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1.
Clinics ; 68(10): 1344-1349, out. 2013. tab
Artículo en Inglés | LILACS | ID: lil-689977

RESUMEN

OBJECTIVE: After acute myocardial infarction, during the cardiac repair phase, periostin is released into the infarct and activates signaling pathways that are essential for the reparative process. However, the role of periostin in chronic cardiac remodeling after myocardial infarction remains to be elucidated. Therefore, the objective of this study was to investigate the relationship between tissue periostin and cardiac variables in the chronic cardiac remodeling induced by myocardial infarction. METHODS: Male Wistar rats were assigned to 2 groups: a simulated surgery group (SHAM; n = 8) and a myocardial infarction group (myocardial infarction; n = 13). After 3 months, morphological, functional and biochemical analyses were performed. The data are expressed as means±SD or medians (including the lower and upper quartiles). RESULTS: Myocardial infarctions induced increased left ventricular diastolic and systolic areas associated with a decreased fractional area change and a posterior wall shortening velocity. With regard to the extracellular matrix variables, the myocardial infarction group presented with higher values of periostin and types I and III collagen and higher interstitial collagen volume fractions and myocardial hydroxyproline concentrations. In addition, periostin was positively correlated with type III collagen levels (r = 0.673, p = 0.029) and diastolic (r = 0.678, p = 0.036) and systolic (r = 0.795, p = 0.006) left ventricular areas. Considering the relationship between periostin and the cardiac function variables, periostin was inversely correlated with both the fractional area change (r = -0.783, p = 0.008) and the posterior wall shortening velocity (r = -0.767, p = 0.012). CONCLUSIONS: Periostin might be a modulator of deleterious cardiac remodeling in the chronic phase after myocardial infarction in rats. .


Asunto(s)
Animales , Masculino , Ratas , Moléculas de Adhesión Celular/metabolismo , Infarto del Miocardio/metabolismo , Remodelación Ventricular/fisiología , Western Blotting , Colágeno Tipo I/análisis , Colágeno Tipo III/análisis , Modelos Animales de Enfermedad , Diástole/fisiología , Hidroxiprolina/análisis , Infarto del Miocardio/fisiopatología , Infarto del Miocardio , Ratas Wistar , Sístole/fisiología , Disfunción Ventricular Izquierda/fisiopatología , Disfunción Ventricular Izquierda , Función Ventricular Izquierda/fisiología
2.
Rev. bras. ecocardiogr. imagem cardiovasc ; 22(3): 20-25, jul.-set. 2009. ilus, tab, graf
Artículo en Portugués | LILACS | ID: lil-522521

RESUMEN

Introdução: A droga antineoplásica doxorrubicina apresenta a cardiotoxicidade como o efeito colateral mais grave. A forma aguda é pouco estudada e pode ser mais bem entendida por meio de avaliações funcionais repetidas. O objetivo deste estudo foi avaliar a utilidade do ecocardiograma no estudo da cardiotoxicidade aguda induzida pela doxorrubicina em ratos. Métodos: Foram utilizados ratos machos Wistar, submetidos à injeção intraperitoneal única de doxorrubicina na dose de 20mg/Kg(n=15) e grupo controle (n=15), com injeção de salina. Foram avaliados por Doppler-ecocardiografia antes e 48h após a infusão. As comparações entre os momentos foram efetuadas pelo teste t pareado, com nível de significância p<0,05. Resultados: Após 48 horas, houve diminuição do peso corporal...


Asunto(s)
Animales , Ratas , Disfunción Ventricular/complicaciones , Disfunción Ventricular/diagnóstico , Doxorrubicina/efectos adversos , Ecocardiografía/métodos , Ecocardiografía , Toxicidad/efectos adversos , Muerte Súbita
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