Efeito da sinvastatina sobre a pressão arterial, metabolismo glicídico, metabolismo lipídico e função endotelial em ratos espontaneamente hipertensos tornados obesos

Detalhes bibliográficos
Autor(a) principal: Ferreira, Diego Faria Marques [UNIFESP]
Data de Publicação: 2018
Tipo de documento: Dissertação
Idioma: por
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: https://sucupira.capes.gov.br/sucupira/public/consultas/coleta/trabalhoConclusao/viewTrabalhoConclusao.jsf?popup=true&id_trabalho=6634816
https://repositorio.unifesp.br/handle/11600/53178
Resumo: INTRODUCTION: Systemic arterial hypertension and obesity are associated with several comorbidities, such as diabetes and endothelial dysfunction. Simvastatin with its pleiotropic effects act on several systems (inflammation, release of vasodilation factors, among others) and show beneficial effects. OBJECTIVE: To evaluate the effects of simvastatin administration on glucose metabolism, lipid metabolism and vascular responsiveness in spontaneously hypertensive rats (SHR) made obese. METHODS: Spontaneous hipertensive rats male with 12 weeks of life were divided into 4 groups: control (SHR, n = 7), SHR + hyperlipidemic diet (SHR + HIPER, n = 5), SHR + simvastatin (n = 7) and group (SHR + HIPER + SINVA, n = 7). The hyperlipidic diet was administered from the weaning period and the dose of simvastatin was 10mg / kg / day, by gavage from the 13th to the 20th week. Body mass and caudal blood pressure were evaluated weekly. At the end of the study, the oral glucose tolerance test (TTGO), insulin tolerance test (TTI), lipid dosage, determination of vascular reactivity and left ventricular mass and epididymal fat were performed. RESULTS: The induction of obesity did not alter the parameters related to tail blood pressure and body weight, even when associated with simvastatin. As for glucose metabolism the administration of a hyperlipidic diet resulted in a significant increase of the area under the glucose curve. The vascular reactivity to acetylcholine, the SHR + SINVA group showed improvement in vasodilatation, whereas the other groups, when the hyperlipidic diet was associated, their effects were abolished. In the dosage of triglycerides, the groups treated with simvastatin obtained a significant reduction in their values, as well as in total cholesterol (TC), low density lipoprotein (LDL) dosage, very low density lipoprotein (VLDL). Regarding the dosage of high density lipoprotein (HDL), the association of pharmacological treatment together with the induction of obesity caused a significant increase in their values. The hyperlipidic diet caused the groups to have a significant increase in the weight of epididymal fat. CONCLUSION: Simvastatin treatment was effective in determining improvement in the endothelial function of SHR rats, but not in SHR + HIPER + SINVA. The increase of the epididymal fat induced by the hyperlipidic diet despite the improvement of the parameters of lipid metabolism, prevented the benefits induced by simvastatin on endothelial function.
