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dc.contributor.author
Leichsenring Silva, Fabiano  
dc.contributor.author
Tavares, Angela Maria Vicente  
dc.contributor.author
Mosele, Francisca  
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Berger, Bruno  
dc.contributor.author
Llesuy, Susana Francisca  
dc.contributor.author
Belló Klein, Adriane  
dc.date.available
2019-01-04T20:27:12Z  
dc.date.issued
2011-12  
dc.identifier.citation
Leichsenring Silva, Fabiano; Tavares, Angela Maria Vicente; Mosele, Francisca; Berger, Bruno; Llesuy, Susana Francisca; et al.; Association of the time course of pulmonary arterial hypertension with changes in oxidative stress in the left ventricle; Wiley Blackwell Publishing, Inc; Clinical and Experimental Pharmacology and Physiology; 38; 12; 12-2011; 804-810  
dc.identifier.issn
0305-1870  
dc.identifier.uri
http://hdl.handle.net/11336/67467  
dc.description.abstract
1. This study investigates the time course of pulmonary arterial hypertension (PAH) due to monocrotaline (MCT) and its association with cardiac function and oxidative stress markers in the left ventricle (LV). 2. Male Wistar rats were divided into six groups: 7days, 21days, and 31days for both control and MCT groups. Following echocardiographic analysis, the heart was removed. The LV was separated and homogenized to analyze oxidized-to-total glutathione ratio and thioredoxin reductase (TrxR) activity as well as hydrogen peroxide (H 2O 2) and ascorbic acid levels. 3. There was significant (P<0.01) cardiac and right ventricle (RV) hypertrophy and pulmonary congestion in the MCT 21day and 31day groups. Echocardiography showed a change in the flow wave of the pulmonary artery at 21days after MCT treatment. There was an increase in the LV ejection time (P<0.05) at 31days after MCT. The LV H 2O 2 concentration was increased (P<0.05) in the MCT 21day and MCT 31day groups compared with controls. There was a reduction (P<0.05) in the LV ascorbic acid concentration and an increase (P<0.05) in TrxR activity in the MCT 31day rats. 4. Our findings showed RV changes due to pulmonary hypertension at 21days after MCT injection. There was a correlation between the degree of dysfunction and the morphometry of the heart chambers, along with impairment of the antioxidant/pro-oxidant balance in the LV 31days after the beginning of the protocol. This study suggests that LV changes follow RV dysfunction subsequent to pulmonary hypertension.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
Wiley Blackwell Publishing, Inc  
dc.rights
info:eu-repo/semantics/openAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/  
dc.subject
Ascorbic Acid  
dc.subject
Cor Pulmonale  
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Glutathione  
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Monocrotaline  
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Right Heart Failure  
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Thioredoxin Reductase  
dc.subject.classification
Otras Medicina Básica  
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Medicina Básica  
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CIENCIAS MÉDICAS Y DE LA SALUD  
dc.title
Association of the time course of pulmonary arterial hypertension with changes in oxidative stress in the left ventricle  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2019-01-04T16:29:52Z  
dc.journal.volume
38  
dc.journal.number
12  
dc.journal.pagination
804-810  
dc.journal.pais
Reino Unido  
dc.journal.ciudad
Londres  
dc.description.fil
Fil: Leichsenring Silva, Fabiano. Universidade Federal do Rio Grande do Sul; Brasil  
dc.description.fil
Fil: Tavares, Angela Maria Vicente. Universidade Federal do Rio Grande do Sul; Brasil  
dc.description.fil
Fil: Mosele, Francisca. Universidade Federal do Rio Grande do Sul; Brasil  
dc.description.fil
Fil: Berger, Bruno. Universidade Federal do Rio Grande do Sul; Brasil  
dc.description.fil
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  
dc.description.fil
Fil: Belló Klein, Adriane. Universidade Federal do Rio Grande do Sul; Brasil  
dc.journal.title
Clinical and Experimental Pharmacology and Physiology  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1111/j.1440-1681.2011.05608.x  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://onlinelibrary.wiley.com/doi/abs/10.1111/j.1440-1681.2011.05608.x