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1.
Clinics ; 68(10): 1344-1349, out. 2013. tab
Article in English | LILACS | ID: lil-689977

ABSTRACT

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. .


Subject(s)
Animals , Male , Rats , Cell Adhesion Molecules/metabolism , Myocardial Infarction/metabolism , Ventricular Remodeling/physiology , Blotting, Western , Collagen Type I/analysis , Collagen Type III/analysis , Disease Models, Animal , Diastole/physiology , Hydroxyproline/analysis , Myocardial Infarction/physiopathology , Myocardial Infarction , Rats, Wistar , Systole/physiology , Ventricular Dysfunction, Left/physiopathology , Ventricular Dysfunction, Left , Ventricular Function, Left/physiology
2.
Arq. bras. cardiol ; 95(5): 635-639, out. 2010. tab
Article in Portuguese | LILACS | ID: lil-570434

ABSTRACT

FUNDAMENTO: A relevância do padrão de remodelamento no modelo de ratos infartados não é conhecida. OBJETIVO: Analisar a presença de diferentes padrões de remodelamento nesse modelo e suas implicações funcionais. MÉTODOS: Ratos infartados (n=46) foram divididos de acordo com o padrão de geometria, analisado pelo ecocardiograma: normal (índice de massa normal e espessura relativa normal), remodelamento concêntrico (índice de massa normal e espessura relativa aumentada), hipertrofia concêntrica (índice de massa aumentado e espessura relativa aumentada) e hipertrofia excêntrica (índice de massa aumentado e espessura relativa normal). Os dados estão em mediana e intervalo interquartil. RESULTADOS: Ratos infartados apresentaram apenas dois dos quatro padrões de geometria: padrão normal (15 por cento) e hipertrofia excêntrica - HE (85 por cento). Os grupos de padrão normal e HE não apresentaram diferenças nos valores de fração de variação de área (Normal = 32,1 - 28,8 a 50,7; HE = 31,3 - 26,5 a 36,7; p=0,343). Dos animais infartados, 34 (74 por cento) apresentaram disfunção sistólica, detectada pela fração de variação de área. Considerando os dois padrões de geometria, 77 por cento dos animais com hipertrofia excêntrica e 57 por cento com geometria normal apresentaram disfunção sistólica (p=0,355). A espessura relativa da parede, os padrões de geometria e o índice de massa não foram fator de predição de disfunção ventricular (p>0,05). Por outro lado, o tamanho do infarto foi fator de predição de disfunção ventricular na análise univariada (p<0,001) e na análise multivariada (p=0,004). CONCLUSÃO: Ratos submetidos à oclusão coronariana apresentam dois diferentes padrões de remodelamento, os quais não se constituem em fator de predição de disfunção ventricular.


BACKGROND: The relevance of the remodeling pattern in the model of infarcted rats is not known. OBJECTIVE: To analyze the presence of different patterns of remodeling in this model and its functional implications. METHODS: Infarcted rats (n=47) have been divided according to the geometry pattern, analyzed by echocardiogram: normal (normal mass index and normal relative thickness), concentric remodeling (normal mass index and increased relative thickness), concentric hypertrophy (increased mass index and increased relative thickness) and eccentric hypertrophy (increased mass index and normal relative thickness). Data are median and interquartile range. RESULTS: Infarcted rats showed only two of the four geometric patterns: normal pattern (15 percent) and eccentric hypertrophy - EH (85 percent). Groups of normal pattern and EH showed no differences in the values of fractional area change (Normal = 32.1 - 28.8 to 50.7; EH = 31.3 - 26.5 to 36.7; p = 0.343). Out of the infarcted animals, 34 (74 percent) had systolic dysfunction, detected by fractional area change. Considering these two geometry patterns, 77 percent of animals with eccentric hypertrophy and 57 percent with normal geometry presented systolic dysfunction (p=0.355). The relative wall thickness, the geometric patterns and the body mass index were not predictors of ventricular dysfunction (p> 0.05). On the other hand, infarct size was a predictive factor for ventricular dysfunction in univariate analysis (p<0.001) and multivariate analysis (p = 0.004). CONCLUSION: Rats that underwent coronary occlusion showed two different patterns of remodeling, which do not constitute a predictor of ventricular dysfunction.


Subject(s)
Animals , Male , Rats , Myocardial Infarction/pathology , Ventricular Dysfunction, Left/pathology , Ventricular Remodeling/physiology , Disease Models, Animal , Myocardial Infarction/complications , Random Allocation , Rats, Wistar , Statistics, Nonparametric , Ventricular Dysfunction, Left/etiology
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