Mechanism of continuous venovenous hemofiltration combined with ulinastatin for the treatment of septic shock / 南方医科大学学报
Journal of Southern Medical University
;
(12): 1189-1196, 2015.
Artículo
en Chino
| WPRIM
| ID: wpr-333658
ABSTRACT
<p><b>OBJECTIVE</b>To investigate the molecular mechanisms of continuous venovenous hemofiltration (CVVH) combined with ulinastatin (ULI) (CVVH-ULI) for the treatment of septic shock.</p><p><b>METHODS</b>Human umbilical endothelial cells (HUVECs) were incubated with serums isolated from normal healthy people (control), septic shock patients treated with conventional therapy (CT) or treated with CVVH combined with ULI (CVVH-ULI). Endothelial permeability was evaluated by the leakage of FITC-labeled albumin. The morphological changes of F-actin was evaluated by Rhodamine-phalloidin. The phosphorylated levels of p38 were determined by Western blot. Cells were then treated with p38inhibitor (SB203580), or DMSO, followed by incubation with serum from septic shock patients treated with conventional therapy. Endothelial permeability and F-actin rearrangements were also evaluated as noted above.</p><p><b>RESULTS</b>Serum from CT group increased endothelial permeability, F-actin rearrangements, and phosphorylated levels of p38, which were inhibited by CVVH-ULI treatment. Moreover, in CT group, the serum-induced endothelial hyperpermeability and F-actin rearrangements were inhibited by SB203580, the inhibitor of p38.</p><p><b>CONCLUSION</b>CVVH combined with ulinastatin decreases endothelial hyperpermeability induced by septic shock through inhibiting p38 MAPK pathways.</p>
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Piridinas
/
Choque Séptico
/
Terapéutica
/
Glicoproteínas
/
Células Cultivadas
/
Actinas
/
Hemofiltración
/
Sistema de Señalización de MAP Quinasas
/
Usos Terapéuticos
/
Proteínas Quinasas p38 Activadas por Mitógenos
Límite:
Humanos
Idioma:
Chino
Revista:
Journal of Southern Medical University
Año:
2015
Tipo del documento:
Artículo
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