The hepatoprotective effect of jaboticaba peel powder in a rat model of type 2 Diabetes Mellitus involves the modulation of thiol/disulfide redox state through the upregulation of glutathione synthesis

Detalhes bibliográficos
Autor(a) principal: Quatrin, Andréia
Data de Publicação: 2018
Outros Autores: Conte, Lisiane, Silva, Dariane Trivisiol da, Figueiredo, Cassiele G, Somacal, Sabrina, Roehrs, Miguel, Teixeira, Cibele Ferreira, Barbisan, Fernanda, Augusti, Paula Rossini, Maróstica Júnior, Mário, Cruz, Ivana Beatrici Manica da, Emanuelli, Tatiana
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFRGS
Texto Completo: http://hdl.handle.net/10183/225799
Resumo: Jaboticaba peel powder (JPP) is rich in bioactive compounds, mainly soluble and insoluble polyphenols with great antioxidant properties. ,e aim of this study is to evaluate the effects of JPP supplementation on the oxidative stress and hepatic damage in a rat model of type 2 diabetes mellitus (T2DM). Diabetic rats received vehicle or JPP at 2.7 (JPP-I), 5.4 (JPP-II), or 10.8 (JPP-III) g/L in drinking water during 8 weeks. JPP-III attenuated hyperglycaemia and dyslipidemia increased by 86% the liver content of nonprotein thiol groups and by 90% the GSH/GSSG ratio by activating glutathione synthesis. Accordingly, JPP supplementation prevented the loss of activity of the sulfhydryl-dependent enzyme δ-aminolaevulinic acid dehydratase and attenuated hepatic injury assessed by the reduction of serum aspartate aminotransferase activity and liver hypertrophy. Our results support that JPP supplementation to T2DM rats decreases hepatic damage most likely by increasing glutathione synthesis and modulating the thiol/disulfide redox balance.
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spelling Quatrin, AndréiaConte, LisianeSilva, Dariane Trivisiol daFigueiredo, Cassiele GSomacal, SabrinaRoehrs, MiguelTeixeira, Cibele FerreiraBarbisan, FernandaAugusti, Paula RossiniMaróstica Júnior, MárioCruz, Ivana Beatrici Manica daEmanuelli, Tatiana2021-08-18T04:31:37Z20182090-0724http://hdl.handle.net/10183/225799001074100Jaboticaba peel powder (JPP) is rich in bioactive compounds, mainly soluble and insoluble polyphenols with great antioxidant properties. ,e aim of this study is to evaluate the effects of JPP supplementation on the oxidative stress and hepatic damage in a rat model of type 2 diabetes mellitus (T2DM). Diabetic rats received vehicle or JPP at 2.7 (JPP-I), 5.4 (JPP-II), or 10.8 (JPP-III) g/L in drinking water during 8 weeks. JPP-III attenuated hyperglycaemia and dyslipidemia increased by 86% the liver content of nonprotein thiol groups and by 90% the GSH/GSSG ratio by activating glutathione synthesis. Accordingly, JPP supplementation prevented the loss of activity of the sulfhydryl-dependent enzyme δ-aminolaevulinic acid dehydratase and attenuated hepatic injury assessed by the reduction of serum aspartate aminotransferase activity and liver hypertrophy. Our results support that JPP supplementation to T2DM rats decreases hepatic damage most likely by increasing glutathione synthesis and modulating the thiol/disulfide redox balance.application/pdfengJournal of Nutrition and Metabolism. London. Vol. 2018, ID 9794629, 13 p.JabuticabaDiabetes mellitusCompostos bioativosCarotenóideThe hepatoprotective effect of jaboticaba peel powder in a rat model of type 2 Diabetes Mellitus involves the modulation of thiol/disulfide redox state through the upregulation of glutathione synthesisEstrangeiroinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSTEXT001074100.pdf.txt001074100.pdf.txtExtracted Texttext/plain60508http://www.lume.ufrgs.br/bitstream/10183/225799/2/001074100.pdf.txtd45843c3b7a7f0a01eac1d1ead524f6dMD52ORIGINAL001074100.pdfTexto completo (inglês)application/pdf1717135http://www.lume.ufrgs.br/bitstream/10183/225799/1/001074100.pdf8596e34ad3bf8c80f8ded54367bf5e7fMD5110183/2257992023-05-17 03:27:14.072557oai:www.lume.ufrgs.br:10183/225799Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2023-05-17T06:27:14Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false
dc.title.pt_BR.fl_str_mv The hepatoprotective effect of jaboticaba peel powder in a rat model of type 2 Diabetes Mellitus involves the modulation of thiol/disulfide redox state through the upregulation of glutathione synthesis
