad de las células SH-SY5Y pretratadas con taurina y estresadas con hidrocortisona, en comparación con el grupo expuesto solo a hidrocortisona, que también se observó morfológicamente. Por tanto, la taurina puede representar un importante candidato terapéutico en la prevención de enfermedades neurodegenerativas como la EA.A doença de Alzheimer (DA) é o distúrbio neurodegenerativo mais comum, progressivo e irreversível, caracterizado por perda de memória, prejuízo cognitivo e anormalidades comportamentais. Embora não haja cura, várias estratégias de estudo buscam elucidar os mecanismos da doença. Estudos recentes abordam os benefícios da taurina. Assim, o presente estudo tem como objetivo analisar o efeito neuroprotetor da taurina em neuroblastoma humano (SH-SY5Y), utilizando um modelo experimental in vitro de estresse oxidativo induzido por hidrocortisona. Este trabalho mostrou pela primeira vez que a taurina pode promover a neuroproteção nas células SH-SY5Y sob o estresse oxidativo causado pela hidrocortisona. A viabilidade celular foi avaliada utilizando cristal violeta e a avaliação da morfologia celular foi realizada por microscopia eletrônica de varredura (MEV). A viabilidade das células SH-SY5Y pré-tratadas com taurina e estressadas com hidrocortisona foi preservada, em comparação com o grupo exposto apenas à hidrocortisona, o que foi também observado morfologicamente. Portanto, a taurina pode representar um importante candidato terapêutico na prevenção de doenças neurodegenerativas, como a DA.Research, Society and Development2021-08-03info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://rsdjournal.org/index.php/rsd/article/view/1842610.33448/rsd-v10i9.18426Research, Society and Development; Vol. 10 No. 9; e55510918426Research, Society and Development; Vol. 10 Núm. 9; e55510918426Research, Society and Development; v. 10 n. 9; e555109184262525-3409reponame:Research, Society and Developmentinstname:Universidade Federal de Itajubá (UNIFEI)instacron:UNIFEIenghttps://rsdjournal.org/index.php/rsd/article/view/18426/16516Copyright (c) 2021 Rafaella Carvalho Rossato; Alessandro Eustaquio Campos Granato; Carlos Dailton Guedes de Oliveira Moraes; Geisa Nogueira Salles; Cristina Pacheco Soareshttps://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessRossato, Rafaella Carvalho Granato, Alessandro Eustaquio Campos Moraes, Carlos Dailton Guedes de Oliveira Salles, Geisa Nogueira Soares, Cristina Pacheco 2021-09-12T14:28:06Zoai:ojs.pkp.sfu.ca:article/18426Revistahttps://rsdjournal.org/index.php/rsd/indexPUBhttps://rsdjournal.org/index.php/rsd/oairsd.articles@gmail.com2525-34092525-3409opendoar:2024-01-17T09:38:34.262765Research, Society and Development - Universidade Federal de Itajubá (UNIFEI)false |
dc.title.none.fl_str_mv |
Neuroprotective effects of taurine on SH-SY5Y cells under hydrocortisone induced stress Efectos neuroprotectivos de la taurina en células SH-SY5Y bajo estrés por hidrocortisona Efeitos neuroprotetores da taurina em células SH-SY5Y sob estresse induzido por hidrocortisona |
title |
Neuroprotective effects of taurine on SH-SY5Y cells under hydrocortisone induced stress |
spellingShingle |
Neuroprotective effects of taurine on SH-SY5Y cells under hydrocortisone induced stress Rossato, Rafaella Carvalho Doença de Alzheimer Estresse Oxidativo Neuroproteção Hidrocortisona. Enfermedad de Alzheimer Estrés oxidativo Neuroprotección Hidrocortisona. Alzheimer's Disease Oxidative Stress Neuroprotection Hydrocortisone. |
title_short |
Neuroprotective effects of taurine on SH-SY5Y cells under hydrocortisone induced stress |
title_full |
Neuroprotective effects of taurine on SH-SY5Y cells under hydrocortisone induced stress |
title_fullStr |
Neuroprotective effects of taurine on SH-SY5Y cells under hydrocortisone induced stress |
title_full_unstemmed |
