Mecanismos envolvidos na proteção do disseleneto de difenila sobre a toxicidade induzida por metilmercúrio em Saccharomyces cerevisiae

Detalhes bibliográficos
Autor(a) principal: Lovato, Fabricio Luís
Data de Publicação: 2015
Tipo de documento: Dissertação
Idioma: por
Título da fonte: Manancial - Repositório Digital da UFSM
Texto Completo: http://repositorio.ufsm.br/handle/1/17374
Resumo: Humans are usually exposed to organic form of mercury, the organometallic cation methylmercury ([CH3Hg]+, MeHg), by eating fish and seafood. The neurotoxic effects of MeHg are already widely known. Individuals exposed to high concentrations of this compound showed sensory disorders in the hands and feet, hearing and visual impairment, weakness and, in extreme cases, paralysis and death. Although the exact mechanisms underlying the toxicity of MeHg are not yet completely understood, there is evidence that oxidative stress plays a central role. The organic compound derived from selenium, diphenyl diselenide [(PhSe)2] is a simple electrophilic synthetic intermediate in the synthesis of various organic compounds of pharmaceutical interest containing selenium and have already presented antioxidant, anti-nociceptive, anti-inflammatory, antihyperglycemic, antiteratogenic, among others properties. The aim of this study was to investigate some mechanisms involved in the protective effect of (PhSe)2 on the toxicity induced by MeHg, using wild and knockout strains of S. cerevisiae for different enzymes and proteins linked to the antioxidant defense system. Using these strains, as well as different concentrations (PhSe)2 and/or MeHg, the specific objectives of this study were: i) to evaluate the growth inhibition; ii) to quantify the production of reactive oxygen species; iii) to evaluate the permeability of cell membranes; iv) to quantify the intracellular GSH content. This study sheds light on the mechanisms involved in the protection of diphenyl diselenide against MeHg indicating the involvement of the antioxidant defense system of S. cerevisiae and the sequestering of Hg in (PhSe)2 protection. The compound diphenyl diselenide protects against the toxicity induced by methylmercury, as noted in the recovery of growth and lower levels of reactive oxygen species, membrane permeability and restoration of intracellular GSH content in yeasts treated with both compounds. The protective effect triggered by diphenyl diselenide seems to be related with the activation of some enzymes of antioxidant system of yeasts. Not all analyzed antioxidant enzymes had the same participation or importance in the protection mechanism. Functional and genetic similarities between yeast and mammalian cells suggests that the elucidation of these mechanisms will help direct the search to human.
id UFSM_fef72880249cec7ad67de8c2a5e3cf27
oai_identifier_str oai:repositorio.ufsm.br:1/17374
network_acronym_str UFSM
network_name_str Manancial - Repositório Digital da UFSM
repository_id_str
spelling Mecanismos envolvidos na proteção do disseleneto de difenila sobre a toxicidade induzida por metilmercúrio em Saccharomyces cerevisiaeMechanisms involved in the action of diphenyl diselenide on methylmercury-induced toxicity in Saccharomyces cerevisiaeMetilmercúrioDisseleneto de difenilaSaccharomyces cerevisiaeEstresse oxidativoDefesas antioxidantesMethylmercuryDiphenyl diselenideOxidative stressAntioxidant defensesCNPQ::CIENCIAS BIOLOGICAS::BIOQUIMICAHumans are usually exposed to organic form of mercury, the organometallic cation methylmercury ([CH3Hg]+, MeHg), by eating fish and seafood. The neurotoxic effects of MeHg are already widely known. Individuals exposed to high concentrations of this compound showed sensory disorders in the hands and feet, hearing and visual impairment, weakness and, in extreme cases, paralysis and death. Although the exact mechanisms underlying the toxicity of MeHg are not yet completely understood, there is evidence that oxidative stress plays a central role. The organic compound derived from selenium, diphenyl diselenide [(PhSe)2] is a simple electrophilic synthetic intermediate in the synthesis of various organic compounds of pharmaceutical interest containing selenium and have already presented antioxidant, anti-nociceptive, anti-inflammatory, antihyperglycemic, antiteratogenic, among others properties. The aim of this study was to investigate some mechanisms involved in the protective effect of (PhSe)2 on the toxicity induced by MeHg, using wild and knockout strains of S. cerevisiae for different enzymes and proteins linked to the antioxidant defense system. Using these strains, as well as different concentrations (PhSe)2 and/or MeHg, the specific objectives of this study were: i) to evaluate the growth inhibition; ii) to quantify the production of reactive oxygen species; iii) to evaluate the permeability of cell membranes; iv) to quantify the intracellular GSH