Cardiac Energy Metabolism and Oxidative Stress Biomarkers in Diabetic Rat Treated with Resveratrol

Detalhes bibliográficos
Autor(a) principal: Santos, Klinsmann Carolo dos [UNESP]
Data de Publicação: 2014
Outros Autores: Braga, Camila Pereira [UNESP], Barbanera, Pedro Octavio [UNESP], Ferreira Seiva, Fabio Rodrigues, Fernandes Junior, Ary [UNESP], Henrique Fernandes, Ana Angelica [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1371/journal.pone.0102775
http://hdl.handle.net/11449/117391
Resumo: Resveratrol (RSV), polyphenol from grape, was studied to evaluate its effects on calorimetric parameters, energy metabolism, and antioxidants in the myocardium of diabetic rats. The animals were randomly divided into four groups (n = 8): C (control group): normal rats; C-RSV: normal rats receiving RSV; DM: diabetic rats; and DM-RSV: diabetics rats receiving RSV. Type 1 diabetes mellitus was induced with administration of streptozotocin (STZ; 60 mg(-1) body weight, single dose, i.p.). After 48 hours of STZ administration, the animals received RSV (1.0 mg/kg/day) for gavage for 30 days. Food, water, and energy intake were higher in the DM group, while administration of RSV caused decreases (p<0.05) in these parameters. The glycemia decreased and higher final body weight increased in DM-RSV when compared with the DM group. The diabetic rats showed higher serum-free fatty acid, which was normalized with RSV. Oxygen consumption (VO2) and carbon dioxide production (VCO2) decreased (p<0.05) in the DM group. This was accompanied by reductions in RQ. The C-RSV group showed higher VO2 and VCO2 values. Pyruvate dehydrogenase activity was lower in the DM group and normalizes with RSV. The DM group exhibited higher myocardial beta-hydroxyacyl coenzyme-A dehydrogenase and citrate synthase activity, and RSV decreased the activity of these enzymes. The DM group had higher cardiac lactate dehydrogenase compared to the DM-RSV group. Myocardial protein carbonyl was increased in the DM group. RSV increased reduced glutathione in the cardiac tissue of diabetic animals. The glutathione reductase activity was higher in the DM-RSV group compared to the DM group. In conclusion, diabetes is accompanied by cardiac energy metabolism dysfunction and change in the biomarkers of oxidative stress. The cardioprotective effect may be mediated through RVS's ability to normalize free fatty acid oxidation, enhance utilization glucose, and control the biomarkers' level of oxidative stress under diabetic conditions.
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spelling Cardiac Energy Metabolism and Oxidative Stress Biomarkers in Diabetic Rat Treated with ResveratrolResveratrol (RSV), polyphenol from grape, was studied to evaluate its effects on calorimetric parameters, energy metabolism, and antioxidants in the myocardium of diabetic rats. The animals were randomly divided into four groups (n = 8): C (control group): normal rats; C-RSV: normal rats receiving RSV; DM: diabetic rats; and DM-RSV: diabetics rats receiving RSV. Type 1 diabetes mellitus was induced with administration of streptozotocin (STZ; 60 mg(-1) body weight, single dose, i.p.). After 48 hours of STZ administration, the animals received RSV (1.0 mg/kg/day) for gavage for 30 days. Food, water, and energy intake were higher in the DM group, while administration of RSV caused decreases (p<0.05) in these parameters. The glycemia decreased and higher final body weight increased in DM-RSV when compared with the DM group. The diabetic rats showed higher serum-free fatty acid, which was normalized with RSV. Oxygen consumption (VO2) and carbon dioxide production (VCO2) decreased (p<0.05) in the DM group. This was accompanied by reductions in RQ. The C-RSV group showed higher VO2 and VCO2 values. Pyruvate dehydrogenase activity was lower in the DM group and normalizes with RSV. The DM group exhibited higher myocardial beta-hydroxyacyl coenzyme-A dehydrogenase and citrate synthase activity, and RSV decreased the activity of these enzymes. The DM group had higher cardiac lactate dehydrogenase compared to the DM-RSV group. Myocardial protein carbonyl was increased in the DM group. RSV increased reduced glutathione in the cardiac tissue of diabetic animals. The glutathione reductase activity was higher in the DM-RSV group compared to the DM group. In conclusion, diabetes is accompanied by cardiac energy metabolism dysfunction and change in the biomarkers of oxidative stress. The cardioprotective effect may be mediated through RVS's ability to normalize free fatty acid oxidation, enhance utilization glucose, and control the biomarkers' level of oxidative stress under diabetic conditions.