Selective bowel decontamination improves the survival of 90% hepatectomy in rats

J Surg Res. 2015 May 15;195(2):454-64. doi: 10.1016/j.jss.2015.01.024. Epub 2015 Jan 19.

Abstract

Background: Clinically, hepatectomy is a clean procedure performed without routine antimicrobial prophylaxis, regardless of the extent of liver loss. Translocation of endotoxin has been recognized as a fatal complication leading to liver failure. After extended hepatectomy, the portal hypertension, mucosal damage, intrahepatic bile acid retention, inhibited enterokinesia, and so forth are likely to contribute to enhanced endotoxin absorption. The effect of selective bowel decontamination (SBD) on the prognosis of hepatectomy were investigated.

Methods: We adopted rat models of partial hepatectomy (70%, PHx) and subtotal hepatectomy (90%, SHx), gentamicin or saline of the same amount was administrated preoperatively. Liver damage makers, portal and systemic lipopolysaccharide, mucosal damage, signaling pathways, liver regeneration, and bile canalicular networks reconstruction were investigated.

Results: We found that SHx but not PHx resulted in significantly enhanced portal and systemic endotoxin. Inhibition of gastrointestinal gram-negative bacteria by gentamicin significantly reduced lipopolysaccharide levels and improved survival after SHx (56% with gentamicin, 24% with saline, P < 0.05). We also found SBD with gentamicin protected intestinal mucosa barrier, alleviated liver parenchymal damage, and promoted liver regeneration and bile canalicular networks reconstruction after extended liver resection.

Conclusions: We conclude that SBD is beneficial and necessary for extended hepatectomy.

Keywords: Endotoxin; Extended hepatectomy; Liver failure; Liver regeneration; Selective bowel decontamination.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Decontamination*
  • Epidermal Growth Factor / physiology
  • Gastrointestinal Tract / microbiology*
  • Gentamicins / pharmacology
  • Hepatectomy / mortality*
  • Intestinal Mucosa / metabolism
  • Lipopolysaccharides / metabolism
  • Liver Regeneration
  • Male
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Gentamicins
  • Lipopolysaccharides
  • Epidermal Growth Factor