Ação farmacológica do 4,4’-dicloro-difenil disseleneto em modelos de hiperglicemia e obesidade em ratos

Detalhes bibliográficos
Ano de defesa: 2017
Autor(a) principal: Quines, Caroline Brandão lattes
Orientador(a): Nogueira, Cristina Wayne lattes
Banca de defesa: Bem, Andreza Fabro de lattes, Premaor, Melissa Orlandin lattes, Mathias, Paulo Cezar de Freitas lattes, Emanuelli, Tatiana lattes
Tipo de documento: Tese
Tipo de acesso: Acesso aberto
Idioma: por
Instituição de defesa: Universidade Federal de Santa Maria
Centro de Ciências Naturais e Exatas
Programa de Pós-Graduação: Programa de Pós-Graduação em Ciências Biológicas: Bioquímica Toxicológica
Departamento: Bioquímica
País: Brasil
Palavras-chave em Português:
Palavras-chave em Inglês:
Área do conhecimento CNPq:
Link de acesso: http://repositorio.ufsm.br/handle/1/18425
Resumo: The obesity epidemic is a worldwide public health problem and is considered one of the leading causes of death and disability worldwide. This is because the pathophysiology of this disease is extremely complex and involves a series of events in cascades that can even evolve into irreversible damage. Regarding treatment, drugs currently available for the treatment of obesity are often inefficient and have adverse effects, so the search for new drugs for the treatment of metabolic diseases has been growing so much in recent years. In this context, organic compounds of selenium have been studied in the last decades, mainly due to their diverse pharmacological activities, among them, antioxidant, neuroprotective, anticancer, antiviral, immunosuppressive, antimicrobial, anxiolytic, antidepressant-like and anti-inflammatory. However, these compounds have recently attracted attention because of their beneficial effects on the regulation of metabolic homeostasis. The present thesis aimed to investigate the pharmacological effects of 4,4'-dichloro-diphenyl diselenide, (p-ClPhSe)2 in hyperglycemia and obesity models induced by the administration of fructose or monosodium glutamate (MSG) in rats. In the manuscript 1, an insulin-mimetic effect of (p-ClPhSe)2 was demonstrated in vitro; this compound stimulated the glucose uptake into skeletal muscle and its acute antihyperglycemic effect in a model of hyperglycemia induced by the administration of fructose in rats. Furthermore, in the manuscript 1, acute treatment with (p-ClPhSe)2 protected against liver metabolic alterations induced by fructose; this compound redirected the carbohydrate metabolism. In that sense, in the article 1, a homeostatic effect of subchronic treatment with (p-ClPhSe)2 was demonstrated, this compound reduced the first signs of obesity induced with the administration of GMS in rats. Whereas in the manuscript 2, it was possible to observe a hepatoprotective effect of subchronic treatment with (p-ClPhSe)2 against the mitochondrial dysfunction, oxidative stress and inflammation induced by the administration of GMS in rats. In addition, a beneficial effect of subchronic treatment with (p-ClPhSe)2 against metabolic dysfunction in blood, liver and skeletal muscle induced by the administration of GMS in rats was demonstrated in manuscript 3. Taken together, the present results demonstrated that the compound, (p-ClPhSe)2, has several pharmacological properties, such as antihyperglycemic, insulin-mimetic, anti-inflammatory and antioxidant. It is known that drugs used for the treatment of obesity are often inefficient due to the complications present during the progression of obesity. Considering the pharmacological effects of (p-ClPhSe)2 demonstrated in the present study, this organic compound of selenium may be a future therapeutic alternative for the treatment of this pathology and its complications.
