Short-term diabetes attenuates left ventricular dysfunction and mortality rates after myocardial infarction in rodents
- Autores
- Rodrigues, Bruno; Figueroa, Diego Mendrot Taboas; Fang, Jiao; Rosa, Kaleizu Teodoro; Llesuy, Susana Francisca; de Angelis, Kátia; Irigoyen, Maria Cláudia
- Año de publicación
- 2011
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Objectives: To investigate the effects of hyperglycemia on left ventricular dysfunction, morphometry, myocardial infarction area, hemodynamic parameters, oxidative stress profile, and mortality rate in rats that had undergone seven days of myocardial infarction. Introduction: Previous research has demonstrated that hyperglycemia may protect the heart against ischemic injury. Methods: Male Wistar rats were divided into four groups: control-sham, diabetes-sham, myocardial infarction, and diabetes + myocardial infarction. Myocardial infarction was induced 14 days after diabetes induction. Ventricular function and morphometry, as well as oxidative stress and hemodynamic parameters, were evaluated after seven days of myocardial infarction. Results: The myocardial infarction area, which was similar in the infarcted groups at the initial evaluation, was reduced in the diabetes + myocardial infarction animals (23 ± 3%) when compared with the myocardial infarction (42 ± 7%, p<0.001) animals at the final evaluation. The ejection fraction (22%, p = 0.003), velocity of circumferential fiber shortening (30%, p = 0.001), and left ventricular isovolumetric relaxation time (26%, p = 0.002) were increased in the diabetes + myocardial infarction group compared with the myocardial infarction group. The diabetes-sham and diabetes + myocardial infarction groups displayed increased catalase concentrations compared to the control-sham and myocardial infarction groups (diabetes-sham: 32± 3; diabetes + myocardial infarction: 35± 0.7; control-sham: 12 ± 2; myocardial infarction: 16 ± 0.1 pmol min -1 mg -1 protein). The levels of thiobarbituric acid-reactive substances were reduced in the diabetes-sham rats compared to the control-sham rats. These positive adaptations were reflected in a reduced mortality rate in the diabetes + myocardial infarction animals (18.5%) compared with the myocardial infarction animals (40.7%, p = 0.001). Conclusions: These data suggest that short-term hyperglycemia initiates compensatory mechanisms, as demonstrated by increased catalase levels, which culminate in improvements in the ventricular response, infarcted area, and mortality rate in diabetic rats exposed to ischemic injury.
Fil: Rodrigues, Bruno. Universidade São Judas Tadeu; Brasil. Universidade de Sao Paulo; Brasil
Fil: Figueroa, Diego Mendrot Taboas. Universidade de Sao Paulo; Brasil
Fil: Fang, Jiao. Universidade de Sao Paulo; Brasil
Fil: Rosa, Kaleizu Teodoro. Universidade de Sao Paulo; Brasil
Fil: Llesuy, Susana Francisca. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Bioquímica y Medicina Molecular. Universidad de Buenos Aires. Facultad Medicina. Instituto de Bioquímica y Medicina Molecular; Argentina
Fil: de Angelis, Kátia. Universidade Nove de Julho; Brasil
Fil: Irigoyen, Maria Cláudia. Universidade de Sao Paulo; Brasil - Materia
-
DIABETES
MORTALITY RATE
MYOCARDIAL INFARCTION
OXIDATIVE STRESS
VENTRICULAR FUNCTION - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/67798
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Short-term diabetes attenuates left ventricular dysfunction and mortality rates after myocardial infarction in rodentsRodrigues, BrunoFigueroa, Diego Mendrot TaboasFang, JiaoRosa, Kaleizu TeodoroLlesuy, Susana Franciscade Angelis, KátiaIrigoyen, Maria CláudiaDIABETESMORTALITY RATEMYOCARDIAL INFARCTIONOXIDATIVE STRESSVENTRICULAR FUNCTIONhttps://purl.org/becyt/ford/3.1https://purl.org/becyt/ford/3Objectives: To investigate the effects of hyperglycemia on left ventricular dysfunction, morphometry, myocardial infarction area, hemodynamic parameters, oxidative stress profile, and mortality rate in rats that had undergone seven days of myocardial infarction. Introduction: Previous research has demonstrated that hyperglycemia may protect the heart against ischemic injury. Methods: Male Wistar rats were divided into four groups: control-sham, diabetes-sham, myocardial infarction, and diabetes + myocardial infarction. Myocardial infarction was induced 14 days after diabetes induction. Ventricular function and morphometry, as well as oxidative stress and hemodynamic parameters, were evaluated after seven days of myocardial infarction. Results: The myocardial infarction area, which was similar in the infarcted groups at the initial evaluation, was reduced in the diabetes + myocardial infarction animals (23 ± 3%) when compared with the myocardial infarction (42 ± 7%, p<0.001) animals at the final evaluation. The ejection fraction (22%, p = 0.003), velocity of circumferential fiber shortening (30%, p = 0.001), and left ventricular isovolumetric relaxation time (26%, p = 0.002) were increased in the diabetes + myocardial infarction group compared with the myocardial infarction group. The diabetes-sham and diabetes + myocardial infarction groups displayed increased catalase concentrations compared to the control-sham and myocardial infarction groups (diabetes-sham: 32± 3; diabetes + myocardial infarction: 35± 0.7; control-sham: 12 ± 2; myocardial infarction: 16 ± 0.1 pmol min -1 mg -1 protein). The levels of thiobarbituric acid-reactive substances were reduced in the diabetes-sham rats compared to the control-sham rats. These positive adaptations were reflected in a reduced mortality rate in the diabetes + myocardial infarction animals (18.5%) compared with the myocardial infarction animals (40.7%, p = 0.001). Conclusions: These data suggest that short-term hyperglycemia initiates compensatory mechanisms, as demonstrated by increased catalase levels, which culminate in improvements in the ventricular response, infarcted area, and mortality rate in diabetic rats exposed to ischemic injury.Fil: Rodrigues, Bruno. Universidade São Judas Tadeu; Brasil. Universidade de Sao Paulo; BrasilFil: Figueroa, Diego Mendrot Taboas. Universidade de Sao Paulo; BrasilFil: Fang, Jiao. Universidade de Sao Paulo; BrasilFil: Rosa, Kaleizu Teodoro. Universidade de Sao Paulo; BrasilFil: Llesuy, Susana Francisca. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Bioquímica y Medicina Molecular. Universidad de Buenos Aires. Facultad Medicina. Instituto de Bioquímica y Medicina Molecular; ArgentinaFil: de Angelis, Kátia. Universidade Nove de Julho; BrasilFil: Irigoyen, Maria Cláudia. Universidade de Sao Paulo; BrasilUniversidade de São Paulo. Faculdade de Medicina. Hospital das Clínicas2011-11info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/67798Rodrigues, Bruno; Figueroa, Diego Mendrot Taboas; Fang, Jiao; Rosa, Kaleizu Teodoro; Llesuy, Susana Francisca; et al.; Short-term diabetes attenuates left ventricular dysfunction and mortality rates after myocardial infarction in rodents; Universidade de São Paulo. Faculdade de Medicina. Hospital das Clínicas; Clinics; 66; 8; 11-2011; 1437-14421807-59321980-5322CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1590/S1807-59322011000800022info:eu-repo/semantics/altIdentifier/url/https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3161225/info:eu-repo/semantics/altIdentifier/url/http://ref.scielo.org/z8gc4pinfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T09:57:21Zoai:ri.conicet.gov.ar:11336/67798instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-03 09:57:21.82CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Short-term diabetes attenuates left ventricular dysfunction and mortality rates after myocardial infarction in rodents |
title |
Short-term diabetes attenuates left ventricular dysfunction and mortality rates after myocardial infarction in rodents |
spellingShingle |
Short-term diabetes attenuates left ventricular dysfunction and mortality rates after myocardial infarction in rodents Rodrigues, Bruno DIABETES MORTALITY RATE MYOCARDIAL INFARCTION OXIDATIVE STRESS VENTRICULAR FUNCTION |
title_short |
Short-term diabetes attenuates left ventricular dysfunction and mortality rates after myocardial infarction in rodents |
title_full |
Short-term diabetes attenuates left ventricular dysfunction and mortality rates after myocardial infarction in rodents |
title_fullStr |
Short-term diabetes attenuates left ventricular dysfunction and mortality rates after myocardial infarction in rodents |