id UFSP_d34455a0dc5abbb6f89e4beedcfb882f
oai_identifier_str oai:repositorio.unifesp.br/:11600/53178
network_acronym_str UFSP
network_name_str Repositório Institucional da UNIFESP
repository_id_str 3465
spelling Efeito da sinvastatina sobre a pressão arterial, metabolismo glicídico, metabolismo lipídico e função endotelial em ratos espontaneamente hipertensos tornados obesosEffect of simvastatin on blood pressure, glucose metabolism, lipid metabolism and endothelial function in spontaneously hypertensive rats becoming obeseSimvastatinHypertensionResistance to insulinInbred rats ShrVasodilationSinvastatinaHipertensãoResistência á insulinaRatos endogâmicos ShrVasodilataçãoINTRODUCTION: Systemic arterial hypertension and obesity are associated with several comorbidities, such as diabetes and endothelial dysfunction. Simvastatin with its pleiotropic effects act on several systems (inflammation, release of vasodilation factors, among others) and show beneficial effects. OBJECTIVE: To evaluate the effects of simvastatin administration on glucose metabolism, lipid metabolism and vascular responsiveness in spontaneously hypertensive rats (SHR) made obese. METHODS: Spontaneous hipertensive rats male with 12 weeks of life were divided into 4 groups: control (SHR, n = 7), SHR + hyperlipidemic diet (SHR + HIPER, n = 5), SHR + simvastatin (n = 7) and group (SHR + HIPER + SINVA, n = 7). The hyperlipidic diet was administered from the weaning period and the dose of simvastatin was 10mg / kg / day, by gavage from the 13th to the 20th week. Body mass and caudal blood pressure were evaluated weekly. At the end of the study, the oral glucose tolerance test (TTGO), insulin tolerance test (TTI), lipid dosage, determination of vascular reactivity and left ventricular mass and epididymal fat were performed. RESULTS: The induction of obesity did not alter the parameters related to tail blood pressure and body weight, even when associated with simvastatin. As for glucose metabolism the administration of a hyperlipidic diet resulted in a significant increase of the area under the glucose curve. The vascular reactivity to acetylcholine, the SHR + SINVA group showed improvement in vasodilatation, whereas the other groups, when the hyperlipidic diet was associated, their effects were abolished. In the dosage of triglycerides, the groups treated with simvastatin obtained a significant reduction in their values, as well as in total cholesterol (TC), low density lipoprotein (LDL) dosage, very low density lipoprotein (VLDL). Regarding the dosage of high density lipoprotein (HDL), the association of pharmacological treatment together with the induction of obesity caused a significant increase in their values. The hyperlipidic diet caused the groups to have a significant increase in the weight of epididymal fat. CONCLUSION: Simvastatin treatment was effective in determining improvement in the endothelial function of SHR rats, but not in SHR + HIPER + SINVA. The increase of the epididymal fat induced by the hyperlipidic diet despite the improvement of the parameters of lipid metabolism, prevented the benefits induced by simvastatin on endothelial function.INTRODUÇÃO: A hipertensão arterial sistêmica e a obesidade estão associadas a diversas comorbidades, como diabetes e a disfunção endotelial. A sinvastatina com seus efeitos pleiotrópicos agem em diversos sistemas (inflamação, liberação de fatores de vasodilatação, entre outros) e demostram efeitos benéficos. OBJETIVO: Avaliar os efeitos da administração de sinvastatina sobre o metabolismo glicídico, lipídico e a responsividade vascular em ratos espontaneamente hipertensos (SHR) tornados obesos. METODOLOGIA: Foram incluídos ratos espontaneamente hipertensos machos com 12 semanas de vida que foram divididos em 4 grupos: Controle (SHR, n=7), SHR + Dieta hiperlipídica (SHR + HIPER, n=5), SHR + Sinvastatina (SHR + SINVA, n=7) e grupo dieta hiperlipídica + sinvastatina (SHR + HIPER + SINVA, n=7). A dieta hiperlipídica foi administrada desde o período do desmame e a dose de sinvastatina foi 10mg/Kg/dia, por gavagem da 13ª a 20ª semana. Foram avaliados semanalmente: massa corporal e pressão arterial caudal. Ao final do estudo foram realizados o teste de tolerância oral à glicose (TTGO), teste de tolerância à insulina (TTI), dosagem dos lipídeos, determinação da reatividade vascular e massa ventrículo