Avaliação da Vanillosmopsis arborea Baker e (-)-α-bisabolol frente a parâmetros oxidativos e toxicológicos

Detalhes bibliográficos
Autor(a) principal: Leite, Gerlânia de Oliveira
Data de Publicação: 2017
Tipo de documento: Tese
Idioma: por
Título da fonte: Manancial - Repositório Digital da UFSM
Texto Completo: http://repositorio.ufsm.br/handle/1/14030
Resumo: Vanillosmopsis arborea Baker belongs to the Asteraceae family and has a recognized economic value due to its anti-inflammatory properties, derived from sesquiterpene (-)-α-bisabolol (BISA), which is present in high concentrations in the essential oil of its wood (OEVA). BISA is used in a wide variety of dermatological products. Some studies suggest that the pharmacological effects of this sesquiterpene, as well as the OEVA, may be related to its antioxidant activity. Rotenone, a pesticide which acts as mitochondrial inhibitor of the complex I from electron chain transporter, has been used in experimental models of parkinsonism by causing an increase in the production of reactive oxygen species (ROS). The aim of this study was to evaluate the antioxidant activity of V. arborea, as well as the antioxidant, neuroprotective and toxicological potential of (-)-α-bisabolol in different experimental models. Firstly, it was evaluated the in vitro effect of the OEVA and the extract of de V. arborea on the Fe (II)-induced thiobarbituric acid (TBARS) production and dichlorofluorescein (DCFH) oxidation in rat brain homogenates, the antioxidant potential through the DPPH radical scavenging test (2 , 2-diphenyl-1-picrylhydrazyl) and the chelating activity. The extracts of V. arborea presented antioxidant activity in vitro demonstrated through a decrease in lipid peroxidation induced by Fe(II), and by its ability in to scavenging DPPH radical. Moreover, the OEVA and BISA reduced the oxidation of DCFH induced by H2O2.The effect of BISA was also in a model of cytotoxicity and genotoxicity in peripheral blood mononuclear (PBMC) and red blood cells from humans. The BISA reduced the cellular viability, caused a nuclear damage and hemolytic activity only when the cells were exposed to high concentrations. After, the antioxidant and neuroprotective effect of BISA was evaluated in vivo using Drosophila melanogaster as organism model. The fruit flies were exposed to rotenone and/or BISA and it were observed behavioral parameters using negative geotaxis and mortality tests. In this model, it were also determined the expression of genes of superoxide dismutase (SOD), catalase and Keap 1 (related to the oxidative stress signaling pathway), also the thiol content and mitochondrial I complex activity. BISA showed no toxicity in the D. melanogaster model. BISA decreased the mortality and increased the locomotor activity in D. melanogaster exposed to rotenone. The alteration in the expression of SOD mRNA caused by rotenone was normalized by treatment with BISA (250 μM). BISA did not change the other parameters tested. In conclusion, V. arborea presents antioxidant activity. BISA, the main constituent of the essential oil, demonstrated antioxidant and neuroprotective activity, besides not showing toxicity in an experimental model using D. melanogaster. The cytotoxicity and genotoxicity of this compound was observed only at high concentrations and over a long period of exposure to PBMC. Therefore, our results show that BISA protects against the toxicity induced by rotenone. Our study reports the antioxidant, neuroprotective effects of V. arborea and its major compound, with low toxicity and suggests its potential as a possible therapeutic agent.
