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Artigo em Chinês | WPRIM (Pacífico Ocidental) | ID: wpr-339085

RESUMO

<p><b>OBJECTIVE</b>To investigate the effect of losartan on cardiac mineralocorticoid receptor (MR) mRNA in rats after acute myocardial infarction (AMI).</p><p><b>METHOD</b>AMI was induced in male SD rats by ligation of the left coronary artery. The survived rats were randomly divided into AMI group, losartan group, and sham-operated group. The cardiac functions of the rats were assessed by echocardiogram and hemodynamics, and the contents of angiotensin II (Ang II) and aldosterone (Ald) in the myocardial tissues were determined by radioimmunoassay. The collagen density in the myocardial tissues were calculated by Masson's trichrome staining and the expression of MR mRNA were determined by real-time quantitative fluorescent PCR.</p><p><b>RESULTS</b>Both the contents of AngII and Ald in the myocardial tissues increased significantly in AMI group compared with those in the sham-operated group (P<0.01). The expression of MR mRNA and collagen density in the myocardial tissues also increased significantly than that in sham-operated group (P<0.01). After four weeks of losartan treatment, the contents of AngII and Ald in the myocardial tissues decreased significantly (P<0.05) and the expression of MR mRNA was also considerably lowered (P<0.01) in comparison with those in the AMI group. Treatment with losartan also resulted in significant decrease of the collagen density in the myocardial tissues.</p><p><b>CONCLUSIONS</b>Losartan may reduce reactive fibrosis not only by attenuating the Ald signaling pathway but also by decreasing the expression of MR.</p>


Assuntos
Animais , Masculino , Ratos , Aldosterona , Metabolismo , Angiotensina II , Metabolismo , Bloqueadores do Receptor Tipo 1 de Angiotensina II , Usos Terapêuticos , Fibrose , Losartan , Usos Terapêuticos , Infarto do Miocárdio , Tratamento Farmacológico , Metabolismo , Miocárdio , Patologia , RNA Mensageiro , Genética , Metabolismo , Distribuição Aleatória , Ratos Sprague-Dawley , Receptores de Mineralocorticoides , Genética , Metabolismo
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