Neuroprotective effects of taurine on SH-SY5Y cells under hydrocortisone induced stress |
title_sort |
Neuroprotective effects of taurine on SH-SY5Y cells under hydrocortisone induced stress |
author |
Rossato, Rafaella Carvalho |
author_facet |
Rossato, Rafaella Carvalho Granato, Alessandro Eustaquio Campos Moraes, Carlos Dailton Guedes de Oliveira Salles, Geisa Nogueira Soares, Cristina Pacheco |
author_role |
author |
author2 |
Granato, Alessandro Eustaquio Campos Moraes, Carlos Dailton Guedes de Oliveira Salles, Geisa Nogueira Soares, Cristina Pacheco |
author2_role |
author author author author |
dc.contributor.author.fl_str_mv |
Rossato, Rafaella Carvalho Granato, Alessandro Eustaquio Campos Moraes, Carlos Dailton Guedes de Oliveira Salles, Geisa Nogueira Soares, Cristina Pacheco |
dc.subject.por.fl_str_mv |
Doença de Alzheimer Estresse Oxidativo Neuroproteção Hidrocortisona. Enfermedad de Alzheimer Estrés oxidativo Neuroprotección Hidrocortisona. Alzheimer's Disease Oxidative Stress Neuroprotection Hydrocortisone. |
topic |
Doença de Alzheimer Estresse Oxidativo Neuroproteção Hidrocortisona. Enfermedad de Alzheimer Estrés oxidativo Neuroprotección Hidrocortisona. Alzheimer's Disease Oxidative Stress Neuroprotection Hydrocortisone. |
description |
Alzheimer's disease (AD) is the most common, progressive and irreversible neurodegenerative disorder, characterized by memory loss, cognitive impairment and behavioral abnormalities. Although there is no cure, several study strategies seek to elucidate mechanisms of the disease. Recent studies address the benefits of taurine. Thus, the present study aims to analyze neuroprotective effects of taurine in human neuroblastoma (SH-SY5Y), using an in vitro experimental model of oxidative stress induced by hydrocortisone. This work showed for the first time that taurine can promote neuroprotection in SH-SY5Y under oxidative stress caused by hydrocortisone. Cell viability was evaluated using crystal violet and the evaluation of cell morphology was performed by scanning electron microscopy (SEM). The viability of SH-SY5Y pre-treated with taurine and stressed with hydrocortisone was preserved, compared to the stressed only group, which was also morphologically observed. Therefore, taurine can represent a considerable therapeutic candidate in the prevention of neurodegenerative diseases, such as AD. |
publishDate |
2021 |
dc.date.none.fl_str_mv |
2021-08-03 |
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://rsdjournal.org/index.php/rsd/article/view/18426 10.33448/rsd-v10i9.18426 |
url |
https://rsdjournal.org/index.php/rsd/article/view/18426 |
identifier_str_mv |
10.33448/rsd-v10i9.18426 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
https://rsdjournal.org/index.php/rsd/article/view/18426/16516 |
dc.rights.driver.fl_str_mv |
https://creativecommons.org/licenses/by/4.0 info:eu-repo/semantics/openAccess |
rights_invalid_str_mv |
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 |
Research, Society and Development |
publisher.none.fl_str_mv |
Research, Society and Development |
dc.source.none.fl_str_mv |
Research, Society and Development; Vol. 10 No. 9; e55510918426 Research, Society and Development; Vol. 10 Núm. 9; e55510918426 Research, Society and Development; v. 10 n. 9; e55510918426 2525-3409 reponame:Research, Society and Development instname:Universidade Federal de Itajubá (UNIFEI) instacron:UNIFEI |
instname_str |
Universidade Federal de Itajubá (UNIFEI) |
instacron_str |
UNIFEI |
institution |
UNIFEI |
reponame_str |
Research, Society and Development |
collection |
Research, Society and Development |
repository.name.fl_str_mv |
Research, Society and Development - Universidade Federal de Itajubá (UNIFEI) |
repository.mail.fl_str_mv |
rsd.articles@gmail.com |
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1797052684746883072 |