Dyslipidemia’s influence on the secretion ovarian’s steroids in female mice

Detalhes bibliográficos
Autor(a) principal: Abreu, Juliana Maganha
Data de Publicação: 2021
Outros Autores: Santos, Gérsika Bitencourt, Carvalho, Maria das Graças de Souza, Mencarelli, Juliana Marques, Cândido, Bruna Rayanne Moreira, Prado, Brunno Borges de Paula, Caixeta, Ester Siqueira, Pereira Neto , Sebastião Orestes, Corsetti, Patricia Paiva, Oliveira, Nelma de Mello Silva, Garcia, Erika Kristina Incerpi, Silvério, Alessandra Cristina Pupin, Anjos, Jander Alves dos, Alves , Lais Roncato de Carvalho, Garcia , José Antonio Dias
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Research, Society and Development
Texto Completo: https://rsdjournal.org/index.php/rsd/article/view/21369
Resumo: Introduction: The synthesis ovarian’s steroids is a process thats depends on the supply of cholesterol. Objective: to evaluate the influence of dyslipidemia on the secretion ovarian’s steroids. Methodology: wild female mice were used (C57BL6) and LDL (LDLR-/-), which they were separated into 4 groups (n = 10): WTS: fed a standard diet; WTHL: fed a high-fat diet; KOS: fed a standard diet; KOHL: fed a high-fat diet. After 60 days, the estrous cycle was analyzed and after anesthetized, blood was collected for the to assess the lipid profile, glucose, plasma insulin level and HOMA index was calculated. In addition, plasma levels of C-reactive protein, estrogen and progesterone were determined. Results: The hyperlipidic diet in both the WTHL and the KOHL group generated hypercholesterolemia when compared to the WTS and KOS, respectively, with a decrease in HDLc, associated with an increase in CRP levels. Severe hypercholesterolemia in the KOHL group generated insulin resistance, marked by an increase in HOMAir. Food hypercholesterolemia in the WTHL group, food and genetics in the KOHL group, compared to their WTS and KOS controls, was definitive in reducing plasma levels of estrogen and progesterone. The genetic hypercholesterolemia associated with insulin resistance observed in the KOS and KOHL groups reduced the levels of progesterone, this reduction being more severe in the KOHL group, which had the highest HOMAir. Conclusion: dyslipidemia affected ovarian steroidogenesis in mice by means of oxidative stress, inflammation and insulin resistance and / or by decreasing HDL cholesterol levels.
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spelling Dyslipidemia’s influence on the secretion ovarian’s steroids in female mice Influencia de la dislipidemia en la secreción de esteroides ováricos en ratonesInfluência da Dislipidemia na Secreção de esteroides ovarianos em CamundongasHipercolesterolemiahipercolesterolemiaestrogenoEstrógenoprogesteronaProgesteronaestresse oxidativoEstresse oxidativo. HypercholesterolemiahypercholesterolemiaEstrogenestrogenProgesteroneprogesteroneOxidative stress.oxidative stresshipercolesterolemiaHipercolesterolemiaEstrógenoestrógenoprogesteronaProgesteronaEstrés oxidativo.Estrés oxidativoIntroduction: The synthesis ovarian’s steroids is a process thats depends on the supply of cholesterol. Objective: to evaluate the influence of dyslipidemia on the secretion ovarian’s steroids. Methodology: wild female mice were used (C57BL6) and LDL (LDLR-/-), which they were separated into 4 groups (n = 10): WTS: fed a standard diet; WTHL: fed a high-fat diet; KOS: fed a standard diet; KOHL: fed a high-fat diet. After 60 days, the estrous cycle was analyzed and after anesthetized, blood was collected for the to assess the lipid profile, glucose, plasma insulin level and HOMA index was calculated. In addition, plasma levels of C-reactive protein, estrogen and progesterone were determined. Results: The hyperlipidic diet in both the WTHL and the KOHL group generated hypercholesterolemia when compared to the WTS and KOS, respectively, with a decrease in HDLc, associated with an increase in CRP levels. Severe hypercholesterolemia in the KOHL group generated insulin resistance, marked by an increase in HOMAir. Food hypercholesterolemia in the WTHL group, food and genetics in the KOHL group, compared to their WTS and KOS controls, was definitive in reducing plasma levels of estrogen and progesterone. The genetic