title_full_unstemmed |
Short-term diabetes attenuates left ventricular dysfunction and mortality rates after myocardial infarction in rodents |
title_sort |
Short-term diabetes attenuates left ventricular dysfunction and mortality rates after myocardial infarction in rodents |
dc.creator.none.fl_str_mv |
Rodrigues, Bruno Figueroa, Diego Mendrot Taboas Fang, Jiao Rosa, Kaleizu Teodoro Llesuy, Susana Francisca de Angelis, Kátia Irigoyen, Maria Cláudia |
author |
Rodrigues, Bruno |
author_facet |
Rodrigues, Bruno Figueroa, Diego Mendrot Taboas Fang, Jiao Rosa, Kaleizu Teodoro Llesuy, Susana Francisca de Angelis, Kátia Irigoyen, Maria Cláudia |
author_role |
author |
author2 |
Figueroa, Diego Mendrot Taboas Fang, Jiao Rosa, Kaleizu Teodoro Llesuy, Susana Francisca de Angelis, Kátia Irigoyen, Maria Cláudia |
author2_role |
author author author author author author |
dc.subject.none.fl_str_mv |
DIABETES MORTALITY RATE MYOCARDIAL INFARCTION OXIDATIVE STRESS VENTRICULAR FUNCTION |
topic |
DIABETES MORTALITY RATE MYOCARDIAL INFARCTION OXIDATIVE STRESS VENTRICULAR FUNCTION |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/3.1 https://purl.org/becyt/ford/3 |
dc.description.none.fl_txt_mv |
Objectives: To investigate the effects of hyperglycemia on left ventricular dysfunction, morphometry, myocardial infarction area, hemodynamic parameters, oxidative stress profile, and mortality rate in rats that had undergone seven days of myocardial infarction. Introduction: Previous research has demonstrated that hyperglycemia may protect the heart against ischemic injury. Methods: Male Wistar rats were divided into four groups: control-sham, diabetes-sham, myocardial infarction, and diabetes + myocardial infarction. Myocardial infarction was induced 14 days after diabetes induction. Ventricular function and morphometry, as well as oxidative stress and hemodynamic parameters, were evaluated after seven days of myocardial infarction. Results: The myocardial infarction area, which was similar in the infarcted groups at the initial evaluation, was reduced in the diabetes + myocardial infarction animals (23 ± 3%) when compared with the myocardial infarction (42 ± 7%, p<0.001) animals at the final evaluation. The ejection fraction (22%, p = 0.003), velocity of circumferential fiber shortening (30%, p = 0.001), and left ventricular isovolumetric relaxation time (26%, p = 0.002) were increased in the diabetes + myocardial infarction group compared with the myocardial infarction group. The diabetes-sham and diabetes + myocardial infarction groups displayed increased catalase concentrations compared to the control-sham and myocardial infarction groups (diabetes-sham: 32± 3; diabetes + myocardial infarction: 35± 0.7; control-sham: 12 ± 2; myocardial infarction: 16 ± 0.1 pmol min -1 mg -1 protein). The levels of thiobarbituric acid-reactive substances were reduced in the diabetes-sham rats compared to the control-sham rats. These positive adaptations were reflected in a reduced mortality rate in the diabetes + myocardial infarction animals (18.5%) compared with the myocardial infarction animals (40.7%, p = 0.001). Conclusions: These data suggest that short-term hyperglycemia initiates compensatory mechanisms, as demonstrated by increased catalase levels, which culminate in improvements in the ventricular response, infarcted area, and mortality rate in diabetic rats exposed to ischemic injury. Fil: Rodrigues, Bruno. Universidade São Judas Tadeu; Brasil. Universidade de Sao Paulo; Brasil Fil: Figueroa, Diego Mendrot Taboas. Universidade de Sao Paulo; Brasil Fil: Fang, Jiao. Universidade de Sao Paulo; Brasil Fil: Rosa, Kaleizu Teodoro. Universidade de Sao Paulo; Brasil Fil: Llesuy, Susana Francisca. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Bioquímica y Medicina Molecular. Universidad de Buenos Aires. Facultad Medicina. Instituto de Bioquímica y Medicina Molecular; Argentina Fil: de Angelis, Kátia. Universidade Nove de Julho; Brasil Fil: Irigoyen, Maria Cláudia. Universidade de Sao Paulo; Brasil |
description |