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spelling 2019-09-25T20:06:53Z2019-09-25T20:06:53Z2017-03-03http://repositorio.ufsm.br/handle/1/18425The obesity epidemic is a worldwide public health problem and is considered one of the leading causes of death and disability worldwide. This is because the pathophysiology of this disease is extremely complex and involves a series of events in cascades that can even evolve into irreversible damage. Regarding treatment, drugs currently available for the treatment of obesity are often inefficient and have adverse effects, so the search for new drugs for the treatment of metabolic diseases has been growing so much in recent years. In this context, organic compounds of selenium have been studied in the last decades, mainly due to their diverse pharmacological activities, among them, antioxidant, neuroprotective, anticancer, antiviral, immunosuppressive, antimicrobial, anxiolytic, antidepressant-like and anti-inflammatory. However, these compounds have recently attracted attention because of their beneficial effects on the regulation of metabolic homeostasis. The present thesis aimed to investigate the pharmacological effects of 4,4'-dichloro-diphenyl diselenide, (p-ClPhSe)2 in hyperglycemia and obesity models induced by the administration of fructose or monosodium glutamate (MSG) in rats. In the manuscript 1, an insulin-mimetic effect of (p-ClPhSe)2 was demonstrated in vitro; this compound stimulated the glucose uptake into skeletal muscle and its acute antihyperglycemic effect in a model of hyperglycemia induced by the administration of fructose in rats. Furthermore, in the manuscript 1, acute treatment with (p-ClPhSe)2 protected against liver metabolic alterations induced by fructose; this compound redirected the carbohydrate metabolism. In that sense, in the article 1, a homeostatic effect of subchronic treatment with (p-ClPhSe)2 was demonstrated, this compound reduced the first signs of obesity induced with the administration of GMS in rats. Whereas in the manuscript 2, it was possible to observe a hepatoprotective effect of subchronic treatment with (p-ClPhSe)2 against the mitochondrial dysfunction, oxidative stress and inflammation induced by the administration of GMS in rats. In addition, a beneficial effect of subchronic treatment with (p-ClPhSe)2 against metabolic dysfunction in blood, liver and skeletal muscle induced by the administration of GMS in rats was demonstrated in manuscript 3. Taken together, the present results demonstrated that the compound, (p-ClPhSe)2, has several pharmacological properties, such as antihyperglycemic, insulin-mimetic, anti-inflammatory and antioxidant. It is known that drugs used for the treatment of obesity are often inefficient due to the complications present during the progression of obesity. Considering the pharmacological effects of (p-ClPhSe)2 demonstrated in the present study, this organic compound of selenium may be a future therapeutic alternative for the treatment of this pathology and its complications.A epidemia de obesidade é um problema de saúde pública mundial e é considerada uma das principais causas de morte e incapacidades em todo o mundo. Isso porque a patofisiologia dessa doença é extremamente complexa e envolve uma série de eventos que podem inclusive evoluir para um dano irreversível. Em relação ao tratamento, as drogas disponíveis, atualmente, para o tratamento da obesidade são muitas vezes ineficientes e apresentam efeitos adversos, por isso a busca por novos fármacos para o tratamento de doenças metabólicas vem crescendo nos últimos anos. Nesse contexto, os compostos orgânicos de selênio têm sido bastante estudados nas últimas décadas principalmente devido as suas diversas atividades farmacológicas, dentre elas, destaca-se as propriedades antioxidantes, neuroprotetora, anticâncer, antiviral, imunossupressora, antimicrobiana, ansiolítica, antidepressiva e anti-inflamatória. Entretanto, recentemente esses compostos têm chamado atenção devido aos seus efeitos benéficos na regulação da homeostase metabólica. Esta tese teve como objetivo investigar os efeitos farmacológicos do 4,4’-dicloro-difenil disseleneto, (p-ClPhSe)2 em modelos de hiperglicemia e obesidade induzidos pela administração de frutose ou glutamato monossódico (GMS) em ratos. No manuscrito 1 foi demonstrado um efeito insulino-mimético do (p-ClPhSe)2 in vitro, este composto estimulou a captação de glicose no músculo esquelético, bem como apresentou efeito anti-hiperglicêmico agudo em um modelo de hiperglicemia induzida pela administração de frutose em ratos. Além disso, no manuscrito 1, também foi demonstrado que o tratamento agudo com o (p-ClPhSe)2 protegeu das alterações metabólicas hepáticas induzidas pela frutose, através de um redirecionamento no metabolismo de carboidratos. Nesse sentido, no artigo 1 foi observado um efeito homeostático do tratamento subcrônico com o (p-ClPhSe)2 