esquerdo e da gordura epididimal. RESULTADOS: A indução da obesidade não alterou os parâmetros relacionados a pressão arterial de cauda e no peso corporal, mesmo quando associada com a sinvastatina. Quanto ao metabolismo glicídico a administração de dieta hiperlipídica determinou um aumento significante da área sob a curva de glicose. A reatividade vascular à acetilcolina, o grupo SHR + SINVA apresentou melhora na vasodilatação que os demais grupos, quando a dieta hiperlipídica foi associada, seus efeitos foram abolidos. Na dosagem do triglicérides, os grupos que fizeram tratamento com sinvastatina obtiveram uma redução significante dos seus valores, assim como na dosagem do colesterol total (CT), dosagem da lipoproteínas de baixa densidade (LDL), dosagem de lipoproteínas muito baixa densidade (VLDL). Quanto a dosagem da lipoproteína de alta densidade (HDL) a associação do tratamento farmacológico junto com a indução da obesidade causou aumento significante dos seus valores. A dieta hiperlipídica fez com que os grupos tivessem aumento significativo do peso da gordura epididimal. CONCLUSÃO: O tratamento com sinvastatina foi eficaz em determinar melhora na função endotelial de ratos SHR, mas não nos SHR+HIPER+SINVA. O aumento da gordura epididimal induzida pela dieta hiperlipídica apesar da melhora dos parâmetros do metabolismo lipídico, impediu os benefícios induzidos pela sinvastatina sobre a função endotelial.Dados abertos - Sucupira - Teses e dissertações (2018)Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Universidade Federal de São Paulo (UNIFESP)Cesaretti, Mario Luis Ribeiro [UNIFESP]http://lattes.cnpq.br/6026967513178490http://lattes.cnpq.br/5770785379698382Ferreira, Diego Faria Marques [UNIFESP]2020-03-25T12:11:04Z2020-03-25T12:11:04Z2018-01-18info:eu-repo/semantics/masterThesisinfo:eu-repo/semantics/publishedVersion89 f.application/pdfhttps://sucupira.capes.gov.br/sucupira/public/consultas/coleta/trabalhoConclusao/viewTrabalhoConclusao.jsf?popup=true&id_trabalho=66348162018-1123.pdfhttps://repositorio.unifesp.br/handle/11600/53178porSão Pauloinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-08-02T21:22:37Zoai:repositorio.unifesp.br/:11600/53178Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-08-02T21:22:37Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv Efeito da sinvastatina sobre a pressão arterial, metabolismo glicídico, metabolismo lipídico e função endotelial em ratos espontaneamente hipertensos tornados obesos
Effect of simvastatin on blood pressure, glucose metabolism, lipid metabolism and endothelial function in spontaneously hypertensive rats becoming obese
title Efeito da sinvastatina sobre a pressão arterial, metabolismo glicídico, metabolismo lipídico e função endotelial em ratos espontaneamente hipertensos tornados obesos
spellingShingle Efeito da sinvastatina sobre a pressão arterial, metabolismo glicídico, metabolismo lipídico e função endotelial em ratos espontaneamente hipertensos tornados obesos
Ferreira, Diego Faria Marques [UNIFESP]
Simvastatin
Hypertension
Resistance to insulin
Inbred rats Shr
Vasodilation
Sinvastatina
Hipertensão
Resistência á insulina
Ratos endogâmicos Shr
Vasodilatação
title_short Efeito da sinvastatina sobre a pressão arterial, metabolismo glicídico, metabolismo lipídico e função endotelial em ratos espontaneamente hipertensos tornados obesos
title_full Efeito da sinvastatina sobre a pressão arterial, metabolismo glicídico, metabolismo lipídico e função endotelial em ratos espontaneamente hipertensos tornados obesos
title_fullStr Efeito da sinvastatina sobre a pressão arterial, metabolismo glicídico, metabolismo lipídico e função endotelial em ratos espontaneamente hipertensos tornados obesos
title_full_unstemmed Efeito da sinvastatina sobre a pressão arterial, metabolismo glicídico, metabolismo lipídico e função endotelial em ratos espontaneamente hipertensos tornados obesos
title_sort Efeito da sinvastatina sobre a pressão arterial, metabolismo glicídico, metabolismo lipídico e função endotelial em ratos espontaneamente hipertensos tornados obesos
author Ferreira, Diego Faria Marques [UNIFESP]
author_facet Ferreira, Diego Faria Marques [UNIFESP]
author_role author
dc.contributor.none.fl_str_mv Cesaretti, Mario Luis Ribeiro [UNIFESP]
http://lattes.cnpq.br/6026967513178490
http://lattes.cnpq.br/5770785379698382
