Amburana cearensis seed extracts protect PC-12 cells against toxicity induced by glutamate

Detalhes bibliográficos
Autor(a) principal: Pereira,Erica P.L.
Data de Publicação: 2017
Outros Autores: Braga-de-Souza,Suzana, Santos,Cleonice C., Santos,Leticia O., Cerqueira,Martins D., Ribeiro,Paulo R., Fernandez,Luzimar G., Silva,Victor D.A., Costa,Silvia L.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Revista Brasileira de Farmacognosia (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0102-695X2017000200199
Resumo: ABSTRACT Amburana cearensis (Allemão) A.C. Sm., Fabaceae, has been widely studied for its medicinal activities. Many neurodegenerative disorders are caused by oxidative stress, mitochondrial dysfunction, excitotoxicity induced by glutamate and ultimately cell death. This study describes the chemical profile of the ethanolic, hexane, dichloromethane, and ethyl acetate extracts obtained from seeds of A. cearensis. The objective of this study was to investigate the chemical profile of extracts obtained from seeds of A. cearensis, as well as their cytotoxicity and neuroprotective effects in cultures of neural PC12 cells. Metabolite profile was performed by GC–MS. PC12 cells were treated with increasing concentrations of the extracts (0.01–2000 µg/ml) and the cell viability was analyzed after 24 and 72 h using an MTT test. For the excitotoxicity assay, PC12 cells were pre-treated with glutamate (1 mM) for 6 h and treated with increasing concentrations (0.1–1000 µg/ml) of the extracts. The chromatographic analysis of the extracts detected various compounds with antioxidant properties, with the majority of peaks corresponding to the isoflavone coumarin. Only the hexane extract showed toxicity after 72 h exposure at the highest concentration (1000 µg/ml). By contrast, all extracts increased the cellular viability of PC12 cells against the toxicity caused by glutamate. Therefore, the extracts from the seeds of A. cearensis showed no toxicity and have neuroprotective potential against neuronal damage induced by glutamate, which may be related to their antioxidant properties.
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spelling Amburana cearensis seed extracts protect PC-12 cells against toxicity induced by glutamateAmburana cearensisGlutamatePC12 cellsExcitotoxicityNeuroprotectionABSTRACT Amburana cearensis (Allemão) A.C. Sm., Fabaceae, has been widely studied for its medicinal activities. Many neurodegenerative disorders are caused by oxidative stress, mitochondrial dysfunction, excitotoxicity induced by glutamate and ultimately cell death. This study describes the chemical profile of the ethanolic, hexane, dichloromethane, and ethyl acetate extracts obtained from seeds of A. cearensis. The objective of this study was to investigate the chemical profile of extracts obtained from seeds of A. cearensis, as well as their cytotoxicity and neuroprotective effects in cultures of neural PC12 cells. Metabolite profile was performed by GC–MS. PC12 cells were treated with increasing concentrations of the extracts (0.01–2000 µg/ml) and the cell viability was analyzed after 24 and 72 h using an MTT test. For the excitotoxicity assay, PC12 cells were pre-treated with glutamate (1 mM) for 6 h and treated with increasing concentrations (0.1–1000 µg/ml) of the extracts. The chromatographic analysis of the extracts detected various compounds with antioxidant properties, with the majority of peaks corresponding to the isoflavone coumarin. Only the hexane extract showed toxicity after 72 h exposure at the highest concentration (1000 µg/ml). By contrast, all extracts increased the cellular viability of PC12 cells against the toxicity caused by glutamate. Therefore, the extracts from the seeds of A. cearensis showed no toxicity and have neuroprotective potential against neuronal damage induced by glutamate, which may be related to their antioxidant properties.Sociedade Brasileira de Farmacognosia2017-04-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0102-695X2017000200199Revista Brasileira de Farmacognosia v.27 n.2 2017reponame:Revista Brasileira de Farmacognosia (Online)instname:Sociedade Brasileira de Farmacognosia (SBFgnosia)instacron:SBFGNOSIA10.1016/j.bjp.2016.08.010info:eu-repo/semantics/openAccessPereira,Erica P.L.Braga-de-Souza,SuzanaSantos,Cleonice C.Santos,Leticia O.Cerqueira,Martins D.Ribeiro,Paulo R.Fernandez,Luzimar G.Silva,Victor D.A.Costa,Silvia L.eng2017-04-20T00:00:00Zoai:scielo:S0102-695X2017000200199Revistahttp://www.sbfgnosia.org.br/revista/https://old.scielo.br/oai/scielo-oai.phprbgnosia@ltf.ufpb.br1981-528X0102-695Xopendoar:2017-04-20T00:00Revista Brasileira de Farmacognosia (Online) - Sociedade Brasileira de Farmacognosia (SBFgnosia)false
dc.title.none.fl_str_mv Amburana cearensis seed extracts protect PC-12 cells against toxicity induced by glutamate
title Amburana cearensis seed extracts protect PC-12 cells against toxicity induced by glutamate
spellingShingle Amburana cearensis seed extracts protect PC-12 cells against toxicity induced by glutamate
Pereira,Erica P.L.