hypercholesterolemia associated with insulin resistance observed in the KOS and KOHL groups reduced the levels of progesterone, this reduction being more severe in the KOHL group, which had the highest HOMAir. Conclusion: dyslipidemia affected ovarian steroidogenesis in mice by means of oxidative stress, inflammation and insulin resistance and / or by decreasing HDL cholesterol levels.Introducción: La producción de esteroides ováricos es un proceso dependiente del aporte de colesterol. Objetivo: evaluar la influencia de la dislipidemia en la secreción de esteroides ováricos. Metodología: Se utilizaron ratones de tipo salvaje (C57BL6) y knockout del gen del receptor de LDL (LDLR - / -). Se dividieron en 4 grupos (n = 10): WTS: recibió comida estándar; WTHL: recibió una dieta alta en grasas; KOS: LDLR - / -, recibió comida estándar; KOHL: LDLR - / -, recibió una dieta alta en grasas. Después de 60 días, se analizó el ciclo estral y se extrajo sangre para evaluar el perfil de lípidos, la glucosa, el nivel de insulina en plasma y se calculó el índice HOMA. Además, se determinaron los niveles plasmáticos de proteína C reactiva, estrógeno y progesterona. Resultados: La dieta alta en grasas en los grupos WTHL y KOHL generó hipercolesterolemia en comparación con los grupos WTS y KOS, respectivamente, con una disminución de cHDL, asociada con un aumento en los niveles de PCR. La hipercolesterolemia severa en el grupo KOHL generó resistencia a la insulina, marcada por un aumento en HOMAir. La hipercolesterolemia dietética en el grupo WTHL, la hipercolesterolemia dietética y genética en el grupo KOHL, en comparación con sus controles WTS y KOS, fue fundamental para reducir los niveles plasmáticos de estrógeno y progesterona. La hipercolesterolemia genética asociada con la resistencia a la insulina observada en los grupos KOS y KOHL redujo los niveles de progesterona, siendo esta reducción más severa en el grupo KOHL, que tenía mayor HOMAir. Conclusión: la dislipidemia afectó la esteroidogénesis ovárica en ratones a través de vías que implican estrés oxidativo, inflamación y resistencia a la insulina y / o mediante la disminución de los niveles de colesterol HDL.Introdução: A produção de esteroides ovarianos é um processo dependente do suprimento de colesterol. Objetivo: avaliar a influência da dislipidemia na secreção dos esteroides ovarianos. Metodologia: Utilizou-se camundongas “wild type” (C57BL6) e knockout para o gene do receptor de LDL (LDLR-/-). Foram separadas em 4 grupos (n=10): WTS: receberam ração padrão; WTHL: receberam ração hiperlipídica; KOS: LDLR-/-, receberam ração padrão; KOHL: LDLR-/-, receberam ração hiperlipídica. Após 60 dias, foi analisado o ciclo estral e o sangue foi coletado para a avaliar o perfil lipídico, glicose, nível plasmático da insulina, e o índice de HOMA foi calculado. Além disso, os níveis plasmáticos de proteína C reativa, estrógeno e progesterona foram determinados. Resultados: A dieta hiperlipídica tanto no grupo WTHL quanto KOHL gerou uma hipercolesterolemia quando comparadas aos WTS e KOS, respectivamente, com diminuição de HDLc, associada ao aumento dos níveis da PCR. A hipercolesterolemia severa no grupo KOHL gerou uma resistência insulínica, marcada por aumento do HOMAir. A hipercolesterolemia alimentar no grupo WTHL, alimentar e genética no grupo KOHL, comparada com seus controles WTS e KOS, foi determinante para reduzir os níveis plasmáticos de estrógeno e progesterona. A hipercolesterolemia genética associada à resistência insulínica observada nos grupos KOS e KOHL reduziu os níveis de progesterona, sendo essa redução mais grave no grupo KOHL, que apresentou maior HOMAir. Conclusão: a dislipidemia afetou a esteroidogênese ovariana em camundongas por vias que envolvem o estresse oxidativo, inflamação e resistência insulínica e/ou pela diminuição dos níveis de HDL colesterol.Research, Society and Development2021-10-12info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://rsdjournal.org/index.php/rsd/article/view/2136910.33448/rsd-v10i13.21369Research, Society and Development; Vol. 10 No. 13; e298101321369Research, Society and Development; Vol. 10 Núm. 13; e298101321369Research, Society and Development; v. 10 n. 13; e2981013213692525-3409reponame:Research, Society