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spelling Avaliação da Vanillosmopsis arborea Baker e (-)-α-bisabolol frente a parâmetros oxidativos e toxicológicosEvaluation of Vanillosmopsis arborea Baker and (-) - α-bisabolol on oxidative and toxicological parameters.Vanillosmopsis arborea(-)-α-bisabololEstresse oxidativoVanillosmopsis arborea(-) - α-bisabololOxidative stressCNPQ::CIENCIAS DA SAUDE::FARMACIAVanillosmopsis arborea Baker belongs to the Asteraceae family and has a recognized economic value due to its anti-inflammatory properties, derived from sesquiterpene (-)-α-bisabolol (BISA), which is present in high concentrations in the essential oil of its wood (OEVA). BISA is used in a wide variety of dermatological products. Some studies suggest that the pharmacological effects of this sesquiterpene, as well as the OEVA, may be related to its antioxidant activity. Rotenone, a pesticide which acts as mitochondrial inhibitor of the complex I from electron chain transporter, has been used in experimental models of parkinsonism by causing an increase in the production of reactive oxygen species (ROS). The aim of this study was to evaluate the antioxidant activity of V. arborea, as well as the antioxidant, neuroprotective and toxicological potential of (-)-α-bisabolol in different experimental models. Firstly, it was evaluated the in vitro effect of the OEVA and the extract of de V. arborea on the Fe (II)-induced thiobarbituric acid (TBARS) production and dichlorofluorescein (DCFH) oxidation in rat brain homogenates, the antioxidant potential through the DPPH radical scavenging test (2 , 2-diphenyl-1-picrylhydrazyl) and the chelating activity. The extracts of V. arborea presented antioxidant activity in vitro demonstrated through a decrease in lipid peroxidation induced by Fe(II), and by its ability in to scavenging DPPH radical. Moreover, the OEVA and BISA reduced the oxidation of DCFH induced by H2O2.The effect of BISA was also in a model of cytotoxicity and genotoxicity in peripheral blood mononuclear (PBMC) and red blood cells from humans. The BISA reduced the cellular viability, caused a nuclear damage and hemolytic activity only when the cells were exposed to high concentrations. After, the antioxidant and neuroprotective effect of BISA was evaluated in vivo using Drosophila melanogaster as organism model. The fruit flies were exposed to rotenone and/or BISA and it were observed behavioral parameters using negative geotaxis and mortality tests. In this model, it were also determined the expression of genes of superoxide dismutase (SOD), catalase and Keap 1 (related to the oxidative stress signaling pathway), also the thiol content and mitochondrial I complex activity. BISA showed no toxicity in the D. melanogaster model. BISA decreased the mortality and increased the locomotor activity in D. melanogaster exposed to rotenone. The alteration in the expression of SOD mRNA caused by rotenone was normalized by treatment with BISA (250 μM). BISA did not change the other parameters tested. In conclusion, V. arborea presents antioxidant activity. BISA, the main constituent of the essential oil, demonstrated antioxidant and neuroprotective activity, besides not showing toxicity in an experimental model using D. melanogaster. The cytotoxicity and genotoxicity of this compound was observed only at high concentrations and over a long period of exposure to PBMC. Therefore, our results show that BISA protects against the toxicity induced by rotenone. Our study reports the antioxidant, neuroprotective effects of V. arborea and its major compound, with low toxicity and suggests its potential as a possible therapeutic agent.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - CAPESA Vanillosmopsis arborea Baker pertence à família Asteraceae e apresenta reconhecido valor econômico devido às suas propriedades anti-inflamatórias, provenientes do sesquiterpeno (-)-α-bisabolol (BISA), o qual está presente em concentrações elevadas no óleo essencial de sua madeira (OEVA). O BISA é utilizado em uma grande variedade de produtos dermatológicos. Alguns estudos sugerem que os efeitos farmacológicos deste sesquiterpeno, bem como do OEVA, podem estar relacionados a sua atividade antioxidante. A rotenona, um pesticida que atua como inibidor do complexo I da cadeia transportadora de elétrons mitocondrial, tem sido utilizada em modelos experimentais de parkinsonismo por causar aumento na produção de espécies reativas de oxigênio (EROs). O objetivo deste estudo foi avaliar a atividade antioxidante de V. arborea, bem como o potencial antioxidante, neuroprotetor e toxicológico do (-)-α-bisabolol em diferentes modelos experimentais. Primeiramente, foi avaliado o efeito in vitro do OEVA e extrato de V. arborea na produção de substâncias reativas ao ácido tiobarbitúrico (TBARS) induzido por Fe(II) e oxidação da diclorofluoresceína (DCFH) em homogeneizado de cérebro de ratos, o potencial antioxidante através do