Amburana cearensis
Glutamate
PC12 cells
Excitotoxicity
Neuroprotection
title_short Amburana cearensis seed extracts protect PC-12 cells against toxicity induced by glutamate
title_full Amburana cearensis seed extracts protect PC-12 cells against toxicity induced by glutamate
title_fullStr Amburana cearensis seed extracts protect PC-12 cells against toxicity induced by glutamate
title_full_unstemmed Amburana cearensis seed extracts protect PC-12 cells against toxicity induced by glutamate
title_sort Amburana cearensis seed extracts protect PC-12 cells against toxicity induced by glutamate
author Pereira,Erica P.L.
author_facet Pereira,Erica P.L.
Braga-de-Souza,Suzana
Santos,Cleonice C.
Santos,Leticia O.
Cerqueira,Martins D.
Ribeiro,Paulo R.
Fernandez,Luzimar G.
Silva,Victor D.A.
Costa,Silvia L.
author_role author
author2 Braga-de-Souza,Suzana
Santos,Cleonice C.
Santos,Leticia O.
Cerqueira,Martins D.
Ribeiro,Paulo R.
Fernandez,Luzimar G.
Silva,Victor D.A.
Costa,Silvia L.
author2_role author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Pereira,Erica P.L.
Braga-de-Souza,Suzana
Santos,Cleonice C.
Santos,Leticia O.
Cerqueira,Martins D.
Ribeiro,Paulo R.
Fernandez,Luzimar G.
Silva,Victor D.A.
Costa,Silvia L.
dc.subject.por.fl_str_mv Amburana cearensis
Glutamate
PC12 cells
Excitotoxicity
Neuroprotection
topic Amburana cearensis
Glutamate
PC12 cells
Excitotoxicity
Neuroprotection
description ABSTRACT Amburana cearensis (Allemão) A.C. Sm., Fabaceae, has been widely studied for its medicinal activities. Many neurodegenerative disorders are caused by oxidative stress, mitochondrial dysfunction, excitotoxicity induced by glutamate and ultimately cell death. This study describes the chemical profile of the ethanolic, hexane, dichloromethane, and ethyl acetate extracts obtained from seeds of A. cearensis. The objective of this study was to investigate the chemical profile of extracts obtained from seeds of A. cearensis, as well as their cytotoxicity and neuroprotective effects in cultures of neural PC12 cells. Metabolite profile was performed by GC–MS. PC12 cells were treated with increasing concentrations of the extracts (0.01–2000 µg/ml) and the cell viability was analyzed after 24 and 72 h using an MTT test. For the excitotoxicity assay, PC12 cells were pre-treated with glutamate (1 mM) for 6 h and treated with increasing concentrations (0.1–1000 µg/ml) of the extracts. The chromatographic analysis of the extracts detected various compounds with antioxidant properties, with the majority of peaks corresponding to the isoflavone coumarin. Only the hexane extract showed toxicity after 72 h exposure at the highest concentration (1000 µg/ml). By contrast, all extracts increased the cellular viability of PC12 cells against the toxicity caused by glutamate. Therefore, the extracts from the seeds of A. cearensis showed no toxicity and have neuroprotective potential against neuronal damage induced by glutamate, which may be related to their antioxidant properties.
publishDate 2017
dc.date.none.fl_str_mv 2017-04-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0102-695X2017000200199
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dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1016/j.bjp.2016.08.010
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Sociedade Brasileira de Farmacognosia
publisher.none.fl_str_mv Sociedade Brasileira de Farmacognosia
dc.source.none.fl_str_mv Revista Brasileira de Farmacognosia v.27 n.2 2017
reponame:Revista Brasileira de Farmacognosia (Online)
instname:Sociedade Brasileira de Farmacognosia (SBFgnosia)
instacron:SBFGNOSIA
instname_str Sociedade Brasileira de Farmacognosia (SBFgnosia)
instacron_str SBFGNOSIA
institution SBFGNOSIA
reponame_str Revista Brasileira de Farmacognosia (Online)
collection Revista Brasileira de Farmacognosia (Online)
repository.name.fl_str_mv Revista Brasileira de Farmacognosia (Online) - Sociedade Brasileira de Farmacognosia (SBFgnosia)
repository.mail.fl_str_mv rbgnosia@ltf.ufpb.br
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