reduzindo os primeiros sinais de obesidade induzidos pela administração de GMS em ratos. Enquanto que, no manuscrito 2 foi possível observar um efeito hepatoprotetor do tratamento subcrônico com o (p-ClPhSe)2 na disfunção mitocondrial, no estresse oxidativo e na inflamação induzidos pela administração de GMS em ratos. Além disso, no manuscrito 3 foi demonstrado um efeito benéfico do tratamento subcrônico com o (p-ClPhSe.2 contra a disfunção metabólica no sangue, fígado e músculo esquelético induzida pela administração de GMS em ratos. Em conjunto, os resultados desta tese demonstram que o composto, (p-ClPhSe2 possui diversas propriedades farmacológicas, tais como, anti-hiperglicêmica, insulino-mimética, anti-inflamatória e antioxidante. Sabe-se que as drogas utilizadas para o tratamento da obesidade são muitas vezes ineficientes devido às complicações presentes durante a progressão da obesidade. Considerando os efeitos farmacológicos do (p-ClPhSe)2 demonstrados no presente estudo, esse composto orgânico de selênio pode ser uma futura alternativa terapêutica para o tratamento desta patologia e de suas complicações.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - CAPESporUniversidade Federal de Santa MariaCentro de Ciências Naturais e ExatasPrograma de Pós-Graduação em Ciências Biológicas: Bioquímica ToxicológicaUFSMBrasilBioquímicaAttribution-NonCommercial-NoDerivatives 4.0 Internationalhttp://creativecommons.org/licenses/by-nc-nd/4.0/info:eu-repo/semantics/openAccessSelênioObesidadeAlterações metabólicasInflamaçãoEstresse oxidativoSeleniumObesityMetabolic alterationsInflammationOxidative stressInsulin-mimeticCNPQ::CIENCIAS BIOLOGICAS::BIOQUIMICAAção farmacológica do 4,4’-dicloro-difenil disseleneto em modelos de hiperglicemia e obesidade em ratosPharmacological action of 4,4'-dichloro-diphenyl diselenide in rat hyperglycemia and obesity modelsinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/doctoralThesisNogueira, Cristina Waynehttp://lattes.cnpq.br/2877042401245169Bem, Andreza Fabro dehttp://lattes.cnpq.br/0383092486694460Premaor, Melissa Orlandinhttp://lattes.cnpq.br/1919693261808995Mathias, Paulo Cezar de Freitashttp://lattes.cnpq.br/5279465385771687Emanuelli, Tatianahttp://lattes.cnpq.br/2165391096880394http://lattes.cnpq.br/7387078165930666Quines, Caroline Brandão2008000000026000186436d-f662-4a5e-b36e-8c8ab8e10bf81862079d-2a66-4ad7-8489-93549016c5c8d24b0de7-f430-430e-8b90-29fe73da7315e54845f9-9f23-46cb-b394-215d71d7a4b2a5e512d3-f13f-4e16-92df-8ded179abb3322aa7bd2-5905-49f4-b5ac-e7167850124freponame:Biblioteca Digital de Teses e Dissertações do UFSMinstname:Universidade Federal de Santa Maria (UFSM)instacron:UFSMORIGINALTES_PPGBT_2017_QUINES_CAROLINE.pdfTES_PPGBT_2017_QUINES_CAROLINE.pdfTese de Doutoradoapplication/pdf12742093http://repositorio.ufsm.br/bitstream/1/18425/1/TES_PPGBT_2017_QUINES_CAROLINE.pdf30230f0f48f4af10be426c7945d96ef4MD51CC-LICENSElicense_rdflicense_rdfapplication/rdf+xml; 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dc.title.por.fl_str_mv Ação farmacológica do 4,4’-dicloro-difenil disseleneto em modelos de hiperglicemia e obesidade em ratos
dc.title.alternative.eng.fl_str_mv Pharmacological action of 4,4'-dichloro-diphenyl diselenide in rat hyperglycemia and obesity models
title Ação farmacológica do 4,4’-dicloro-difenil disseleneto em modelos de hiperglicemia e obesidade em ratos
spellingShingle Ação farmacológica do 4,4’-dicloro-difenil disseleneto em modelos de hiperglicemia e obesidade em ratos
Quines, Caroline Brandão
Selênio
Obesidade
Alterações metabólicas
Inflamação
Estresse oxidativo
Selenium
Obesity
Metabolic alterations
Inflammation
Oxidative stress
Insulin-mimetic
CNPQ::CIENCIAS BIOLOGICAS::BIOQUIMICA
title_short Ação farmacológica do 4,4’-dicloro-difenil disseleneto em modelos de hiperglicemia e obesidade em ratos
title_full Ação farmacológica do 4,4’-dicloro-difenil disseleneto em modelos de hiperglicemia e obesidade em ratos
title_fullStr Ação farmacológica do 4,4’-dicloro-difenil disseleneto em modelos de hiperglicemia e obesidade em ratos
title_full_unstemmed Ação farmacológica do 4,4’-dicloro-difenil disseleneto em modelos de hiperglicemia e obesidade em ratos
title_sort Ação farmacológica do 4,4’-dicloro-difenil disseleneto em modelos de hiperglicemia e obesidade em ratos
author Quines, Caroline Brandão
author_facet Quines, Caroline Brandão
author_role author
dc.contributor.advisor1.fl_str_mv Nogueira, Cristina Wayne
dc.contributor.advisor1Lattes.fl_str_mv http://lattes.cnpq.br/2877042401245169
dc.contributor.referee1.fl_str_mv Bem, Andreza Fabro de
dc.contributor.referee1Lattes.fl_str_mv http://lattes.cnpq.br/0383092486694460
dc.contributor.referee2.fl_str_mv Premaor, Melissa Orlandin
dc.contributor.referee2Lattes.fl_str_mv http://lattes.cnpq.br/1919693261808995
dc.contributor.referee3.fl_str_mv Mathias, Paulo Cezar de Freitas
dc.contributor.referee3Lattes.fl_str_mv http://lattes.cnpq.br/5279465385771687