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Sao Paulo State Univ UNESP, Inst Biosci, Dept Chem & Biochem, Botucatu, SP, BrazilNorth Parana State Univ UENP, Inst Biol, Bandeirantes, Parana, BrazilSao Paulo State Univ UNESP, Inst Biosci, Dept Microbiol & Immunol, Botucatu, SP, BrazilSao Paulo State Univ UNESP, Inst Biosci, Dept Chem & Biochem, Botucatu, SP, BrazilSao Paulo State Univ UNESP, Inst Biosci, Dept Microbiol & Immunol, Botucatu, SP, BrazilFAPESP: 13/12957-8Public Library ScienceUniversidade Estadual Paulista (Unesp)North Parana State Univ UENPSantos, Klinsmann Carolo dos [UNESP]Braga, Camila Pereira [UNESP]Barbanera, Pedro Octavio [UNESP]Ferreira Seiva, Fabio RodriguesFernandes Junior, Ary [UNESP]Henrique Fernandes, Ana Angelica [UNESP]2015-03-18T15:56:01Z2015-03-18T15:56:01Z2014-07-22info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article8application/pdfhttp://dx.doi.org/10.1371/journal.pone.0102775Plos One. San Francisco: Public Library Science, v. 9, n. 7, 8 p., 2014.1932-6203http://hdl.handle.net/11449/11739110.1371/journal.pone.0102775WOS:000339551100056WOS000339551100056.pdfWeb of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengPlos One2.7661,164info:eu-repo/semantics/openAccess2023-12-29T06:17:38Zoai:repositorio.unesp.br:11449/117391Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462023-12-29T06:17:38Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Cardiac Energy Metabolism and Oxidative Stress Biomarkers in Diabetic Rat Treated with Resveratrol
title Cardiac Energy Metabolism and Oxidative Stress Biomarkers in Diabetic Rat Treated with Resveratrol
spellingShingle Cardiac Energy Metabolism and Oxidative Stress Biomarkers in Diabetic Rat Treated with Resveratrol
Santos, Klinsmann Carolo dos [UNESP]
title_short Cardiac Energy Metabolism and Oxidative Stress Biomarkers in Diabetic Rat Treated with Resveratrol
title_full Cardiac Energy Metabolism and Oxidative Stress Biomarkers in Diabetic Rat Treated with Resveratrol
title_fullStr Cardiac Energy Metabolism and Oxidative Stress Biomarkers in Diabetic Rat Treated with Resveratrol
title_full_unstemmed Cardiac Energy Metabolism and Oxidative Stress Biomarkers in Diabetic Rat Treated with Resveratrol
title_sort Cardiac Energy Metabolism and Oxidative Stress Biomarkers in Diabetic Rat Treated with Resveratrol
author Santos, Klinsmann Carolo dos [UNESP]
author_facet Santos, Klinsmann Carolo dos [UNESP]
Braga, Camila Pereira [UNESP]
Barbanera, Pedro Octavio [UNESP]
Ferreira Seiva, Fabio Rodrigues
Fernandes Junior, Ary [UNESP]
Henrique Fernandes, Ana Angelica [UNESP]
author_role author
author2 Braga, Camila Pereira [UNESP]
Barbanera, Pedro Octavio [UNESP]
Ferreira Seiva, Fabio Rodrigues
Fernandes Junior, Ary [UNESP]
Henrique Fernandes, Ana Angelica [UNESP]
author2_role author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
North Parana State Univ UENP
dc.contributor.author.fl_str_mv Santos, Klinsmann Carolo dos [UNESP]
Braga, Camila Pereira [UNESP]
Barbanera, Pedro Octavio [UNESP]
Ferreira Seiva, Fabio Rodrigues
Fernandes Junior, Ary [UNESP]
Henrique Fernandes, Ana Angelica [UNESP]
description Resveratrol (RSV), polyphenol from grape, was studied to evaluate its effects on calorimetric parameters, energy metabolism, and antioxidants in the myocardium of diabetic rats. The animals were randomly divided into four groups (n = 8): C (control group): normal rats; C-RSV: normal rats receiving RSV; DM: diabetic rats; and DM-RSV: diabetics rats receiving RSV. Type 1 diabetes mellitus was induced with administration of streptozotocin (STZ; 60 mg(-1) body weight, single dose, i.p.). After 48 hours of STZ administration, the animals received RSV (1.0 mg/kg/day) for gavage for 30 days. Food, water, and energy intake were higher in the DM group, while administration of RSV caused decreases (p<0.05) in these parameters. The glycemia decreased and higher final body weight increased in DM-RSV when compared with the DM group. The diabetic rats showed higher serum-free fatty acid, which was normalized with RSV. Oxygen consumption (VO2) and carbon dioxide production (VCO2) decreased (p<0.05) in the DM group. This was accompanied by reductions in RQ. The C-RSV group showed higher VO2 and VCO2 values. Pyruvate dehydrogenase activity was lower in the DM group and normalizes with RSV. The DM group exhibited higher myocardial beta-hydroxyacyl coenzyme-A dehydrogenase and citrate synthase activity, and RSV decreased the activity of these enzymes. The DM group had higher cardiac lactate dehydrogenase compared to the DM-RSV group. Myocardial protein carbonyl was increased in the DM group. RSV increased reduced glutathione in the cardiac tissue of diabetic animals. The glutathione reductase activity was higher in the DM-RSV group compared to the DM group. In conclusion, diabetes is accompanied by cardiac energy metabolism dysfunction and change in the biomarkers of oxidative stress. The cardioprotective effect may be mediated through RVS's ability to normalize free fatty acid oxidation, enhance utilization glucose, and control the biomarkers' level of oxidative stress under diabetic conditions.
publishDate 2014
dc.date.none.fl_str_mv 2014-07-22
2015-03-18T15:56:01Z
2015-03-18T15:56:01Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1371/journal.pone.0102775
Plos One. San Francisco: Public Library Science, v. 9, n. 7, 8 p., 2014.
1932-6203
http://hdl.handle.net/11449/117391
10.1371/journal.pone.0102775
WOS:000339551100056
WOS000339551100056.pdf
url http://dx.doi.org/10.1371/journal.pone.0102775
http://hdl.handle.net/11449/117391
identifier_str_mv Plos One. San Francisco: Public Library Science, v. 9, n. 7, 8 p., 2014.
1932-6203
10.1371/journal.pone.0102775
WOS:000339551100056
WOS000339551100056.pdf
dc.language.iso.fl_str_mv eng
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dc.relation.none.fl_str_mv Plos One
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dc.publisher.none.fl_str_mv Public Library Science
publisher.none.fl_str_mv Public Library Science
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