dc.contributor.author.fl_str_mv Ferreira, Diego Faria Marques [UNIFESP]
dc.subject.por.fl_str_mv Simvastatin
Hypertension
Resistance to insulin
Inbred rats Shr
Vasodilation
Sinvastatina
Hipertensão
Resistência á insulina
Ratos endogâmicos Shr
Vasodilatação
topic Simvastatin
Hypertension
Resistance to insulin
Inbred rats Shr
Vasodilation
Sinvastatina
Hipertensão
Resistência á insulina
Ratos endogâmicos Shr
Vasodilatação
description INTRODUCTION: Systemic arterial hypertension and obesity are associated with several comorbidities, such as diabetes and endothelial dysfunction. Simvastatin with its pleiotropic effects act on several systems (inflammation, release of vasodilation factors, among others) and show beneficial effects. OBJECTIVE: To evaluate the effects of simvastatin administration on glucose metabolism, lipid metabolism and vascular responsiveness in spontaneously hypertensive rats (SHR) made obese. METHODS: Spontaneous hipertensive rats male with 12 weeks of life were divided into 4 groups: control (SHR, n = 7), SHR + hyperlipidemic diet (SHR + HIPER, n = 5), SHR + simvastatin (n = 7) and group (SHR + HIPER + SINVA, n = 7). The hyperlipidic diet was administered from the weaning period and the dose of simvastatin was 10mg / kg / day, by gavage from the 13th to the 20th week. Body mass and caudal blood pressure were evaluated weekly. At the end of the study, the oral glucose tolerance test (TTGO), insulin tolerance test (TTI), lipid dosage, determination of vascular reactivity and left ventricular mass and epididymal fat were performed. RESULTS: The induction of obesity did not alter the parameters related to tail blood pressure and body weight, even when associated with simvastatin. As for glucose metabolism the administration of a hyperlipidic diet resulted in a significant increase of the area under the glucose curve. The vascular reactivity to acetylcholine, the SHR + SINVA group showed improvement in vasodilatation, whereas the other groups, when the hyperlipidic diet was associated, their effects were abolished. In the dosage of triglycerides, the groups treated with simvastatin obtained a significant reduction in their values, as well as in total cholesterol (TC), low density lipoprotein (LDL) dosage, very low density lipoprotein (VLDL). Regarding the dosage of high density lipoprotein (HDL), the association of pharmacological treatment together with the induction of obesity caused a significant increase in their values. The hyperlipidic diet caused the groups to have a significant increase in the weight of epididymal fat. CONCLUSION: Simvastatin treatment was effective in determining improvement in the endothelial function of SHR rats, but not in SHR + HIPER + SINVA. The increase of the epididymal fat induced by the hyperlipidic diet despite the improvement of the parameters of lipid metabolism, prevented the benefits induced by simvastatin on endothelial function.
publishDate 2018
dc.date.none.fl_str_mv 2018-01-18
2020-03-25T12:11:04Z
2020-03-25T12:11:04Z
dc.type.driver.fl_str_mv info:eu-repo/semantics/masterThesis
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format masterThesis
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://sucupira.capes.gov.br/sucupira/public/consultas/coleta/trabalhoConclusao/viewTrabalhoConclusao.jsf?popup=true&id_trabalho=6634816
2018-1123.pdf
https://repositorio.unifesp.br/handle/11600/53178
url https://sucupira.capes.gov.br/sucupira/public/consultas/coleta/trabalhoConclusao/viewTrabalhoConclusao.jsf?popup=true&id_trabalho=6634816
https://repositorio.unifesp.br/handle/11600/53178
identifier_str_mv 2018-1123.pdf
dc.language.iso.fl_str_mv por
language por
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 89 f.
application/pdf
dc.coverage.none.fl_str_mv São Paulo
dc.publisher.none.fl_str_mv Universidade Federal de São Paulo (UNIFESP)
publisher.none.fl_str_mv Universidade Federal de São Paulo (UNIFESP)
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
instname:Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
instname_str Universidade Federal de São Paulo (UNIFESP)
instacron_str UNIFESP
institution UNIFESP
reponame_str Repositório Institucional da UNIFESP
collection Repositório Institucional da UNIFESP
repository.name.fl_str_mv Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)
repository.mail.fl_str_mv biblioteca.csp@unifesp.br
_version_ 1814268411382857728