dc.contributor.referee4.fl_str_mv Emanuelli, Tatiana
dc.contributor.referee4Lattes.fl_str_mv http://lattes.cnpq.br/2165391096880394
dc.contributor.authorLattes.fl_str_mv http://lattes.cnpq.br/7387078165930666
dc.contributor.author.fl_str_mv Quines, Caroline Brandão
contributor_str_mv Nogueira, Cristina Wayne
Bem, Andreza Fabro de
Premaor, Melissa Orlandin
Mathias, Paulo Cezar de Freitas
Emanuelli, Tatiana
dc.subject.por.fl_str_mv Selênio
Obesidade
Alterações metabólicas
Inflamação
Estresse oxidativo
topic Selênio
Obesidade
Alterações metabólicas
Inflamação
Estresse oxidativo
Selenium
Obesity
Metabolic alterations
Inflammation
Oxidative stress
Insulin-mimetic
CNPQ::CIENCIAS BIOLOGICAS::BIOQUIMICA
dc.subject.eng.fl_str_mv Selenium
Obesity
Metabolic alterations
Inflammation
Oxidative stress
Insulin-mimetic
dc.subject.cnpq.fl_str_mv CNPQ::CIENCIAS BIOLOGICAS::BIOQUIMICA
description The obesity epidemic is a worldwide public health problem and is considered one of the leading causes of death and disability worldwide. This is because the pathophysiology of this disease is extremely complex and involves a series of events in cascades that can even evolve into irreversible damage. Regarding treatment, drugs currently available for the treatment of obesity are often inefficient and have adverse effects, so the search for new drugs for the treatment of metabolic diseases has been growing so much in recent years. In this context, organic compounds of selenium have been studied in the last decades, mainly due to their diverse pharmacological activities, among them, antioxidant, neuroprotective, anticancer, antiviral, immunosuppressive, antimicrobial, anxiolytic, antidepressant-like and anti-inflammatory. However, these compounds have recently attracted attention because of their beneficial effects on the regulation of metabolic homeostasis. The present thesis aimed to investigate the pharmacological effects of 4,4'-dichloro-diphenyl diselenide, (p-ClPhSe)2 in hyperglycemia and obesity models induced by the administration of fructose or monosodium glutamate (MSG) in rats. In the manuscript 1, an insulin-mimetic effect of (p-ClPhSe)2 was demonstrated in vitro; this compound stimulated the glucose uptake into skeletal muscle and its acute antihyperglycemic effect in a model of hyperglycemia induced by the administration of fructose in rats. Furthermore, in the manuscript 1, acute treatment with (p-ClPhSe)2 protected against liver metabolic alterations induced by fructose; this compound redirected the carbohydrate metabolism. In that sense, in the article 1, a homeostatic effect of subchronic treatment with (p-ClPhSe)2 was demonstrated, this compound reduced the first signs of obesity induced with the administration of GMS in rats. Whereas in the manuscript 2, it was possible to observe a hepatoprotective effect of subchronic treatment with (p-ClPhSe)2 against the mitochondrial dysfunction, oxidative stress and inflammation induced by the administration of GMS in rats. In addition, a beneficial effect of subchronic treatment with (p-ClPhSe)2 against metabolic dysfunction in blood, liver and skeletal muscle induced by the administration of GMS in rats was demonstrated in manuscript 3. Taken together, the present results demonstrated that the compound, (p-ClPhSe)2, has several pharmacological properties, such as antihyperglycemic, insulin-mimetic, anti-inflammatory and antioxidant. It is known that drugs used for the treatment of obesity are often inefficient due to the complications present during the progression of obesity. Considering the pharmacological effects of (p-ClPhSe)2 demonstrated in the present study, this organic compound of selenium may be a future therapeutic alternative for the treatment of this pathology and its complications.
publishDate 2017
dc.date.issued.fl_str_mv 2017-03-03
dc.date.accessioned.fl_str_mv 2019-09-25T20:06:53Z
dc.date.available.fl_str_mv 2019-09-25T20:06:53Z
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url http://repositorio.ufsm.br/handle/1/18425
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language por
dc.relation.cnpq.fl_str_mv 200800000002
dc.relation.confidence.fl_str_mv 600
dc.relation.authority.fl_str_mv 0186436d-f662-4a5e-b36e-8c8ab8e10bf8
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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.publisher.none.fl_str_mv Universidade Federal de Santa Maria
Centro de Ciências Naturais e Exatas
dc.publisher.program.fl_str_mv Programa de Pós-Graduação em Ciências Biológicas: Bioquímica Toxicológica
dc.publisher.initials.fl_str_mv UFSM
dc.publisher.country.fl_str_mv Brasil
dc.publisher.department.fl_str_mv Bioquímica
publisher.none.fl_str_mv Universidade Federal de Santa Maria
Centro de Ciências Naturais e Exatas
dc.source.none.fl_str_mv reponame:Biblioteca Digital de Teses e Dissertações do UFSM
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