content. This study sheds light on the mechanisms involved in the protection of diphenyl diselenide against MeHg indicating the involvement of the antioxidant defense system of S. cerevisiae and the sequestering of Hg in (PhSe)2 protection. The compound diphenyl diselenide protects against the toxicity induced by methylmercury, as noted in the recovery of growth and lower levels of reactive oxygen species, membrane permeability and restoration of intracellular GSH content in yeasts treated with both compounds. The protective effect triggered by diphenyl diselenide seems to be related with the activation of some enzymes of antioxidant system of yeasts. Not all analyzed antioxidant enzymes had the same participation or importance in the protection mechanism. Functional and genetic similarities between yeast and mammalian cells suggests that the elucidation of these mechanisms will help direct the search to human.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - CAPESOs seres humanos normalmente são expostos à forma orgânica do Hg, o cátion organometálico metilmercúrio ([CH3Hg]+, MeHg), através da alimentação com peixes e frutos do mar. Os efeitos neurotóxicos do MeHg já são amplamente conhecidos. Indivíduos expostos a altas concentrações desse composto apresentaram distúrbios sensoriais nas mãos e pés, disfunção auditiva e visual, fraqueza e, em casos extremos, paralisia e morte. Embora os mecanismos exatos subjacentes à toxicidade do MeHg ainda não estejam totalmente elucidados, há evidências de que o estresse oxidativo desempenha um papel central nesse processo. O composto orgânico derivado do selênio, disseleneto de difenila [(PhSe)2] é um intermediário sintético eletrofílico simples na síntese de vários compostos orgânicos de interesse farmacológico contendo selênio, tendo apresentado as propriedades antioxidante, anti-nociceptiva, anti-inflamatória, antihiperglicêmica, antiteratogênica, entre outras. O objetivo principal deste trabalho foi investigar alguns mecanismos envolvidas no efeito protetor do (PhSe)2 sobre a toxicidade induzida por MeHg, utilizando cepas selvagem e knockout de Saccharomyces cerevisiae para diferentes enzimas e proteínas ligadas ao sistema de defesa antioxidante. Utilizando-se dessas linhagens, bem como diferentes concentrações de (PhSe)2 e/ou MeHg, os objetivos específicos desse trabalho foram: i) avaliar a inibição do crescimento; ii) quantificar a produção de espécies reativas do oxigênio; iii) avaliar a permeabilidade das membranas celulares; iv) quantificar o conteúdo intracelular de GSH. O presente estudo lança luz sobre os mecanismos envolvidos na proteção do disseleneto de difenila contra o MeHg indicando o envolvimento do sistema de defesa antioxidante de S. cerevisiae e o sequestro de Hg na proteção do (PhSe)2. O composto disseleneto de difenila protege contra a toxicidade induzida pelo metilmercúrio, conforme observou-se na recuperação do crescimento e menores índices de espécies reativas de oxigênio, permeabilidade de membrana e restauração do conteúdo intracelular de GSH, em leveduras tratadas com ambos os compostos. O efeito protetor desencadeado pelo disseleneto de difenila parece estar relacionado com a ativação de algumas enzimas do sistema antioxidante das leveduras. Nem todas as enzimas antioxidantes analisadas tiveram a mesma participação ou importância no mecanismo de proteção. A similaridade funcional e genética entre células de leveduras e de mamíferos sugere que a elucidação desses mecanismos ajudará a direcionar a pesquisa para humanos.Universidade Federal de Santa MariaBrasilBioquímicaUFSMPrograma de Pós-Graduação em Ciências Biológicas: Bioquímica ToxicológicaCentro de Ciências Naturais e ExatasDalla Corte, Cristiane Lenzhttp://lattes.cnpq.br/5296284169605317Rocha, Joao Batista Teixeira dahttp://lattes.cnpq.br/3935055744673018Rosemberg, Denis Broockhttp://lattes.cnpq.br/7713953979203056Saffi, Jeniferhttp://lattes.cnpq.br/3179264934205423Lovato, Fabricio Luís2019-07-09T22:32:16Z2019-07-09T22:32:16Z2015-12-14info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisapplication/pdfhttp://repositorio.ufsm.br/handle/1/17374porAttribution-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:UFSM2019-07-10T06:00:34Zoai:repositorio.ufsm.br:1/17374Biblioteca Digital de Teses e Dissertaçõeshttps://repositorio.ufsm.br/ONGhttps://repositorio.ufsm.br/oai/requestatendimento.sib@ufsm.br||tedebc@gmail.comopendoar:2019-07-10T06:00:34Manancial - Repositório Digital da UFSM - Universidade Federal de Santa Maria (UFSM)false
dc.title.none.fl_str_mv Mecanismos envolvidos na proteção do disseleneto de difenila sobre a toxicidade induzida por metilmercúrio em Saccharomyces cerevisiae
Mechanisms involved in the action of diphenyl diselenide on methylmercury-induced toxicity in Saccharomyces cerevisiae
title Mecanismos envolvidos na proteção do disseleneto de difenila sobre a toxicidade induzida por metilmercúrio em Saccharomyces cerevisiae