Objectives: To investigate the effects of hyperglycemia on left ventricular dysfunction, morphometry, myocardial infarction area, hemodynamic parameters, oxidative stress profile, and mortality rate in rats that had undergone seven days of myocardial infarction. Introduction: Previous research has demonstrated that hyperglycemia may protect the heart against ischemic injury. Methods: Male Wistar rats were divided into four groups: control-sham, diabetes-sham, myocardial infarction, and diabetes + myocardial infarction. Myocardial infarction was induced 14 days after diabetes induction. Ventricular function and morphometry, as well as oxidative stress and hemodynamic parameters, were evaluated after seven days of myocardial infarction. Results: The myocardial infarction area, which was similar in the infarcted groups at the initial evaluation, was reduced in the diabetes + myocardial infarction animals (23 ± 3%) when compared with the myocardial infarction (42 ± 7%, p<0.001) animals at the final evaluation. The ejection fraction (22%, p = 0.003), velocity of circumferential fiber shortening (30%, p = 0.001), and left ventricular isovolumetric relaxation time (26%, p = 0.002) were increased in the diabetes + myocardial infarction group compared with the myocardial infarction group. The diabetes-sham and diabetes + myocardial infarction groups displayed increased catalase concentrations compared to the control-sham and myocardial infarction groups (diabetes-sham: 32± 3; diabetes + myocardial infarction: 35± 0.7; control-sham: 12 ± 2; myocardial infarction: 16 ± 0.1 pmol min -1 mg -1 protein). The levels of thiobarbituric acid-reactive substances were reduced in the diabetes-sham rats compared to the control-sham rats. These positive adaptations were reflected in a reduced mortality rate in the diabetes + myocardial infarction animals (18.5%) compared with the myocardial infarction animals (40.7%, p = 0.001). Conclusions: These data suggest that short-term hyperglycemia initiates compensatory mechanisms, as demonstrated by increased catalase levels, which culminate in improvements in the ventricular response, infarcted area, and mortality rate in diabetic rats exposed to ischemic injury. |
publishDate |
2011 |
dc.date.none.fl_str_mv |
2011-11 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
format |
article |
status_str |
publishedVersion |
dc.identifier.none.fl_str_mv |
http://hdl.handle.net/11336/67798 Rodrigues, Bruno; Figueroa, Diego Mendrot Taboas; Fang, Jiao; Rosa, Kaleizu Teodoro; Llesuy, Susana Francisca; et al.; Short-term diabetes attenuates left ventricular dysfunction and mortality rates after myocardial infarction in rodents; Universidade de São Paulo. Faculdade de Medicina. Hospital das Clínicas; Clinics; 66; 8; 11-2011; 1437-1442 1807-5932 1980-5322 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/67798 |
identifier_str_mv |
Rodrigues, Bruno; Figueroa, Diego Mendrot Taboas; Fang, Jiao; Rosa, Kaleizu Teodoro; Llesuy, Susana Francisca; et al.; Short-term diabetes attenuates left ventricular dysfunction and mortality rates after myocardial infarction in rodents; Universidade de São Paulo. Faculdade de Medicina. Hospital das Clínicas; Clinics; 66; 8; 11-2011; 1437-1442 1807-5932 1980-5322 CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/doi/10.1590/S1807-59322011000800022 info:eu-repo/semantics/altIdentifier/url/https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3161225/ info:eu-repo/semantics/altIdentifier/url/http://ref.scielo.org/z8gc4p |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc/2.5/ar/ |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by-nc/2.5/ar/ |
dc.format.none.fl_str_mv |
application/pdf application/pdf |
dc.publisher.none.fl_str_mv |
Universidade de São Paulo. Faculdade de Medicina. Hospital das Clínicas |
publisher.none.fl_str_mv |
Universidade de São Paulo. Faculdade de Medicina. Hospital das Clínicas |
dc.source.none.fl_str_mv |
reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
reponame_str |
CONICET Digital (CONICET) |
collection |
CONICET Digital (CONICET) |
instname_str |
Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.name.fl_str_mv |
CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.mail.fl_str_mv |
dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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1842269458349948928 |
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13.13397 |