Effects of the administration of pentoxifylline and prednisolone on the evolution of portal fibrogenesis secondary to biliary obstruction-an experimental study in growing animals
Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
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Data(s) |
19/10/2012
19/10/2012
2009
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Resumo |
Background: Many chronic liver diseases lead to progressive hepatic fibrosis, a condition that can ultimately result in loss of organ function and severe portal hypertension necessitating hepatic transplantation. Within the last few decades, studies have been conducted to demonstrate the possibility of drug modulation of hepatic fibrogenesis. Regarding biliary obstruction, it has been suggested that administration of corticosteroids could promote better late outcomes for children with biliary atresia submitted to Kasai`s portoenterostomy. Models used to test potential antifibrogenic drugs such as pentoxifylline (PTX) have not included growing animals. Methods: In this experimental study, 119 young rats (21st or 22nd days) were submitted to laparotomy and common bile duct ligation (CBDL) or to sham surgery (SHAM). Animals were allocated into 5 groups, according to surgical procedure, and administered the following solutions: (1) CBDL + distilled water, (2) SHAM + distilled water, (3) CBDL + PTX, (4) CBDL + prednisolone (PRED), and (5) CBDL + PTX + PRED (PTX + PRED). Each group was further divided into 2 subgroups according to the length of the experiment (15 or 30 days). At the end of the defined period, animals were weighed, and a hepatic fragment was collected from each one for analyses. Results: The PTX animals exhibited increased weight gain compared to animals in the PRED or PTX + PRED groups. Animals from the 3 therapeutic groups (PTX, PRED, and PTX + PRED) showed diminished collagen-filled area in portal spaces. Total portal space area was increased in the PTX group. Conclusions: Hepatic fibrosis induced by bile duct ligation in young rats could be modulated by pharmacologic interventions. Administration of PTX or PRED, or the combination of both, resulted in diminished collagen-filled areas in portal spaces. (C) 2009 Elsevier Inc. All rights reserved. |
Identificador |
JOURNAL OF PEDIATRIC SURGERY, v.44, n.11, p.2071-2077, 2009 0022-3468 http://producao.usp.br/handle/BDPI/22802 10.1016/j.jpedsurg.2009.05.020 |
Idioma(s) |
eng |
Publicador |
W B SAUNDERS CO-ELSEVIER INC |
Relação |
Journal of Pediatric Surgery |
Direitos |
restrictedAccess Copyright W B SAUNDERS CO-ELSEVIER INC |
Palavras-Chave | #Biliary atresia #Liver fibrogenesis #Pediatric liver disease #Experimental cholestasis #Glucocorticoids #Biliary congenital disorders #PLACEBO-CONTROLLED TRIAL #HEPATIC STELLATE CELLS #BILE-DUCT LIGATION #CORTICOSTEROID-THERAPY #KASAI PORTOENTEROSTOMY #ATRESIA #FIBROSIS #RATS #ALPHA #MODEL #Pediatrics #Surgery |
Tipo |
article original article publishedVersion |