and Developmentinstname:Universidade Federal de Itajubá (UNIFEI)instacron:UNIFEIenghttps://rsdjournal.org/index.php/rsd/article/view/21369/18924Copyright (c) 2021 Juliana Maganha Abreu; Gérsika Bitencourt Santos; Maria das Graças de Souza Carvalho; Juliana Marques Mencarelli; Bruna Rayanne Moreira Cândido; Brunno Borges de Paula Prado; Ester Siqueira Caixeta; Sebastião Orestes Pereira Neto ; Patricia Paiva Corsetti; Nelma de Mello Silva Oliveira; Erika Kristina Incerpi Garcia; Alessandra Cristina Pupin Silvério; Jander Alves dos Anjos; Lais Roncato de Carvalho Alves ; José Antonio Dias Garcia https://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessAbreu, Juliana Maganha Santos, Gérsika Bitencourt Carvalho, Maria das Graças de SouzaMencarelli, Juliana Marques Cândido, Bruna Rayanne Moreira Prado, Brunno Borges de Paula Caixeta, Ester SiqueiraPereira Neto , Sebastião Orestes Corsetti, Patricia Paiva Oliveira, Nelma de Mello Silva Garcia, Erika Kristina Incerpi Silvério, Alessandra Cristina Pupin Anjos, Jander Alves dos Alves , Lais Roncato de Carvalho Garcia , José Antonio Dias 2021-11-21T18:26:28Zoai:ojs.pkp.sfu.ca:article/21369Revistahttps://rsdjournal.org/index.php/rsd/indexPUBhttps://rsdjournal.org/index.php/rsd/oairsd.articles@gmail.com2525-34092525-3409opendoar:2024-01-17T09:40:48.089521Research, Society and Development - Universidade Federal de Itajubá (UNIFEI)false
dc.title.none.fl_str_mv Dyslipidemia’s influence on the secretion ovarian’s steroids in female mice
Influencia de la dislipidemia en la secreción de esteroides ováricos en ratones
Influência da Dislipidemia na Secreção de esteroides ovarianos em Camundongas
title Dyslipidemia’s influence on the secretion ovarian’s steroids in female mice
spellingShingle Dyslipidemia’s influence on the secretion ovarian’s steroids in female mice
Abreu, Juliana Maganha
Hipercolesterolemia
hipercolesterolemia
estrogeno
Estrógeno
progesterona
Progesterona
estresse oxidativo
Estresse oxidativo.
Hypercholesterolemia
hypercholesterolemia
Estrogen
estrogen
Progesterone
progesterone
Oxidative stress.
oxidative stress
hipercolesterolemia
Hipercolesterolemia
Estrógeno
estrógeno
progesterona
Progesterona
Estrés oxidativo.
Estrés oxidativo
title_short Dyslipidemia’s influence on the secretion ovarian’s steroids in female mice
title_full Dyslipidemia’s influence on the secretion ovarian’s steroids in female mice
title_fullStr Dyslipidemia’s influence on the secretion ovarian’s steroids in female mice
title_full_unstemmed Dyslipidemia’s influence on the secretion ovarian’s steroids in female mice
title_sort Dyslipidemia’s influence on the secretion ovarian’s steroids in female mice
author Abreu, Juliana Maganha
author_facet Abreu, Juliana Maganha
Santos, Gérsika Bitencourt
Carvalho, Maria das Graças de Souza
Mencarelli, Juliana Marques
Cândido, Bruna Rayanne Moreira
Prado, Brunno Borges de Paula
Caixeta, Ester Siqueira
Pereira Neto , Sebastião Orestes
Corsetti, Patricia Paiva
Oliveira, Nelma de Mello Silva
Garcia, Erika Kristina Incerpi
Silvério, Alessandra Cristina Pupin
Anjos, Jander Alves dos
Alves , Lais Roncato de Carvalho
Garcia , José Antonio Dias
author_role author
author2 Santos, Gérsika Bitencourt
Carvalho, Maria das Graças de Souza
Mencarelli, Juliana Marques
Cândido, Bruna Rayanne Moreira
Prado, Brunno Borges de Paula
Caixeta, Ester Siqueira
Pereira Neto , Sebastião Orestes
Corsetti, Patricia Paiva
Oliveira, Nelma de Mello Silva
Garcia, Erika Kristina Incerpi
Silvério, Alessandra Cristina Pupin
Anjos, Jander Alves dos
Alves , Lais Roncato de Carvalho
Garcia , José Antonio Dias
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Abreu, Juliana Maganha
Santos, Gérsika Bitencourt
Carvalho, Maria das Graças de Souza
Mencarelli, Juliana Marques
Cândido, Bruna Rayanne Moreira
Prado, Brunno Borges de Paula
Caixeta, Ester Siqueira
Pereira Neto , Sebastião Orestes
Corsetti, Patricia Paiva
Oliveira, Nelma de Mello Silva
Garcia, Erika Kristina Incerpi
Silvério, Alessandra Cristina Pupin
Anjos, Jander Alves dos
Alves , Lais Roncato de Carvalho
Garcia , José Antonio Dias
dc.subject.por.fl_str_mv Hipercolesterolemia
hipercolesterolemia
estrogeno
Estrógeno
progesterona
Progesterona
estresse oxidativo
Estresse oxidativo.