teste de sequestro do radical DPPH (2,2-difenil-1-picril-hidrazil) e a atividade quelante. Os extratos de V. arborea apresentam atividade antioxidante in vitro demonstrado através da diminuição da peroxidação lipídica induzida por Fe(II), e também pela capacidade de sequestrar o radical DPPH. Além disso, o OEVA e BISA reduziram a oxidação da DCFH induzida pelo H2O2. O efeito do BISA foi também avaliado em modelo de citotoxicidade e genotoxicidade em células monocucleares e hemácias de sangue periféricos (CMSP) humano. O BISA reduziu a viabilidade celular, causou dano nuclear e atividade hemolítica somente quando as células foram expostas à altas concentrações. Após, o efeito antioxidante e neuroprotetor do BISA foi avaliado in vivo utilizando Drosophila melanogaster como organismo modelo. As moscas da fruta foram expostas à rotenona e/ou BISA e foram observados parâmetros comportamentais, utilizando os testes de geotaxia negativa e mortalidade. Neste modelo, também foi determinada a immunorreatividade da tirosina hidroxilase (TH), a expressão dos genes superóxido dismutase (SOD), catalase e Keap 1 (relacionados à via de sinalização do estresse oxidativo), além do conteúdo de tióis e atividade do complexo I mitocondrial. O BISA não demonstrou toxicidade no modelo de D. Melanogaster. O BISA diminuiu a mortalidade e a perda da atividade locomotora em D. Melanogaster expostas a rotenona. A alteração na expressão de RNAm da SOD causada pela rotenona foi normalizada pelo tratamento com BISA (250 μM). O co-tratamento com BISA não modificou os outros parâmetros testados. Em conclusão a V. arborea apresenta atividade antioxidante. O BISA, principal constituinte do óleo essencial, demonstrou atividade antioxidante e neuroprotetora, além de não demonstrar toxicidade em modelo experimental utilizando D. melanogaster. A citotoxicidade e a genotoxicidade deste composto foi observada somente em altas concentrações e por um longo período de exposição em CMSP. Assim sendo, nossos resultados mostram que o BISA protege contra a toxicidade induzida por rotenona. Nossos estudos demonstraram que V. arborea e seu composto majoritário apresentam efeito antioxidante, neuroprotetor, com baixa toxicidade e sugere sua potencialidade como possível agente terapêutico.Universidade Federal de Santa MariaBrasilFarmacologiaUFSMPrograma de Pós-Graduação em FarmacologiaCentro de Ciências da SaúdeWagner, Carolinehttp://lattes.cnpq.br/4004565241849091Fachinetto, Roseleihttp://lattes.cnpq.br/7203076675431306Posser, Thaishttp://lattes.cnpq.br/2277857386983441Barros, Adriana Rolim Camposhttp://lattes.cnpq.br/3791336333658295Corte, Cristiane Lenz Dallahttp://lattes.cnpq.br/5296284169605317Bochi, Guilherme Vargashttp://lattes.cnpq.br/4191221572795869Leite, Gerlânia de Oliveira2018-08-07T18:38:13Z2018-08-07T18:38:13Z2017-08-18info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/doctoralThesisapplication/pdfhttp://repositorio.ufsm.br/handle/1/14030porAttribution-NonCommercial-NoDerivatives 4.0 Internationalhttp://creativecommons.org/licenses/by-nc-nd/4.0/info:eu-repo/semantics/openAccessreponame:Manancial - Repositório Digital da UFSMinstname:Universidade Federal de Santa Maria (UFSM)instacron:UFSM2022-04-07T16:40:01Zoai:repositorio.ufsm.br:1/14030Biblioteca Digital de Teses e Dissertaçõeshttps://repositorio.ufsm.br/ONGhttps://repositorio.ufsm.br/oai/requestatendimento.sib@ufsm.br||tedebc@gmail.comopendoar:2022-04-07T16:40:01Manancial - Repositório Digital da UFSM - Universidade Federal de Santa Maria (UFSM)false
dc.title.none.fl_str_mv Avaliação da Vanillosmopsis arborea Baker e (-)-α-bisabolol frente a parâmetros oxidativos e toxicológicos
Evaluation of Vanillosmopsis arborea Baker and (-) - α-bisabolol on oxidative and toxicological parameters.
title Avaliação da Vanillosmopsis arborea Baker e (-)-α-bisabolol frente a parâmetros oxidativos e toxicológicos
spellingShingle Avaliação da Vanillosmopsis arborea Baker e (-)-α-bisabolol frente a parâmetros oxidativos e toxicológicos
Leite, Gerlânia de Oliveira
Vanillosmopsis arborea
(-)-α-bisabolol
Estresse oxidativo
Vanillosmopsis arborea
(-) - α-bisabolol
Oxidative stress
CNPQ::CIENCIAS DA SAUDE::FARMACIA
title_short Avaliação da Vanillosmopsis arborea Baker e (-)-α-bisabolol frente a parâmetros oxidativos e toxicológicos
title_full Avaliação da Vanillosmopsis arborea Baker e (-)-α-bisabolol frente a parâmetros oxidativos e toxicológicos
title_fullStr Avaliação da Vanillosmopsis arborea Baker e (-)-α-bisabolol frente a parâmetros oxidativos e toxicológicos
title_full_unstemmed Avaliação da Vanillosmopsis arborea Baker e (-)-α-bisabolol frente a parâmetros oxidativos e toxicológicos
title_sort Avaliação da Vanillosmopsis arborea Baker e (-)-α-bisabolol frente a parâmetros oxidativos e toxicológicos
author Leite, Gerlânia de Oliveira
author_facet Leite, Gerlânia de Oliveira
author_role author
dc.contributor.none.fl_str_mv Wagner, Caroline
http://lattes.cnpq.br/4004565241849091
