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Potencial tóxico e anticarcinogênico da alga Prasiola crispa

Detalhes bibliográficos
Ano de defesa: 2015
Autor(a) principal: Zemolin, Ana Paula Pegoraro
Orientador(a): Não Informado pela instituição
Banca de defesa: Não Informado pela instituição
Tipo de documento: Tese
Tipo de acesso: Acesso aberto
dARK ID: ark:/26339/001300000b9fz
Idioma: por
Instituição de defesa: Universidade Federal de Santa Maria
Brasil
Bioquímica
UFSM
Programa de Pós-Graduação em Ciências Biológicas: Bioquímica Toxicológica
Centro de Ciências Naturais e Exatas
Programa de Pós-Graduação: Não Informado pela instituição
Departamento: Não Informado pela instituição
País: Não Informado pela instituição
Palavras-chave em Português:
Link de acesso: http://repositorio.ufsm.br/handle/1/17548
Resumo: Toxic and anticarcinogenic effects of Prasiola Seaweed extract crispa (PCE) were investigated in Drosophila melanogaster, Nauphoeta cinérea and leukemic cells. In fruit flies, toxicity was assessed as mortality and biochemical changes, including acetylcholinesterase (AChE) and oxidative stress markers. The cardiotoxic action of PCE was examined in a semi-isolated heart model cheap. They were also analyzed the antiproliferative properties of Prasiola crispa (Pc) in leukemic K562 cells. The PCE administration (2 mg / ml) in flies, lasted 24 hours and resulted in a significant increase in mortality (7.6 fold increase compared to control). Activity of AChE (GSH) glutathione levels and the hydroperoxide formation was unchanged. Glutathione S-transferase (GST) and catalase (CAT) were significantly altered after treatment PCE. The fraction III (ethyl acetate) PCE was significantly more toxic to the flies compared to fractions I (methanol) and II (ethanol). A significant decrease in heart function inexpensive semi isolated heart model was observed. Addition of 5,5'-dithiobis acid (2-nitrobenzoic acid (DTNB), an oxidizing agent, concomitantly with the extract significantly blocked this effect. The PCE insecticidal properties can be related to changes in the important antioxidant detoxification system as well as to changes in insect cardiac function. To assess the antiproliferative activities of ethanolic fraction (EF) and ethyl acetate (EAF) of Prasiola crispa extract, cancerous leukemic K562 cells were exposed for 24 hours to different concentrations of PCE fractions. After treatment, cell viability, PARP cleavage and apoptosis Nrf2 expression of HO-1 and HSP70 were determined. The EAF showed a higher cytotoxic activity on leukemic cells as compared to EF. Cell proliferation was inhibited, a fact which was accompanied by a marked increase in the expression of Nrf2, HO-1 and HSP70 protein levels, indicating signs of oxidative stress. The results indicate the potential antitumor effect of Prasiola crispa algae.
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spelling Potencial tóxico e anticarcinogênico da alga Prasiola crispaPotential toxic and anticarcinogenic seaweed Prasiola crispaPrasiola crispaInseticidaEfeito antitumoralInsecticideAntitumoral effectCNPQ::CIENCIAS BIOLOGICAS::BIOQUIMICAToxic and anticarcinogenic effects of Prasiola Seaweed extract crispa (PCE) were investigated in Drosophila melanogaster, Nauphoeta cinérea and leukemic cells. In fruit flies, toxicity was assessed as mortality and biochemical changes, including acetylcholinesterase (AChE) and oxidative stress markers. The cardiotoxic action of PCE was examined in a semi-isolated heart model cheap. They were also analyzed the antiproliferative properties of Prasiola crispa (Pc) in leukemic K562 cells. The PCE administration (2 mg / ml) in flies, lasted 24 hours and resulted in a significant increase in mortality (7.6 fold increase compared to control). Activity of AChE (GSH) glutathione levels and the hydroperoxide formation was unchanged. Glutathione S-transferase (GST) and catalase (CAT) were significantly altered after treatment PCE. The fraction III (ethyl acetate) PCE was significantly more toxic to the flies compared to fractions I (methanol) and II (ethanol). A significant decrease in heart function inexpensive semi isolated heart model was observed. Addition of 5,5'-dithiobis acid (2-nitrobenzoic acid (DTNB), an oxidizing agent, concomitantly with the extract significantly blocked this effect. The PCE insecticidal properties can be related to changes in the important antioxidant detoxification system as well as to changes in insect cardiac function. To assess the antiproliferative activities of ethanolic fraction (EF) and ethyl acetate (EAF) of Prasiola crispa extract, cancerous leukemic K562 cells were exposed for 24 hours to different concentrations of PCE fractions. After treatment, cell viability, PARP cleavage and apoptosis Nrf2 expression of HO-1 and HSP70 were determined. The EAF showed a higher cytotoxic activity on leukemic cells as compared to EF. Cell proliferation was inhibited, a fact which was accompanied by a marked increase in the expression of Nrf2, HO-1 and HSP70 protein levels, indicating signs of oxidative stress. The results indicate the potential antitumor effect of Prasiola crispa algae.