Hypercholesterolemia
hypercholesterolemia
Estrogen
estrogen
Progesterone
progesterone
Oxidative stress.
oxidative stress
hipercolesterolemia
Hipercolesterolemia
Estrógeno
estrógeno
progesterona
Progesterona
Estrés oxidativo.
Estrés oxidativo
topic Hipercolesterolemia
hipercolesterolemia
estrogeno
Estrógeno
progesterona
Progesterona
estresse oxidativo
Estresse oxidativo.
Hypercholesterolemia
hypercholesterolemia
Estrogen
estrogen
Progesterone
progesterone
Oxidative stress.
oxidative stress
hipercolesterolemia
Hipercolesterolemia
Estrógeno
estrógeno
progesterona
Progesterona
Estrés oxidativo.
Estrés oxidativo
description Introduction: The synthesis ovarian’s steroids is a process thats depends on the supply of cholesterol. Objective: to evaluate the influence of dyslipidemia on the secretion ovarian’s steroids. Methodology: wild female mice were used (C57BL6) and LDL (LDLR-/-), which they were separated into 4 groups (n = 10): WTS: fed a standard diet; WTHL: fed a high-fat diet; KOS: fed a standard diet; KOHL: fed a high-fat diet. After 60 days, the estrous cycle was analyzed and after anesthetized, blood was collected for the to assess the lipid profile, glucose, plasma insulin level and HOMA index was calculated. In addition, plasma levels of C-reactive protein, estrogen and progesterone were determined. Results: The hyperlipidic diet in both the WTHL and the KOHL group generated hypercholesterolemia when compared to the WTS and KOS, respectively, with a decrease in HDLc, associated with an increase in CRP levels. Severe hypercholesterolemia in the KOHL group generated insulin resistance, marked by an increase in HOMAir. Food hypercholesterolemia in the WTHL group, food and genetics in the KOHL group, compared to their WTS and KOS controls, was definitive in reducing plasma levels of estrogen and progesterone. The genetic hypercholesterolemia associated with insulin resistance observed in the KOS and KOHL groups reduced the levels of progesterone, this reduction being more severe in the KOHL group, which had the highest HOMAir. Conclusion: dyslipidemia affected ovarian steroidogenesis in mice by means of oxidative stress, inflammation and insulin resistance and / or by decreasing HDL cholesterol levels.
publishDate 2021
dc.date.none.fl_str_mv 2021-10-12
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://rsdjournal.org/index.php/rsd/article/view/21369
10.33448/rsd-v10i13.21369
url https://rsdjournal.org/index.php/rsd/article/view/21369
identifier_str_mv 10.33448/rsd-v10i13.21369
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv https://rsdjournal.org/index.php/rsd/article/view/21369/18924
dc.rights.driver.fl_str_mv https://creativecommons.org/licenses/by/4.0
info:eu-repo/semantics/openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by/4.0
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Research, Society and Development
publisher.none.fl_str_mv Research, Society and Development
dc.source.none.fl_str_mv Research, Society and Development; Vol. 10 No. 13; e298101321369
Research, Society and Development; Vol. 10 Núm. 13; e298101321369
Research, Society and Development; v. 10 n. 13; e298101321369
2525-3409
reponame:Research, Society and Development
instname:Universidade Federal de Itajubá (UNIFEI)
instacron:UNIFEI
instname_str Universidade Federal de Itajubá (UNIFEI)
instacron_str UNIFEI
institution UNIFEI
reponame_str Research, Society and Development
collection Research, Society and Development
repository.name.fl_str_mv Research, Society and Development - Universidade Federal de Itajubá (UNIFEI)
repository.mail.fl_str_mv rsd.articles@gmail.com
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