spellingShingle Mecanismos envolvidos na proteção do disseleneto de difenila sobre a toxicidade induzida por metilmercúrio em Saccharomyces cerevisiae
Lovato, Fabricio Luís
Metilmercúrio
Disseleneto de difenila
Saccharomyces cerevisiae
Estresse oxidativo
Defesas antioxidantes
Methylmercury
Diphenyl diselenide
Oxidative stress
Antioxidant defenses
CNPQ::CIENCIAS BIOLOGICAS::BIOQUIMICA
title_short Mecanismos envolvidos na proteção do disseleneto de difenila sobre a toxicidade induzida por metilmercúrio em Saccharomyces cerevisiae
title_full Mecanismos envolvidos na proteção do disseleneto de difenila sobre a toxicidade induzida por metilmercúrio em Saccharomyces cerevisiae
title_fullStr Mecanismos envolvidos na proteção do disseleneto de difenila sobre a toxicidade induzida por metilmercúrio em Saccharomyces cerevisiae
title_full_unstemmed Mecanismos envolvidos na proteção do disseleneto de difenila sobre a toxicidade induzida por metilmercúrio em Saccharomyces cerevisiae
title_sort Mecanismos envolvidos na proteção do disseleneto de difenila sobre a toxicidade induzida por metilmercúrio em Saccharomyces cerevisiae
author Lovato, Fabricio Luís
author_facet Lovato, Fabricio Luís
author_role author
dc.contributor.none.fl_str_mv Dalla Corte, Cristiane Lenz
http://lattes.cnpq.br/5296284169605317
Rocha, Joao Batista Teixeira da
http://lattes.cnpq.br/3935055744673018
Rosemberg, Denis Broock
http://lattes.cnpq.br/7713953979203056
Saffi, Jenifer
http://lattes.cnpq.br/3179264934205423
dc.contributor.author.fl_str_mv Lovato, Fabricio Luís
dc.subject.por.fl_str_mv Metilmercúrio
Disseleneto de difenila
Saccharomyces cerevisiae
Estresse oxidativo
Defesas antioxidantes
Methylmercury
Diphenyl diselenide
Oxidative stress
Antioxidant defenses
CNPQ::CIENCIAS BIOLOGICAS::BIOQUIMICA
topic Metilmercúrio
Disseleneto de difenila
Saccharomyces cerevisiae
Estresse oxidativo
Defesas antioxidantes
Methylmercury
Diphenyl diselenide
Oxidative stress
Antioxidant defenses
CNPQ::CIENCIAS BIOLOGICAS::BIOQUIMICA
description Humans are usually exposed to organic form of mercury, the organometallic cation methylmercury ([CH3Hg]+, MeHg), by eating fish and seafood. The neurotoxic effects of MeHg are already widely known. Individuals exposed to high concentrations of this compound showed sensory disorders in the hands and feet, hearing and visual impairment, weakness and, in extreme cases, paralysis and death. Although the exact mechanisms underlying the toxicity of MeHg are not yet completely understood, there is evidence that oxidative stress plays a central role. The organic compound derived from selenium, diphenyl diselenide [(PhSe)2] is a simple electrophilic synthetic intermediate in the synthesis of various organic compounds of pharmaceutical interest containing selenium and have already presented antioxidant, anti-nociceptive, anti-inflammatory, antihyperglycemic, antiteratogenic, among others properties. The aim of this study was to investigate some mechanisms involved in the protective effect of (PhSe)2 on the toxicity induced by MeHg, using wild and knockout strains of S. cerevisiae for different enzymes and proteins linked to the antioxidant defense system. Using these strains, as well as different concentrations (PhSe)2 and/or MeHg, the specific objectives of this study were: i) to evaluate the growth inhibition; ii) to quantify the production of reactive oxygen species; iii) to evaluate the permeability of cell membranes; iv) to quantify the intracellular GSH content. This study sheds light on the mechanisms involved in the protection of diphenyl diselenide against MeHg indicating the involvement of the antioxidant defense system of S. cerevisiae and the sequestering of Hg in (PhSe)2 protection. The compound diphenyl diselenide protects against the toxicity induced by methylmercury, as noted in the recovery of growth and lower levels of reactive oxygen species, membrane permeability and restoration of intracellular GSH content in yeasts treated with both compounds. The protective effect triggered by diphenyl diselenide seems to be related with the activation of some enzymes of antioxidant system of yeasts. Not all analyzed antioxidant enzymes had the same participation or importance in the protection mechanism. Functional and genetic similarities between yeast and mammalian cells suggests that the elucidation of these mechanisms will help direct the search to human.
publishDate 2015
dc.date.none.fl_str_mv 2015-12-14
2019-07-09T22:32:16Z
2019-07-09T22:32:16Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/masterThesis
format masterThesis
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://repositorio.ufsm.br/handle/1/17374
url http://repositorio.ufsm.br/handle/1/17374
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
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
_version_ 1805922044673523712