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - CAPESOs efeitos tóxicos e anticarcinogênicos do extrato da alga Prasiola crispa (PCE) foram investigados em Drosophila melanogaster, Nauphoeta cinérea e células leucêmicas. Em moscas, a toxicidade foi avaliada como mortalidade e alterações bioquímicas, incluindo acetilcolinesterase (AChE) e marcadores de estresse oxidativo. A ação cardiotóxica do PCE foi examinado em um modelo de coração semi-isolado de barata. Foram analisadas ainda, as propriedades antiproliferativas de Prasiola crispa (Pc), em células K562 leucêmicas. A administração de PCE (2 mg / ml) em moscas, durou 24 horas e resultou num aumento significativo na taxa de mortalidade (aumento de 7,6 vezes em relação ao controle). Atividade da AChE, (GSH) os níveis de glutationa, e a formação de hidroperóxido manteve-se inalterada. Glutationa S-transferase (GST) e catalase (CAT) foram significativamente alterados após tratamento PCE. A fração acetato de etilo de PCE foi significativamente mais tóxica para as moscas em comparação com as frações I (metanol) e II (etanol). Uma diminuição significativa na função cardíaca em modelo de coração semi isolado de barata foi observada. A adição de ácido 5,5'-ditiobis- (ácido 2-nitrobenzóico (DTNB), um agente oxidante, concomitante com o extrato bloqueou significativamente este efeito. As propriedades inseticidas do PCE podem estar relacionada a mudanças no importante sistema antioxidante de desintoxicação, bem como a alterações na função cardíaca do inseto. Para avaliar as atividades antiproliferativas das frações etanólica ( EF) e acetato de etila( EAF) do extrato de Prasiola crispa, células leucêmicas cancerosas K562 foram expostas durante 24 horas a diferentes concentrações de frações do PCE. Após os tratamentos, a viabilidade celular , clivagem de PARP, apoptose e a expressão de Nrf2, HO-1 e HSP70 foram determinadas. A EAF mostrou uma maior atividade citotóxica em células leucêmicas, quando comparado com EF. A proliferação celular foi inibida, fato que foi acompanhado por um aumento acentuado na expressão de Nrf2, HO-1 e nos níveis de proteína HSP70, indicando sinais de estresse oxidativo. Os resultados indicam o potencial efeito antitumoral da alga Prasiola crispa.Universidade Federal de Santa MariaBrasilBioquímicaUFSMPrograma de Pós-Graduação em Ciências Biológicas: Bioquímica ToxicológicaCentro de Ciências Naturais e ExatasFranco, Jeferson Luishttp://lattes.cnpq.br/1680065573338339Soares, Félix Alexandre Antuneshttp://lattes.cnpq.br/8752453650114092Rubin, Maribel Antonellohttp://lattes.cnpq.br/7237734243628134Rosemberg, Denis Broockhttp://lattes.cnpq.br/7713953979203056Zemolin, Ana Paula Pegoraro2019-07-24T17:29:11Z2019-07-24T17:29:11Z2015-12-22info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/doctoralThesisapplication/pdfhttp://repositorio.ufsm.br/handle/1/17548ark:/26339/001300000b9fzporAttribution-NonCommercial-NoDerivatives 4.0 Internationalinfo:eu-repo/semantics/openAccessreponame:Manancial - Repositório Digital da UFSMinstname:Universidade Federal de Santa Maria (UFSM)instacron:UFSM2019-07-25T06:02:11Zoai:repositorio.ufsm.br:1/17548Biblioteca Digital de Teses e Dissertaçõeshttps://repositorio.ufsm.br/PUBhttps://repositorio.ufsm.br/oai/requestatendimento.sib@ufsm.br||tedebc@gmail.com||manancial@ufsm.bropendoar:2019-07-25T06:02:11Manancial - Repositório Digital da UFSM - Universidade Federal de Santa Maria (UFSM)false
dc.title.none.fl_str_mv Potencial tóxico e anticarcinogênico da alga Prasiola crispa
Potential toxic and anticarcinogenic seaweed Prasiola crispa
title Potencial tóxico e anticarcinogênico da alga Prasiola crispa
spellingShingle Potencial tóxico e anticarcinogênico da alga Prasiola crispa
Zemolin, Ana Paula Pegoraro
Prasiola crispa
Inseticida
Efeito antitumoral
Insecticide
Antitumoral effect
CNPQ::CIENCIAS BIOLOGICAS::BIOQUIMICA
title_short Potencial tóxico e anticarcinogênico da alga Prasiola crispa
title_full Potencial tóxico e anticarcinogênico da alga Prasiola crispa
title_fullStr Potencial tóxico e anticarcinogênico da alga Prasiola crispa