title The hepatoprotective effect of jaboticaba peel powder in a rat model of type 2 Diabetes Mellitus involves the modulation of thiol/disulfide redox state through the upregulation of glutathione synthesis
spellingShingle The hepatoprotective effect of jaboticaba peel powder in a rat model of type 2 Diabetes Mellitus involves the modulation of thiol/disulfide redox state through the upregulation of glutathione synthesis
Quatrin, Andréia
Jabuticaba
Diabetes mellitus
Compostos bioativos
Carotenóide
title_short The hepatoprotective effect of jaboticaba peel powder in a rat model of type 2 Diabetes Mellitus involves the modulation of thiol/disulfide redox state through the upregulation of glutathione synthesis
title_full The hepatoprotective effect of jaboticaba peel powder in a rat model of type 2 Diabetes Mellitus involves the modulation of thiol/disulfide redox state through the upregulation of glutathione synthesis
title_fullStr The hepatoprotective effect of jaboticaba peel powder in a rat model of type 2 Diabetes Mellitus involves the modulation of thiol/disulfide redox state through the upregulation of glutathione synthesis
title_full_unstemmed The hepatoprotective effect of jaboticaba peel powder in a rat model of type 2 Diabetes Mellitus involves the modulation of thiol/disulfide redox state through the upregulation of glutathione synthesis
title_sort The hepatoprotective effect of jaboticaba peel powder in a rat model of type 2 Diabetes Mellitus involves the modulation of thiol/disulfide redox state through the upregulation of glutathione synthesis
author Quatrin, Andréia
author_facet Quatrin, Andréia
Conte, Lisiane
Silva, Dariane Trivisiol da
Figueiredo, Cassiele G
Somacal, Sabrina
Roehrs, Miguel
Teixeira, Cibele Ferreira
Barbisan, Fernanda
Augusti, Paula Rossini
Maróstica Júnior, Mário
Cruz, Ivana Beatrici Manica da
Emanuelli, Tatiana
author_role author
author2 Conte, Lisiane
Silva, Dariane Trivisiol da
Figueiredo, Cassiele G
Somacal, Sabrina
Roehrs, Miguel
Teixeira, Cibele Ferreira
Barbisan, Fernanda
Augusti, Paula Rossini
Maróstica Júnior, Mário
Cruz, Ivana Beatrici Manica da
Emanuelli, Tatiana
author2_role author
author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Quatrin, Andréia
Conte, Lisiane
Silva, Dariane Trivisiol da
Figueiredo, Cassiele G
Somacal, Sabrina
Roehrs, Miguel
Teixeira, Cibele Ferreira
Barbisan, Fernanda
Augusti, Paula Rossini
Maróstica Júnior, Mário
Cruz, Ivana Beatrici Manica da
Emanuelli, Tatiana
dc.subject.por.fl_str_mv Jabuticaba
Diabetes mellitus
Compostos bioativos
Carotenóide
topic Jabuticaba
Diabetes mellitus
Compostos bioativos
Carotenóide
description Jaboticaba peel powder (JPP) is rich in bioactive compounds, mainly soluble and insoluble polyphenols with great antioxidant properties. ,e aim of this study is to evaluate the effects of JPP supplementation on the oxidative stress and hepatic damage in a rat model of type 2 diabetes mellitus (T2DM). Diabetic rats received vehicle or JPP at 2.7 (JPP-I), 5.4 (JPP-II), or 10.8 (JPP-III) g/L in drinking water during 8 weeks. JPP-III attenuated hyperglycaemia and dyslipidemia increased by 86% the liver content of nonprotein thiol groups and by 90% the GSH/GSSG ratio by activating glutathione synthesis. Accordingly, JPP supplementation prevented the loss of activity of the sulfhydryl-dependent enzyme δ-aminolaevulinic acid dehydratase and attenuated hepatic injury assessed by the reduction of serum aspartate aminotransferase activity and liver hypertrophy. Our results support that JPP supplementation to T2DM rats decreases hepatic damage most likely by increasing glutathione synthesis and modulating the thiol/disulfide redox balance.
publishDate 2018
dc.date.issued.fl_str_mv 2018
dc.date.accessioned.fl_str_mv 2021-08-18T04:31:37Z
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dc.identifier.issn.pt_BR.fl_str_mv 2090-0724
dc.identifier.nrb.pt_BR.fl_str_mv 001074100
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dc.language.iso.fl_str_mv eng
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dc.relation.ispartof.pt_BR.fl_str_mv Journal of Nutrition and Metabolism. London. Vol. 2018, ID 9794629, 13 p.
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