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Journal of Southern Medical University ; (12): 1633-1636, 2006.
Artículo en Chino | WPRIM | ID: wpr-232817

RESUMEN

<p><b>OBJECTIVE</b>To investigate the effect of calcineurin AalphacDNA (AdCnAalpha) overexpression as a result of adenovirally mediated gene transfer on neonatal rat cardiac myocyte apoptosis induced by hypoxia-reoxygenation (H/R) and adrenergic receptors.</p><p><b>METHODS</b>Neonatal rat cardiac myocytes were cultured for 20 h after AdCnAalpha transfection, and treated with isoproterenol (10 micromol/L) and 24 h of hypoxia followed by 4 h of reoxygenation (24H/4R). The cardiac myocyte apoptosis induced by the treatments was assessed by flow cytometry and DNA laddering, and the levels of calcineurin, p38 and phosphorylation p38 (p-p38) were determined by Western blotting and (or) RT-PCR.</p><p><b>RESULTS</b>AdCnAalpha transfection promoted cultured neonatal rat cardiac myocyte apoptosis induced by isoproterenol+24H/4R as compared with the treated cells without transfection (14.247-/+0.525 vs 10.763-/+1.554, P<0.01), along with greater phosphorylation p38 protein expression (1.60-/+0.22 vs 2.42-/+0.19, P<0.01). The levels of p38 underwent no obvious change after AdCnAalpha transfection (P<0.05).</p><p><b>CONCLUSIONS</b>AdCnAalpha transfection can promote cardiac myocyte apoptosis induced by H/R and adrenergic receptors, the mechanism of which might be associated with p38 mitongen-activated protein kinase (p38MAPK) activation.</p>


Asunto(s)
Animales , Femenino , Masculino , Ratas , Adenoviridae , Genética , Agonistas Adrenérgicos beta , Farmacología , Animales Recién Nacidos , Apoptosis , Genética , Fisiología , Western Blotting , Calcineurina , Genética , Metabolismo , Hipoxia de la Célula , Células Cultivadas , Citometría de Flujo , Vectores Genéticos , Genética , Isoproterenol , Farmacología , Miocitos Cardíacos , Biología Celular , Metabolismo , Oxígeno , Farmacología , Fosforilación , ARN Mensajero , Genética , Metabolismo , Ratas Wistar , Receptores Adrenérgicos , Fisiología , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa , Transfección , Proteínas Quinasas p38 Activadas por Mitógenos , Metabolismo
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