title_full_unstemmed Potencial tóxico e anticarcinogênico da alga Prasiola crispa
title_sort Potencial tóxico e anticarcinogênico da alga Prasiola crispa
author Zemolin, Ana Paula Pegoraro
author_facet Zemolin, Ana Paula Pegoraro
author_role author
dc.contributor.none.fl_str_mv Franco, Jeferson Luis
http://lattes.cnpq.br/1680065573338339
Soares, Félix Alexandre Antunes
http://lattes.cnpq.br/8752453650114092
Rubin, Maribel Antonello
http://lattes.cnpq.br/7237734243628134
Rosemberg, Denis Broock
http://lattes.cnpq.br/7713953979203056
dc.contributor.author.fl_str_mv Zemolin, Ana Paula Pegoraro
dc.subject.por.fl_str_mv Prasiola crispa
Inseticida
Efeito antitumoral
Insecticide
Antitumoral effect
CNPQ::CIENCIAS BIOLOGICAS::BIOQUIMICA
topic Prasiola crispa
Inseticida
Efeito antitumoral
Insecticide
Antitumoral effect
CNPQ::CIENCIAS BIOLOGICAS::BIOQUIMICA
description Toxic and anticarcinogenic effects of Prasiola Seaweed extract crispa (PCE) were investigated in Drosophila melanogaster, Nauphoeta cinérea and leukemic cells. In fruit flies, toxicity was assessed as mortality and biochemical changes, including acetylcholinesterase (AChE) and oxidative stress markers. The cardiotoxic action of PCE was examined in a semi-isolated heart model cheap. They were also analyzed the antiproliferative properties of Prasiola crispa (Pc) in leukemic K562 cells. The PCE administration (2 mg / ml) in flies, lasted 24 hours and resulted in a significant increase in mortality (7.6 fold increase compared to control). Activity of AChE (GSH) glutathione levels and the hydroperoxide formation was unchanged. Glutathione S-transferase (GST) and catalase (CAT) were significantly altered after treatment PCE. The fraction III (ethyl acetate) PCE was significantly more toxic to the flies compared to fractions I (methanol) and II (ethanol). A significant decrease in heart function inexpensive semi isolated heart model was observed. Addition of 5,5'-dithiobis acid (2-nitrobenzoic acid (DTNB), an oxidizing agent, concomitantly with the extract significantly blocked this effect. The PCE insecticidal properties can be related to changes in the important antioxidant detoxification system as well as to changes in insect cardiac function. To assess the antiproliferative activities of ethanolic fraction (EF) and ethyl acetate (EAF) of Prasiola crispa extract, cancerous leukemic K562 cells were exposed for 24 hours to different concentrations of PCE fractions. After treatment, cell viability, PARP cleavage and apoptosis Nrf2 expression of HO-1 and HSP70 were determined. The EAF showed a higher cytotoxic activity on leukemic cells as compared to EF. Cell proliferation was inhibited, a fact which was accompanied by a marked increase in the expression of Nrf2, HO-1 and HSP70 protein levels, indicating signs of oxidative stress. The results indicate the potential antitumor effect of Prasiola crispa algae.
publishDate 2015
dc.date.none.fl_str_mv 2015-12-22
2019-07-24T17:29:11Z
2019-07-24T17:29:11Z
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dc.type.driver.fl_str_mv info:eu-repo/semantics/doctoralThesis
format doctoralThesis
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://repositorio.ufsm.br/handle/1/17548
dc.identifier.dark.fl_str_mv ark:/26339/001300000b9fz
url http://repositorio.ufsm.br/handle/1/17548
identifier_str_mv ark:/26339/001300000b9fz
dc.language.iso.fl_str_mv por
language por
dc.rights.driver.fl_str_mv Attribution-NonCommercial-NoDerivatives 4.0 International
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Attribution-NonCommercial-NoDerivatives 4.0 International
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Universidade Federal de Santa Maria
Brasil
Bioquímica
UFSM
Programa de Pós-Graduação em Ciências Biológicas: Bioquímica Toxicológica
Centro de Ciências Naturais e Exatas
publisher.none.fl_str_mv Universidade Federal de Santa Maria
Brasil
Bioquímica
UFSM
Programa de Pós-Graduação em Ciências Biológicas: Bioquímica Toxicológica
Centro de Ciências Naturais e Exatas
dc.source.none.fl_str_mv reponame:Manancial - Repositório Digital da UFSM
instname:Universidade Federal de Santa Maria (UFSM)
instacron:UFSM
instname_str Universidade Federal de Santa Maria (UFSM)
instacron_str UFSM
institution UFSM
reponame_str Manancial - Repositório Digital da UFSM
collection Manancial - Repositório Digital da UFSM
repository.name.fl_str_mv Manancial - Repositório Digital da UFSM - Universidade Federal de Santa Maria (UFSM)
repository.mail.fl_str_mv atendimento.sib@ufsm.br||tedebc@gmail.com||manancial@ufsm.br
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