Influence of biliary drainage on the repair of hepatic lesions in biliary fibrosis

J Surg Res. 2011 Aug;169(2):e127-36. doi: 10.1016/j.jss.2011.04.028. Epub 2011 May 14.

Abstract

Background: Bilioduodenal (BD) and biliojejunal (BJ) derivation induce enterobiliary reflux and bile stasis. Decompression of the excluded loop of the Roux-en-Y (BJD) was proposed to minimize these effects. The aim of this study was to compare the influence of these three modalities of biliary bypass on hepatic lesion repair in rats with secondary biliary fibrosis.

Materials and methods: Rats with 15 d of biliary obstruction underwent BD, BJ, and BJD drainage and were compared with a group submitted to simulated operation (SO) and biliary obstruction (CBO). The serum values of total and fractional bilirubin, alkaline phosphatase (ALP), and aminotransferases (AST and ALT), as well as hepatobiliointestinal excretion determined with (99m)Tc-Disida, were used for comparison. In addition, we used morphometric analyses to estimate the mass of the hepatocytes, bile ducts, and liver fibrosis. We also counted hepatic stellate cells (SC).

Results: For each of the three modalities of biliary drainage, there were significant reductions in bilirubin, AST, ALP, and the number of SCs. The recovery of the estimated mass of all histologic components occurred only after BJ and BJD; in the BD group, the estimated hepatocyte mass was reduced compared with the SO group. The residual hepatic radioactivity of (99m)Tc-Disida was greater in the BJD group than in the SO group.

Conclusions: The interposition of the jejunal loop between the biliary tree and the intestine may slow hepatobiliary clearance of radioactivity, even though it provides the resolution of cholestasis and is effective in recovering from hepatic lesions.

MeSH terms

  • Alkaline Phosphatase / metabolism
  • Anastomosis, Roux-en-Y / methods
  • Animals
  • Bile Ducts / surgery*
  • Cholestasis / metabolism
  • Cholestasis / pathology
  • Cholestasis / surgery*
  • Digestive System Surgical Procedures / methods*
  • Disease Models, Animal
  • Duodenum / surgery
  • Hepatic Stellate Cells / pathology
  • Jejunum / surgery
  • Liver / metabolism
  • Liver / pathology*
  • Liver / surgery*
  • Liver Cirrhosis / metabolism
  • Liver Cirrhosis / pathology
  • Liver Cirrhosis / surgery*
  • Male
  • Rats
  • Rats, Wistar
  • Transaminases / metabolism

Substances

  • Transaminases
  • Alkaline Phosphatase