Fachinetto, Roselei
http://lattes.cnpq.br/7203076675431306
Posser, Thais
http://lattes.cnpq.br/2277857386983441
Barros, Adriana Rolim Campos
http://lattes.cnpq.br/3791336333658295
Corte, Cristiane Lenz Dalla
http://lattes.cnpq.br/5296284169605317
Bochi, Guilherme Vargas
http://lattes.cnpq.br/4191221572795869
dc.contributor.author.fl_str_mv Leite, Gerlânia de Oliveira
dc.subject.por.fl_str_mv Vanillosmopsis arborea
(-)-α-bisabolol
Estresse oxidativo
Vanillosmopsis arborea
(-) - α-bisabolol
Oxidative stress
CNPQ::CIENCIAS DA SAUDE::FARMACIA
topic Vanillosmopsis arborea
(-)-α-bisabolol
Estresse oxidativo
Vanillosmopsis arborea
(-) - α-bisabolol
Oxidative stress
CNPQ::CIENCIAS DA SAUDE::FARMACIA
description Vanillosmopsis arborea Baker belongs to the Asteraceae family and has a recognized economic value due to its anti-inflammatory properties, derived from sesquiterpene (-)-α-bisabolol (BISA), which is present in high concentrations in the essential oil of its wood (OEVA). BISA is used in a wide variety of dermatological products. Some studies suggest that the pharmacological effects of this sesquiterpene, as well as the OEVA, may be related to its antioxidant activity. Rotenone, a pesticide which acts as mitochondrial inhibitor of the complex I from electron chain transporter, has been used in experimental models of parkinsonism by causing an increase in the production of reactive oxygen species (ROS). The aim of this study was to evaluate the antioxidant activity of V. arborea, as well as the antioxidant, neuroprotective and toxicological potential of (-)-α-bisabolol in different experimental models. Firstly, it was evaluated the in vitro effect of the OEVA and the extract of de V. arborea on the Fe (II)-induced thiobarbituric acid (TBARS) production and dichlorofluorescein (DCFH) oxidation in rat brain homogenates, the antioxidant potential through the DPPH radical scavenging test (2 , 2-diphenyl-1-picrylhydrazyl) and the chelating activity. The extracts of V. arborea presented antioxidant activity in vitro demonstrated through a decrease in lipid peroxidation induced by Fe(II), and by its ability in to scavenging DPPH radical. Moreover, the OEVA and BISA reduced the oxidation of DCFH induced by H2O2.The effect of BISA was also in a model of cytotoxicity and genotoxicity in peripheral blood mononuclear (PBMC) and red blood cells from humans. The BISA reduced the cellular viability, caused a nuclear damage and hemolytic activity only when the cells were exposed to high concentrations. After, the antioxidant and neuroprotective effect of BISA was evaluated in vivo using Drosophila melanogaster as organism model. The fruit flies were exposed to rotenone and/or BISA and it were observed behavioral parameters using negative geotaxis and mortality tests. In this model, it were also determined the expression of genes of superoxide dismutase (SOD), catalase and Keap 1 (related to the oxidative stress signaling pathway), also the thiol content and mitochondrial I complex activity. BISA showed no toxicity in the D. melanogaster model. BISA decreased the mortality and increased the locomotor activity in D. melanogaster exposed to rotenone. The alteration in the expression of SOD mRNA caused by rotenone was normalized by treatment with BISA (250 μM). BISA did not change the other parameters tested. In conclusion, V. arborea presents antioxidant activity. BISA, the main constituent of the essential oil, demonstrated antioxidant and neuroprotective activity, besides not showing toxicity in an experimental model using D. melanogaster. The cytotoxicity and genotoxicity of this compound was observed only at high concentrations and over a long period of exposure to PBMC. Therefore, our results show that BISA protects against the toxicity induced by rotenone. Our study reports the antioxidant, neuroprotective effects of V. arborea and its major compound, with low toxicity and suggests its potential as a possible therapeutic agent.
publishDate 2017
dc.date.none.fl_str_mv 2017-08-18
2018-08-07T18:38:13Z
2018-08-07T18:38:13Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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/1/14030
url http://repositorio.ufsm.br/handle/1/14030
dc.language.iso.fl_str_mv por
language por
dc.rights.driver.fl_str_mv Attribution-NonCommercial-NoDerivatives 4.0 International
http://creativecommons.org/licenses/by-nc-nd/4.0/
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Attribution-NonCommercial-NoDerivatives 4.0 International
http://creativecommons.org/licenses/by-nc-nd/4.0/
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
Farmacologia
UFSM
Programa de Pós-Graduação em Farmacologia
Centro de Ciências da Saúde
publisher.none.fl_str_mv Universidade Federal de Santa Maria
Brasil
Farmacologia
UFSM
Programa de Pós-Graduação em Farmacologia
Centro de Ciências da Saúde
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
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